Corcept Therapeutics
Annual Report 2012

Plain-text annual report

Table of Contents UNITED STATESSECURITIES AND EXCHANGE COMMISSIONWashington, D.C. 20549 FORM 10-K xANNUAL REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934For the fiscal year ended December 31, 2012or ¨TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF1934For the transition period from to Commission File Number: 000-50679CORCEPT THERAPEUTICS INCORPORATED(Exact Name of Corporation as Specified in Its Charter) Delaware 77-0487658(State or other jurisdiction of incorporation or organization) (I.R.S. Employer Identification No.)149 Commonwealth DriveMenlo Park, CA 94025(Address of principal executive offices) (zip code) (650) 327-3270(Registrant’s telephone number, including area code) Securities registered pursuant to Section 12 (b) of the Act: Title of Each Class: Name of Each Exchange on which Registered:Common Stock, $0.001 par value The NASDAQ Capital MarketSecurities registered pursuant to Section 12 (g) of the Act:NoneIndicate by check mark if the registrant is a well-known seasoned issuer, as defined in Rule 405 of the Securities Act. Yes ¨ No xIndicate by check mark if the registrant is not required to file reports pursuant to Section 13 or Section 15 (d) of the Act. Yes ¨ No xIndicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filingrequirements for the past 90 days. Yes x No ¨Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Web site, if any, every Interactive Data Filerequired to be submitted and posted pursuant to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorterperiod that the registrant was required to submit and post such files). Yes x No ¨Indicate by check mark if disclosure of delinquent filers pursuant to Item 405 of Regulation S-K is not contained herein, and will not be contained, tothe best of the Registrant’s knowledge, in definitive proxy or information statements incorporated by reference to Part III of this Form 10-K or anyamendment to this Form 10-K. ¨Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer or a smaller reporting company. Seethe definitions of “large accelerated filer”, “accelerated filer” and “smaller reporting company” in Rule 12b-2 of the Exchange Act. Large accelerated filer ¨ Accelerated filer x Non-accelerated filer ¨ (Do not check if a smaller reporting company) Smaller reporting company ¨ Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes ¨ No xThe aggregate market value of voting and non-voting common equity held by non-affiliates of the Registrant was $241,382,000 as of June 30, 2012based upon the closing price on the NASDAQ Capital Market reported for such date. This calculation does not reflect a determination that certain persons areaffiliates of the Registrant for any other purpose.On March 1, 2013 there were 99,814,250 shares of common stock outstanding at a par value of $0.001 per share.DOCUMENTS INCORPORATED BY REFERENCEPortions of the Registrant’s definitive proxy statement for its 2013 Annual Meeting of Stockholders are incorporated by reference in Items 10, 11, 12,13 and 14 of Part III. Table of ContentsTABLE OF CONTENTSForm 10-KFor the year ended December 31, 2012 Page PART I ITEM 1. Business 1 ITEM 1A. Risk Factors 20 ITEM 1B. Unresolved Staff Comments 45 ITEM 2. Properties 45 ITEM 3. Legal Proceedings 45 ITEM 4. Mine Safety Disclosures 45 PART II ITEM 5. Market for Registrant’s Common Equity, Related Stockholder Matters and Issuer Purchases of Equity Securities 46 ITEM 6. Selected Financial Data 48 ITEM 7. Management’s Discussion and Analysis of Financial Condition and Results of Operations 49 ITEM 7A. Quantitative and Qualitative Disclosures About Market Risk 63 ITEM 8. Financial Statements and Supplementary Data 63 ITEM 9. Changes in and Disagreements with Accountants on Accounting and Financial Disclosure 63 ITEM 9A. Controls and Procedures 63 ITEM 9B. Other Information 65 PART III ITEM 10. Directors, Executive Officers and Corporate Governance 66 ITEM 11. Executive Compensation 66 ITEM 12. Security Ownership of Certain Beneficial Owners and Management and Related Stockholder Matters 66 ITEM 13. Certain Relationships and Related Transactions, and Director Independence 66 ITEM 14. Principal Accounting Fees and Services 66 PART IV ITEM 15. Exhibits, Financial Statement Schedules 67 Signatures and Power of Attorney 71 Table of ContentsPART IThis Annual Report on Form 10-K (Form 10-K) contains forward-looking statements within the meaning of Section 21E of the Securities ExchangeAct of 1934, as amended (Exchange Act), and Section 27A of the Securities Act of 1933, as amended (Securities Act). All statements contained in this Form10-K, other than statements of historical fact, are forward-looking statements. When used in this report or elsewhere by management from time to time, thewords “believe,” “anticipate,” “intend,” “plan,” “estimate,” “expect,” “may,” “will,” “should,” “seeks” and similar expressions are forward-lookingstatements. Such forward-looking statements are based on current expectations, but the absence of these words does not necessarily mean that a statement isnot forward-looking. Forward-looking statements made in this Form 10-K include, but are not limited to, statements about: • our ability to manufacture, market and sell Korlym (mifepristone) 300mg Tablets; • our ability to realize the benefits of Orphan Drug Designation of Korlym in the United States; • the progress and timing of our research, development and clinical programs and the timing of regulatory activities for mifepristone for thetreatment of the psychotic features of psychotic depression; • our estimates regarding enrollment in and the dates by which we expect to report results of our clinical trials and the anticipated results of thesetrials; • our ability to achieve marketing approval of Korlym in the European Union (EU) and realize the benefits of Orphan Drug Designation there; • the timing of the market introduction of future product candidates, including any compound in our families of selective GR-II antagonists; • our ability to manufacture, market, commercialize and achieve market acceptance for our future product candidates, including mifepristone for thetreatment of the psychotic features of psychotic depression and any compound in our families of selective GR-II antagonists; • uncertainties associated with obtaining and enforcing patents; • our estimates for future performance, including revenue and profits; and • our estimates regarding our capital requirements.Forward-looking statements are not guarantees of future performance and involve risks and uncertainties. Actual events or results may differmaterially from those discussed in the forward-looking statements as a result of various factors. For a more detailed discussion of such forward-lookingstatements and the potential risks and uncertainties that may impact upon their accuracy, see the “Risk Factors” section of this Form 10-K and the“Overview” and “Liquidity and Capital Resources” sections of the “Management’s Discussion and Analysis of Financial Condition and Results ofOperations” section of this Form 10-K. These forward-looking statements reflect our view only as of the date of this report. Except as required by law, weundertake no obligations to update any forward-looking statements. Accordingly, you should also carefully consider the factors set forth in other reports ordocuments that we file from time to time with the Securities and Exchange Commission (SEC). ITEM 1. BUSINESSOverviewWe are a pharmaceutical company engaged in the discovery, development and commercialization of drugs for the treatment of severe metabolic andpsychiatric disorders. Our focus is on those disorders that are associated with a steroid hormone called cortisol. Elevated levels and abnormal release patternsof cortisol have been implicated in a broad range of human disorders. Since our inception in May 1998, we have been developing mifepristone — a potentglucocorticoid receptor II (GR-II) antagonist that blocks the activity of cortisol — for the treatment of a number of severe metabolic and psychiatric disorders.We have also discovered three series of novel selective GR-II antagonists and have moved a compound from one of these series into clinical development. 1™Table of ContentsOn February 17, 2012, the United States Food and Drug Administration (FDA) approved Korlym (mifepristone) 300 mg Tablets as a once-daily oralmedication for treatment of hyperglycemia secondary to hypercortisolism in adult patients with endogenous Cushing’s syndrome who have type 2 diabetesmellitus or glucose intolerance and have failed surgery or are not candidates for surgery. FDA approval means that we can market the drug for the approvedindication in the United States. We made Korlym available to patients in April 2012 and continue to develop the sales, marketing, medical affairs andlogistical infrastructure needed to commercialize the drug. We also have an on-going Phase 3 study of mifepristone, the active ingredient in Korlym, for thepsychotic features of psychotic depression.Unless otherwise stated, all references in this document to “we,” “us,” “our,” “Corcept,” the “Company,” “our company” and similar designations referto Corcept Therapeutics Incorporated.Cushing’s Syndrome. Cushing’s syndrome is a disorder caused by prolonged exposure of the body’s tissues to high levels of the hormone cortisol.Sometimes called “hypercortisolism,” it is relatively uncommon and most often affects adults aged 20 to 50. An estimated 10 to 15 of every one millionpeople are newly diagnosed with this syndrome each year, resulting in approximately 3,000 new patients and an estimated prevalence of 20,000 patients withCushing’s syndrome in the United States.We received Orphan Drug Designation from the FDA in July 2007 for Korlym for the treatment of endogenous Cushing’s syndrome. In the UnitedStates, Orphan Drug Designation is a special status granted by the FDA to encourage the development of treatments for diseases or conditions that affectfewer than 200,000 patients. Drugs that receive Orphan Drug Designation obtain seven years of marketing exclusivity for the approved indication from thedate of drug approval, as well as tax credits for clinical trial costs, marketing application filing fee waivers and assistance from the FDA in the drugdevelopment process.In October 2011 we received Orphan Drug Designation in the EU. Orphan Drug Designation in the EU confers benefits similar to those in the U.S., butincludes ten years of marketing exclusivity for the approved indication in all 27 member states, free scientific advice during drug development, access to acentralized review process and a reduction or complete waiver of fees levied by the European Medicines Agency (EMA). We are working with the EMA nowto prepare a Marketing Authorization Application (MAA) that, subject to filing with and review by the EMA, could serve as the basis for Korlym’s approvalin the EU.As discussed above, in February 2012, the FDA approved our New Drug Application (NDA) for Korlym as a once-daily oral medication for treatment ofhyperglycemia secondary to hypercortisolism in adult patients with endogenous Cushing’s syndrome who have type 2 diabetes mellitus or glucoseintolerance and have failed surgery or are not candidates for surgery.Psychotic Depression. We are also developing mifepristone, Korlym’s active ingredient, for treatment of the psychotic features of psychoticdepression under an exclusive patent license from Stanford University. The FDA has granted “fast track” status to evaluate the safety and efficacy ofmifepristone for the treatment of the psychotic features of psychotic depression.In March 2008, we began enrollment in Study 14, our ongoing Phase 3 trial in psychotic depression. The protocol for this trial incorporates what wehave learned from our three previously completed Phase 3 trials. It attempts to address the established relationship between increased drug plasma levels andclinical response and attempts to decrease the random variability observed in the results of the psychometric instruments used to measure efficacy. In one ofthe previously completed Phase 3 trials, Study 06, we prospectively tested and confirmed that patients whose plasma levels rose above a predeterminedthreshold statistically separated from both those patients whose plasma levels were below the threshold and those patients who received placebo; thisthreshold was established from data produced in earlier studies.As expected, the group of patients who took 1200 milligrams (mg) of mifepristone in Study 06 developed higher drug plasma levels than did thegroups of patients who received lower doses. Further, there was no 2™Table of Contentsdiscernible difference in the incidence of adverse events between patients who received placebo in Study 06 and those who received 300 mg, 600 mg or 1200mg of mifepristone in that study. In August 2011, we published our analysis of these data in The Journal of Clinical Psychopharmacology. Based on thisinformation, we are using a mifepristone dose of 1200 mg once per day for seven days in Study 14.In addition, we are utilizing a third party centralized rating service to independently evaluate patients for entry into the study as well as to evaluatetheir level of response throughout their participation. We believe the centralization of this process will improve the consistency of rating across clinical trialsites and reduce the background noise that was experienced in earlier studies and is endemic to psychopharmacologic studies. We believe that this change indose, as well as the other modifications to the protocol, should allow us to demonstrate the efficacy of mifepristone in the treatment of the psychoticsymptoms of psychotic depression. In mid-2009, in order to conserve financial resources, we reduced the number of clinical sites to eight and extended thetimeline for the study’s completion. To increase the pace of patient enrollment, we began adding clinical sites in the fourth quarter of 2012 and plan to have20 clinical sites participating by the end of the first quarter of 2013. Our goal is to enroll a sufficient number of patients by the end of 2013 to be able toperform a successful interim analysis.Antipsychotic-induced Weight Gain Mitigation. In 2005, we published the results of studies in rats that demonstrated that mifepristone both reversedthe weight gain associated with the ongoing use of olanzapine and mitigated the weight gain associated with the initiation of treatment with olanzapine (theactive ingredient in Zyprexa). The results from this study were published in the journal Brain Behavioral Research in early 2006. The study was paid for byEli Lilly and Company (Eli Lilly).During 2007 we announced positive results from our clinical proof-of-concept study in lean healthy male volunteers evaluating the ability ofmifepristone to mitigate weight gain associated with the use of Zyprexa. The results show a statistically significant reduction in weight gain in those subjectswho took Zyprexa plus mifepristone compared to those who took Zyprexa plus placebo. Also, the addition of mifepristone to treatment with Zyprexa had abeneficial impact on secondary metabolic measures such as fasting insulin, triglycerides and abdominal fat, as indicated by waist circumference. Eli Lillyprovided Zyprexa and financial support for this study and its results were published in the journal Advances in Therapy in 2009. In January 2009, weannounced positive results from a similar proof-of-concept study evaluating the ability of mifepristone to mitigate weight gain associated with the use ofJohnson & Johnson’s Risperdal. This study confirmed and extended the earlier results seen with mifepristone and Zyprexa, demonstrating a statisticallysignificant reduction in weight and secondary metabolic endpoints of fasting insulin, triglycerides and abdominal fat, as indicated by waist circumference.The results from the study of mifepristone and Risperdal were presented at several scientific conferences, including the American Diabetes Associationmeeting in June 2009, and were published in the journal Obesity in 2010.The combination of Zyprexa or Risperdal and mifepristone is not approved for any indication. The purpose of these studies was to explore thehypothesis that GR-II antagonists, such as mifepristone and our next generation of selective GR-II antagonists, would mitigate weight gain associated withantipsychotic medications. The group of medications known as second generation antipsychotic medication, including Zyprexa, Risperdal, Clozaril andSeroquel, are widely used to treat schizophrenia and bipolar disorder. All medications in this group are associated with treatment-emergent weight gain ofvarying degrees and carry a warning in their labels relating to treatment-emergent hyperglycemia and diabetes mellitus.Selective GR-II Receptor Antagonists. In 2003, we initiated a discovery research program to identify and patent selective GR-II antagonists. Ourintent is to develop a pipeline of products for proprietary use. Three distinct series of selective GR-II antagonists have been identified. These compounds, likethe active ingredient in our lead product Korlym, potently block the cortisol receptor (GR-II) but, unlike Korlym, do not appear to block the PR(progesterone), ER (estrogen), AR (androgen) or GR-I (mineralocorticoid) receptors. Both the United 3®®®®Table of ContentsStates Patent & Trademark Office (USPTO) and the European Patent Office (EPO) have issued to us composition of matter patents in each of the three series.Two additional composition of matter patent applications are pending. See “Business — Intellectual Property.”Several of our new compounds have demonstrated positive results in animal models for the prevention and reversal of anti-psychotic-induced weightgain, as well as animal and in vitro models of other metabolic and common central nervous system disorders. One of these new compounds, CORT 108297, isin exploratory Phase 2 clinical trials and we plan to explore its potential use in several indications. See Business — Next-Generation Selective GR-IIAntagonists for the Prevention and Reversal of Anti-Psychotic-Induced Weight Gain. We have identified other selective GR-II antagonists from ourproprietary series that we believe may have utility as therapeutic agents in a variety of diseases. We intend to continue our discovery research program withthe goal of identifying new selective GR-II antagonists and to perform manufacturing and pre-clinical development on several of these compounds and tosubmit Investigational New Drug applications (INDs) with respect to the most promising of them, as we deem appropriate.The Role of Cortisol in DiseaseCortisol is a steroid hormone that plays a significant role in the way the body reacts to stressful conditions and is essential for survival. Cortisolsignificantly influences metabolism, exerts a clinically useful anti-inflammatory effect and contributes to emotional stability. Insufficient levels of cortisolmay lead to dehydration, hypotension, shock, fatigue, low resistance to infection, trauma, stress and hypoglycemia. Excessive levels of cortisol may lead toimpaired glucose tolerance, diabetes, obesity, depressed mood, psychosis, wasting of the arms and legs, edema, fatigue, hypertension, and other problems.Elevated levels and abnormal release patterns of cortisol have also been linked to a broad range of metabolic and psychiatric conditions, such asweight gain, diabetes, hypertension, mood changes, psychosis and cognitive impairment.While excess cortisol may play a role in numerous diseases, Cushing’s syndrome (sometimes called “hypercortisolism”) is the archetypal disease ofexcess cortisol, as Cushing’s syndrome patients have tumors that produce excess levels of cortisol or adrenocorticotropic hormone (ACTH), which stimulatesthe production of cortisol. Exposure to high levels of cortisol can result in weight gain, diabetes, hypertension, infections, severe fatigue and psychosis.Many studies have shown that patients with psychotic depression have elevated levels and abnormal release patterns of cortisol. This abnormal cortisolactivity is not usually present in patients with nonpsychotic depression. More than 20 years ago, one of our scientific co-founders postulated that elevatedlevels of cortisol in patients with psychotic depression lead to elevated levels of dopamine, an important chemical substance found in the brain. Elevatedlevels of dopamine have been implicated in both delusional thinking and hallucinations. This hypothesis led to the concept that, by regulating the level andrelease patterns of cortisol, one could normalize dopamine levels in the brain, which may, in turn, ameliorate the symptoms of psychotic depression. Inaddition to cortisol’s effect on dopamine levels, research has shown that prolonged elevated cortisol may also play a direct role in causing the symptoms ofpsychotic depression.The challenge in regulating levels of cortisol is that cortisol is needed for natural processes in the human body. Destroying the ability of the body tomake cortisol or to drastically reduce its presence would result in serious detrimental effects. To have a viable therapeutic effect, a compound must be able toselectively modulate cortisol’s effects.Glucocorticoid Receptor AntagonistsCortisol is produced by the adrenal glands and is carried via the bloodstream throughout the body, including to the brain, where it directly influencesneuronal function. In the brain, cortisol binds to two receptors, 4Table of ContentsGlucocorticoid Receptor I and Glucocorticoid Receptor II, also known as GR-I and GR-II. GR-I is a high-affinity receptor that is involved in the routinefunctions of cortisol in the brain. It has approximately ten times the affinity of GR-II for cortisol and its binding sites are filled with cortisol nearly all thetime. In general, GR-II binding sites do not fill until levels of cortisol become elevated. Short-term activation of GR-II has benefits, which include helping theindividual to be more alert and better able to function under stressful conditions. Long-term activation of GR-II, however, has been shown to have significanttoxicity and appears to be linked to multiple metabolic and psychiatric disease states, such as Cushing’s syndrome and psychotic depression. The action ofcortisol can be moderated by the use of blockers, or antagonists, that prevent the binding of the hormone to its receptors. These antagonists, referred to asglucocorticoid or cortisol receptor antagonists, may prevent the undesirable effects of elevated levels and abnormal release patterns of cortisol.Mifepristone, the active ingredient in Korlym, works by selectively blocking the binding of cortisol to GR-II. It is neither an antagonist nor agonist ofGR-I. It also blocks the binding of progesterone to the progesterone receptor (PR). Because of its selective affinity, we believe that mifepristone can have atherapeutic benefit by modulating the effects of abnormal levels and release patterns of cortisol without compromising the necessary normal functions ofcortisol. We have also discovered three series of additional compounds that, like mifepristone, potently block the GR-II receptor, but, unlike mifepristone, donot block the progesterone receptor. One of these compounds, CORT 108297, is now being studied in the clinic. We have identified other compoundssuitable for advancement and plan to begin pre-clinical work on several of them in 2013.Overview of Cushing’s SyndromeEndogenous Cushing’s syndrome is caused by prolonged exposure of the body’s tissues to high levels of the hormone cortisol produced by a tumor ortumors. In endogenous Cushing’s syndrome, the excess cortisol is stimulated or directly produced by pituitary, adrenal or ectopic tumors. Cushing’ssyndrome is an orphan indication which most commonly affects adults aged 20 to 50. An estimated 10 to 15 of every one million people are newly diagnosedwith this syndrome each year, resulting in approximately 3,000 new patients in the United States. An estimated 20,000 patients in the United States havebeen diagnosed with Cushing’s syndrome. Symptoms vary, but most people have one or more of the following manifestations: high blood sugar, diabetes,high blood pressure, upper body obesity, rounded face, increased fat around the neck, thinning arms and legs, severe fatigue and weak muscles. Irritability,anxiety, cognitive disturbances and depression are also common. Cushing’s syndrome can affect every organ system in the body and can be lethal if nottreated effectively.The preferred treatment for Cushing’s syndrome patients is surgery, which if successful can cure the disease. Depending on the type of tumor, surgerycan result in a range of complications and has varying rates of success. In approximately half of the patients, surgery is not successful, either because thetumor cannot be removed completely or the disease returns.Commercialization of KorlymKorlym is the first approved therapy for patients with endogenous Cushing’s syndrome. On February 17, 2012, Korlym was approved by the FDA forhyperglycemia secondary to hypercortisolism in adult patients with endogenous Cushing’s syndrome who have type 2 diabetes mellitus or glucoseintolerance and have failed surgery or are not candidates for surgery. As indicated in the medicine’s prescribing information, physicians prescribing Korlymmay determine the appropriate dose for each patient by assessing tolerability and degree of improvement in manifestations of Cushing’s syndrome. In the firstsix weeks, these manifestations may include changes in glucose control, anti-diabetic medication requirements, insulin levels and psychiatric symptoms.After two months, assessment may also be based on improvements in cushingoid appearance, acne, hirsutism, striae, decreased body weight, along withfurther changes in glucose control.We have begun marketing Korlym in the United States, without a partner, because we believe that the market is highly concentrated and accessible.Following the drug’s approval by the FDA in February 2012, 5Table of Contentswe began hiring a small number of experienced medical science liaisons (MSLs), supported by medical affairs and other infrastructure, to educate health careproviders about Korlym. To reach more physicians, in October 2012 we began deploying a small force of experienced field sales personnel. We intend for ourMSLs and sales representatives to focus on patients who are in the care of an endocrinologist and in active treatment for their disease. We estimate that wewould need to target approximately 500 endocrinologists to reach a large portion of the Cushing’s syndrome population in active treatment. We also reachpatients directly through web-based initiatives and interactions with patient groups. We have executed agreements with a specialty pharmacy, a specialtydistributor, a contract sales organization, and a third-party logistics company to distribute Korlym and provide logistical support.A large percentage of the people who suffer from Cushing’s syndrome remain undiagnosed or inadequately treated. We intend to develop programs toeducate the medical community and patients about early diagnosis of this syndrome and to increase awareness regarding the role of GR-II antagonists for thissyndrome. We have retained a vendor to help patients with the reimbursement process. This vendor also administers our financial assistance programs foruninsured or under-insured patients who cannot otherwise afford the cost of Korlym.Both the FDA and the European Commission have granted Orphan Drug Designation for Korlym. In the United States, Orphan drugs receive sevenyears of marketing exclusivity for the approved indication from the date of approval, as well as tax credits for clinical trial costs, marketing application filingfee waivers and assistance from the FDA in the drug development process. Benefits of Orphan Drug Designation in the EU are similar to those in the U.S., butinclude ten years of marketing exclusivity for the approved indication in all 27 member states, free scientific advice during drug development, access to acentralized review process and a reduction or complete waiver of fees levied by the European Medicines Agency (EMA). In 2013, we plan to commence astudy of Korlym in pediatric Cushing’s syndrome patients. If we complete the study and submit the data to the FDA and EMA pursuant to protocols andwithin timelines that we may agree upon with these agencies, our Orphan Drug marketing exclusivity period will be extended by six months in the UnitedStates and two years in the EU.Additional Trials and Preclinical StudiesAs part of its approval for Korlym, the FDA has required us to study the interactions, if any, between Korlym and ketoconazole, an anti-fungal agentthat is sometimes used to treat Cushing’s syndrome, although it is not approved by the FDA for that purpose. Further, the FDA has required us to perform adrug utilization study to better characterize the reporting rates of adverse events associated with the long-term use of Korlym. On our own initiative, weconducted a long-term extension study in patients who completed the Phase 3 trial to assess safety of chronic dosing. Upon the approval of Korlym wetransitioned study patients to commercial product and terminated the study.Overview of Psychotic DepressionPsychotic depression is a serious psychiatric disease in which a patient suffers from severe depression accompanied by delusions, hallucinations orboth. These psychotic features typically develop after the onset of a depressed mood, but may develop concurrently as well. Once psychotic symptoms occur,they usually reappear with each subsequent depressive episode. Of particular importance, when the patient’s mood returns to normal the psychosis alsoresolves.Data from the National Institute of Mental Health published in 2005 indicate that depressive disorders affect an estimated 9.5% of adults in the UnitedStates, or about 19 million people each year. Of these 19 million people, many published studies show that approximately 15-20%, or about three millionpeople, have psychotic depression. Most patients with psychotic depression suffer their first episode of major depression between the ages of 30 and 40 andthe majority will experience more than one episode in their lifetime. People with psychotic depression are approximately 70 times more likely to commitsuicide in their lifetime than the general population and often require lengthy and expensive hospital stays. 6Table of ContentsCurrent Treatments for Psychotic DepressionThere are two treatment approaches for the psychotic features of psychotic depression currently used by psychiatrists: electroconvulsive therapy (ECT)and combination drug therapy, which is a combination of antidepressant and antipsychotic medication. Neither of these treatments has been approved by theFDA for the psychotic features of psychotic depression and both approaches almost always have a slow onset of action, which may result in lengthy andcostly hospitalization. Each of these treatments can have debilitating side effects. Of the two treatments, ECT is generally considered to be more effective. • ECT involves passing an electrical current through the brain until the patient has a seizure. At least 100,000 patients receive ECT each year inthe United States, with each patient requiring approximately six to twelve procedures over a period of three to five weeks. • Combination drug therapy is an alternative treatment for the psychotic features of psychotic depression that involves taking antipsychotic drugssuch as olanzapine, haloperidol or chlorpromazine in combination with antidepressant drugs, such as fluoxetine, imipramine or venlafaxine.Patients on combination drug therapy often require three weeks or more to show improvement in their symptoms and treatment can take monthsbefore the symptoms are resolved entirely. Antipsychotic drugs can cause significant adverse side effects, including weight gain, diabetes,sedation, permanent movement disorders and sexual dysfunction.Mifepristone for the Psychotic Features of Psychotic DepressionWe are developing mifepristone as an oral medication to treat the psychotic features of psychotic depression. As a GR-II antagonist, mifepristoneappears to mitigate the effects of the elevated and abnormal release patterns of cortisol in patients suffering from psychotic depression. We intendmifepristone to be a once-daily treatment given to patients with psychotic depression over seven consecutive days in a controlled setting, such as a hospitalor physician’s office.We believe that mifepristone may significantly reduce psychotic symptoms of psychotic depression in many patients within one week and allowpatients to be more easily maintained on antidepressant therapy alone without the need for ECT or antipsychotic medication. We believe that mifepristonemay be superior to currently available treatments because we believe that mifepristone will enable patients with psychotic depression to improve theirquality of life more quickly and with fewer side effects than with ECT or combination drug therapy.Completed Clinical Trials of Mifepristone for Psychotic DepressionWe have completed seven prior clinical trials evaluating mifepristone for treatment of the psychotic features of psychotic depression, in addition to ourongoing Phase 3 trial. The trials include three Phase 3 trials conducted from 2004 through 2007, in addition to four earlier stage clinical trials withmifepristone. These completed trials generated important data confirming the safety profile of mifepristone (alone and in combination with commonlyprescribed antipsychotic and antidepressant medications), demonstrated positive efficacy trends, and provided insights into the design of future clinical trialswhich might improve the probability of clinical success.Completed Phase 3 Clinical Trials. In addition to Phase 1 and 2 studies, we have completed three randomized, double-blind, placebo-controlledPhase 3 clinical trials to further assess the safety and efficacy of mifepristone for the treatment of the psychotic features of psychotic depression. Two of thesetrials (Study 06 and Study 07) were conducted primarily in the United States. The third trial (Study 09) was conducted in Eastern Europe.The primary endpoint for Study 06 and Study 07 was the proportion of patients with at least a 50% improvement in the Brief Psychiatric Rating ScalePositive Symptom Subscale (BPRS PSS) at both Day 7 and 7Table of ContentsDay 56. The primary endpoint for Study 09 was the proportion of patients with at least a 50% improvement in the BPRS PSS, at both Day 7 and Day 28, withday 56 as a secondary endpoint. Patients must have had at least mild psychotic symptoms (BPRS PSS 12) to enter the studies and were hospitalized ifclinically necessary. • Study 07: The first of these trials, which began in September 2004, enrolled 257 patients randomized one-to-one to either treatment or placebo.Patients in the treatment arm received 600 mg of mifepristone once daily for seven days. Patients did not take any antidepressant orantipsychotic medication for at least one week before beginning the seven day treatment period. After the seven days of mifepristone treatment,all patients received antidepressant therapy through Day 56. Treatment with antipsychotic medications or ECT was not allowed at any timeduring the study.In this study patients receiving mifepristone did not have a statistically significant difference in response rate at the primary endpoint than didthe patients receiving placebo. A retrospective analysis of the data showed that patients achieving drug plasma levels higher than 1800nanograms per milliliter (ng/ml) had a statistically significant greater response rate than placebo. There was also a statistically significant site bytreatment effect in this trial. Among the twenty sites who participated from the trial onset, patients who were given mifepristone had asignificantly higher response rate than patients who received placebo. Among the sites added later in the trial, there was no significant differencein response rate between mifepristone and placebo patients. These findings were published in 2009 by Contemporary Clinical Trials. • Study 09: This study, which commenced in May 2005, was a randomized, double-blind, placebo-controlled study in which 247 patients wereenrolled at sites in Eastern Europe. Patients in the treatment arm received 600 mg of mifepristone once daily for seven days. The primaryendpoint was the proportion of patients with at least a 50% improvement in the BPRS PSS score at both Day 7 and Day 28. The study did notdemonstrate a significant difference in response between patients receiving mifepristone and patients receiving placebo as measured by theprimary endpoint. The results at the two key secondary endpoints of Study 09 also were not statistically significant. Study 09 had an extremelyhigh placebo response rate. • Study 06: This trial began in October 2004, and enrolled 443 patients. These patients were randomly assigned to three active dose groups (300mg, 600 mg and 1200 mg) or a placebo group, with patients receiving once daily dosing for a period of seven days. The three dosing levelsresponded to the FDA’s request to supplement data on a range of doses to augment the data provided by our open label dose ranging studycompleted in 2001.The study did not achieve statistical significance with respect to the primary endpoint. However, there was a statistically significant correlationbetween plasma levels and clinical outcome achieved during treatment. Response rates for patients whose plasma levels rose above apredetermined threshold of 1661 ng/ml were statistically different than those patients whose plasma levels were below the threshold and thosepatients who received placebo. Further, the incidence of serious adverse events did not differ between placebo and any of the three mifepristonedose groups. In August 2011, we published an analysis of these results in The Journal of Clinical Psychopharmacology.Ongoing Phase 3 trial – Study 14: We believe that the confirmation of a correlation between drug concentration and clinical response, as well asother observations from Study 06 and our two other completed Phase 3 clinical trials, served as a strong basis for the design of our ongoing Phase 3 study,which commenced in March 2008. The protocol for this trial incorporates information learned from the three completed Phase 3 trials in that it addresses theestablished relationship between increased drug plasma levels and clinical response, and it attempts to decrease the random variability observed in the resultsof the psychometric instruments used to confirm diagnosis and measure efficacy. • Increased “Signal”: In this trial we are administering a mifepristone dose of 1200 mg once per day for seven days instead of 600 mg once perday for seven days. 8Table of Contents • Decreased “Noise”: We also are utilizing a third party centralized rating service to independently evaluate the patient’s diagnosis prior to entryinto the study as well as to assess response. We believe the centralization of this process will improve the accuracy of diagnosis and theconsistency of rating across clinical trial sites and reduce the background noise that is endemic to psychopharmacologic studies and clearlyvisible in our earlier studies.We believe that these changes in the protocol should allow us to establish the efficacy of mifepristone in the treatment of the psychotic features ofpsychotic depression. Given the serious nature of psychotic depression, the lack of any approved drugs for the disorder and the data from our first clinicaltrial, the FDA granted a fast track designation for mifepristone for the treatment of the psychotic features of psychotic depression. In addition, the FDA hasindicated that mifepristone will receive a priority review if no other treatment is approved for the psychotic features of psychotic depression at the time wesubmit our NDA.Enrollment in Study 14 is ongoing. Our goal is to enroll a sufficient number of patients by the end of 2013 to be able to perform a successful interimanalysis. To help reach this goal, we plan to increase the number of clinical sites from eight to approximately 20 by the end of the first quarter of 2013.Clinical Trial Agreements. Many of our Phase 3 clinical trials are conducted through the use of clinical research organizations (CROs.) At ourrequest, these organizations oversee clinical trials at various institutions to test the safety and efficacy of our product candidates for the targeted indications.Our ongoing Phase 3 clinical trial, Study 14, evaluating mifepristone for the treatment of the psychotic features of psychotic depression is being conductedunder an agreement with ICON Clinical Research, LP (ICON). We may terminate this agreement with 60 days notice to ICON, or sooner based on mutualagreement of the parties. In addition, we entered into an agreement with MedAvante, Inc. (MedAvante), in March 2008, to provide the centralized psychiatricdiagnosis and rating services for patients being screened and enrolled in Study 14. We may terminate this agreement with 30 days notice to MedAvante.Discovery Research: Next-Generation Selective GR-II AntagonistsIn 2003, we initiated a discovery research program to identify and patent selective GR-II antagonists at a contract research organization in the UnitedKingdom. Through this program we have identified and filed patent applications for three distinct series of selective GR-II antagonists. These compoundsappear to be as potent as our lead product mifepristone in blocking cortisol but, unlike mifepristone, they do not appear to block the progesterone or othersteroid receptors. Currently, we are investigating several compounds in our research programs. We plan to submit INDs for such additional compounds as ourresearch indicates may be promising and as we deem appropriate.We have assembled a patent portfolio covering both a broad range of uses and the composition of our new chemical entities. • We have composition of matter claims on three patent families of novel selective glucocorticoid receptor (GR-II) antagonists. Applications for allthree families have been allowed or issued in both the United States and Europe. Two additional composition of matter patent applications arepending in both the United States and Europe. • We also have a portfolio of patents describing the use of drugs that block the GR-II receptor for the treatment of metabolic and psychiatricdisorders. In addition to psychotic depression, we own or have exclusively licensed issued patents for the use of GR-II antagonists for treatmentand / or prevention of: • weight gain following treatment with antipsychotic medication; • mild cognitive impairment; • stress disorders; • early dementia, including early Alzheimer’s disease; 9Table of Contents • delirium; • gastroesophageal reflux disease; • cognitive deterioration in adults with Down’s Syndrome; • psychosis associated with cocaine addiction; • catatonia; and • increased therapeutic response to ECT.See “Business — Intellectual Property.”Next-Generation Selective GR-II Antagonists for the Prevention and Reversal of Antipsychotic-Induced Weight GainIn January 2009, we announced results from two preclinical studies of our first next-generation selective GR-II receptor antagonist, CORT 108297, forthe prevention and reversal of weight gain caused by olanzapine, a medication marketed by Eli Lilly as Zyprexa. Using the same experimental rat model usedpreviously with mifepristone, the preclinical studies demonstrated that CORT 108297 1) reversed and 2) prevented the weight gain caused by olanzapine inrats. Eli Lilly provided olanzapine and funded the cost of the studies. • In the first of these two studies, seventy-two female rats (n=12 per group) were allowed to eat a normal diet for 56 days. During an “induction”phase of weight gain (study days 1-34), 12 rats were administered placebo, whereas 48 were administered olanzapine. Animals receivingolanzapine gained significantly more weight than animals receiving placebo (p<.000001). On Day 35, the 48 animals that had receivedolanzapine during the weight induction phase were randomized (n=12 per group) to receive one of the following regimens: placebo, CORT108297 (20mg/kg), CORT 108297 (60mg/kg), CORT 108297 (120mg/kg) for the subsequent 21 days. There were robust, statistically significant,differences in weight between the olanzapine plus placebo and olanzapine plus CORT 108297 groups: Animals receiving olanzapine andplacebo continued to gain significant body weight from day 35 to 56 (p<.0001) while animals receiving olanzapine plus CORT 108297 (alldoses) exhibited significant weight reduction (p<.00001). At the highest dose tested (120 mg/kg), the animals’ weight returned to levelsobserved prior to initial olanzapine ingestion. The results of this first study suggest that after significant weight gain from olanzapine has alreadyoccurred, CORT 108297 can be introduced while olanzapine is continued and reverse the weight gain caused by olanzapine. • In the second study, rats (n = 96) were dosed with placebo, olanzapine (2.4 mg/kg), or, olanzapine plus CORT 108297 (2, 6, 20, 60, or120 mg/kg) for 21 days. From baseline to day 21, rats administered olanzapine plus CORT 108297 gained significantly less weight than ratsreceiving olanzapine and placebo (p <.00001). Larger doses of CORT 108297 were significantly correlated with greater weight reduction(p<.00001). This second study suggests that when CORT 108297 is administered concomitantly with olanzapine, weight gain associated withthe use of olanzapine can be prevented or at least attenuated.These first two studies used dose levels of 20 mg/kg, 60 mg/kg and 120 mg/kg of CORT 108297. The results of these two experiments replicated thefindings from previous animal studies of mifepristone, and were also consistent with results from randomized trials conducted in humans. The results werepresented at the International Society of Psychoneuroendocrinology and the World Congress of Biological Psychiatry conferences in July 2009 and werepublished in the peer-reviewed journal, Diabetes Obesity and Metabolism in 2010.A third study in the rat further evaluated the dose response relationship of CORT 108297 in preventing olanzapine induced weight gain with dosesfrom 2 mg/kg to 20 mg/kg. 10Table of ContentsAt the American Diabetes Association conference in June 2009 there was also a presentation of preclinical data from a study which demonstrated thatCORT 108297 suppresses body weight gain and improves insulin sensitivity in healthy mice fed a 60% fat diet and high sucrose liquid. In 2011, these studyresults were published in the peer-reviewed publication, The Journal of Nutrition and Metabolism.The manufacturing and preclinical development of CORT 108297 began late in 2008 and resulted in the submission of an IND to the FDA inDecember 2009. Dosing of healthy volunteers in the first Phase 1 study of CORT 108297 was completed in July 2010. This initial study was a single doseescalation study in healthy volunteers. We continue to evaluate CORT 108297 in exploratory Phase 2a studies in models of antipsychotic induced weightgain and changes in biomarkers induced by prednisone, a steroid.If any of our selective GR-II antagonists prove to mitigate the weight gain and metabolic disturbances associated with the use of antipsychoticmedication, they could potentially be of benefit to the millions of people currently taking this important pharmacotherapy.Proof-of-Concept StudiesMetabolic DisordersIn April 2005, we announced results from two preclinical studies conducted in a rat model of olanzapine-induced weight gain. These studiesdemonstrated that mifepristone’s GR-II antagonist action has the potential to both reverse the weight gain associated with olanzapine and to prevent theweight gain associated with the initiation of treatment with olanzapine, which led to our studies in humans.In 2007, we announced results of our human clinical proof-of-concept study evaluating the ability of mifepristone to mitigate weight gain associatedwith the administration of Eli Lilly’s Zyprexa (olanzapine). The results indicated a statistically significant reduction in weight gain in those subjects whotook Zyprexa plus mifepristone compared to those who took Zyprexa plus placebo. Eli Lilly provided Zyprexa and financial support for this study. During2009, we announced results from another proof-of-concept study evaluating the ability of mifepristone to mitigate weight gain associated with theadministration of Johnson & Johnson’s Risperdal (risperidone). The results indicated a statistically significant reduction in weight gain in those subjects whotook Risperdal plus mifepristone compared to those who took Risperdal plus placebo. Both Zyprexa and Risperdal are indicated for the treatment ofschizophrenia and bipolar disorder.In the study of mifepristone and Zyprexa, 57 lean, healthy men (body mass index of 25 or less) were randomized to receive either Zyprexa plus placebo(n=22), Zyprexa plus mifepristone (n=24) or mifepristone plus placebo (n=11). This study took place in an institutional setting where daily weights wererecorded and a range of metabolic parameters were measured. In the two week study, subjects in the Zyprexa plus placebo group gained an average of 7.0pounds and subjects in the Zyprexa plus mifepristone group gained an average of 4.4 pounds; which is a statistically significant difference (p<.001). Subjectsin the mifepristone plus placebo group gained an average of 4.4 pounds. The difference in weight gain trajectory was apparent in the first days of the study,reaching statistical significance during the first week. The increase in waist circumference, a surrogate for abdominal fat, in subjects who received Zyprexaplus placebo was also significantly greater than subjects who received Zyprexa plus mifepristone (p<.01). The study was not designed to enroll a sufficientnumber of patients to have statistical power to detect significant effects on metabolic measures; however, the effect of mifepristone in this model was greaterthan expected. In addition to the finding about waist circumference, notable additional non-statistically significant group differences were observed. Patientstaking Zyprexa plus placebo experienced greater increases from baseline to end of study in both triglycerides and fasting insulin compared to patients takingZyprexa plus mifepristone. No unexpected study drug related adverse events were observed. These results were published in Advances in Therapy in 2009.In the study of mifepristone and Risperdal, 75 lean, healthy men (body mass index of 23 or less) were randomized to receive either Risperdal plusplacebo (n=30), Risperdal plus mifepristone (n=30) or mifepristone plus placebo (n=15). This study also took place in an institutional setting where dailyweights were recorded and 11Table of Contentsa range of metabolic parameters were measured. In this four-week randomized double-blind controlled study, subjects in the Risperdal plus placebo groupgained an average of 9.2 pounds, compared to a gain of 5.1 pounds in the Risperdal plus mifepristone group. This difference was statistically significant(p<0.0001). Additional important metabolic parameters, including fasting insulin, triglycerides and abdominal fat, as reflected by waist circumference, werealso measured. The addition of mifepristone to Risperdal resulted in a statistically significant reduction in fasting insulin levels, triglyceride levels, andabdominal fat (as measured by waist circumference). Consistent with prior studies, mifepristone appeared to be well tolerated. These results were published inObesity in 2010.The combinations of Zyprexa and mifepristone or Risperdal and mifepristone are not approved for any indication. The purpose of these studies was toexplore the hypothesis that GR-II antagonists would mitigate weight gain and other metabolic effects associated with antipsychotic medications. The groupof medications sometimes referred to as “atypical antipsychotics,” including Zyprexa, Risperdal, Clozaril (clozapine) and Seroquel (quetiapine), are widelyused to treat schizophrenia and bipolar disorder. All medications in this group are associated with treatment-emergent weight gain of varying degrees andcarry a warning in the label relating to treatment-emergent hyperglycemia and diabetes mellitus.Other DisordersWe have collaborated with researchers investigating the utility of mifepristone and some of our next-generation selective GR-II antagonists in pre-clinical and human proof-of-concept studies in a wide range of disorders, including alcoholism, post-traumatic stress disorder, Alzheimer’s disease, andovarian cancer.Research and DevelopmentWe incurred approximately $14.1 million, $21.0 million and $18.9 million of research and development expenses in the years ended December 31,2012, 2011 and 2010, respectively, which accounted for approximately 36%, 65% and 69% of our total operating expenses in these respective fiscal years.For a further discussion, see Part II, Item 7, Management’s Discussion and Analysis of Financial Conditions and Results of Operations — Results ofOperations.Manufacturing KorlymAs a drug discovery, development and commercialization company, we intend to continue to utilize our financial resources to commercialize Korlymand advance other product candidates rather than diverting resources to establishing our own manufacturing facilities.We intend to continue to rely on experienced contract manufacturers to produce our product candidates. We have entered into a manufacturingagreement with one contract manufacturer, Produits Chimiques Auxiliaires et de Synthese SA (PCAS), to produce the active pharmaceutical ingredient (API)for Korlym. The FDA approved our commercial use of material produced by PCAS as part of our NDA submission for Korlym. The agreement with PCAS,which was executed in November 2006, was for an initial period of five years with an automatic extension for one additional year and has been extended toJune 2013. We are pursuing discussions to continue the relationship thereafter. The agreement calls for us to purchase from PCAS at least 75 percent of ourrequirements until the expiration of the agreement. If PCAS is unable to manufacture the product for a consecutive six-month period, we have the right toterminate the agreement, without penalty.We have also entered into an agreement with another contract manufacturer, PharmaForm, L.L.C. (PharmaForm), for the production of Korlym tablets.The agreement with PharmaForm was executed in March 2012 for an initial period of two years. The agreement will be automatically extended for additionalone year periods unless one Party gives six months’ prior written notice that it does not want such an extension. The agreement with PharmaForm may beterminated by either party upon 180 days written notice; we may terminate projects initiated under this agreement with 30 days written notice. There are nominimum purchase amounts under this agreement. 12Table of ContentsWe are currently in negotiations for a commercial manufacturing agreement with AAI Pharma, our second tablet manufacturer whose facility wasapproved by the FDA for manufacture of our commercial Korlym tablets in November 2012.Competition for KorlymKorlym competes with established treatments, including surgery, radiation, and approved medicines prescribed “off-label.” Korlym will also competewith Novartis’ drug, Signifor (pasireotide) Injection, which the FDA approved in December 2012 for the treatment of adult patients with Cushing’s disease (asubset of Cushing’s syndrome) who are not candidates for pituitary surgery or for whom surgery did not work. In April 2012, Signifor received marketingapproval in the EU. It has Orphan Drug designation in both the United States and the EU. Signifor is a somatostatin analogue that inhibits ACTH productionby the pituitary, which leads to reduced cortisol production. In the Phase 3 study that served as the basis for Novartis’ NDA, the drug normalized cortisollevels in 26 percent of patients. Sixty-seven percent of patients developed hyperglycemia or diabetes. Signifor must be taken twice daily, by injection.Korlym may also experience competition from compounds under development for Cushing’s syndrome. We are aware that Laboratoire HRA Pharma(HRA) has received an Orphan Drug Designation in the United States and Europe for the use of mifepristone to treat a subtype of Cushing’s syndrome and hasbegun a clinical trial in Europe and the United States. If this product is approved for commercialization in the United States and the EU, our potential futurerevenue could be reduced. We are also aware that Exelgyn Laboratories, which operates as a subsidiary of Medi Challenge (Pty) Ltd., received Orphan DrugDesignation for endogenous Cushing’s syndrome in Europe, but they have stated that they have not yet conducted any clinical trials.Many colleges, universities and public and private research organizations are also active in the human health care field. While these entities focus oneducation, they may develop or acquire proprietary technology that we may require for the development of our product candidates. We may attempt to obtainlicenses to this proprietary technology.Our ability to compete successfully will be based on our ability to develop proprietary products, attract and retain scientific personnel, obtain patent orother protection for our product candidates, obtain required regulatory approvals and manufacture and successfully market Korlym and our future productseither alone or through outside parties.Intellectual PropertyPatents and other proprietary rights are important to our business. It is our policy to seek patent protection for our inventions, and to rely upon tradesecrets, know-how, continuing technological innovations and licensing opportunities to develop and maintain our competitive position.Under an agreement with Stanford University, we have licensed exclusive rights to the following issued U.S. patents and any corresponding foreignpatents: U.S. Patent Number Subject Matter Expiration Date6,150,349 Use of GR-II antagonists in the treatment of psychotic majordepression October 5, 20186,362,173 Use of GR-II antagonists in the treatment of cocaine-inducedpsychosis October 5, 20186,369,046 Use of GR-II antagonists in the treatment of early dementia February 4, 2019The corresponding foreign patents expire in 2018. 13®Table of ContentsWe are required to make milestone payments and pay royalties to Stanford University on sales of products commercialized under any of the abovepatents. We are currently in compliance with our obligations under the agreement. If Stanford University were to terminate any of our exclusive licenses dueto breach of the license on our part, we would not be able to commercialize mifepristone for the treatment of the psychotic features of psychotic depression,cocaine-induced psychosis or early dementia.We also own issued U.S. patents for the use of GR-II antagonists in the treatment of mild cognitive impairment, for the treatment of weight gainfollowing treatment with antipsychotic medication, for the prevention and treatment of stress disorders, for increasing the therapeutic response to ECT, for thetreatment of delirium, for the treatment of catatonia, for the treatment of gastroesophageal reflux disease and for inhibiting cognitive deterioration in adultswith Down’s Syndrome. The expiration dates of these patents and their foreign counterparts range from 2020 to 2028.In addition, we have nine U.S. method-of-use applications covering certain GR-II antagonists, including the treatment of: • patients suffering from mental disorders by optimizing mifepristone levels in plasma serum; • neurological damage in premature infants; • muscular dystrophy; • migraine headaches; • psychosis associated with interferon-alpha therapy; • depression in patients taking Interleukin-2 (IL-2); and • amyotrophic lateral sclerosis (ALS).The approximate expiration dates of the patents that could issue from these applications and their foreign counterparts range from 2023 to 2032.We have composition of matter claims on three patent families of novel selective GR-II antagonists. Applications for all of the three families have beenallowed in both the United States and Europe. The expiration dates of these U.S. and European patents range from 2026 to 2027. Two additional compositionof matter patent applications are pending.We have also filed, where we deemed appropriate, foreign patent applications corresponding to our U.S. patents and applications.However, we cannot assure you that any of our patent applications will result in the issuance of patents, that any issued patent will include claims ofthe breadth sought in these applications, or that competitors will not successfully challenge or circumvent our patents if they are issued.Although three of our patents have claims directed to the composition of compounds, we do not have a patent with claims directed to the compositionof mifepristone. Our rights under our issued patents related to mifepristone cover only the use of that compound in the treatment of specific diseases.The composition of matter patent covering mifepristone has expired. The only previously FDA-approved use of mifepristone is to terminate pregnancy.The FDA has imposed significant restrictions on the use of mifepristone to terminate pregnancy. To protect our market for Korlym we plan to rely on (1) theexclusive marketing rights conferred as a benefit of Orphan Drug Designation in the United States and EU, (2) the restrictions imposed by the FDA on the useof mifepristone to terminate pregnancy, (3) the different patient populations, administering physicians and treatment settings between the use of mifepristoneto terminate pregnancy and to treat Cushing’s syndrome and (4) our method of use patents described above. 14Table of ContentsThe patent positions of companies in the pharmaceutical industry are highly uncertain, involve complex legal and factual questions and have been andcontinue to be the subject of much litigation. Our product candidates may give rise to claims that we infringe on the products or proprietary rights of others. Ifit is determined that our drug candidates infringe on others’ patent rights, we may be required to obtain licenses to those rights. If we fail to obtain licenseswhen necessary, we may experience delays in commercializing our product candidates while attempting to design around other patents, or determine that weare unable to commercialize our product candidates at all. If we do become involved in intellectual property litigation, we are likely to incur considerablecosts in defending or prosecuting the litigation. We believe that we do not currently infringe any third party’s patents or other proprietary rights, and we arenot obligated to pay royalties relating to the use of intellectual property to any third party other than Stanford University.In 2004 Akzo Nobel filed an observation to the grant of our exclusively licensed European patent application with claims directed to psychoticdepression. In February 2006, the EPO allowed our patent application. We are not aware of any other disputes related to patent issues.License AgreementUnder our exclusive license agreement with Stanford University to patents covering the use of mifepristone to treat the psychotic features of psychoticdepression and for the treatment of early dementia, we are required to pay Stanford $50,000 annually as a nonrefundable royalty payment. This payment iscreditable against future royalties. We are also obligated to pay Stanford a $50,000 milestone upon the filing of the NDA for mifepristone for the treatment ofpsychotic depression and a further $200,000 milestone payment upon FDA approval of mifepristone for that indication. The milestone payments are alsocreditable against future royalties. This license agreement expires upon expiration of the related patents or upon notification by us to Stanford relating to theuse of intellectual property. See “Intellectual Property.”Government RegulationPrescription pharmaceutical products are subject to extensive pre- and post-approval regulation, including regulations that govern the testing,manufacturing, safety, efficacy, labeling, storage, record keeping, advertising, and promotion of the products under the Federal Food, Drug and Cosmetic Act.All of our product candidates will require regulatory approval by government agencies prior to commercialization. The process required by the FDA before anew drug may be marketed in the United States generally involves the following: completion of preclinical laboratory and animal testing; submission of anIND, which must become effective before clinical trials may begin; performance of adequate and well-controlled human clinical trials to establish the safetyand efficacy of the proposed drug or biologic’s intended use; and, in the case of a new drug, approval by the FDA of an NDA. The process of complying withthese and other federal and state statutes and regulations in order to obtain the necessary approvals and subsequently complying with federal and statestatutes and regulations involves significant time and expense.Preclinical studies are generally conducted in laboratory animals to evaluate the potential safety and the efficacy of a product. Drug developers submitthe results of preclinical studies to the FDA as a part of an IND, which must be approved before beginning clinical trials in humans. Typically, human clinicaltrials are conducted in three sequential phases that may overlap. • Phase 1. Clinical trials are conducted with a small number of subjects to determine the early safety profile, maximum tolerated dose andpharmacokinetics of the product candidate in human volunteers. • Phase 2. Clinical trials are conducted with groups of patients afflicted with a specific disease to determine preliminary efficacy, optimaldosages and expanded evidence of safety. • Phase 3. Large-scale, multi-center, comparative trials are conducted with patients afflicted with a target disease to establish the overallrisk/benefit ratio of the drug and to provide enough data to demonstrate with substantial evidence the efficacy and safety of the product, asrequired by the FDA. 15Table of ContentsThe FDA and the Institutional Review Boards closely monitor the progress of each of the three phases of clinical trials that are conducted in the UnitedStates and may reevaluate, alter, suspend or terminate the testing at any time for various reasons, including a belief that the subjects are being exposed to anunacceptable health risk. The FDA may also require that additional studies be conducted, such as studies demonstrating that the drug being tested does notcause cancer.After Phase 3 trials are completed, drug developers submit the results of preclinical studies, clinical trials, formulation studies and data supportingmanufacturing to the FDA in the form of an NDA for approval to commence commercial sales. The FDA reviews all NDAs submitted before it accepts them forfiling. The FDA may request additional information rather than accept an NDA for filing. If the FDA accepts an NDA for filing, it may grant marketingapproval, request additional information or deny the application if it determines that the application does not meet regulatory approval criteria. Once an NDAhas been accepted for filing, by law the FDA has 180 days to examine the application and respond to the applicant. However, the review process is oftensignificantly extended by FDA requests for additional information or clarification. Under the Prescription Drug User Fee Act, the FDA has a goal ofresponding to NDAs within ten months of the filing date for standard review, and 6 months for priority review if a sponsor shows that its drug candidateprovides a significant improvement compared to marketed drugs. The FDA has indicated to us that it will grant us a priority review of our NDA ofmifepristone for the treatment of the psychotic features of psychotic depression if no other medications have been approved for this indication at the time ofour submission. FDA approvals may not be granted on a timely basis, or at all.If the FDA approves an NDA, the subject drug becomes available for physicians to prescribe in the United States. Once approved, the FDA maywithdraw the product approval if compliance with pre- and post-approval regulatory standards is not maintained. The drug developer must submit periodicreports to the FDA. Adverse experiences with the product must be reported to the FDA and could result in the imposition of marketing restrictions throughlabeling changes or product removal. Product approvals may be withdrawn if problems with safety or efficacy occur after the product reaches the marketplace.In addition, the FDA may require post-marketing studies, referred to as Phase 4 studies, to monitor the effect of approved products, and may limit furthermarketing of the product based on the results of these post-approval studies.Facilities used to manufacture drugs are subject to periodic inspection by the FDA and other authorities where applicable, and must comply withcurrent Good Manufacturing Practices regulations (cGMP). Failure to comply with the statutory and regulatory requirements subjects the manufacturer topossible legal or regulatory action, such as suspension of manufacturing, seizure of product or voluntary recall of a product.With respect to post-approval product advertising and promotion, the FDA imposes a number of complex regulations on entities that advertise andpromote pharmaceuticals, which include, among others, standards and regulations for direct-to-consumer advertising, off-label promotion, industry sponsoredscientific and educational activities, and promotional activities involving the Internet. The FDA has very broad enforcement authority under the FederalFood, Drug and Cosmetic Act, and failure to abide by these regulations can result in penalties including the issuance of a warning letter directing a companyto correct deviations from FDA standards, a requirement that future advertising and promotional materials be pre-cleared by the FDA, and state and federalcivil and criminal investigations and prosecutions.In addition to studies requested by the FDA after approval, a drug developer may conduct other studies to explore use of the approved compound fortreatment of new indications. The purpose of these trials and studies and related publications is to broaden the application and use of the drug and itsacceptance in the medical community. Data supporting the use of a drug for these new indications must be submitted to the FDA in a new or supplementalNDA that must be approved by the FDA before the drug can be marketed for the new indications.Orphan Drug Designation. We have received Orphan Drug designation for Korlym for the treatment of endogenous Cushing’s syndrome in both theUnited States and the EU. In the United States, Orphan Drug 16Table of Contentsdesignation provides special status to a product to treat a rare disease or condition providing that the product meets certain criteria. Orphan designationqualifies the sponsor of the product for the tax credit and marketing incentives of the Orphan Drug Act, including seven years of exclusive marketing rightsfor the specific drug for the orphan indication, if it receives the first regulatory approval for that indication, with limited exceptions. A marketing applicationfor a prescription drug product that has been designated as a drug for a rare disease or condition is not subject to a prescription drug user fee unless theapplication includes an indication for other than a rare disease or condition. Orphan Drug designation does not prevent competitors from developing ormarketing different drugs for an indication. It also does not convey an advantage in, or shorten the duration of, the review and approval process for a drug bythe applicable regulatory authority.Benefits of Orphan Drug Designation in the EU are similar to those in the U.S., but include ten years of marketing exclusivity in all 27 member states,free scientific advice during drug development, access to a centralized review process and a reduction or complete waiver of fees levied by the EuropeanMedicines Agency.Approvals outside the United States. Other than applying for and receiving Orphan Drug Designation for Korlym for Cushing’s syndrome in the EU,we have not started the regulatory approval process in any jurisdiction other than the United States and we are unable to estimate when, if ever, we willcommence the regulatory approval process in any foreign jurisdiction. We or our potential future partners will have to complete an approval process similarto the U.S. approval process in foreign target markets for our product candidates before we can commercialize our product candidates in those countries. Theapproval procedure and the time required for approval vary from country to country and can involve additional testing. Foreign approvals may not begranted on a timely basis, or at all. Regulatory approval of pricing is required in most countries other than the United States. The prices approved may be toolow to generate an acceptable return to us.Fast Track Designation. The FDA sometimes grants “fast track” status under the Food and Drug Administration Modernization Act of 1997. The fasttrack mechanism is intended to facilitate the development and approval of new drugs intended for the treatment of serious or life-threatening diseases orconditions and which demonstrate the potential to address unmet medical needs for the disease or condition. The fast track process includes scheduling ofmeetings to seek FDA input into development plans, the option of submitting an NDA serially in sections rather than submitting all componentssimultaneously, the option to request evaluation of studies using surrogate endpoints, and the potential for a priority review.We have been granted fast track status for mifepristone for the treatment of the psychotic features of psychotic depression. However, the fast trackdesignation may be withdrawn by the FDA at any time. The fast track designation does not guarantee that we will qualify for or be able to take advantage ofthe expedited review procedures and does not increase the likelihood that mifepristone will receive regulatory approval.Priority Review. The FDA has indicated to us that it will grant us a priority review of our NDA of mifepristone for the treatment of the psychoticfeatures of psychotic depression if no other medications have been approved for this indication at the time of our submission.Executive OfficersThe following table sets forth, as of March 1, 2013, information about our executive officers: Name Age Position Joseph K. Belanoff, M.D. 55 Chief Executive Officer and DirectorRobert L. Roe, M.D. 72 President and SecretaryG. Charles Robb 50 Chief Financial OfficerSteven Lo 45 Vice President of Commercial OperationsAnne M. LeDoux 65 Vice President, Controller and Chief Accounting Officer 17Table of ContentsJoseph K. Belanoff, M.D. is a co-founder of our company and has served as a member of our Board and as our Chief Executive Officer since 1999.Dr. Belanoff is currently a clinical faculty member and has held various positions in the Department of Psychiatry and Behavioral Sciences at StanfordUniversity since 1992. Dr. Belanoff received his B.A. from Amherst College and his M.D. from Columbia University’s College of Physicians & Surgeons. OurBoard selected Dr. Belanoff to serve as a director because, as our Chief Executive Officer, he brings expertise and knowledge regarding our business andoperations to our Board of Directors. Dr. Belanoff also has expertise in clinical medicine and psychopharmacology.Robert L. Roe, M.D. joined us as President in October 2001. Dr. Roe has spent more than 35 years in the pharmaceutical and biotechnology industries.From 1999 to 2001, he served as President and Chief Executive Officer of Allergenics, Inc. From 1996 to 1999, he was Executive Vice President, ChiefOperating Officer and a director of Cytel Corporation. From 1995 to 1996, he was Executive Vice President, Chief Operating Officer and a director of ChugaiBiopharmaceuticals, Inc. From 1992 to 1995, Dr. Roe served as President of the Development Research Division and Senior Vice President of SyntexCorporation. Dr. Roe received his B.A. from Stanford University and his M.D. from the University of California, San Francisco.G. Charles Robb joined us as Chief Financial Officer in September 2011. Mr. Robb has more than 25 years of experience in executive management,operations and finance. From April 2005 through August 2011 Mr. Robb served as the Senior Vice President of Operations, Administration and Finance ofFitness Anywhere, Inc. (FAI), a private fitness equipment and training company with operations in the United States, Europe and Asia. From 2003 to 2005,Mr. Robb was engaged in the private practice of law. From 2000 to 2002 he was Senior Vice President of Citadon, Inc. He also held positions in businessdevelopment for Normura Asset Capital Corporation from 1998 to 1999 and in sales and marketing for Legal Research Network, Inc. from 1996 to 1998.From 1992 to 1996 Mr. Robb practiced law at Howard, Rice, Nemerovski, Canady, Falk & Rabkin. Mr. Robb earned a B.A. in English and PoliticalPhilosophy from Yale and a J.D. from Harvard Law School, where he was a member of the Harvard Law Review.Steven Lo joined us as Vice President of Commercial Operations in September 2010. Mr. Lo has more than 18 years of commercial experience in thepharmaceutical and biotechnology industry. From 1997 to 2010, Mr. Lo held various positions in marketing, sales and managed markets at Genentech, Inc., abiotechnology company that became a member of the Roche Group in March 2009, most recently as Franchise Head, leading that company’s endocrinologymarketing and sales organization. Mr. Lo received his B.S. degree from the University of California, Davis and his Master of Health Administration from theUniversity of Southern California.Anne M. LeDoux joined us as Controller in 2004 and was promoted to the position of Vice President, Controller and Chief Accounting Officer in April2007. Ms. LeDoux has over 20 years of financial and accounting management experience with public pharmaceutical and biotechnology companies. Prior tojoining Corcept in 2004, Ms. LeDoux served in various financial positions at Aviron, Roche Biosciences and Syntex Corporation. She was also VicePresident and Chief Financial Officer at the Northern California Health Center and Vice President, Finance for the Children’s Hospital of San Francisco.Ms. LeDoux is a Certified Public Accountant with over 13 years of experience in public accounting, primarily at Coopers and Lybrand. Ms. LeDoux receivedher Bachelor of Arts degree in Business from the University of Massachusetts and a law degree from Western New England College, School of Law.EmployeesWe are managed by a core group of experienced pharmaceutical executives with a track record of bringing new drugs to market. To facilitateadvancement of development programs, we also enlist the expertise of associates and advisors with extensive pharmaceutical development experience. 18Table of ContentsAs of December 31, 2012, we had 38 full-time employees, six part-time employees, a contracted sales force of 13 sales representatives and 12 long-termcontract staff. Four of our employees have M.D.s. We consider our employee relations to be good. None of our employees is covered by a collectivebargaining agreement.GeneralWe were incorporated in the State of Delaware on May 13, 1998. Our registered trademarks include Corcept and CORLUX. A trademark is pendingwith respect to Korlym. Other service marks, trademarks and trade names referred to in this document are the property of their respective owners.Available InformationWe are subject to the information requirements of the Securities Exchange Act of 1934, as amended, and we therefore file periodic reports, proxystatements and other information with the SEC relating to our business, financial statements and other matters. The reports, proxy statements and otherinformation we file may be inspected and copied at prescribed rates at the SEC’s Public Reference Room, 100 F Street, N.E., Washington, D.C. 20549, onofficial business days during the hours of 10:00 A.M. to 3:00 P.M. You may obtain information on the operation of the SEC’s Public Reference Room bycalling the SEC at 1-800-SEC-0330. The SEC also maintains an Internet site that contains reports, proxy statements and other information regarding issuerslike us that file electronically with the SEC. The address of the SEC’s Internet site is www.sec.gov. For more information about us, please visit our website atwww.corcept.com. You may also obtain a free copy of our annual reports on Form 10-K, quarterly reports on Form 10-Q, current reports on Form 8-K andamendments to those reports on the day the reports or amendments are filed with or furnished to the SEC by visiting our website at www.corcept.com. Theinformation found on, or otherwise accessible through, our website, is not incorporated information, and does not form a part of, this Form 10-K. 19®®™Table of ContentsITEM 1A.RISK FACTORSAn investment in our common stock involves significant risks. You should carefully consider the risks described below and the other information inthis Annual Report on Form 10-K, including our financial statements and related notes, before you decide to invest in our common stock. If any of thefollowing risks or uncertainties actually occurs, our business, results of operations or financial condition could be materially harmed, the trading price ofour common stock could decline and you could lose all or part of your investment. The risks and uncertainties described below are those that we currentlybelieve may materially affect us; however, they may not be the only ones that we face. Additional risks and uncertainties of which we are unaware orcurrently deem immaterial may also become important factors that may harm our business. Except as required by law, we undertake no obligations toupdate any risk factors.Risks Related to the Commercialization of Korlymand Development of Mifepristone and Our Other Proprietary GR-II AntagonistsWe depend heavily on the success of Korlym, which we only recently began to sell. If we are unable to commercialize Korlym successfully, orexperience significant delays in doing so, we may not generate revenues as quickly as or at the levels that we or investors expect and our stock price willlikely decline.We anticipate that for the foreseeable future our ability to generate meaningful revenues and achieve profitability will be solely dependent on thesuccessful commercialization of Korlym. Many factors could harm our efforts to commercialize Korlym, including: • an inability to generate meaningful revenue due to low product usage, inadequate coverage and reimbursement or other factors; • competition from Novartis’s Signifor and from other companies with greater financial, technical and marketing resources than ours. • an inability to manufacture Korlym or the active ingredient in Korlym in commercial quantities and at an acceptable cost; • political concerns relating to other uses of mifepristone, or RU-486, that could limit the market acceptance of Korlym; • negative, inconclusive or otherwise unfavorable results from any post-approval studies we conduct; • previously unknown, serious side effects that may be identified; and • rapid technological change making Korlym obsolete.Even if we are able to commercialize Korlym successfully, we cannot predict the rate at which success will occur.As our current ability to generate revenue is wholly dependent upon the commercialization of Korlym, its rate of sale will directly and materially affectour results of operations. There are inherent difficulties in predicting the volumes of Korlym that will be sold, which are heightened by our relativeinexperience commercializing Korlym or other products. Failure of our revenue to meet the expectations of investors could cause our stock price to decline.See also the discussion below under “The failure of our financial results to meet estimates published by research analysts or other investor expectations couldcause our stock price to decline.”Physicians may accept Korlym slowly or may never accept it, which would adversely affect our financial results.Many factors may affect the market acceptance and commercial success of Korlym.Even though the FDA has approved Korlym, physicians may not adopt it as a treatment for their eligible patients. Physicians will prescribe Korlymonly if they determine, based on experience, clinical data, side effect 20Table of Contentsprofiles and other factors, that it is preferable to other products or treatments currently in use, even if those products are not approved for Cushing’s syndrome.Because Cushing’s syndrome is rare, most physicians are inexperienced in the care of patients with the illness and it may be difficult to persuade them toprescribe a new treatment, such as Korlym, even with clinical trial results that suggest that it may be a compelling treatment for them to consider.Other factors that may affect the market acceptance and commercial success of Korlym include: • the effectiveness of Korlym, including any side effects, as compared to alternative treatment methods; • the rate of adoption of Korlym by physicians and by target patient populations; • the possible preference of some physicians for more familiar, long-standing off-label treatments for Cushing’s syndrome or for Novartis’ drug,Signifor, for the treatment of Cushing’s disease; • the cost-effectiveness of Korlym and the availability of third-party insurance coverage and reimbursement, in particular from government payorssuch as Medicare and Medicaid, for patients using Korlym; • the product labeling required by the FDA for Korlym; • the extent and success of our efforts to manufacture, commercialize, market, distribute and sell Korlym; and • negative publicity concerning Korlym, RU-486, Mifeprex or mifepristone.The failure of Korlym to achieve market acceptance would prevent us from generating meaningful revenue.The Orphan Drug Designation for Korlym may not provide protection from competition and other benefits as anticipated.In July 2007, we received Orphan Drug Designation from the FDA for Korlym for the treatment of hyperglycemia secondary to hypercortisolism inadult patients with endogenous Cushing’s syndrome who have type 2 diabetes mellitus or glucose intolerance and have failed surgery or are not candidatesfor surgery. Drugs that receive Orphan Drug Designation are eligible to obtain seven years of marketing exclusivity for the approved indication from the dateof drug approval, with limited exceptions, as well as tax credits for clinical trial costs, marketing application filing fee waivers and assistance from the FDA inthe drug development process.In October 2011, the European Commission granted us Orphan Drug Designation for Korlym for the treatment of endogenous Cushing’s syndrome(hypercortisolism) in the EU. Benefits of Orphan Drug Designation in the EU are similar to those in the United States, but include ten years of marketingexclusivity for the approved indication in all 27 member states, free scientific advice during drug development, access to a centralized review process and areduction or complete waiver of fees levied by the European Medicines Agency.Although we have received Orphan Drug Designation in both the United States and the EU, we cannot be assured that we will recognize the potentialbenefits of these designations. Even after an orphan drug is approved for its orphan indication, the FDA can subsequently approve a different drug for thesame condition if the FDA concludes that the later drug is safer, more effective or makes a major contribution to patient care. In addition, the FDA may,during the seven-year orphan drug exclusivity period, approve the same drug for a different indication.Notwithstanding Korlym’s Orphan status in both the United States and the EU, in 2012 Novartis received approval in both jurisdictions to market itssomatostatin analogue Signifor for adult patients with Cushing’s disease (a subset of Cushing’s syndrome that afflicts approximately 70 percent of allCushing’s syndrome patients) for whom pituitary surgery is not an option or has not been curative. Novartis has substantially more resources and experiencethan Corcept and may provide significant competition. 21®Table of ContentsFurther, we are aware that Laboratoire HRA Pharma has received Orphan Drug Designation in the United States and the EU for the use of mifepristoneto treat a subtype of Cushing’s syndrome and has begun a Phase 2 clinical trial in Europe and the United States for this indication. We are also aware thatExelgyn Laboratories, which operates as a subsidiary of Medi Challenge (Pty) Ltd., received Orphan Drug Designation for Cushing’s syndrome in the EU, butit has stated that it has not yet conducted any clinical trials.If another drug with mifepristone as its active ingredient is approved in the EU for Cushing’s syndrome before Korlym, we will not receive the ten yearsof marketing exclusivity from the date of drug approval in the EU and other potential benefits. Any delay in our commercialization of Korlym may have anegative impact on the revenue that we might be able to realize from the exclusivity provided during the applicable periods.We will face competition from companies that attempt to develop mifepristone or other compounds for the treatment of Cushing’s syndrome, whichcould limit our future revenues from the commercialization of Korlym and which could have a negative impact on future revenues from thecommercialization of Korlym for any indication. These companies may have significantly more resources than we do.We will experience competition from Novartis, which has received approval in the United States and the EU to market Signifor (pasireotide), aninjectable somatostatin analogue, for the treatment of adult patients with Cushing’s disease (a subset of the patients with Cushing’s syndrome) for whompituitary surgery is not an option or has not been curative. We expect Novartis to begin promoting Signifor in the United States.In addition, we are aware that Laboratoire HRA Pharma has begun a Phase 2 clinical trial in Europe and the United States evaluating the use ofmifepristone to treat a subtype of Cushing’s syndrome, and that Exelgyn Laboratories may be planning to develop a Cushing’s syndrome product, althoughit has stated that it has not conducted any clinical trials to date. See also the discussion above under “The Orphan Drug Designation for Korlym may notprovide protection from competition and other benefits as anticipated.” If another product for treatment of Cushing’s syndrome or Cushing’s disease isapproved for commercialization, our potential future revenue could be reduced.If we are unable to continue to obtain acceptable prices or adequate coverage and reimbursement for Korlym from third-party payors, we will beunable to generate significant revenues.There is significant uncertainty related to the availability of third-party insurance coverage and reimbursement for newly approved medications. Thecommercial success of our medications in both domestic and international markets depends on whether third-party coverage and reimbursement is availablefor them. Government payors, including Medicare and Medicaid, health maintenance organizations and other third-party payors are increasingly attemptingto contain healthcare costs by limiting both coverage and the level of reimbursement of new medicines, and, as a result, they may not cover or provideadequate payment for our medications. Our near-term dependence on the commercial success of Korlym makes us particularly susceptible to any such costcontainment or reduction efforts. Accordingly, even though Korlym has been approved for commercial sale, unless government and other third-party payorscontinue to provide adequate and timely coverage and reimbursement, physicians may not prescribe it and patients may not purchase it. In addition,meaningful delays in insurance coverage for individual patients may increase our costs and reduce our revenues. Further, we will need to obtain approvalsfrom hospital formularies before Korlym can be reimbursed for in-patient treatment. If we fail to obtain such approvals, this will reduce the level of revenuesthat we are able to attain.In some foreign markets, pricing and profitability of prescription pharmaceuticals are subject to government control. In the United States, we expectthat there will continue to be federal and state proposals for similar controls. Also, the trends toward managed health care in the United States and recent lawsand legislation intended to reduce the cost of government insurance programs could significantly influence the purchase of health care services and productsand may result in lower prices for our products or the exclusion of such products from reimbursement programs. 22Table of ContentsIn March 2010, the Patient Protection and Affordable Care Act, as amended by the Health Care and Education Affordability Reconciliation Act,collectively referred to as the PPACA, was passed. The PPACA included, among other things, the following measures: • annual, non-deductible fees on any entity that manufactures or imports certain prescription drugs and biologics; • increases in Medicaid rebates owed by manufacturers under the Medicaid Drug Rebate Program for both branded and generic drugs; • a new Patient-Centered Outcomes Research Institute to oversee, identify priorities in and conduct comparative clinical research; • new requirements for manufacturers to discount drug prices to eligible patients by 50 percent at the pharmacy level and for mail order services inorder for their outpatient drugs to be covered under Medicare Part D; • an increase in the number of entities eligible for discounts under the Public Health Service pharmaceutical pricing program; and • establishment of a licensure framework for follow-on biologic products.The PPACA provisions on comparative clinical effectiveness research extended the initiatives of the American Recovery and Reinvestment Act of2009, also known as the stimulus package, which included $1.1 billion in funding to study the comparative effectiveness of health care treatments. Thisstimulus funding was designated for, among other things, conducting, supporting or synthesizing research that compares and evaluates the risks and benefits,clinical outcomes, effectiveness and appropriateness of products. The PPACA also appropriated additional funding to comparative clinical effectivenessresearch. Although Congress has indicated that this funding is intended to improve the quality of health care, it remains unclear how the research will impactcurrent Medicare coverage and reimbursement or how new information will influence other third-party payor policies.Since its passage, a number of state governors have strenuously opposed the mandatory purchase of insurance, referred to as the individual mandate,and aspects of voluntary Medicaid expansion under PPACA, and initiated lawsuits challenging its constitutionality. On June 28, 2012, the United StatesSupreme Court upheld the constitutionality of the individual mandate, and invalidated requirements that states forfeit certain federal funding if they do notexpand Medicaid coverage as prescribed by PPACA. The Court left the remainder of PPACA intact.In addition, other legislative changes have been proposed and adopted in the United States since the PPACA was enacted. Most recently, on August 2,2011, the Budget Control Act of 2011 among other things, created the Joint Select Committee on Deficit Reduction to recommend proposals in spendingreductions to Congress. The Joint Select Committee did not achieve its targeted deficit reduction of at least $1.2 trillion for the years 2013 through 2021,triggering the legislation’s automatic reduction to several government programs. This includes aggregate reductions to Medicare payments to providers of upto 2 percent per fiscal year, starting in 2013. On January 2, 2013, President Obama signed into law the American Taxpayer Relief Act of 2012, or the ATRA,which, among other things, delayed for another two months the budget cuts mandated by these sequestration provisions of the Budget Control Act of 2011.The ATRA also reduced Medicare payments to several providers, including hospitals, imaging centers and cancer treatment centers, and increased the statuteof limitations period for the government to recover overpayments to providers from three to five years. These new laws may result in additional reductions inMedicare and other health care funding, which could have a material adverse effect on our customers and accordingly, our financial operations.These new laws and the regulations and policies implementing them, as well as other healthcare reform measures that may be adopted in the future,may have a material adverse effect on our industry generally and on our ability to successfully develop and commercialize our products. 23Table of ContentsWe will need to continue to develop our medical education, sales and marketing capabilities to successfully commercialize Korlym and our otherproprietary, selective GR-II antagonists.To achieve commercial success for any approved product, we must either develop sales and marketing capabilities internally or enter into arrangementswith third parties to market and sell our current and future products, and we may not be successful in doing so. We continue to hire experienced field andinternal personnel to commercialize Korlym in the United States, which is expensive and time consuming. Although we received approval to market and sellKorlym in February 2012, our efforts to staff, deploy and train a marketing and medical education organization remain in an early stage. Any failure or delayin the development or failure to maintain effectively our internal capabilities for the marketing and sales of Korlym would adversely impact thecommercialization of the product. If our efforts to develop an internal commercial marketing and sales team are not successful, cost-effective and timely, wemay not achieve profitability.We will need to increase the size of our organization, and we may experience difficulties in managing growth.We expect that the development of our commercial organization and the likely future expansion of our research and development efforts will strain ouradministrative, operational and management resources. Future growth will impose significant added responsibilities on members of management, includingthe need to identify, recruit, maintain and integrate additional employees. To date, we have relied on a small management team, including a number of part-time contributors. Our future financial performance and our ability to compete effectively will depend, in part, on our ability to manage any future growtheffectively.To that end, we must be able to: • integrate additional management, clinical development, administrative and sales and marketing personnel; • expand the size and composition of our management team; • develop our administrative, accounting and management information systems and controls; • hire and train additional qualified personnel; • manage our sales and marketing efforts effectively; • maintain our supply chain effectively; • manage our clinical trials effectively; and • manage our research and development efforts effectively.We may not be able to accomplish these tasks, and our failure to accomplish any of them could harm our business.Public perception of the active ingredient in Korlym, mifepristone (also known as “RU-486”), may limit our ability to market and sell Korlym.The active ingredient in Korlym, mifepristone (RU-486), is approved by the FDA in another drug for the termination of early pregnancy. As a result,mifepristone has been and continues to be the subject of considerable ethical and political debate in the United States and elsewhere. Public perception ofmifepristone may limit our ability to engage alternative manufacturers and may limit the commercial acceptance of Korlym by patients and physicians. Eventhough we have taken measures to minimize the likelihood of the prescribing of Korlym to a pregnant woman, physicians may choose not to prescribeKorlym to a woman simply to avoid any risk of unintentionally terminating a pregnancy. We have taken measures to control the distribution of Korlym toreduce the potential for diversion and this controlled distribution may negatively impact sales of Korlym. 24Table of ContentsWe have no manufacturing capabilities and we currently depend on third parties to manufacture the active ingredient and the tablets for Korlym, bothof which are single-source suppliers. If these suppliers are unable or unwilling to continue manufacturing Korlym and we are unable to contract quicklywith alternative sources, or if these third-party manufacturers fail to comply with FDA regulations or otherwise fail to meet our requirements, ourbusiness will be harmed.We currently have no experience in, and we do not own facilities for, nor do we plan to develop facilities for, manufacturing any products. We dependon third-party contract manufacturers to supply the active pharmaceutical ingredient, or API, in Korlym and to manufacture the Korlym tablet. In addition, weexpect to use third-party manufacturers and suppliers if and when our product candidates are approved. The facilities used by our contract manufacturers tomanufacture our products must be approved by the FDA pursuant to inspections. We do not control the manufacturing processes of, and are completelydependent on, our contract manufacturing partners for compliance with the regulatory requirements, known as current good manufacturing practices, orcGMPs. If our contract manufacturers cannot successfully manufacture material that conforms to our specifications and the strict regulatory requirements ofthe FDA or others, they will not be able to secure and/or maintain regulatory approval for their manufacturing facilities. In addition, we have no control overthe ability of our contract manufacturers to maintain adequate quality control, quality assurance and qualified personnel. If the FDA or a comparable foreignregulatory authority does not approve these facilities for the manufacture of our products or if it withdraws any such approval in the future, we may need tofind alternative manufacturing facilities, which would significantly impact our ability to develop, obtain regulatory approval for or market our products. Inaddition, sanctions could be imposed on us, including fines, injunctions, civil penalties, failure of regulatory authorities to grant marketing approval of ourproduct candidates, delays, suspension or withdrawal of approvals, seizures or recalls of products, operating restrictions and criminal prosecutions, any ofwhich could harm our business.We have only one approved manufacturer of the API in Korlym, with whom our agreement expires in June 2013. We intend to continue therelationship and are in the process of negotiating a new agreement. We have a memorandum of understanding with a second API manufacturer. However,there are no activities currently being conducted at this second manufacturer’s site to develop or qualify the manufacturing processes or facilities and we didnot request approval of material produced by this second manufacturer when we submitted our NDA for Cushing’s syndrome.We have an agreement with a tablet manufacturer that we included in our NDA submission for Korlym. This tablet manufacturer has temporarilysuspended commercial production while it relocates to, and seeks regulatory approval to begin operation of, a new facility. On November 1, 2012, the FDAapproved our second Korlym tablet manufacturer as a qualified site for the manufacture of Korlym tablets, with whom we are now negotiating a commercialsupply agreement. We cannot assure you that our tablet suppliers will be able or willing to meet our future demands. If our original tablet manufacturer is notable to qualify its new site or if our second Korlym tablet manufacturer is unable to prepare Korlym tablets in the quantities and time frame required, we maynot be able to manufacture our product in a timely manner. If our suppliers were to fail to manufacture tablets on a timely basis in the quantities that werequire, or fail to maintain manufacturing capabilities that meet FDA standards, we would likely experience a lengthy delay in our manufacturing processes.Our current arrangements with these manufacturers are terminable by such manufacturers. If we are unable, for whatever reason, to obtain the API orKorlym tablets from our contract manufacturers, we may not be able to manufacture our required quantities or identify alternate manufacturers of mifepristoneor Korlym tablets in a timely manner or on reasonable terms, if at all, which would harm our business. 25Table of ContentsIf we or others identify previously unknown, serious side effects of mifepristone, we may be required to perform lengthy additional clinical trials,change the labeling of Korlym or withdraw it from the market, any of which would hinder or preclude our ability to generate revenues.The FDA’s approval of Korlym requires that we conduct a study of the interactions between Korlym and ketoconazole, an anti-fungal agent sometimesused to treat patients with Cushing’s syndrome. It also requires us to study drug utilization to better characterize the reporting rates of adverse eventsassociated with the long-term use of Korlym. If we or others identify previously unknown, serious side effects of mifepristone: • regulatory authorities may withdraw their approvals; • we may be required to conduct additional clinical trials, make changes in labeling, implement changes to or obtain re-approvals of ourmanufacturing facilities; • we may experience a significant drop in the sales of Korlym; • our reputation in the marketplace may suffer; and • we may become the target of lawsuits, including class action lawsuits.Any of these events could harm or prevent sales of the affected products or could increase the costs and expenses of commercializing and marketingKorlym.We may have substantial exposure to product liability claims and may not have adequate insurance to cover those claims.We may be subject to product liability or other claims based on allegations that the use of our products has resulted in adverse effects or that ourproduct candidates are not effective, whether by participants in our clinical trials for Korlym or other product candidates, or by patients using Korlym. Aproduct liability claim may damage our reputation by raising questions about Korlym or any of our product candidates’ safety or efficacy and could limit ourability to sell a product by preventing or interfering with product commercialization. In some cases, less common adverse effects of a pharmaceutical productare not known until long after the FDA approves the product for marketing. The active ingredient in Korlym is used to terminate pregnancy. Therefore,clinicians using the medicine in our clinical trials and physicians prescribing the medicine to women with childbearing potential must take necessary andstrict precautions to ensure that the medicine is not administered to pregnant women. The failure to observe these precautions could result in significantproduct claims.We have only limited product liability insurance coverage, with limits that we believe to be customary for a company beginning to commercialize itsfirst pharmaceutical product. We intend to expand our product liability insurance coverage to any product candidates for which we obtain marketingapproval. However, this insurance may be prohibitively expensive or may not fully cover our potential liabilities. Our inability to obtain adequate insurancecoverage at an acceptable cost could prevent or inhibit the commercialization of Korlym or any of our product candidates, or result in meaningfulunderinsured or uninsured liability. Defending a lawsuit could be costly and significantly divert management’s attention from conducting our business. If athird party successfully sues us for any injury caused by our product candidates, our liability could exceed our total assets.Even if we receive regulatory approval for our product candidates, we will be subject to ongoing and continued regulatory review, and if we are unableto maintain regulatory approval of Korlym, or if we fail to comply with regulatory requirements, we will be unable to generate revenue or may besubject to penalties and our business will be harmed.Even after we obtain U.S. regulatory approval for a product, the FDA may still impose significant restrictions on the approved indicated uses for whichthe product may be marketed or on the conditions of approval. For example, a product’s approval may contain requirements for potentially costly post-approval studies and surveillance, including phase 4 clinical trials, to monitor the safety and efficacy of the product. The 26Table of ContentsFDA’s approval of Korlym was subject to limitations on the indicated uses for which the product may be marketed and requirements for post-marketingfollow-up studies and information reporting. In addition, the FDA’s approval of Korlym requires that we conduct a study of the interactions between Korlymand ketoconazole, an anti-fungal agent sometimes used to treat patients with Cushing’s syndrome. It also requires us to conduct a drug utilization study tobetter characterize the reporting rates of adverse events associated with the long-term use of Korlym.We will also be subject to ongoing obligations and continued regulatory review by the FDA and other regulatory authorities in the United States andother countries with respect to the research, testing, manufacturing, labeling, distribution, adverse event reporting, storage, selling, advertising, promotion,recordkeeping and marketing of products. These requirements include submissions of safety and other post-marketing information and reports, annualupdates on manufacturing activities and continued compliance with cGMPs and cGCPs for any clinical trials that we conduct post-approval. Later discoveryof previously unknown problems with a product, including adverse events of unanticipated severity or frequency, or with our third-party manufacturers ormanufacturing processes, or failure to comply with FDA regulations and other applicable foreign and U.S. regulatory requirements may result in, among otherthings, warning letters, civil and criminal penalties, injunctions, holds on clinical trials, product seizure or detention, refusal to permit the import or export ofproducts, restrictions on product marketing, withdrawal of the product from the market, voluntary or mandatory product recalls, total or partial suspension ofproduction, refusal to approve pending NDAs or supplements to approved NDAs, and suspension or revocation of product approvals.The FDA’s policies may change and additional governmental regulations may be enacted that could prevent, limit or delay regulatory approval of ourproduct candidates. If we are slow or unable to adapt to changes in existing requirements or the adoption of new requirements or policies, or if we are not ableto maintain regulatory compliance, we may place at risk any marketing approval that we may have obtained, which would adversely affect our business,prospects and ability to achieve or sustain profitability.The sale of our products is subject to regulatory approvals, and our business is subject to extensive regulatory requirements, and if we are unable toobtain regulatory approval for future product candidates, including mifepristone for the treatment of the psychotic features of psychotic depression, wewill be limited in our ability to commercialize such product candidates and our business will be harmed.We are not permitted to market or promote any of our product candidates before we receive regulatory approval from the FDA or comparable foreignregulatory authorities, and we may never receive such regulatory approval for any of our product candidates. Obtaining regulatory approval of a new drug isan uncertain, lengthy and expensive process, and success is never guaranteed. Despite the time, resources and effort expended, failure can occur at any stage.In order to receive approval from the FDA for each product candidate, we must demonstrate that the new drug product is safe and effective for its intended useand that our manufacturing processes for the product candidate comply with the FDA’s cGMPs. cGMPs include requirements related to production processes,quality control and assurance, and recordkeeping. The FDA has substantial discretion in the approval process for human medicines. The FDA may requiresubstantial additional clinical testing or find our drug products do not satisfy the standards for approval. Our inability or the inability of our suppliers tocomply with applicable FDA and other regulatory requirements can result in, among other things, delays in or denials of new product approvals, warningletters, fines, consent decrees restricting or suspending manufacturing operations, injunctions, civil penalties, recall or seizure of products, total or partialsuspension of sales, and/or criminal prosecution. Any of these or other regulatory actions could materially adversely affect our business and our financialcondition.Future governmental action or changes in FDA law, policy or personnel may also result in delays or rejection of an NDA in the United States. Inaddition, because the only other currently FDA-approved use of mifepristone is the termination of pregnancy, we expect that the label for mifepristone forany indication will include, as Korlym’s does, some limitations, including a so-called “black-box” warning that it should not be used by pregnant women orwomen seeking to become pregnant. 27Table of ContentsIf we receive regulatory approval for our future product candidates, including mifepristone for the treatment of psychotic depression, we will be subjectto ongoing FDA obligations and continued regulatory oversight and review, such as continued safety reporting requirements; and we may also be subject toadditional FDA post-marketing restrictions and obligations, such as a Risk Evaluation and Mitigation Strategy. If we are not able to maintain regulatorycompliance, we may not be permitted to market our product candidates and/or may be subject to product recalls or seizures.Any regulatory approvals that we receive for our future product candidates may also be subject to limitations on the indicated uses for which themedicine may be marketed or contain requirements for potentially costly post-marketing follow-up studies. In addition, if the FDA approves any of ourproduct candidates, we will be subject to ongoing and continuing regulatory requirements. See also the discussion above under “Even if we receiveregulatory approval for our product candidates, we will be subject to ongoing and continued regulatory review, and if we are unable to maintain regulatoryapproval of Korlym, or if we fail to comply with regulatory requirements, we will be unable to generate revenue or may be subject to penalties and ourbusiness will be harmed.”If we market products in a manner that violates FDA regulations or health care fraud and abuse laws, we may be subject to civil or criminal penalties.In the United States, we are subject to FDA regulations governing the promotion of health care products. Although physicians are permitted, based ontheir medical judgment, to prescribe drugs for indications other than those approved by the FDA, manufacturers are prohibited from promoting their productsfor such “off-label” uses. In the United States, we are marketing Korlym for treatment of hyperglycemia secondary to hypercortisolism in adult patients withendogenous Cushing’s syndrome who have type 2 diabetes mellitus or glucose intolerance and have failed surgery or are not candidates for surgery andprovide promotional materials and training programs to physicians regarding the use of Korlym for this indication. Although we believe our marketingmaterials and training programs for physicians do not constitute “off-label” promotion of Korlym, the FDA may disagree. If the FDA determines that ourpromotional materials, training or other activities by our employees or agents constitute “off-label” promotion of Korlym, it could request that we modify ourtraining or promotional materials or other activities or subject us to regulatory enforcement actions, including the issuance of a warning letter, injunction,seizure, civil fine and criminal penalties. It is also possible that other federal or state enforcement authorities might take action if they believe that the allegedimproper promotion led to the submission and payment of claims for an unapproved use, which could result in significant fines or penalties under otherstatutory authorities, such as laws prohibiting false claims for reimbursement. Even if it is later determined that we are not in violation of these laws, we maybe faced with negative publicity, incur significant expenses defending our position and have to divert significant management resources from other matters.In addition, there are health care fraud and abuse regulations and enforcement by both the federal government and the states in which we conduct ourbusiness. The laws that may affect our ability to operate include: • the federal health care programs’ Anti-Kickback Statute, which prohibits, among other things, persons from knowingly and willfully soliciting,receiving, offering or paying remuneration, directly or indirectly, in exchange for or to induce either the referral of an individual for, or thepurchase, order or recommendation of, any good or service for which payment may be made under federal health care programs such as theMedicare and Medicaid programs; • federal false claims laws, which prohibit any person from knowingly presenting, or causing to be presented, a false claim for payment to thefederal government, or knowingly making, or causing to be made, a false statement to get a false claim paid. Pharmaceutical companies havebeen prosecuted under these laws for a variety of promotional and marketing activities, such as allegedly providing free product to or enteringinto “sham” consulting arrangements with customers to induce such customers to purchase, order or recommend the company’s products inviolation of the Anti-Kickback Statute and 28Table of Contents federal false claims laws and regulations; reporting to pricing services inflated average wholesale prices that were then used by certaingovernmental programs to set reimbursement rates; engaging in the promotion of “off-label” uses that caused customers to submit claims to andobtain reimbursement from governmental payors for non-covered “off-label” uses; and submitting inflated best price information to theMedicaid Drug Rebate Program; • the federal Health Insurance Portability and Accountability Act of 1996 (HIPAA), which created federal criminal laws that prohibit executing ascheme to defraud any health care benefit program or making false statements relating to health care matters; • federal “sunshine” laws that require transparency regarding financial arrangements with health care providers, such as the reporting anddisclosure requirements imposed by the PPACA on drug manufacturers regarding any “transfer of value” made or distributed to prescribers andother health care providers. Manufacturers will be required to begin data collection on August 1, 2013 and report such data to the Centers forMedicare and Medicaid Services (known as “CMS”) by March 31, 2014; and • state law equivalents of each of the above federal laws, such as anti-kickback and false claims laws which may apply to items or servicesreimbursed by any third-party payor, including commercial insurers.Some states, such as California, Massachusetts, Minnesota, Nevada, Vermont and Washington, as well as the District of Columbia, mandateimplementation of commercial compliance programs to ensure compliance with these laws.The risk of our being found in violation of these laws and regulations is increased by the fact that many of them have not been fully interpreted by theregulatory authorities or the courts, and their provisions are open to a variety of interpretations. Moreover, recent health care reform legislation hasstrengthened these laws. For example, the PPACA, among other things, amended the intent requirement of the federal anti-kickback and criminal health carefraud statutes; a person or entity no longer needs to have actual knowledge of these statutes or specific intent to violate them. In addition, the PPACAprovided that the government may assert that a claim including items or services resulting from a violation of the federal anti-kickback statute constitutes afalse or fraudulent claim for purposes of the false claims statutes. If our operations are found to be in violation of any of the laws described above or any othergovernmental regulations that apply to us, we may be subject to penalties, including civil and criminal penalties, damages, fines, exclusion fromgovernmental health care programs, and the curtailment or restructuring of our operations, any of which could adversely affect our ability to operate ourbusiness and our financial results.Clinical drug development involves a lengthy and expensive process with an uncertain outcome, and results of earlier studies and trials may not bepredictive of future trial results.Clinical development is a long, expensive and uncertain process, and data obtained from clinical trials and supportive studies are susceptible tovarying interpretations, which could delay, limit or prevent regulatory approval. The results from early clinical trials may not be predictive of results to beobtained in later clinical trials. Product candidates in later stages of clinical trials may fail to show the desired safety and efficacy traits despite havingprogressed through preclinical studies and initial clinical trials. A number of companies in the biopharmaceutical industry have suffered significant setbacksin advanced clinical trials due to lack of efficacy or adverse safety profiles, notwithstanding promising results in earlier trials. Clinical trials may notdemonstrate sufficient safety and efficacy to obtain the necessary regulatory approvals or a commercially viable product. To gain regulatory approval fromthe FDA to market mifepristone for the psychotic features of psychotic depression, our ongoing phase 3 clinical trial must demonstrate the safety and efficacyof mifepristone for that indication. The ongoing phase 3 clinical trial of mifepristone for the treatment of the psychotic features of psychotic depression maynot demonstrate efficacy or safety results sufficient for approval, and we may need to conduct other studies in support of a potential NDA in that indication. Ifour ongoing phase 3 clinical trial is not 29Table of Contentscompleted or conducted as planned or if mifepristone does not prove to be safe and effective or does not receive required regulatory approvals, thecommercialization of mifepristone for the psychotic features of psychotic depression would be delayed or prevented, and our ability to generate revenueswould be impaired.Moreover, the commencement and completion of clinical trials may be delayed by many factors that are beyond our control, including: • delays obtaining regulatory approval to commence a trial; • reaching agreement on acceptable terms with contract research organizations, or CROs, and clinical trial sites; • obtaining institutional review board, or IRB, approval at each site; • slower than anticipated patient enrollment; • scheduling conflicts with participating clinicians and clinical institutions; • lack of funding; • negative or inconclusive results; • patient noncompliance with the protocol; • adverse medical events or side effects among patients during the clinical trials; • negative or problematic FDA inspections of our clinical operations or manufacturing operations; and • real or perceived lack of effectiveness or safety of mifepristone.We could encounter delays if a clinical trial is suspended or terminated by us, the IRBs of the clinical trial sites in which such trials are beingconducted, by the Data Safety Monitoring Board, or DSMB, for such trial or by the FDA or other regulatory authorities. Such authorities may impose such asuspension or termination due to a number of factors, including failure to conduct the clinical trial in accordance with regulatory requirements or our clinicalprotocols, inspection of the clinical trial operations or trial site by the FDA or other regulatory authorities resulting in the imposition of a clinical hold,unforeseen safety issues or adverse side effects, failure to demonstrate a benefit from using a drug, changes in governmental regulations or administrativeactions or lack of adequate funding to continue the clinical trial.We may decide, or the FDA or other regulatory authorities may require us, to pursue additional clinical or preclinical studies on mifepristone for thetreatment of the psychotic features of psychotic depression. Additional trials or studies may require additional funding, the availability of which is notassured. Also, it is possible that additional trials or studies that we decide are necessary or desirable will delay or prevent the completion of the developmentof mifepristone for treating the psychotic features of psychotic depression. Even if we are able to conduct all of the clinical trials and supportive studies thatwe consider appropriate for an optimal NDA, we may never receive regulatory approval to market mifepristone for psychotic depression.Our use of MedAvante to provide centralized psychiatric rating services in Study 14, our ongoing clinical trial evaluating mifepristone for thepsychotic features of psychotic depression, may not result in any improvement in the accuracy and consistency of the psychiatric assessments and maycontinue to slow the pace of enrollment in Study 14.In connection with our ongoing phase 3 trial evaluating mifepristone for the psychotic features of psychotic depression, Study 14, we engagedMedAvante to provide centralized psychiatric rating services. MedAvante is providing centralized psychometric assessments via high resolution video-conferencing. The use of MedAvante’s centralized rating services is intended to increase the accuracy and consistency of the psychiatric assessments. 30Table of ContentsMedAvante has provided similar centralized rating services to companies conducting clinical studies in various psychiatric disorders. However, theyhave not previously provided centralized rating services to any study in patients with psychotic depression. Although we and MedAvante conducted a smallpilot evaluation in patients with psychotic depression to assess patient receptivity, we cannot be certain that centralized rating will be successful with thepatients enrolled in our study.If patients are uncomfortable or unwilling to participate in the centralized rating process or if MedAvante is unable to provide services in a satisfactorymanner over the course of the trial, we may not see any improvement in the accuracy or reliability of the psychiatric assessments. Such a result mightdiminish the likelihood of a successful trial or a definitive demonstration of the efficacy of mifepristone in treating the psychotic features of psychoticdepression.During screening for Study 14, there has been a higher than anticipated incidence of potential patients who do not meet appropriate criteria forentrance into the trial for diagnostic and other clinical reasons. Although we believe that this is the result of improved accuracy in the screening processresulting from the use of the MedAvante centralized rating services as an additional step in the selection of patients appropriate for inclusion in the study,MedAvante’s diagnostic screening may not actually improve trial performance. In addition, in mid-2009, in order to lower expenses and to conserve financialresources, we scaled back our planned rate of spending on this trial and extended the timeline for its completion. Our current plan is to increase the number ofclinical sites from eight to approximately 20, which will increase our rate of spending on the trial, with an unknown effect on the likelihood of success.In order to meet our goal of enrolling a sufficient number of patients in Study 14 by the end of 2013 to perform a successful interim analysis, we willneed to increase the pace of enrollment which will be costly and may not be successful.The pace of enrollment in Study 14 is subject to a number of factors, including our ability to identify, qualify and enlist new trial sites, our ability toidentify potential study subjects and enroll them in the trial, and the ability and willingness of patients in the trial to complete the study protocol.Furthermore, we will need to work with our existing third-party service providers and may need to retain additional personnel to support our effort to increasethe rate of Study 14 enrollment, which will be costly, and we may not be successful in these efforts. Finally, even if we succeed in increasing the rate ofenrollment in Study 14, this will not necessarily allow us to demonstrate the efficacy of the medicine.If we conduct an interim analysis of the data from our on-going Phase 3 trial of mifepristone for the treatment of psychotic depression (Trial 14), theresults may not show efficacy. If the interim results are inconclusive and we continue the study, conducting an interim analysis will make achieving apositive result more difficult.One of our goals is to enroll a sufficient number of patients in Trial 14 by the end of 2013 so that we can, if we choose, perform an interim analysis ofthe study’s data. We have not yet determined whether we will perform such an analysis or what its parameters might be. Regardless of how many patients weenroll in Trial 14 by the end of 2013, there can be no assurance that an interim analysis will take place.Even if we reach our patient enrollment goal and choose to perform an interim analysis, its results may be negative or inconclusive. If they arenegative, then we will terminate the trial and either incur the substantial additional expense and delay of undertaking a new trial, or discontinue the study ofmifepristone for the psychotic features of psychotic depression, which may reduce our future revenue. If the results are inconclusive, and we choose tocontinue the trial, we will incur additional expense and delay the possibility of our obtaining regulatory approval of a treatment for this disease.In addition, performing an interim analysis makes the measure of statistical significance in any continued trial more rigorous and more difficult tomeet. Therefore, a continued trial following an interim analysis is generally less likely to achieve a statistically meaningful positive outcome, making it moredifficult to achieve a positive result. 31Table of ContentsWe depend on third parties to conduct and manage many of our clinical trials and to perform related data collection and analysis and, if these thirdparties do not successfully carry out their contractual duties or meet expected timelines, we may face costs and delays that may prevent or delay usfrom obtaining regulatory approval for or commercializing our product candidates, which could substantially harm our business.We rely on clinical investigators and clinical sites to enroll patients and other third parties such as clinical research organizations, or CROs, to managemany of our trials and to perform related data collection and analysis. We control only certain aspects of these third parties’ activities. Nevertheless, we areresponsible for ensuring that each of our studies is conducted in accordance with the applicable protocol, legal, regulatory and scientific standards, and ourreliance on third parties does not relieve us of our regulatory responsibilities. We and these third parties are required to comply with current good clinicalpractices, or cGCP, which are regulations and guidelines enforced by the FDA and comparable foreign regulatory authorities through periodic inspections oftrial sponsors, clinical investigators and clinical sites. If we or any of the third parties working on or conducting our trials fail to comply with applicablecGCPs, the clinical data generated in our clinical trials may be deemed unreliable and the FDA or comparable foreign regulatory authorities may require us toperform additional clinical trials before approval of our marketing applications, if at all. We cannot assure you that upon inspection by a given regulatoryauthority, such regulatory authority will determine that any of our clinical trials complies with cGCP requirements. In addition, our clinical trials must beconducted with product produced under cGMP regulations. Our failure to comply with these regulations may require us to repeat clinical trials, which woulddelay the regulatory approval process. Moreover, we may not be able to control the timing of identification and selection of appropriate sites for our plannedtrials and the amount and timing of resources that the clinical sites that conduct the clinical testing may devote to our clinical trials. If our clinicalinvestigators and clinical sites fail to enroll a sufficient number of patients in our clinical trials or fail to enroll them on our planned schedules, we will beunable to complete our trials or to complete them as planned, which could delay or prevent us from completing the clinical development of mifepristone forthe psychotic features of psychotic depression or other development programs.We have an agreement with a CRO that is conducting our ongoing phase 3 trial evaluating mifepristone for the treatment of the psychotic features ofpsychotic depression (Study 14) to supervise and monitor clinical site performance and to perform investigator supervision, data collection and analysis forthis trial. The conduct of future clinical trials may also be conducted through the use of CROs and third party clinical sites. We may not be able to maintainrelationships with this or other CROs or with the clinical investigators and the clinical sites through the completion of all trial activities without delays inanticipated timing of trial activities or excessive expenditures. If any of our relationships with CROs or other third parties terminates, we may not be able toenter into arrangements with alternative CROs or third parties on commercially reasonable terms, or at all. If these CROs, clinical investigators, clinical sitesor other third parties do not carry out their contractual duties or obligations or fail to meet expected deadlines, or if they need to be replaced or if the qualityor accuracy of the clinical data they obtain is compromised due to their failure to adhere to our clinical protocols or regulatory requirements or for otherreasons, our clinical trials may be extended, delayed or terminated and we may be unable to obtain regulatory approval for, or successfully commercialize,mifepristone for the psychotic features of psychotic depression.Failure to obtain regulatory approval in foreign jurisdictions will prevent us from commercializing Korlym and our other product candidates abroad.We may seek to commercialize our products and product candidates in international markets with the help of one or more partners or on our own.Outside the United States, we may commercialize a product only if we receive a marketing authorization and, in many cases, pricing approval, from theappropriate regulatory authorities, whose approval processes include all of the risks associated with the FDA approval process, and, in some cases, additionalrisks. The approval procedure varies among countries and can involve additional testing, and the time required to obtain approval may differ from thatrequired to obtain FDA approval. Other than seeking and receiving Orphan Drug Designation in the EU, we have not taken any actions to obtain foreignapprovals. We may not develop our product candidates in the clinic in order to obtain foreign regulatory approvals on a timely basis, if at all. 32Table of ContentsApproval by the FDA does not ensure approval by regulatory authorities in other countries, and approval by one foreign regulatory authority does notensure approval by regulatory authorities in other foreign countries or by the FDA, but a failure or delay in obtaining regulatory approval in one country mayhave a negative effect on the regulatory process in others. We may not be able to file for regulatory approvals and may not receive necessary approvals tocommercialize our product candidates in any foreign market.The “fast track” designation for the development program of mifepristone for the treatment of the psychotic features of psychotic depression may notlead to a faster development or regulatory review or approval process.If a human medicine is intended for the treatment of a serious or life-threatening disease or condition and the medicine demonstrates the potential toaddress unmet medical needs for this disease or condition, the sponsor of an IND may apply for FDA “fast track” designation for a particular indication.Marketing applications submitted by sponsors of product candidates in fast track development may qualify for expedited FDA review under the policies andprocedures offered by the FDA, but the fast track designation does not assure any such qualification. Although we have obtained a fast track designation fromthe FDA for mifepristone for the treatment of the psychotic features of psychotic depression, we may not experience a faster development process, review orapproval compared to applications considered for approval under conventional FDA procedures. In addition, the FDA may withdraw our fast trackdesignation at any time. If we lose our fast track designation, the approval process may be delayed. In addition, our fast track designation does not guaranteethat we will qualify for or be able to take advantage of the expedited review procedures and does not increase the likelihood that mifepristone will receiveregulatory approval for the treatment of the psychotic features of psychotic depression.We face competition from companies with substantial financial, technical and marketing resources, which could limit our future revenues from thecommercialization of mifepristone for the treatment of the psychotic features of psychotic depression or for other indications.The biotechnology and pharmaceutical industries are intensely competitive and subject to rapid and significant technological change. If approved forcommercial use as a treatment for the psychotic features of psychotic depression, mifepristone will compete with established treatments, including ECT andcombination medicinal therapy.Combination medicinal therapy consists of the use of antipsychotic and antidepressant medicines not currently approved for the treatment of psychoticdepression. The antipsychotics are prescribed by physicians for off-label use to treat the psychotic features of psychotic depression, which is the clinicaltarget of mifepristone. Antipsychotics include Abilify (Bristol-Myers Squibb), Clozaril (Novartis), Geodon and Navane (Pfizer), Haldol (Ortho-McNeil),Mellaril (Mylan), Risperdal (Janssen Pharmaceuticals), Seroquel (AstraZeneca), Stelazine and Thorazine (GlaxoSmithKline) and Zyprexa (Eli Lilly).Mifepristone may not compete effectively with these established treatments. We are aware of one clinical trial conducted by Organon, for a new chemicalentity for the treatment of psychotic depression. Organon was the pharmaceutical division of Akzo Nobel, which was purchased by Schering Plough whichwas then subsequently acquired by Merck & Co. Organon’s new chemical entity is a GR-II antagonist; we believe that its commercial use would be coveredby our patent.Our present and potential competitors include major pharmaceutical companies such as the makers of the drugs identified above, as well as specializedpharmaceutical firms, universities and public and private research institutions. Moreover, we expect competition to intensify as technical advances are made.These competitors, either alone or with collaborative parties, may succeed with the development and commercialization of medicinal products that aresuperior to and more cost-effective than mifepristone. Many of our competitors and related private and public research and academic institutions have greaterexperience, more financial and marketing resources and larger research and development staffs than we do. In addition, many of these competitors, eitheralone or together with their collaborative partners, have significantly greater experience than we do in developing human medicines, obtaining regulatoryapprovals, manufacturing and commercializing products. 33®®®®®®®®®®®Table of ContentsAccordingly, mifepristone may not be an effective competitor against established treatments and our present or potential competitors may succeed indeveloping medicinal products that are superior to mifepristone or render mifepristone obsolete or non-competitive. If we are unable to establish mifepristoneas a superior and cost-effective treatment for the psychotic features of psychotic depression, or any future use, we may be unable to generate the revenuesnecessary to support our business.Our efforts to discover, develop and commercialize new product candidates beyond mifepristone are at a very early stage. If we fail to identify anddevelop additional uses for GR-II antagonists, we may be unable to market additional products.To develop additional potential sources of revenue, we believe that we must identify and develop additional product candidates. We own or haveexclusively licensed issued U.S. patents covering the use of GR-II antagonists to treat psychotic depression, mild cognitive impairment, weight gain due totreatment with antipsychotic medication, stress disorders, early dementia, delirium, gastroesophageal reflux disease, Down’s Syndrome, catatonia andpsychosis associated with cocaine addiction, and to increase the therapeutic response to electroconvulsive therapy (ECT). In addition, we have nine U.S.method-of-use patent applications covering GR-II antagonists for the treatment of a number of other metabolic and psychiatric disorders, three U.S.composition of matter patents covering specific GR-II antagonists, and two additional U.S. composition of matter patents are pending. We have also filedpatent applications in the major international markets.The use of GR-II antagonists may not be effective to treat these conditions or any other indications. Moreover, we could discover that the use of GR-IIantagonists in these patient populations has unacceptable side effects or is otherwise not safe. Due to the risks of efficacy and side effects inherent indeveloping novel compounds, we are likely to enter multiple compounds into development, which would increase our rate of spending with no assurancethat we will be successful in developing new drugs that are safe and effective.In addition, we may not develop or continue to develop product candidates for any of the indications or compounds covered by our patents and patentapplications. Typically, there is a high rate of attrition for product candidates in preclinical and clinical trials, and our product development efforts may notlead to commercially viable products.We may elect to enter into collaboration arrangements with respect to one or more of our product candidates. If we do enter into such an arrangement,we would be dependent on a collaborative partner for the success of the product candidates developed under the arrangement. Any future collaborativepartner may fail to successfully develop or commercialize a product candidate under a collaborative arrangement.We only have significant clinical experience with mifepristone and we may determine that mifepristone is not desirable for uses other than for thetreatment of hyperglycemia secondary to hypercortisolism in adult patients with endogenous Cushing’s syndrome who have type 2 diabetes mellitus orglucose intolerance and have failed surgery or are not candidates for surgery and, potentially, for the psychotic features of psychotic depression. For example,we do not intend to develop mifepristone for mitigation of the weight gain associated with the use of Zyprexa, Risperdal or other atypical antipsychotics,even though we have reported positive results in the proof of concept studies described in Part I, Item 1, Business - Overview - Mifepristone Proof-of-ConceptStudies, Other Metabolic Disorders of our Annual Report on Form 10-K for the year ended December 31, 2012. We are pursuing other GR-II antagonists forthis use. The compounds developed pursuant to our early clinical, preclinical and discovery research programs, including CORT 108297, may fail to becomeviable product candidates regardless of the resources we may dedicate to the program. Even if product candidates are identified, we may abandon furtherdevelopment efforts before we reach clinical trials or after expending significant expense and time conducting clinical trials due to financial constraints,concerns over the safety or efficacy of the product candidates, manufacturing difficulties or other reasons. Moreover, governmental authorities may enact newlegislation or regulations that could limit or restrict our development efforts. If we are unable to successfully discover and commercialize new uses for GR-IIantagonists, we may be unable to generate sufficient revenue to support our operations. 34Table of ContentsIf we lose our key personnel or are unable to attract and retain additional skilled personnel, we may be unable to pursue our product development andcommercialization efforts.Our ability to operate successfully and manage our potential future growth depends significantly upon retaining key research, technical, sales,marketing, managerial and financial personnel, and attracting and retaining additional highly qualified personnel in these areas. We depend substantially onthe principal members of our management and scientific staff. We do not have agreements with any of our executive officers that provide for their continuedemployment with us or employment insurance covering any of our key personnel. Any officer or employee can terminate his or her relationship with us at anytime and work for one of our competitors. The loss of these key individuals could result in competitive harm because we could experience delays in ourproduct research, development and commercialization efforts without their expertise.We face intense competition for qualified personnel from numerous companies, as well as universities and nonprofit research organizations in thehighly competitive San Francisco Bay Area. Although we believe that we have been successful in attracting and retaining qualified personnel to date, wemay not be able to attract and retain sufficient qualified personnel in the future. The inability to attract and retain these personnel could result in delays in theresearch, development and commercialization of our potential products.Rapid technological change could make our product candidates obsolete.Pharmaceutical technologies have undergone rapid and significant change and we expect that they will continue to do so. Our future will depend inlarge part on our ability to maintain a competitive position with respect to these technologies. Any products and processes that we develop may becomeobsolete or uneconomical before we recover any or all expenses incurred in connection with their development. Rapid technological change could make ourproduct candidates obsolete or uneconomical, which could materially adversely affect our business, financial condition and results of operations.The occurrence of a catastrophic disaster or other similar events could cause damage to our own or our manufacturers’ facilities and equipment, whichcould require us to cease or curtail operations.Because our executive offices are located in the San Francisco Bay Area and some of our current manufacturers are also located in earthquake-proneareas, our business is vulnerable to damage from various types of disasters or other similarly disruptive events, including earthquake, fire, flood, power lossand communications failures. In addition, political considerations relating to mifepristone may put us and our manufacturers at increased risk for terroristattacks, protests or other disruptive events. If any disaster or other similar event were to occur, we may not be able to operate our business and ourmanufacturers may not be able to produce our product candidates. Our insurance may not be adequate to cover, and our insurance policies may excludecoverage for, our losses resulting from disasters or other business interruptions.We rely significantly on information technology and any failure, inadequacy, interruption or security lapse of that technology, including any cybersecurity incidents, could harm our ability to operate our business effectively.Despite the implementation of security measures, our internal computer systems and those of third parties with which we contract are vulnerable todamage from cyber-attacks, computer viruses, unauthorized access, natural disasters, terrorism, war and telecommunication and electrical failures. Systemfailures, accidents or security breaches could cause interruptions in our operations, and could result in a material disruption of our clinical andcommercialization activities and business operations, in addition to possibly requiring substantial expenditures of resources to remedy. The loss of clinicaltrial data could result in delays in our regulatory approval efforts and significantly increase our costs to recover or reproduce the data. To the extent that anydisruption or security breach were to result in a loss of, or damage to, our data or applications, or inappropriate disclosure of confidential or proprietaryinformation, we could incur liability and our product research, development and commercialization efforts could be delayed. 35Table of ContentsRisks Related to Our Capital Needs and Financial ResultsWe may need additional capital in order to complete the development and commercialization of our proprietary, selective GR-II antagonists.Additional capital may not be available to us at all or on favorable terms, which could adversely affect our business.We may have to perform more clinical trials, in addition to our ongoing phase 3 trial, prior to submitting an NDA for mifepristone for the treatment ofthe psychotic features of psychotic depression. If so, we may need to raise additional funds to complete the development of mifepristone for that indication.In addition, we may need to raise additional funds to continue and expand the development of our proprietary, selective GR-II antagonists in variousindications. We may also raise additional funds for other research and development activities, including clinical trials, and working capital and for othergeneral corporate purposes, or to acquire or invest in businesses, products and technologies that are complementary to our own.Factors impacting our cash position and future prospects of liquidity include the following: • the amount and timing of revenues from the commercialization of Korlym; • the pace at which physicians adopt Korlym as a treatment; • the willingness of insurance companies, the government and other third-party payors to provide coverage for Korlym at reasonable rates; • changes in the coverage and reimbursement policies of third-party insurance companies or government agencies; • the costs, timing of site selection and enrollment of our clinical trials; • the results of our research efforts and clinical trials; • the need to perform additional clinical trials and other supportive studies; • the timing of the submission of an NDA to the FDA, the acceptance of the NDA submission, and the outcome of the FDA approval process for themarketing of mifepristone for the treatment of the psychotic features of psychotic depression; • the timing of commercialization of mifepristone for the treatment of psychotic depression; • developments or disputes concerning patents or proprietary rights, including announcements of claims of infringement, interference or litigationagainst us or our licensors; • actual or anticipated fluctuations in our operating results; • changes in our growth rates; and • changes in our research and development plans for our proprietary, selective GR-II antagonists.Consequently, we may need additional funding sooner than anticipated. In addition, we may choose to raise additional capital due to marketconditions or strategic considerations even if we believe we have sufficient funds for our current and future operating plans.We cannot be certain that additional funding will be available on acceptable terms or at all. Even though we have raised funds a number of times in thepast, market and economic conditions may make it difficult for us to raise any or sufficient additional capital. Our sales of common stock and warrants andthe exercises of warrants have been dilutive to stockholders and any exercise of outstanding warrants and additional equity financing could cause furtherdilution to stockholders. Debt financing, if available, may involve restrictive covenants. If we obtain funds through collaborations with others, thesearrangements may be on unfavorable terms or may require us to relinquish certain rights to Korlym, our technologies or product candidates, which we wouldotherwise seek to develop on our own. If adequate funds are not available, we may be required to delay, reduce the scope of or eliminate one or more of ourresearch or development programs or we may be required to discontinue operations. 36Table of ContentsWe have incurred losses since inception and anticipate that we will incur continued losses for at least the next few years.We have a limited history of operations and have focused primarily on clinical trials. We have begun to commercialize Korlym and, if the outcome ofour clinical trials supports it, we plan to seek FDA regulatory clearance to market mifepristone for the treatment of the psychotic features of psychoticdepression. Historically, we have funded our operations primarily from the sale of our equity securities. We have incurred losses in each year since ourinception in 1998. As of December 31, 2012, we had an accumulated deficit of $246.6 million. We only began to sell our first commercial product, Korlym,in the United States in April 2012. Based on this limited experience marketing Korlym, it is difficult for us to predict the magnitude or timing of futureproduct sales. We expect our research and development expenses to increase in connection with the clinical trials and other development activities formifepristone for the psychotic features of psychotic depression and for other product candidates. We expect to incur significant expenses related tocommercializing Korlym. As a result, we expect that our losses will increase at least until Korlym is generating material amounts of revenue. We are unable topredict the extent of any future losses or whether or when we will become profitable.We may not be able to pursue all of our product research and development opportunities if we are unable to generate sufficient revenue or secureadequate funding for these programs.The costs required to start or continue many of the programs that our intellectual property allows us to consider for further development arecollectively greater than the funds currently available to us. For example, we have successfully discovered three series of compounds that are selective GR-IIantagonists but, unlike mifepristone, do not appear to block the progesterone receptor. Further development of these proprietary compounds or any furtherdevelopment stemming from our method-of-use patents may be delayed or cancelled if we determine that such development may jeopardize our ability tocomplete the clinical development of mifepristone for the treatment of psychotic depression.Global economic conditions could adversely affect our liquidity and financial condition.In the United States and globally, market and economic conditions have been volatile over the past few years, with significantly tighter creditconditions in the markets in which we conduct our operations. The U.S. and global economies have experienced a recession and face continued concernsabout the systemic impact of adverse economic conditions, such as unstable global financial markets, adverse effects on the cost and availability of capital,high corporate, consumer and governmental debt levels and high unemployment. Concern about the stability of the markets generally, and the strength ofcounterparties specifically, has led and may again lead many lenders and institutional investors to reduce, and in some cases, cease, to provide credit tobusinesses. Renewed or increased turbulence in the global markets and economies may adversely affect our liquidity and financial condition.In addition, our access to funds under any credit facility into which we may enter depends on the ability of the counterparties to such facilities to meettheir funding commitments to us. We cannot assure you that long-term disruptions in the global economy and the return of tighter credit conditions among,and potential failures of, third party financial institutions as a result of such disruptions will not have an adverse effect on such counterparties.If we do not have sufficient cash flow to continue operating our business and are unable to borrow funds or raise equity or debt capital, we may need tofind alternative ways to increase our liquidity. Such alternatives may include, without limitation, curtailing clinical or drug development activity, or limitingour commercial efforts, product manufacturing or sales and marketing support, which would have an adverse effect on our business, results of operations, cashflows and financial condition. 37Table of ContentsIf we acquire other GR-II antagonists or other technologies or potential products, we will incur a variety of costs and may never realize the anticipatedbenefits of the acquisition.If appropriate opportunities become available, we may attempt to acquire other GR-II antagonists, particularly GR-II antagonists that do not terminatepregnancy. We may also be able to acquire other technologies or potential products that are complementary to our operating plan. We currently have nocommitments, agreements or plans for any acquisitions. The process of acquiring rights to another GR-II antagonist or any other potential product ortechnology may result in unforeseen difficulties and expenditures and may absorb significant management attention that would otherwise be available forongoing development of our business. In addition, we may fail to realize the anticipated benefits of any acquired potential product or technology. Futureacquisitions could dilute our stockholders’ ownership interest in us and could cause us to incur debt, expose us to future liabilities and result in amortizationor other expenses related to goodwill and other intangible assets.Failure to meet our obligations under our Financing Agreement with Biopharma Secured Debt Fund II Sub, S.àr.l, could adversely affect our financialresults and liquidity.Pursuant to our Financing Agreement with Biopharma entered into in August 2012, we are obligated to make payments to Biopharma equal to 20percent of our net product sales of Korlym, any future mifepristone-based products and our next-generation selective GR-II antagonists (Covered Products),subject to certain quarterly caps, as well as an un-capped 20 percent of any upfront, milestone or other contingent payments we receive with respect toCovered Products, until such payments to Biopharma total $45 million.Pursuant to this agreement, we may not: (i) incur indebtedness greater than the sum of earnings before interest, taxes, depreciation and amortization,including such items as non-cash stock-based compensation, (EBITDA) for the four calendar quarters preceding such incurrence, which we refer to as theIndebtedness Covenant; (ii) pay a dividend or other cash distribution, unless we have cash and cash equivalents in excess of $50 million after such payment;(iii) amend or restate our certificate of incorporation or bylaws unless such amendments or restatements do not affect Biopharma’s interests under thetransaction; and (iv) encumber any of the collateral securing our performance under the agreement.The percentage used to calculate our payments to Biopharma would increase to 50 percent and any applicable payment caps would lapse if we (i) failto provide Biopharma with certain information regarding our promotion and sales of Covered Products, (ii) do not devote a commercially reasonable amountof resources to the promotion and marketing of the Covered Products or (iii) violate the Indebtedness Covenant and, in each case, fail to cure within theapplicable cure period.Upon a Corcept change of control transaction, as defined in the agreement, Biopharma will be automatically entitled to receive any amounts notpreviously paid, up to our maximum repayment obligation of $45 million. As defined in the agreement, “Change of Control” includes, among other things,(i) a greater than 50 percent change in the ownership of Corcept, (ii) certain changes in Board composition of Corcept and (iii) the licensing of Korlym to athird party for sale in the United States.To secure our obligations under the agreement, we granted Biopharma a security interest in our rights in patents, trademarks, trade names, domainnames, copyrights, know-how and regulatory approvals related to the Covered Products, all books and records relating to the foregoing and all proceeds ofthe foregoing, which we refer to as the Collateral. If we (i) fail to deliver a royalty payment when due and do not remedy that failure within 30 days, (ii) fail tomaintain a first-priority perfected security interest in the Collateral in the United States and do not remedy that failure within five business days of receivingnotice of such failure or (iii) become subject to an event of bankruptcy, then Biopharma may attempt to recover up to $45 million (after deducting anypayments we have already made). 38Table of ContentsThere can be no assurance that we will not breach the covenants or other terms of, or that an event of default will not occur under this agreement and, ifa breach or event of default occurs, there can be no assurance that we will be able to cure the event within the time permitted. Any failure to pay ourobligations when due, any breach or default of our covenants or other obligations, or any other event that causes an acceleration of payment at a time whenwe do not have sufficient resources to meet these obligations, could have a material adverse effect on our business, results of operations, financial conditionand future viability.The acceleration of the payment obligation in the event of a change of control transaction may make us less attractive to potential acquirers, and thepayment of such funds out of our available cash or acquisition proceeds would reduce acquisition proceeds for our stockholders.Risks Relating to Our Intellectual PropertyIf Korlym or future product candidates conflict with the patents of others or if we become involved in other intellectual property disputes, we may haveto engage in costly litigation or obtain a license and we may be unable to commercialize our product candidates.Our success depends in part on our ability to obtain and maintain adequate patent protection for the use of mifepristone for the treatment of thepsychotic features of psychotic depression and other potential uses of GR-II antagonists. If we do not adequately protect our intellectual property,competitors may be able to use our intellectual property and erode our competitive advantage.To date, we own eleven issued U.S. method of use patents and have exclusively licensed three issued U.S. method of use patents. We have nine U.S.method-of-use patent applications pending for GR-II antagonists. We own three composition-of-matter patents and have two composition of matter patentapplications pending. We have applied, and will continue to apply, for patents covering our product candidates as we deem appropriate. We have also filed,where we deemed appropriate, foreign patent applications corresponding to our U.S. patents and applications.We have exclusively licensed three issued U.S. patents from Stanford University for the use of GR-II antagonists in the treatment of psychotic majordepression, which is commonly referred to as psychotic depression, cocaine-induced psychosis and early dementia, including early Alzheimer’s disease. Webear the costs of protecting and defending the rights to these patents. In order to maintain the exclusive license to these patents until their expiration, we areobligated to make milestone and royalty payments to Stanford University. If we become noncompliant with our obligations under this agreement, we maylose the right to commercialize mifepristone for the treatment of psychotic depression, cocaine-induced psychosis and early dementia and our business wouldbe materially harmed. In addition, if Stanford University were to terminate our mifepristone license due to breach of the license on our part, we would not beable to commercialize mifepristone for the treatment of the psychotic features of psychotic depression, cocaine-induced psychosis or early dementia.Our patent applications and patents licensed or issued to us may be challenged by third parties and our patent applications may not result in issuedpatents. For example, in 2004, Akzo Nobel, which was subsequently acquired by Schering Plough which was then subsequently acquired by Merck & Co.,filed an observation challenging the claims of our exclusively licensed European patent application with claims directed to psychotic depression. In thisinstance, the patent later issued and, in 2007, we received notice from the European Patent Office that there will be no opposition proceedings in Europe inregard to this patent.Our presently pending and future patent applications may not issue as patents, and any patent issued to us may be challenged, invalidated, heldunenforceable or circumvented. For example, the arguments presented by Akzo Nobel could be raised in the United States either before the U.S. Patent andTrademark Office or in a court of law. Furthermore, the claims in patents which have been issued to us, or which may be issued to us in the future, may not besufficiently broad to prevent third parties from producing competing products. In addition, the laws of various foreign countries in which we compete maynot protect our intellectual property to the same 39Table of Contentsextent as do the laws of the United States. If we fail to obtain adequate patent protection for our proprietary technology, our competitors may producecompeting products based on our technology, which would impair our ability to compete.If a third party were successful in asserting an infringement claim against us, we could be forced to pay damages and prevented from developing,manufacturing or marketing our potential products. We do not have liability insurance for patent infringements. A third party could require us to obtain alicense to continue to use their intellectual property, and we may not be able to do so on commercially acceptable terms, or at all. We believe that significantlitigation will continue in our industry regarding patent and other intellectual property rights. If we become involved in litigation, it could consume asubstantial portion of our resources. Regardless of the merit of any particular claim, defending a lawsuit takes significant time, is expensive and divertsmanagement’s attention from other business.If we are unable to protect our trade secrets and proprietary information, our ability to compete in the market could be diminished.In addition to patents, we rely on a combination of confidentiality, nondisclosure and other contractual provisions, laws protecting trade secrets andsecurity measures to protect our trade secrets and proprietary information. Nevertheless, these measures may not adequately protect our trade secrets or otherproprietary information. If they do not adequately protect our rights, third parties could use our proprietary information, which could diminish our ability tocompete in the market. In addition, employees, consultants and others who participate in the development of our product candidates may breach theiragreements with us regarding our trade secrets and other proprietary information, and we may not have adequate remedies for the breach. We also realize thatour trade secrets may become known through means not currently foreseen. Notwithstanding our efforts to protect our trade secrets and proprietaryinformation, our competitors may independently develop similar or alternative products that are equal or superior to our product candidates withoutinfringing on any of our proprietary information or trade secrets.Our licensed patent covering the use of mifepristone to treat psychotic depression is a method of use patent rather than a composition of matter patent,which may make it more difficult for us to prove patent infringement if physicians prescribe another manufacturer’s mifepristone for the treatment ofCushing’s syndrome or psychotic depression or if patients acquire mifepristone from other sources, such as the internet or black market.We have an exclusive license from Stanford University to a patent covering the use of GR-II antagonists, including mifepristone, for the treatment ofpsychotic depression. A method of use patent covers only a specified use of a particular compound, not a particular composition of matter. Because none ofour issued patents covers the composition of mifepristone, we cannot prevent others from commercializing mifepristone in indications not covered by ourmethod of use patents. If others receive approval to manufacture and market mifepristone or any other GR-II antagonist, physicians could prescribemifepristone or any other GR-II antagonist for patients with psychotic depression instead of mifepristone. Although any such “off-label” use would violateour licensed patent, effectively monitoring compliance with our licensed patent may be difficult and costly. In addition, if others develop a treatment for thepsychotic features of psychotic depression that works through a mechanism which does not involve the GR-II receptor, physicians could prescribe thattreatment instead of mifepristone.In addition, we cannot be assured that patients will not obtain mifepristone from other sources. As with other pharmaceutical products, patients may beable to purchase mifepristone through the internet or black market. Mifepristone is also sold in the United States by Danco Laboratories for the termination ofearly pregnancy. While distribution is limited to a single dose provided in the physician’s office and covered by other restrictions, we cannot be certain thatCushing’s syndrome patients will not be able to obtain mifepristone from this source or others, should another company receive approval to marketmifepristone for another indication. 40Table of ContentsRisks Related to Our StockThe market price of our common stock has been and is likely to continue to be highly volatile due to the limited number of shares of our common stockheld by non-affiliates or factors influencing the stock market and opportunities for sale at any given time may be limited.We cannot assure you that an active trading market for our common stock will exist at any time. Holders of our common stock may not be able to sellshares quickly or at the market price if trading in our common stock is not active. During the 52-week period ended March 1, 2013, our average daily tradingvolume was approximately 389,000 shares and the intra-day sales prices per share of our common stock on the NASDAQ Stock Market ranged from $1.27 to$4.55. As of March 1, 2013, our officers, directors and principal stockholders controlled approximately 36 percent of our common stock. he trading price ofour common stock has been and is likely to continue to be highly volatile and could be subject to wide fluctuations in price in response to various factors,many of which are beyond our control, including: • the pace of market acceptance of Korlym or the timing and level of coverage and reimbursement attained; • our cash and short-term investment position; • actual or anticipated timing and results of our clinical trials; • new products or services introduced or announced by us or our competitors; • actual or anticipated regulatory approvals of our product candidates or of competing products; • changes in laws or regulations applicable to our product candidates or our competitors’ products; • changes in the expected or actual timing of our development programs or our competitors’ potential development programs; • actual or anticipated variations in quarterly operating results, including potential product returns and timing of revenue recognition; • announcements of technological innovations by us, our collaborators or our competitors; • general market and economic conditions, including those seen as a result of the recent worldwide financial credit crisis; • changes in financial estimates or recommendations by securities analysts; • conditions or trends in the biotechnology and pharmaceutical industries; • changes in the market valuations of similar companies; • announcements by us or our competitors of significant acquisitions, strategic partnerships, joint ventures or capital commitments; • additions or departures of key personnel; • disputes or other developments relating to proprietary rights, including patents, litigation matters and our ability to obtain patent protection forour technologies; • developments concerning collaborations; • trading volume of our common stock; • limited number of shares of our common stock held by our non-affiliates; • maintaining compliance with the listing requirements of the stock exchange on which we are listed; • success of additional financing efforts; and • purchases or sales of our common stock by us, our officers, directors or our stockholders. 41Table of ContentsIn addition, the stock market in general, the NASDAQ Stock Market and the market for biotechnology and life sciences companies in particular haveexperienced extreme price and volume fluctuations that have often been unrelated or disproportionate to the operating performance of those companies.These broad market and industry factors may seriously harm the market price of our common stock, regardless of our operating performance. In the past,following periods of volatility in the market, securities class-action litigation has often been instituted against companies. Such litigation, if institutedagainst us, could result in substantial costs and diversion of management’s attention and resources.The failure of our financial results to meet estimates published by research analysts or other investor expectations could cause our stock price todecline.There are inherent difficulties in predicting the amount of Korlym that will be sold. For example, the rate of physician adoption of Korlym is uncertain.Furthermore, the timing of a single large order for Korlym could substantially affect our revenue, making our levels of revenue potentially volatile and theidentification of revenue trends difficult. Due to such uncertainty, we have not provided any revenue forecasts to investors or research analysts. Researchanalysts who cover our business have, however, put forth a wide range of revenue estimates, based entirely on their own investigation and analysis. We havenot guided or commented on these estimates and you should rely on them at your own discretion. Announcement of financial results that fail to meet analystestimates or the expectations of investors could cause our stock price to decline.Research analysts may not continue to provide or initiate coverage of our common stock or may issue negative reports, which may have a negativeimpact on our common stock’s market price.Securities analysts currently covering our common stock may discontinue research coverage. Additional securities analysts may elect not to provideresearch coverage of our common stock. A lack of research coverage may adversely affect our common stock’s market price. The trading market for ourcommon stock may be affected in part by the research and reports that industry or financial analysts publish about us or our business. If one or more of theanalysts who elects to cover us downgrades our stock, our stock price would likely decline rapidly and significantly. If one or more of these analysts ceasescoverage of our company, we could lose visibility in the market, which in turn could cause our stock price to decline. In addition, rules mandated by theSarbanes-Oxley Act of 2002, and a global settlement reached in 2003 between the SEC, other regulatory analysts and a number of investment banks have ledto a number of fundamental changes in how analysts are reviewed and compensated. In particular, many investment banking firms are required to contractwith independent financial analysts for their stock research. It may be difficult for companies such as ours with smaller market capitalizations to attractindependent financial analysts that will cover our common stock. This could have a negative effect on our market price.A sale of a substantial number of shares of our common stock may cause the price of our common stock to decline.Sales of a substantial number of shares of our common stock in the public market could harm the market price of our common stock. As additionalshares of our common stock become available for resale in the public market, whether as a result of equity financings by us or due to the release of tradingrestrictions, the supply of our common stock will increase, which could decrease the price. Substantially all of the shares of our common stock are eligible forsale, subject to applicable volume and other resale restrictions.We may be required to pay significant amounts if we are not able to meet our obligations under our outstanding registration rights agreements.The registration rights agreement covering the approximately 8.9 million shares of our common stock issued in a private offering in March 2008 andan additional approximately 4.5 million shares of common stock underlying warrants issued in connection with the offering provides that if we fail to file orcause to be declared effective the registration statement covering the resale of these shares prior to specified deadlines, or fail to 42Table of Contentsmaintain the effectiveness of such registration statement (subject to limited permissible suspension periods), we will be required to pay the holders of suchshares and warrants liquidated damages at the rate of 1 percent of the purchase price of these shares and warrants per month, up to a total of 10 percent. Theregistration statement covering the resale of the shares and shares underlying the warrants sold in this transaction was declared effective by the SEC inNovember 2008. Since this registration statement was not declared effective within the time frame specified in the registration rights agreement, we becameobligated to pay liquidated damages of approximately $1.3 million in 2008 to the investors in this financing, which obligation was settled in the form ofstock in lieu of cash in November 2008. As noted above, if we fail to maintain the effectiveness of this registration statement, we may be obligated to payadditional liquidated damage amounts in the future.In addition, in March 2008, we entered into a CEFF with Kingsbridge, under which we granted to Kingsbridge a warrant for the purchase of 330,000shares of common stock. We terminated our CEFF with Kingsbridge effective August 7, 2012 and no further securities will be sold thereunder. However,under the registration rights agreement issued in connection with the CEFF, we are required to continue to use commercially reasonable efforts to maintainthe effectiveness of the registration statement covering the shares sold under this agreement and to be issued upon the exercise of the warrant for a period ofup to two years following the termination of the CEFF, subject to earlier termination on certain events. During this period, if the effectiveness of theregistration statement lapses through actions that were within our control, we may be obligated to pay Kingsbridge for all shares issued upon exercise of thewarrant and still owned by Kingsbridge at any time during the period of ineffectiveness the difference between (a) the volume weighted average price as ofthe day prior to the period of ineffectiveness and (b) the volume weighted average price as of the day following the period of ineffectiveness.If we are required to pay significant amounts under this or future registration rights agreements, it could have a material adverse effect on our financialcondition and ability to finance our operations.Our officers, directors and principal stockholders, acting as a group, will be able to significantly influence corporate actions.As of March 1, 2013, our officers, directors and principal stockholders control approximately 36 percent of our common stock. As a result, thesestockholders, acting together, will be able to significantly influence all matters requiring approval by our stockholders, including the election of directorsand the approval of mergers or other business combination transactions. The interests of this group of stockholders may not always coincide with our interestsor the interests of other stockholders and may prevent or delay a change in control. This significant concentration of share ownership may adversely affect thetrading price of our common stock because investors often perceive disadvantages to owning stock in companies with controlling stockholders.Changes in laws and regulations may result in increased costs to us, which may harm our financial results.New laws and regulations, as well as changes to existing laws and regulations, affecting our company, including the provisions of the PPACA requiringthe reporting of aggregate spending related to health care professionals, the provisions of the Sarbanes-Oxley Act of 2002 and rules adopted by the SEC andby The NASDAQ Stock Market have and will likely continue to result in increased costs to us as we respond to their requirements. We are investing resourcesto comply with evolving laws and regulations, and this investment may result in increased selling, general and administrative expenses and a diversion ofmanagement’s time and attention from revenue-generating activities to compliance activities.In addition, new rules and regulations could make it more difficult or costly for us to obtain certain types of insurance, including director and officerliability insurance, and we may be forced to accept reduced policy limits and coverage or incur higher costs to obtain the same or similar coverage. Theimpact of these events could also make it more difficult for us to attract and retain qualified persons to serve on our Board of Directors, or our boardcommittees, or as executive officers. At present, we cannot predict or estimate the amount of the additional costs related to new rules and regulations or thetiming of such costs. 43Table of ContentsCompliance with public company obligations, including the securities laws and regulations, is costly and requires significant management resources,and we may fail to comply.We are a small company with limited resources.The federal securities laws and regulations, including the corporate governance and other requirements of the Sarbanes-Oxley Act of 2002, imposecomplex and continually changing regulatory requirements on our operations and reporting. These requirements impose comprehensive reporting anddisclosure requirements, set stricter independence and financial expertise standards for audit committee members, and impose civil and criminal penalties forcompanies, their chief executive officers, principal financial officers and directors for securities law violations. These requirements have increased and willcontinue to increase our legal compliance costs, increase the difficulty and expense in obtaining director and officer liability insurance, and make it harderfor us to attract and retain qualified members of our Board of Directors and/or qualified executive officers. Such developments could harm our results ofoperations and divert management’s attention from business operations.In addition, as directed by Section 404 of the Sarbanes-Oxley Act of 2002, the SEC adopted rules requiring public companies to include a report ofmanagement on the company’s internal control over financial reporting in their annual reports on Form 10-K. This requirement first applied to our annualreport on Form 10-K for the year ended December 31, 2007. This same legislation also requires that the independent registered public accounting firmauditing our financial statements must attest to and report on the effectiveness of our internal controls over financial reporting. This requirement first appliedto our annual report on Form 10-K for the year ended December 31, 2010. Uncertainty exists regarding our ability to comply with these requirements byapplicable deadlines and to maintain compliance in future years. If we are unable to complete the required assessment as to the adequacy of our internalcontrol over financial reporting in future years or if our independent registered public accounting firm is unable to provide us with an unqualified report as tothe effectiveness of our internal control over financial reporting as of future year ends, investors could lose confidence in the reliability of our financialreporting.Changes in or interpretations of accounting rules and regulations could result in unfavorable accounting charges or require us to change ouraccounting policies or operating practices.Accounting methods and policies for business and marketing practices of pharmaceutical companies are subject to continual review, interpretation andguidance from relevant accounting authorities, including the SEC. For example, in December 2004, the Financial Accounting Standards Board adopted arevised standard related to stock-based compensation. This standard, which we adopted in 2006, requires the recording of expense for stock options grantedusing fair value-based measurements. As a result, our operating expenses have increased and are likely to continue to increase. We rely heavily on stockoptions to compensate existing employees and attract new employees. Because we are now required to expense stock options using fair value-basedmeasurements, we may choose to reduce our reliance on stock options as a compensation tool. If we reduce our use of stock options, it may be more difficultfor us to attract and retain qualified employees. Although we believe that our accounting practices are consistent with current accounting pronouncements,changes to or interpretations of accounting methods or policies in the future may require us to reclassify, restate or otherwise change or revise our financialstatements. Any such changes could result in corresponding changes to the amounts of assets, liabilities, revenues, expenses and income. Any such changescould have a material adverse effect on our business, financial position and results of operations and could cause the market value of our common stock todecline.If we fail to continue to meet all applicable NASDAQ Stock Market requirements, our stock could be delisted by The NASDAQ Stock Market. If delistingoccurs, it would adversely affect the market liquidity of our common stock and harm our business.If we are unable to meet any of the NASDAQ listing requirements in the future, including, for example, if the closing bid price for our common stock isbelow $1 per share for 30 consecutive trading days, The NASDAQ Stock Market could determine to delist our common stock, the delisting could adverselyaffect the market 44Table of Contentsliquidity of our common stock and the market price of our common stock could decrease. Such delisting could also adversely affect our ability to obtainfinancing for the continuation of our operations and could result in the loss of confidence by investors, suppliers and employees.Anti-takeover provisions in our charter and bylaws and under Delaware law and payment acceleration provisions under the Biopharma FinancingAgreement may make an acquisition of us or a change in our management more expensive or difficult, even if an acquisition or a management changewould be beneficial to our stockholders.Provisions in our charter and bylaws may delay or prevent an acquisition of us or a change in our management. Some of these provisions allow us toissue preferred stock without any vote or further action by the stockholders, require advance notification of stockholder proposals and nominations ofcandidates for election as directors and prohibit stockholders from acting by written consent. In addition, a supermajority vote of stockholders is required toamend our bylaws. Our bylaws provide that special meetings of the stockholders may be called only by our Chairman, President or the Board of Directors andthat the authorized number of directors may be changed only by resolution of the Board of Directors. These provisions may prevent or delay a change in ourBoard of Directors or our management, which is appointed by our Board of Directors. In addition, because we are incorporated in Delaware, we are governedby the provisions of Section 203 of the Delaware General Corporation Law. Section 203 may prohibit large stockholders, in particular those owning 15percent or more of our outstanding voting stock, from merging or combining with us. In addition, our payment obligations to BioPharma accelerate in theevent of a change of control transaction. See “Risk Factors – Failure to meet our obligations under our Financing Agreement with Biopharma Secured DebtFund II Sub, S.à r.l, could adversely affect our financial results and liquidity.” These provisions in our charter and bylaws under Delaware law could reducethe price that investors might be willing to pay for shares of our common stock in the future and result in the market price being lower than it would bewithout these provisions. ITEM 1B.UNRESOLVED STAFF COMMENTSNone. ITEM 2.PROPERTIESWe lease approximately 13,225 square feet of office space in Menlo Park, California for our corporate facilities. Our current lease extended ouroccupancy through December 2013 and provides us with an option to extend the lease for one additional year. We expect that these facilities willaccommodate our operations for the next year. ITEM 3.LEGAL PROCEEDINGSWe are not currently involved in any material legal proceedings. ITEM 4.MINE SAFETY DISCLOSURESNot applicable. 45Table of ContentsPART II ITEM 5.MARKET FOR REGISTRANT’S COMMON EQUITY, RELATED STOCKHOLDER MATTERS AND ISSUER PURCHASES OF EQUITYSECURITIESMarket InformationOur common stock is traded on The NASDAQ Capital Market under the symbol “CORT”. The following table sets forth the high and low intra-day saleprices per share of our common stock on The NASDAQ Capital Market for the periods indicated. These prices represent quotations among dealers withoutadjustments for retail mark-ups, markdowns or commissions, and may not represent prices of actual transactions. High Low 2012 First Quarter $4.90 $2.50 Second Quarter $4.55 $3.49 Third Quarter $4.51 $2.48 Fourth Quarter $2.84 $1.27 2011 First Quarter $4.51 $3.43 Second Quarter $5.07 $3.67 Third Quarter $4.02 $2.51 Fourth Quarter $3.58 $2.70 Stockholders of Record and DividendsAs of March 1, 2013, we had 99,814,250 shares of common stock outstanding held by 116 stockholders of record. We have never declared or paid cashdividends on our capital stock. We currently intend to retain any future earnings to finance the growth and development of our business and therefore, do notanticipate paying any cash dividends in the foreseeable future. In addition, the Biopharma Financing Agreement prohibits payment of dividends unless wehave cash and cash equivalents in excess of $50 million after such payment.Sale of Unregistered SecuritiesAll sales of unregistered securities during the year ended December 31, 2012 have previously been disclosed in filings with the SEC. We have used, orwill use, the net proceeds from these transactions to fund our on-going operations, including the commercialization of Korlym 300 mg Tablets, continuationof our phase 3 clinical trial of mifepristone for the treatment of the psychotic features of psychotic depression, the further development of our portfolio ofnext-generation compounds, as well as to fund working capital and for general corporate purposes.Repurchases of SecuritiesNone.Market Performance GraphThe graph and the accompanying text below is not “soliciting material,” is not deemed filed with the SEC and is not to be incorporated by referencein any filings by us under the Securities Act or the Exchange Act, whether made before or after the date hereof and irrespective of any generalincorporation language in such filing.The rules of the SEC require that we include a line-graph comparing cumulative stockholder returns on our common stock with the NASDAQComposite Index (which tracks the aggregate price performance of equity 46Table of Contentssecurities of companies traded on NASDAQ) and either a published industry or line-of-business standard index or an index of peer companies selected by us.We have elected to use the NASDAQ Biotechnology Index (consisting of a group of approximately 120 companies in the biotechnology sector, including us)for purposes of the performance comparison that appears below.The graph shows the cumulative total stockholder return assuming the investment of $100.00 and the reinvestment of dividends and is based on thereturns of the component companies weighted according to their market capitalizations as of the end of the period for which returns are indicated. Nodividends have been declared on our common stock.The stockholder return shown on the graph below is not necessarily indicative of future performance, and we do not make or endorse any predictions asto future stockholder returns.COMPARISON OF 5 YEAR CUMULATIVE TOTAL RETURN* AMONGCORCEPT THERAPEUTICS, THE NASDAQ CAPITAL MARKET (U.S.) INDEXAND THE NASDAQ BIOTECHNOLOGY INDEX *$100 invested on December 31, 2007 including reinvestment of dividends. Fiscal year ended December 31. 47Table of ContentsITEM 6.SELECTED FINANCIAL DATASELECTED FINANCIAL DATA(in thousands, except per share data)The selected financial data set forth below are derived from our financial statements. The statement of operations data for the years ended December 31,2012, 2011, and 2010 and the balance sheet data as of December 31, 2012 and 2011 are derived from our audited financial statements included in thisAnnual Report on Form 10-K (Form 10-K). The statements of operations data for the years ended December 31, 2009 and 2008, and the balance sheet data asof December 31, 2010, 2009 and 2008 have been derived from our audited financial statements, which are not included in this Form 10-K. The selectedfinancial data set forth below should be read in conjunction with our financial statements, the related notes and “Management’s Discussion and Analysis ofFinancial Condition and Results of Operations” included elsewhere in this Form 10-K. Year Ended December 31, 2012 2011 2010 2009 2008 (In thousands, except per share data) Statement of Operations Data: Revenues: Product sales, net $3,307 $— $— $— $— Collaboration revenue — — — 29 209 Total revenues 3,307 — — 29 209 Operating expenses: Cost of sales 91 — — — — Research and development* 14,074 21,001 18,949 14,402 14,152 Selling, general and administrative* 25,414 11,331 8,488 5,877 5,746 Total operating expenses 39,579 32,332 27,437 20,279 19,898 Loss from operations (36,272) (32,332) (27,437) (20,250) (19,689) Non-operating income (expense), net* (1,776) (22) 1,471 84 (372) Net loss $(38,048) $(32,354) $(25,966) $(20,166) $(20,061) Net loss per share: Basic and diluted $(0.41) $(0.39) $(0.38) $(0.38) $(0.43) Weighted average shares—basic and diluted 93,015 83,309 68,336 52,443 46,721 * Includes significant non-cash expenses, of the following: Stock-based compensation Research and development $546 $547 $220 $263 $268 Selling, general and administrative 4,764 2,888 1,896 1,552 1,360 Total stock-based compensation 5,310 $3,435 2,116 1,815 1,628 Non-operating expense related to accretion of interest on long-termobligation 1,680 — — — — Total significant non-cash expenses $6,990 $3,435 $2,116 $1,815 $1,628 As of December 31, 2012 2011 2010 2009 2008 (In thousands) Balance Sheet Data: Cash, cash equivalents and investments $93,032 $39,635 $24,578 $23,867 $18,309 Working capital 86,703 34,749 21,136 22,001 16,717 Total assets 99,166 39,833 25,104 24,511 19,775 Long-term obligation — current portion 2,650 — — — 6 Long-term obligation, net of current portion 29,030 — — — — Total stockholders’ equity 61,777 34,807 21,244 22,092 16,907 48Table of ContentsITEM 7.MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONSForward-Looking StatementsThis Management Discussion should be read in conjunction with the financial statements and notes thereto appearing elsewhere in this report. Wemake statements in this section that are forward-looking statements within the meaning of the federal securities laws. For a complete discussion of suchforward-looking statements and the potential risks and uncertainties that may impact upon their accuracy, see “Forward-Looking Statements” included inPart I, “Risk Factors” included in Part I of this Form 10-K and the “Overview” and “Liquidity and Capital Resources” sections of this Management’sDiscussion and Analysis of Financial Condition and Results of Operations.OverviewWe are a pharmaceutical company engaged in the discovery, development and commercialization of drugs for the treatment of severe metabolic andpsychiatric disorders. Our focus is on disorders associated with the steroid hormone cortisol. Elevated levels and abnormal release patterns of cortisol havebeen implicated in a broad range of human disorders.Since our inception in May 1998, we have been developing mifepristone, a potent glucocorticoid receptor II (GR-II) antagonist. On February 17, 2012,the FDA approved Korlym™ (mifepristone) 300 mg Tablets in the United States as a once-daily oral medication for treatment of hyperglycemia secondary tohypercortisolism in adult patients with endogenous Cushing’s syndrome who have type 2 diabetes mellitus or glucose intolerance and have failed surgery orare not candidates for surgery. We made Korlym available to patients in April 2012 and have begun marketing the drug in the United States. We continue todevelop the sales, marketing, medical affairs and logistical infrastructure needed to commercialize the drug. We also have an on-going phase 3 study ofmifepristone, the active ingredient in Korlym, for treatment of the psychotic features of psychotic depression. We have discovered three series of novelselective GR-II antagonists.Unless otherwise stated, all references in this document to “we,” “us,” “our,” “Corcept,” the “Company,” “our company” and similar designations referto Corcept Therapeutics Incorporated.Cushing’s Syndrome. Cushing’s syndrome is a disorder caused by prolonged exposure of the body’s tissues to high levels of the hormone cortisol.Sometimes called “hypercortisolism,” it is uncommon and most often affects adults aged 20 to 50. An estimated 10 to 15 of every one million people arenewly diagnosed with this syndrome each year, resulting in approximately 3,000 new patients and an estimated prevalence of 20,000 patients with Cushing’ssyndrome in the United States.The FDA approved our NDA for Korlym on February 17, 2012. This approval allows us to market Korlym in the United States for its approvedindication. We are carrying out our commercialization plans, including hiring a small number of medical science liaisons (MSLs) and sales representatives.We have also developed internet marketing capabilities and patient assistance programs to support physicians and patients. We began shipping Korlym toour specialty pharmacy in early April 2012, and the medicine first became available to patients on April 10, 2012. We finished hiring our team of MSLs inthe third quarter of 2012. Our sales representatives received their initial training and were deployed to the field in the fourth quarter of 2012.We have Orphan Drug Designations for Korlym from the FDA for the approved indication and from the European Commission for the treatment ofendogenous Cushing’s syndrome. Orphan Drug Designation in the United States is a special status granted by the FDA to encourage the development oftreatments for diseases or conditions that affect fewer than 200,000 patients in the United States. Drugs that receive Orphan Drug Designation obtain sevenyears of marketing exclusivity for the approved indication from the date of drug 49Table of Contentsapproval, as well as tax credits for clinical trial costs, marketing application filing fee waivers and assistance from the FDA in the drug development process.Benefits of Orphan Drug Designation in the EU are similar to those in the United States, but include ten years of marketing exclusivity for the approvedindication in all 27 member states, free scientific advice during drug development, access to a centralized review process and a reduction or complete waiverof fees levied by the European Medicines Agency.Psychotic Depression. We are also developing mifepristone, the active ingredient in Korlym, for the treatment of the psychotic features of psychoticdepression under an exclusive patent license from Stanford University. The FDA has granted “fast track” status to evaluate the safety and efficacy ofmifepristone for the treatment of the psychotic features of psychotic depression.In March 2008, we began enrollment in Study 14, our ongoing phase 3 trial in psychotic depression. The protocol for this trial incorporates what wehave learned from our three previously completed phase 3 trials. It attempts to address the established relationship between increased drug plasma levels andclinical response and attempts to decrease the random variability observed in the results of the psychometric instruments used to measure efficacy. In one ofthe previously completed phase 3 trials, Study 06, we prospectively tested and confirmed that patients whose plasma levels rose above a predeterminedthreshold statistically separated from both those patients whose plasma levels were below the threshold and those patients who received placebo; thisthreshold was established from data produced in earlier studies.As expected, the group of patients who took 1200 milligrams (mg) of mifepristone in Study 06 developed higher drug plasma levels than did thegroups of patients who received lower doses. Further, there was no discernable difference in the incidence of adverse events between patients who receivedplacebo in Study 06 and those who received 300 mg, 600 mg or 1200 mg of mifepristone in that study. In August 2011, we published our analysis of thesedata in The Journal of Clinical Psychopharmacology. Based on this information, we are testing a mifepristone dose of 1200 mg once per day for seven daysin Study 14.In addition, we are using a third-party centralized rating service to independently evaluate the patients for entry into the study as well as to evaluatetheir level of response throughout their participation in the study. We believe the centralization of this process will improve the consistency of rating acrossclinical trial sites and reduce the background statistical noise that was observed in earlier studies and is endemic to psychopharmacologic studies. We believethat the change in dose, as well as the other modifications to the protocol described above, should allow us to demonstrate the efficacy of mifepristone in thetreatment of the psychotic symptoms of psychotic depression. In mid-2009, to conserve financial resources, we reduced the number of clinical sites in thisstudy to eight and extended the timeline for its completion.Enrollment in Study 14 is ongoing. Our goal is to enroll a sufficient number of patients by the end of 2013 to be able to perform a successful interimanalysis. To help reach this goal, we began adding clinical sites in the fourth quarter of 2012 and plan to have 20 sites by the end of the first quarter of 2013.Antipsychotic-induced Weight Gain Mitigation. In 2005, we announced the results of studies in rats that demonstrated that mifepristone bothreversed the weight gain associated with the ongoing use of olanzapine and mitigated the weight gain associated with the initiation of treatment witholanzapine (the active ingredient in Zyprexa). The results from this study were published in the journal Brain Behavioral Research in early 2006. This studywas paid for by Eli Lilly and Company (Eli Lilly).During 2007, we announced positive results from our clinical proof-of-concept study in lean healthy male volunteers evaluating the ability ofmifepristone to mitigate weight gain associated with the use of Zyprexa. The results showed a statistically significant reduction in weight gain in thosesubjects who took Zyprexa plus mifepristone compared to those who took Zyprexa plus placebo. Also, the addition of mifepristone to treatment with Zyprexahad a beneficial impact on secondary metabolic measures such as fasting insulin, triglycerides and abdominal fat, as indicated by waist circumference. EliLilly provided Zyprexa and financial support for this 50®Table of Contentsstudy, the results of which were published in the journal Advances in Therapy in 2009. In January 2009, we announced positive results from a similar proof-of-concept study evaluating the ability of mifepristone to mitigate weight gain associated with the use of Johnson & Johnson’s Risperdal. This studyconfirmed and extended the earlier results seen with mifepristone and Zyprexa, demonstrating a statistically significant reduction in weight gain and in thesecondary metabolic endpoints of fasting insulin, triglycerides and abdominal fat, as indicated by waist circumference. The results from the study ofmifepristone and Risperdal were presented at several scientific conferences, including the American Diabetes Association meeting in June 2009, and werepublished in the journal Obesity in 2010.The combination of Zyprexa or Risperdal and mifepristone is not approved for any indication. The purpose of these studies was to explore thehypothesis that GR-II antagonists, such as mifepristone and our next generation of selective GR-II antagonists, would mitigate weight gain associated withantipsychotic medications. The group of medications known as second generation antipsychotic medication, including Zyprexa, Risperdal, Clozaril andSeroquel, are widely used to treat schizophrenia and bipolar disorder. All medications in this group are associated with treatment-emergent weight gain ofvarying degrees and carry a warning in their labels relating to treatment-emergent hyperglycemia and diabetes mellitus.Selective GR-II Receptor Antagonists. In 2003, we initiated a discovery research program to identify and patent selective GR-II antagonists with theintent of developing a pipeline of products for proprietary use. Three distinct series of GR-II antagonists were identified. These compounds, like mifepristone,potently block the cortisol receptor (GR-II) but, unlike mifepristone, they do not appear to block the PR (progesterone), ER (estrogen), AR (androgen) or GR-I(mineralocorticoid) receptors. Both the United States Patent & Trademark Office (USPTO) and the European Patent Office (EPO) have issued composition-of-matter patents to us on each of the three series. Two additional composition-of-matter patent applications are pending.Several of our new compounds have demonstrated positive results in animal models for the prevention and reversal of anti-psychotic-induced weightgain. One of them, CORT 108297, is in exploratory phase 2a clinical trials and we plan to explore its potential use in other indications. We have identifiedother selective GR-II antagonists from our proprietary series that we believe may have utility as therapeutic agents in a variety of diseases. Our intent is tocontinue our discovery research program with the goal of identifying new selective GR-II antagonists and to manufacture and conduct pre-clinicaldevelopment on one or more of these compounds and to submit Investigational New Drug (IND) applications with respect to the most promising of them, aswe deem appropriate.At the American Diabetes Association conference in June 2009, there was also a presentation of preclinical data from another study of CORT 108297conducted at Stanford University. This study demonstrated that CORT 108297 suppresses body weight gain and improves insulin sensitivity in healthy micefed a 60 percent fat diet and high sucrose liquid. The results of these preclinical data were published in April 2011 in the journal Nutrition and Metabolism.In addition, we are continuing research and pre-clinical efforts to identify additional selective GR-II antagonists for clinical study.GeneralOur activities to date have included: • product development, including drug formulation and manufacturing, as well as designing, funding and overseeing clinical trials andconducting non-human clinical investigatory activities, such as toxicological testing; • commercialization of Korlym, including hiring and training medical science liaisons and sales representatives, retention and management ofthird-party distribution partners, establishment of third-party coverage and reimbursement and patient assistance programs and marketingactivities. 51®®®Table of Contents • discovery research; • intellectual property prosecution and expansion; and • regulatory affairs.Historically, we have financed our operations and internal growth primarily through private placements of our preferred and common stock, the publicsale of common stock and our capped royalty financing transaction, rather than through collaborative or partnership agreements.As of December 31, 2012, we had an accumulated deficit of $246.6 million. Our historical operating losses have resulted principally from our researchand development activities, including clinical trial activities for mifepristone, discovery research, non-clinical activities such as toxicology andcarcinogenicity studies, manufacturing process development and regulatory activities, as well as selling, general and administrative expenses, includingpreparations for the commercial launch of Korlym. We may continue to incur net losses over at least the next few years as we continue our mifepristone andselective GR-II antagonist discovery and clinical development programs, apply for regulatory approvals, acquire and / or develop treatments in othertherapeutic areas, establish sales and marketing capabilities and expand our operations.Our business is subject to significant risks, including the risks inherent in our research and development efforts, the results of our mifepristone andother clinical trials, uncertainties associated with securing financing, uncertainties associated with obtaining and enforcing patents, our investment inmanufacturing set-up, the management of our supply chain, the lengthy and expensive regulatory approval process and competition from other products. Ourability to successfully generate revenues in the foreseeable future is dependent upon our ability, alone or with others, to finance our operations and develop,obtain regulatory approval for, manufacture and market our products.Results of OperationsNet Product Sales — Net product sales includes product revenue resulting from sales to our customers, reduced by 1) trade allowances, such asdiscounts for prompt payment and distributor fees, 2) estimated government rebates and chargebacks, 3) reserves for expected product returns and4) estimated costs of our patient assistance program.In April 2012, we made Korlym commercially available in the United States through a specialty pharmacy that sells to individual patients and aspecialty distributor that sells to hospital pharmacies. For the year ended December 31, 2012, we recognized $3.3 million in net product sales. To calculatenet product sales, we deducted from gross sales estimates of prompt-pay discounts, distribution service fees, rebates and chargebacks owed to governmentpayors and patient assistance program costs, which amounts are not material for the year ended December 31, 2012.Based on our limited experience marketing Korlym, it is difficult for us to forecast its sales for any future periods.Cost of sales — Cost of sales includes the cost to manufacture Korlym (which includes material, third-party manufacturing costs and indirect personneland other overhead costs) based on units sold in the current period, as well as the cost of stability testing and distribution. We began capitalizing Korlymproduction costs as inventory following approval by the FDA to market Korlym on February 17, 2012. Prior to Korlym’s approval, we expensed all costsrelated to the manufacturing of product (including stability costs and manufacturing overhead) as incurred, classifying these costs as research anddevelopment expense. A portion of the product manufactured prior to FDA approval is available for us to use commercially.Cost of sales was $91,000 for the year ended December 31, 2012, which equals 2.8 percent of net product sales for the same period. The majority ofthese costs related to stability testing. The amount and timing of 52Table of Contentsstability testing varies from period to period as determined by FDA regulations and our production schedule and is not a fixed percentage of our salesvolumes. In addition, the cost of manufacturing Korlym reflected in our cost of sales in 2012, and for some period thereafter, will not reflect the full cost ofproduction because we have previously expensed the majority of the raw materials, labor and overhead costs incurred to produce the product sold during thisperiod. We expect that our cost of sales of Korlym as a percentage of net product sales will fluctuate from period to period during 2013 and for some timethereafter as product manufactured prior to FDA approval, which is already fully expensed, is consumed.Research and development expenses — Research and development expenses include 1) the personnel costs related to our development activities,including facilities costs and non-cash stock-based compensation, 2) the costs of discovery research, 3) costs associated with IND-enabling activities and pre-clinical studies, 4) costs of clinical trials, including trial preparation, enrollment, site monitoring and data management and analysis expenses, 5) regulatorycosts, 6) the costs of manufacturing development, including the development and activities to qualify a second tablet manufacturing site, 7) the costs ofmanufacture and / or acquisition of clinical trial materials and material used in registration and validation batches included in the NDA submission forKorlym and 8) other costs associated with the preparation and prosecution of the Korlym NDA or other FDA submissions related to Korlym or other productcandidates.Research and development expenses decreased 33 percent to $14.1 million for the year ended December 31, 2012 from $21.0 million for thecomparable period in 2011.During the year ended December 31, 2012 as compared to the corresponding period in 2011, there was an increase of $991,000 in staffing costs, whichincludes bonuses paid on FDA approval of Korlym in the amount of $474,000, and an increase of $164,000 for stock-based compensation expenses related toemployees working in research and development functions. During the year ended December 31, 2012 as compared to the corresponding periods in 2011,there were decreases in consultancy costs of $2.8 million due primarily to the additional resources required during 2011 for the preparation, submission andprosecution of the NDA, which was submitted in April 2011 and filed by the FDA in June 2011. For the year ended December 31, 2012, non-cash stock-basedcompensation expense related to consultant options decreased $165,000 as compared to the corresponding period of 2011 due primarily to the inclusion in2011 of costs related to a stock option award to a consultant that vested in its entirety on the acceptance of the NDA by the FDA in June 2011.Korlym manufacturing costs categorized as research and development expense decreased $3.8 million during the year ended December 31, 2012 ascompared to the corresponding period in 2011, due primarily to capitalizing to inventory the costs of Korlym’s active pharmaceutical ingredient and themanufacture of Korlym tablets for commercial sale following the date of FDA approval.Clinical trial costs reflected a net decrease of $1.6 million during the year ended December 31, 2012, as compared to the corresponding period of 2011.During the year ended December 31, 2012 as compared to the corresponding period in 2011, there were decreases of $1.2 million related to clinical studieswith CORT 108297 and $917,000 related to the clinical trials with Korlym in the treatment of Cushing’s syndrome. These decreases were partially offset byincreases during year ended December 31, 2012, as compared to the corresponding period of 2011, of $487,000 related to the psychotic depression study.In addition, costs related to financial support for medical conferences and seminars in support of our Cushing’s syndrome program decreased $337,000for the year ended December 31, 2012, as compared to the corresponding period of 2011, because, subsequent to product approval, the nature of our activitiesat medical meetings has changed, and now such costs relate to marketing activities that are classified as a component of selling, general and administrativeexpenses. Costs relating to IND-enabling activities and research efforts regarding our new GR-II antagonists increased $363,000 during the year endedDecember 31, 2012, as compared to the corresponding period in 2011.Research and development expenses increased 11% to $21.0 million for the year ended December 31, 2011 from $18.9 million for the comparableperiod in 2010. For the year ended December 31, 2011 as compared to the 53Table of Contentscorresponding period in 2010, there were net increases of $1.8 million in consultancy costs which included the following increases: a) $588,000 related tothe development of the Risk Evaluation and Mitigation System (REMS) that was included in the Korlym NDA submission, b) $834,000 related to thepreparation, submission and prosecution of the NDA, c) $114,000 related to the development of a medical safety program, d) $187,000 related tomanufacturing and quality control activities to prepare for commercialization and e) $192,000 in non-cash stock-based compensation costs related to aperformance-based award to a consultant that vested in June 2011 upon the filing of our NDA for Korlym by the FDA, which were partially offset by thedecrease in consulting fees in other clinical activities of $78,000. For the year ended December 31, 2011, as compared to the corresponding period in 2010,there was also an increase of $300,000 related to attendance of seminars in support of our Cushing’s syndrome program.Korlym manufacturing costs increased $4.2 million during the year ended December 31, 2011, as compared to the corresponding period in 2010, dueprimarily to the acquisition of active pharmaceutical ingredient for Korlym and the initiation of manufacturing development work at a potential back-up sitefor the manufacture of Korlym that were only partially offset by a decrease in manufacturing activities related to our proprietary, selective new GR-IIantagonists.There were decreases in clinical trial costs of $4.3 million during the year ended December 31, 2011, as compared to the corresponding period of 2010.Clinical trial cost decreases included (a) $2.8 million related to drug-drug interaction and other NDA-supportive studies with Korlym that were substantiallycompleted during 2010, (b) $727,000 related to the clinical trials with Korlym for the treatment of Cushing’s syndrome due to patients having completed theinitial study and moving into the long-term extension study, (c) $331,000 related to the clinical trial with mifepristone for the treatment of psychoticdepression and (d) $468,000 related to clinical studies activities with CORT 108297. During the year ended December 31, 2011, as compared to thecorresponding period in 2010, there was also a decrease of $244,000 related to the IND-enabling work on CORT 108297, which was partially offset byincreases of $168,000 related to research efforts on our other selective GR-II antagonists.Below is a summary of our research and development expenses by major project: Year EndedDecember 31, Project 2012 2011 2010 (in thousands) Development programs: Cushing’s syndrome $4,093 $10,925 $5,075 Psychotic depression 2,613 1,779 2,567 Selective GR-II antagonists 4,249 4,546 5,100 Unallocated activities, including NDA supportive studies and manufacturing, regulatory and pre-clinical activities 2,573 3,204 5,987 Stock-based compensation 546 547 220 Total research and development expense $14,074 $21,001 $18,949 We expect that research and development expenditures in 2013 will likely be higher than they were in 2012, due to the cost of expanding enrollmentin our phase 3 study of mifepristone in the treatment of psychotic depression and increased spending on the development of our next-generation selectiveGR-II antagonists. Research and development expenses in 2014 and beyond will depend on our strategic priorities. See also, “Liquidity and CapitalResources”.Many factors can affect the cost and timing of our trials including inconclusive results requiring more clinical trials, slow patient enrollment, adverseside effects in study patients, insufficient supplies for our clinical trials and real or perceived lack of effectiveness or safety of the drug in our trials. The costand timing of 54Table of Contentsdevelopment of our selective GR-II antagonists will depend on the success of our efforts and any difficulties that we may encounter. In addition, thedevelopment of all of our product candidates will be subject to extensive governmental regulation. These factors make it difficult for us to predict the timingand costs of the further development and approval of our product candidates.Selling, general and administrative expenses — Selling, general and administrative expenses include 1) personnel and consultancy costs related toadministrative and commercialization activities, including facilities costs and non-cash stock-based compensation, 2) expenses of third-party vendors that weengage to execute our commercial plans related to Korlym, including conducting market research, providing market analytics, developing reimbursementsupport services and, distribution and other logistical needs related to our commercialization of Korlym and 3) legal, accounting and other professional fees.For the year ended December 31, 2012, selling, general and administrative expenses increased to $25.4 million from $11.3 million for the comparableperiod in 2011.During the year ended December 31, 2012 as compared to the corresponding period in 2011, staffing and consultancy costs increased $6.9 million dueprimarily to additional resources necessary to commercialize Korlym. The increase for the year ended December 31, 2012 included $1.6 million in cashbonuses awarded in the first quarter of 2012 to employees working in selling, general and administrative functions in recognition of the FDA’s approval ofKorlym, $1.3 million of non-cash stock-based compensation costs related to performance-based stock option awards to officers that vested in February 2012upon the FDA approval of Korlym and $600,000 of increases related to other stock options to directors, officers and employees working in selling, generaland administrative functions.In addition, other professional services costs related to commercialization activities and other corporate matters increased $5.8 million during the yearended December 31, 2012 as compared to the corresponding period of 2011. These costs reflect increased vendor activities after FDA approval, pricingstrategy and market analysis, patient registry and reimbursement programs, focus groups, internet marketing and communications.There were also cost increases during the year ended December 31, 2012 as compared to the corresponding period of 2011 related to the infrastructurenecessary to support the commercialization of Korlym including a) $538,000 related to travel, b) 386,000 related to the expansion of facilities andinformation technology support, c) $147,000 related to employee education primarily due to the training of the new medical science liaisons and d) $95,000related to donations.For the year ended December 31, 2011, selling, general and administrative expenses increased 33% to $11.3 million from $8.5 million for the yearended December 31, 2010. During 2010, we had recorded an aggregate amount of $1.3 million related to bonuses awarded to our officers and employeesworking in selling, general and administrative functions in recognition of significant company accomplishments during 2010. We did not award bonuses for2011 performance to any officer or employee in these functions. In addition, during 2011, as compared to 2010, staffing and consultancy costs increased $1.6million due primarily to additional resources necessary to engage in preparations for the potential commercialization of Korlym, which included an increaseof $992,000 in noncash stock-based compensation costs related to stock options granted to employees, directors and consultants. There was also an increaseof $2.0 million during 2011, as compared to 2010, in market research and other commercialization preparation activities and an increase in legal costs relatedto patents, commercialization, compliance and other corporate matters during 2011, as compared to 2010, of $456,000.Selling, general and administrative expenses included stock-based compensation expense related to option grants to individuals performing thesefunctions of $4.8 million, $2.9 million and $1.9 million for the years ended December 31, 2012, 2011 and 2010, respectively.We expect that selling, general and administrative expenses will increase during 2013 as compared to 2012 in regard to activities directly associatedwith product commercialization and the need to continue building our 55Table of Contentsadministrative infrastructure to support these activities. The level of selling, general and administrative activities and related expenses in 2014 and futureyears will be largely dependent on our assessment of the staff and other services necessary to support product commercialization and our continued clinicaldevelopment activities and the availability of additional funds. See also, “Liquidity and Capital Resources.”Interest and other income, net — Interest and other income, net of investment management fees, was $3,000 for the year ended December 31, 2011 ascompared to $1.5 million for the same period in 2010. Other income in 2011 was comprised of income on stockholder notes. Other income in 2010 hadincluded $750,000 in connection with the favorable settlement of a lawsuit brought on our behalf against an individual for defamation and harassment and$733,000 in grants from the United States Treasury’s Therapeutic Discovery Project Grant program.Interest and other expense — Interest and other expense for the year ended December 31, 2012 was $1.8 million as compared to $25,000 for thecomparable period in 2011. This increase is primarily due to the inclusion in the current period of $1.7 million of interest expense related to our FinancingAgreement with Biopharma for the period from August 16, 2012, the date of funding of the agreement to December 31, 2012. Other expense for the yearended December 31, 2011 was $25,000 in 2011 and in 2010 and consisted primarily of a state tax on capital, which is based on our capital and assetpositions as of each year-end. Interest expense will increase during 2013, as compared to 2012, due to the inclusion of interest on the long-term obligation fora full year.Non-GAAP Financial MeasuresOur financial statements and footnotes thereto are prepared in accordance with U.S. Generally Accepted Accounting Principles (GAAP) and areincluded in Part IV, Item 15 of this Annual Report on Form 10-K.To supplement our financial results presented on a GAAP basis, we use non-GAAP measuresof net loss that exclude significant non-cash expenses related to stock-based compensation expense and the accretion of interest expense under our cappedroyalty financing transaction. We use this non-GAAP measure of net loss to manage our business and believe that it may help investors better evaluate ourpast financial performance and potential future results. Non-GAAP measures should not be considered in isolation or as a substitute for comparable GAAPaccounting and investors should read them in conjunction with our financial statements and notes thereto prepared in accordance with GAAP. The non-GAAP measure of net loss we use may be different from, and not directly comparable to, similarly titled measures used by other companies. Year EndedDecember 31, 2012 2011 2010 (in thousands) GAAP net loss $38,048 $32,354 $25,966 Significant non-cash expenses: Stock-based compensation Research and development 546 547 220 Selling, general and administrative 4,764 2,888 1,896 Total stock-based compensation 5,310 3,435 2,116 Accretion of interest expense related to long-term obligation 1,680 — — Non-GAAP net loss, as adjusted for significant non-cash expenses $31,058 $28,919 $23,850 GAAP basic and diluted net loss per share $(0.41) $(0.39) $(0.38) Non-GAAP basic and diluted net loss per share, as adjusted for significant non-cash expenses $(0.33) $(0.35) $(0.35) Shares used in computing basic and diluted net loss per share 93,015 83,309 68,336 56Table of ContentsLiquidity and Capital ResourcesWe have incurred operating losses since inception, and at December 31, 2012, we had an accumulated deficit of $246.6 million. Since our inception,we have relied primarily on the proceeds from public and private sales of our equity securities and our capped royalty financing transaction to fund ouroperations.At December 31, 2012, we had cash and cash equivalents of $93.0 million, compared to $39.6 million at December 31, 2011. Net cash used inoperating activities for the years ended December 31, 2012, 2011 and 2010 was $36.0 million, $27.4 million and $22.3 million, respectively. We used cashin each period primarily for research and development activities, including efforts toward the submission and prosecution of the NDA for Korlym, for thecommercialization of Korlym and to develop administrative infrastructure to support commercialization.In July 2012, we sold 11.0 million shares of our common stock in an underwritten public offering for net proceeds of $46.1 million after deductingexpenses of the offering.In March 2012, we issued approximately 4.2 million shares of our common stock upon the exercise of warrants that had been issued in a privateplacement transaction in April 2010 and sold new warrants to the same investors to purchase approximately 4.2 million shares of common stock. The netproceeds generated in this transaction were $12.8 million, after the deduction of issuance costs. In addition, during the year ended December 31, 2012,additional warrants and stock options were exercised for the purchase of our common generating aggregate net proceeds of $760,000.In March 2008, we entered into a CEFF with Kingsbridge, under which the determination of the timing and amount of any CEFF financings were to bemade solely by us, subject to certain conditions. As discussed in Note 9 of our financial statements included in Part II, Item 8 of this Annual Report on Form10-K, effective August 7, 2012, we terminated the CEFF. No further securities will be sold under this agreement.As discussed in Notes 1 and 6 of our financial statements included in Part II, Item 8 of this Annual Report on Form 10-K, in August 2012, we enteredinto a Purchase and Sale Agreement (Financing Agreement) with Biopharma Secured Debt Fund II Sub, S.à r.l (Biopharma), a private limited liabilitycompany organized under the laws of Luxembourg, under which we received $30 million. Pursuant to the Financing Agreement, beginning with the quarterending June 30, 2013, we will make quarterly payments equal to (i) 20 percent of our net product sales of Korlym and any other products containingmifepristone or any of our proprietary selective GR-II antagonists (Covered Products), subject to certain quarterly payment caps through 2015 and(ii) 20 percent of any upfront, milestone or other contingent payments we receive under co-promotion or out-licensing agreements with respect to CoveredProducts subsequent to entering into the agreement (without application of caps), until we have made cumulative payments of $45 million. Under the termsof the Financing Agreement, our payments are variable, with no fixed minimums. If there are no net sales, upfront, milestone or other contingent payments ina period with respect to Covered Products, then no payment will be due for that period.We expect cash used in operating activities will increase during 2013 as compared to spending levels in 2012 due to the continued commercializationof Korlym, the continuation and scale-up of our phase 3 clinical trial of mifepristone for the treatment of psychotic depression and the continueddevelopment of our selective GR-II antagonists, which will be only partially offset by sales of Korlym. We expect our funding requirements for operatingactivities may increase in 2014 and possibly beyond as costs associated with the continuation of our development program for Cushing’s syndrome,continuation and expansion of our development programs for psychotic depression and our selective GR-II antagonists, research activities,commercialization activities and selling, general and administrative expenses may be only partially offset by revenues from sales of Korlym. In addition, asdiscussed below under the caption Contractual Obligations and Commercial Commitments, beginning in July 2013 we will be required to make paymentsunder the Biopharma Financing Agreement, the amount of which will be variable.We may choose to raise additional funds to finance our strategic priorities. We cannot be certain that additional funding will be available onacceptable terms or at all. Further, any additional equity financing may be 57Table of Contentsdilutive to stockholders, and any debt financing, if available, may involve restrictive covenants. If we obtain funds through collaborations with others, thesearrangements may be on unfavorable terms or may require us to relinquish certain rights to our technologies or product candidates, including potentially ourlead product candidate that we would otherwise seek to develop on our own.While we monitor the cash balance in our checking account and transfer the funds in only as needed, these cash balances and our money market fundcould be impacted if the underlying financial institution were to fail or were subject to other adverse conditions in the financial markets. To date, we haveexperienced no loss or lack of access to cash in our checking accounts or money market fund.Contractual Obligations and Commercial CommitmentsThe following table presents our estimates of obligations under contractual agreements as of December 31, 2012. Contractual Obligations Total Less than1 year 1-3Years 3-5Years More than5 Years (in thousands) Long-term obligation $45,000 Other contractual obligations: Research and development studies $8,214 $5,544 $2,670 $— $— Commercial activities 1,116 466 650 — — Operating lease 428 428 — — — Minimum royalty payments 50 100 100 50 per year Total other contractual obligations $6,488 $3,420 $100 $50 per year As discussed above under the caption “Liquidity and Capital Resources”, in August 2012, we entered into a Financing Agreement with Biopharma under which we received $30 million from Biopharma.In consideration of the $30 million payment, we are obligated to make payments to Biopharma totaling $45 million, calculated as follows: • 20 percent of our net product sales of Covered Products, beginning with the calendar quarter ending June 30, 2013, subject to quarterly payment caps of $2,250,000 during 2013, $3,000,000during 2014, and $3,750,000 during 2015. There is no quarterly cap on payments with respect to net product sales in 2016 and later. • 20 percent of payments received for upfront, milestone or other contingent fees under co-promotion and out-license agreements for Covered Products (without application of quarterly caps),provided however, that any amounts received under such agreements after the transaction’s effective date of August 2, 2012 but before June 30, 2013 would be deferred and made simultaneouslywith the payment for the calendar quarter ending June 30, 2013. • The percentage used to calculate our payments to Biopharma would increase to 50 percent and any applicable payment caps would lapse if we (i) fail to provide Biopharma with certaininformation regarding our promotion and sales of Covered Products, (ii) do not devote a commercially reasonable amount of resources to the promotion and marketing of the Covered Products or(iii) violate the indebtedness covenant by incurring indebtedness greater than the sum of earnings before interest, taxes, depreciation and amortization, including such items as non-cash stock-based compensation, (EBITDA) for the four calendar quarters preceding such incurrence and, in each case, fail to cure within the applicable cure period. • Upon the occurrence of a Corcept change of control transaction or the licensing of Korlym to a third-party for promotion and sale in the United States, the entire $45 million, less any amountsalready paid by us, would become due.Under the terms of the Financing Agreement, our payments are entirely variable, with no fixed minimums. The timing of our payments is determined by future sales and other receipts. If there are no netsales, upfront, milestone or other contingent payments in a period with respect to Covered Products, then no payment will be due for that period. Biopharma’s right to receive payments will expire once ithas received cumulative payments of $45 million. Amounts reflected for research and development studies exclude amounts included in accounts payable and accrued clinical costs reflected on the balance sheet as of December 31, 2012. During 2008, we entered into agreements for services in connection with our ongoing Phase 3 trial to confirm the utility of mifepristone for the treatment of the psychotic features of psychotic depression.The total commitment under these original agreements was $21.1 million. In June 2009, we amended these agreements to reduce the amounts of commitments with these 58(1)(2)and (3)(4)(5)(6)(1)(2)(3)Table of Contents organizations by $5.0 million in accordance with the short-term reduction in the scope of activities under this trial. In December 2012, we further amended these agreements to reflect the increase in trialactivities toward our goal of concluding trial enrolment by the end of 2013, increasing the cost by $2.5 million. The total commitment under these agreements, including amendments through 2012, isnow estimated to be $18.6 million over the course of the trial. We expensed $10.4 million of these costs through December 31, 2012, with the remainder to be incurred over the course of the trial. Underthe master services agreements with these vendors, the project contracts may be terminated upon thirty to sixty days notice. If terminated early, we would be responsible for the costs incurred by thevendors through the effective date of termination plus cancellation charges as stipulated in the agreements. In June 2012, we amended our agreement with United Biosource Corporation for reimbursement support services related to our Support Program for Access and Reimbursement for Korlym (SPARK). Thetotal commitment under the agreement is $2.7 million, of which $1.6 million had been incurred through December 31, 2012, with the remainder to be incurred over the course of the agreement. In June 2012, we signed an amendment to the lease for our office space that reflected an expansion of the space and extended our occupancy through December 2013. The aggregate commitment for baserent through the term of the amendment is $630,000, of which $202,000 was incurred during the second half of 2012, with the remainder to be incurred during 2013. The amended lease provides us withan option to extend the lease for one additional year. Under our cancellable license agreement with Stanford University, we are obligated to make nonrefundable minimum royalty payments of $50,000 annually for as long as we maintain our licenses withStanford; however, these payments are creditable against future royalties.We also have other contractual payment obligations and purchase commitments, the timing of which are contingent on future events. (a)Under our license agreement with Stanford University related to the patent covering the use of GR-II antagonists to treat the psychosis associated with psychotic depression and early dementia, we areobligated to make milestone payments to Stanford of $50,000 upon filing of an NDA covering a licensed product and $200,000 upon FDA approval of a licensed product. The milestone payments payableto Stanford under these licenses are creditable against future royalties. (b)Under the agreement with a contract research company we may be obligated to make milestone payments upon the occurrence of certain events, including: (i) $5,000 upon patent filings in connection withthe project; (ii) $100,000 for each entry into a Phase 1 clinical trial; and (iii) $500,000 in respect of each first national regulatory approval of each product arising from work performed under the agreement,provided that sales of the product by the Company or any future licensees reach $5,000,000. These obligations remain in force after the conclusion of work under the agreement. There are no royaltyobligations associated with this contract. (c)Pursuant to our memorandum of understanding with ScinoPharm, ScinoPharm agrees to manufacture API for mifepristone for the treatment of psychotic depression and we agree to purchase at least$1,000,000 bulk mifepristone per year following the commercial launch of mifepristone in that indication. (d)In November 2006, we entered into an agreement with PCAS for the manufacture of mifepristone, the API in Korlym, for our development and commercial needs for an initial period of five years. Theagreement provides for an automatic extension for one additional year and has been further extended to June 30, 2013. We are currently in discussions for a new contract to continue the relationshipthereafter. The current agreement calls for us to purchase from PCAS at least 75 percent of our requirements through the expiration of the agreement. If PCAS is unable to manufacture the product for aconsecutive six-month period, we have the right to terminate the agreement without penalty.Net Operating Loss CarryforwardsAt December 31, 2012 we had net operating loss carryforwards available to offset any future taxable income that we may generate for federal incometax purposes of $116.2 million, which expire in the years 2019 through 2032, and California net operating loss carryforwards of $110.6 million, which expirein the years 2013 through 2032. We also had federal and California research and development tax credits of $17.9 million and $2.0 million, respectively. Thefederal research credits will expire in the years 2019 through 2032 and the California research credits have no expiration date. Our deferred tax assets havebeen offset by a full valuation allowance as the realization of such assets is uncertain. Utilization of our net operating losses and tax credit carryforwards maybe subject to substantial annual limitation due to the ownership change limitations provided by the Internal Revenue Code and similar state provisions. Suchlimitations could result in the expiration of the net operating losses and tax credit carryforwards before utilization.Off-Balance Sheet ArrangementsNone. 59(4)(5)(6)Table of ContentsCritical Accounting Policies and EstimatesOur financial statements have been prepared in accordance with U.S. generally accepted accounting principles. The preparation of these financialstatements requires us to make estimates and judgments that affect the reported amounts of assets, liabilities and expenses. We base our estimates onhistorical experience and on various other assumptions that we believe to be reasonable under the circumstances, the results of which form the basis formaking judgments about the carrying values of assets and liabilities that are not readily apparent from other sources. Actual results may differ from theseestimates under different assumptions or conditions.Net Product SalesWe sell Korlym to a specialty pharmacy and a specialty distributor, which subsequently resell Korlym to patients and healthcare providers. Werecognize product revenues from sales of Korlym upon delivery to our customers as long as (i) there is persuasive evidence that an arrangement existsbetween ourselves and the customer, (ii) collectability is reasonably assured and (iii) the price is fixed or determinable. In order to conclude that the price isfixed or determinable, we must be able to (i) calculate gross product revenues from the sales to our customers and (ii) reasonably estimate net productrevenues.We calculate gross product revenues based on the price that we charge our customers. We estimate our net product revenues by deducting from ourgross product revenues (a) trade allowances, such as discounts for prompt payment and distributor fees, (b) estimated government rebates and chargebacks,(c) reserves for expected product returns and (d) estimated costs of patient assistance programs. We initially record estimates for these deductions at the timewe recognize the gross revenue. We update our estimates on a recurring basis as new information becomes available.Trade Allowances: We offer our customers a discount on Korlym sales for payment within 30 days. We also offer them a small discount for theprovision of data services. We expect our customers to earn these discounts and accordingly deduct them in full from gross product revenues and tradereceivables at the time we recognize such revenues.Rebates and Chargebacks: We contract with Medicaid and other government agencies so that Korlym will be eligible for purchase by, or qualify forpartial or full reimbursement from, such government programs. We estimate the rebates and chargebacks that we will be obligated to provide to governmentprograms and deduct these estimated amounts from our gross product sales at the time the revenues are recognized. We base our estimates of these rebates andchargebacks upon (i) the discount amounts applicable to government-funded programs and (ii) information obtained from our vendors regarding thepercentage of sales by our customers to patients who are covered by entities or programs that are eligible for such rebates and chargebacks.Allowances for Patient Assistance Program: We provide financial assistance to eligible patients whose insurance policies require them to pay highdeductibles and co-pays. We estimate the cost of assistance to be provided under this program by applying our actual experience regarding such assistance toour estimate of the percentage of our sales in the period that will be provided to patients covered by the program.Sales Returns: Our customers have the right to return Korlym beginning six months before the labeled expiration date and ending 12 months after thelabeled expiration date. This right of return is extended to our specialty distributor channel’s hospital customers who generally have the right to return onlyunopened bottles. The expiration date for our Korlym product sold in 2012 will not occur until late in 2013. We estimate the amount of Korlym that webelieve will be returned and deduct that estimated amount from gross revenue at the time we recognize such revenue. When estimating future returns, weanalyze quantitative and qualitative information including, but not limited to, actual return rates, the amount of product in the distribution channel, theexpected shelf life of such product, current and projected product demand, the introduction of competing products that may erode demand, and broadeconomic and industry-wide indicators. If we cannot reasonably estimate product returns with respect to a particular sale, we defer recognition of revenuefrom that sale until such time as a reasonable estimate can be made. 60Table of ContentsInventory and Cost of SalesWe consider regulatory approval of product candidates to be uncertain, and product manufactured prior to regulatory approval may not be sold unlessregulatory approval is obtained. We expense manufacturing costs for product candidates incurred prior to regulatory approval as research and developmentexpenses as we incur them. When regulatory approval of a product is obtained, we begin capitalizing manufacturing costs related to the approved productinto inventory.We value our inventories at the lower of cost or net realizable value. We determine the cost of inventory using the specific identification method,which approximates a first-in, first-out basis. We analyze our inventory levels quarterly and write down inventory that has become obsolete or has a cost basisin excess of its expected net realizable value, as well as any inventory quantities in excess of expected requirements. Any expired inventory is disposed ofand the related costs are recognized as cost of sales.Cost of sales includes the cost of product (the cost to manufacture Korlym, which includes material, third-party manufacturing costs and indirectpersonnel and other overhead costs) based on units for which revenue is recognized in the current period, as well as costs of stability testing, logistics anddistribution of the product. We began capitalizing Korlym production costs as inventory following approval by the FDA on February 17, 2012. Prior toreceiving FDA approval for Korlym, we expensed all costs related to the manufacturing of the product (including stability costs and manufacturing overhead)as incurred; we classified these costs as research and development expense. A portion of the product manufactured prior to FDA approval is available for us touse commercially.Inventory amounts that are not expected to be consumed within twelve months following the balance sheet date are classified as a noncurrent asset.Accruals of Research and Development CostsWe recorded accruals for estimated costs of research, pre-clinical and clinical studies, and manufacturing development with outstanding balances of$843,000 and $644,000 as of December 31, 2012 and 2011, respectively. These costs are a significant component of our research and development expenses.We make significant judgments and estimates in determining the accrual balance in each reporting period. Accrued clinical trial costs are based on estimatesof the work completed under the service agreements, milestones achieved, patient enrollment and past experience with similar contracts and serviceproviders. Our estimate of the work completed, and associated costs to be accrued, includes our assessment of the information received from our third-partycontract research organizations and the overall status of our clinical trial activities. In the past, we have not experienced any material deviations betweenaccrued and actual clinical trial expenses. However, actual services performed, number of patients enrolled and the rate of patient enrollment may vary fromour estimates, resulting in adjustments to clinical trial expense in future periods.Stock-based compensationStock-based compensation arises from the granting of stock options to employees and directors, as well as to non-employees.Employees and directorsOur accounting practices and the estimates and judgments that are considered in determining fair value in regard to stock option grants to employeesand directors are as follows: • For options granted from January 1, 2006 through September 2009, the expected term used in determining the fair value-based measurement ofoptions was based on the “simplified” method prescribed by the SEC that considers the weighted average of the vesting period and contractuallife of the options. For options granted since September 2009, the expected term has been based on a formula that considers the expected serviceperiod and expected post-vesting termination behavior differentiated by whether the grantee is an employee, an officer or a director. 61Table of Contents • We base the expected volatility of our common stock used in determining the fair value-based measurement of option grants to employees,officers and directors on a weighted-average combination of the volatility of our own stock price and that of a group of peer companies for thosegrants with expected terms longer than the period of time that we have been a public company. For stock options granted to employees withexpected terms of less than the period of time that we have been a public company, the volatility is based on historical data of the price for ourcommon stock for periods of time equivalent to the expected term of these grants. • For service-based awards, we recognize the expense over the requisite service period utilizing the straight-line amortization method. For optionswith performance-based vesting criteria, we recognize the expense at such time as there is a high degree of probability (i.e., greater than 70%) ofachieving the required vesting criteria. • Since we have a limited base of employees and directors and have experienced minimal turnover, we do not apply a forfeiture rate. When anemployee terminates, we will record a change in accounting estimate that represents the difference between the expense recorded in the financialstatements and the expense that would have been recorded based upon the rights to options that vested during the individual’s service as anemployee.As of December 31, 2012, we had $8.9 million of unrecognized compensation expense for employee and director options outstanding as of that date,which had a remaining weighted-average vesting period of 2.7 years.Non-employeesAll stock option grants to consultants vest solely based upon continuing service, with the exception of a performance-based award granted during2010 for 50,000 shares and an award in December 2012 for 10,000 shares. Stock-based compensation related to service-based option grants to non-employeesis charged to expense on a straight line basis over the vesting period of the options, which approximates the period over which the related services arerendered, based on the fair value-based measurement of the options using the Black-Scholes option pricing model. The assumptions used in thesecalculations are similar to those used for the determination of fair value-based measurements for options granted to employees, with the exception that, fornon-employee options, we are required to use the remaining contractual term as the life of the option and the fair value-based measurement related tounvested non-employee options is re-measured quarterly, based on the then current stock price as reflected on the NASDAQ Capital Market. For options withperformance-based vesting criteria, we recognize expense based on the minimum number of shares that will vest over time as the criteria are met based on theBlack-Scholes valuation of the vested shares.Long-term obligationThe accounting for the Financing Agreement with Biopharma requires us to make certain estimates and assumptions, including the timing of royaltypayments due to Biopharma, the expected rate of return to Biopharma, the split between current and long-term portions of the obligation and the accretion ofrelated interest expense. Korlym has only been marketed since April 2012 and the magnitude and timing of Korlym revenue is difficult to predict. Therefore,these estimates and assumptions are subject to significant variability and are likely to change as we gain experience marketing Korlym, which will result inchanges in our classification of the current and long-term portions of the amounts payable pursuant to this financing agreement, as well as the internal rate ofreturn paid to Biopharma and the accretion of interest expense related to this obligation. Actual payment amounts will be based on Korlym receipts over theterm of the Financing Agreement but in no event will the total amount paid to Biopharma exceed $45.0 million. 62Table of ContentsITEM 7A.QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISKQuantitative and Qualitative Disclosures About Market RiskInterest Rate RiskThe primary objective of our investment activities is to preserve principal while at the same time maximizing the income we receive from ourinvestments without significantly increasing risk of loss. As of December 31, 2012, the fair value of our cash and cash equivalents was $93.0 million andconsisted primarily of money market funds maintained at major U.S. financial institutions. To minimize our exposure to interest rate risk, we have limited thematurities of our investments to less than two years with an average maturity not to exceed one year. Due to the short-term nature of these instruments, a 10%increase or decrease in market interest rates would not have a material impact on the total value of our portfolio as of December 31, 2012. ITEM 8.FINANCIAL STATEMENTS AND SUPPLEMENTARY DATAThe financial statements required by this item are set forth beginning at page F-1 of this report and are incorporated herein by reference. ITEM 9.CHANGES IN AND DISAGREEMENTS WITH ACCOUNTANTS ON ACCOUNTING AND FINANCIAL DISCLOSURENone. ITEM 9A.CONTROLS AND PROCEDURES (a)Evaluation of Disclosure Controls and ProceduresWe maintain disclosure controls and procedures that are designed to ensure that information required to be disclosed in our periodic and current reportsthat we file with the SEC is recorded, processed, summarized and reported within the time periods specified in the SEC’s rules and forms, and that suchinformation is accumulated and discussed with our management, including our Chief Executive Officer, Chief Financial Officer and Chief AccountingOfficer, as appropriate, to allow timely decisions regarding required disclosure. In designing and evaluating the disclosure controls and procedures,management recognized that any controls and procedures, no matter how well designed and operated, can provide only reasonable and not absoluteassurance of achieving the desired control objectives. In reaching a reasonable level of assurance, management necessarily was required to apply its judgmentin evaluating the cost-benefit relationship of possible controls and procedures. In addition, the design of any system of controls also is based in part uponcertain assumptions about the likelihood of future events, and there can be no assurance that any design will succeed in achieving its stated goals under allpotential future conditions; over time, control may become inadequate because of changes in conditions, or the degree of compliance with policies orprocedures may deteriorate. Because of the inherent limitations in a cost-effective control system, misstatements due to error or fraud may occur and not bedetected.As of December 31, 2012, our Chief Executive Officer, Chief Financial Officer and Chief Accounting Officer have evaluated our disclosure controlsand procedures (as defined in Rules 13a-15(e) and 15d-15(e) of the Exchange Act) which were designed to ensure that the information required to bedisclosed by us in this Annual Report on Form 10-K was recorded, processed, summarized and reported within the time periods specified in the SEC’s rulesand on Form 10-K. Our disclosure controls and procedures are designed to provide reasonable, not absolute, assurance that the objectives of our disclosurecontrol system are met. Based on the evaluation, our Chief Executive Officer, Chief Financial Officer and Chief Accounting Officer have concluded that ourdisclosure controls and procedures are effective.There were no changes in our internal controls over financial reporting during the quarter ended December 31, 2012 that have materially affected, orare reasonably likely to materially affect, our internal control over financial reporting. 63Table of Contents(b)Management’s Report on Internal Control Over Financial ReportingOur management is responsible for establishing and maintaining adequate internal control over financial reporting, as such term is defined inExchange Act Rule 13a-15(f). Our internal control system is designed to provide reasonable assurance regarding the preparation and fair presentation offinancial statements for external purposes in accordance with generally accepted accounting principles. All internal control systems, no matter how welldesigned, have inherent limitations and can provide only reasonable assurance that the objectives of the internal control system are met.Our management, including our Chief Executive Officer, Chief Financial Officer and Chief Accounting Officer, conducted an evaluation of theeffectiveness of our internal control over financial reporting, based on criteria established in Internal Control — Integrated Framework issued by theCommittee of Sponsoring Organizations of the Treadway Commission (COSO). Based on this evaluation, our management concluded that our internalcontrol over financial reporting was effective as of December 31, 2012.Our independent registered public accounting firm has issued an attestation report on our internal control over financial reporting as included below. (c)Report of Independent Registered Public Accounting FirmThe Board of Directors and Stockholders of Corcept Therapeutics IncorporatedWe have audited Corcept Therapeutics Incorporated’s internal control over financial reporting as of December 31, 2012, based on criteria establishedin Internal Control — Integrated Framework issued by the Committee of Sponsoring Organizations of the Treadway Commission (the COSO criteria). CorceptTherapeutics Incorporated’s management is responsible for maintaining effective internal control over financial reporting, and for its assessment of theeffectiveness of internal control over financial reporting included in the accompanying Management’s Report on Internal Control Over Financial Reporting.Our responsibility is to express an opinion on the Company’s internal control over financial reporting based on our audit.We conducted our audit in accordance with the standards of the Public Company Accounting Oversight Board (United States). Those standards requirethat we plan and perform the audit to obtain reasonable assurance about whether effective internal control over financial reporting was maintained in allmaterial respects. Our audit included obtaining an understanding of internal control over financial reporting, assessing the risk that a material weaknessexists, testing and evaluating the design and operating effectiveness of internal control based on the assessed risk, and performing such other procedures aswe considered necessary in the circumstances. We believe that our audit provides a reasonable basis for our opinion.A company’s internal control over financial reporting is a process designed to provide reasonable assurance regarding the reliability of financialreporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles. A company’sinternal control over financial reporting includes those policies and procedures that (1) pertain to the maintenance of records that, in reasonable detail, 64Table of Contentsaccurately and fairly reflect the transactions and dispositions of the assets of the company; (2) provide reasonable assurance that transactions are recorded asnecessary to permit preparation of financial statements in accordance with generally accepted accounting principles, and that receipts and expenditures of thecompany are being made only in accordance with authorizations of management and directors of the company; and (3) provide reasonable assuranceregarding prevention or timely detection of unauthorized acquisition, use, or disposition of the company’s assets that could have a material effect on thefinancial statements.Because of its inherent limitations, internal control over financial reporting may not prevent or detect misstatements. Also, projections of anyevaluation of effectiveness to future periods are subject to the risk that controls may become inadequate because of changes in conditions, or that the degreeof compliance with the policies or procedures may deteriorate.In our opinion, Corcept Therapeutics Incorporated maintained, in all material respects, effective internal control over financial reporting as ofDecember 31, 2012, based on the COSO criteria.We also have audited, in accordance with the standards of the Public Company Accounting Oversight Board (United States), the 2012 financialstatements of Corcept Therapeutics Incorporated and our report dated March 15, 2013 expressed an unqualified opinion thereon./s/ Ernst & Young LLPRedwood City, CaliforniaMarch 15, 2013 ITEM 9B.OTHER INFORMATIONNone. 65Table of ContentsPART IIICertain information required by Part III is omitted from this Annual Report on Form 10-K because we expect to file with the U.S. Securities andExchange Commission, not later than 120 days after the end of the fiscal year covered by this Annual Report on Form 10-K, a definitive proxy statement (theProxy Statement), pursuant to Regulation 14A in connection with the solicitation of proxies for our 2013 Annual Meeting of Stockholders, and certaininformation included therein is incorporated herein by reference. ITEM 10.DIRECTORS, EXECUTIVE OFFICERS AND CORPORATE GOVERNANCEThe information required by this Item concerning our executive officers is set forth in Part I of this Annual Report on Form 10-K. The remaininginformation required by this Item will be included in the Proxy Statement and is incorporated herein by reference. ITEM 11.EXECUTIVE COMPENSATIONCompensation Discussion and AnalysisThe information required by this Item will be included in the Proxy Statement and is incorporated herein by reference. ITEM 12.SECURITY OWNERSHIP OF CERTAIN BENEFICIAL OWNERS AND MANAGEMENT AND RELATED STOCKHOLDERMATTERSThe information required by this Item will be included in the Proxy Statement and is incorporated herein by reference. ITEM 13.CERTAIN RELATIONSHIPS AND RELATED TRANSACTIONS, AND DIRECTOR INDEPENDENCEThe information required by this Item will be included in the Proxy Statement and is incorporated herein by reference. ITEM 14.PRINCIPAL ACCOUNTING FEES AND SERVICESThe information required by this Item will be included in the Proxy Statement and is incorporated herein by reference. 66Table of ContentsPART IV ITEM 15.EXHIBITS, FINANCIAL STATEMENT SCHEDULESThe following documents are filed as part of this Form 10-K(1) Financial Statements: Page Report of Independent Registered Public Accounting Firm F-2 Audited Financial Statements Balance Sheets F-3 Statements of Comprehensive Loss F-4 Statement of Stockholders’ Equity F-5 Statements of Cash Flows F-6 Notes to Financial Statements F-7 (2) Financial Statement Schedules:All schedules have been omitted because the information required to be set forth therein is not applicable or is shown in the financial statements ornotes thereto.(3) Exhibits:Item 601 of Regulation S-K requires the exhibits listed below. Each management contract or compensatory plan or arrangement required to be filed asan exhibit to this Form 10-K has been identified.(A) EXHIBITS ExhibitNumber Description of Document 3.1 Amended and Restated Certificate of Incorporation, as amended (incorporated by reference to Exhibit 3.1 to the registrant’s QuarterlyReport on Form 10-Q filed on August 9. 2012). 3.2 Amended and Restated Bylaws (incorporated by reference to Exhibit 3.1 to the registrant’s Current Report on Form 8-K filed onSeptember 27, 2007). 4.1 Specimen Common Stock Certificate (incorporated by reference to Exhibit 4.1 to the registrant’s Registration Statement on Form S-1(Registration No. 333-112676) filed on February 10, 2004). 4.2 Registration Rights Agreement by and among Corcept Therapeutics Incorporated and the investors signatory thereto, dated March 14,2008 (incorporated by reference to Exhibit 10.25 to the registrant’s Annual Report on Form 10-K filed on March 31, 2008). 4.3 Registration Rights Agreement by and between Corcept Therapeutics Incorporated and Kingsbridge Capital Limited, dated as of March25, 2008 (incorporated by reference to Exhibit 10.27 to the registrant’s Annual Report on Form 10-K filed on March 31, 2008). 4.4 Amendment to Registration Rights Agreement by and among Corcept Therapeutics Incorporated and the investors signatory thereto,dated November 11, 2008 (incorporated by reference to Exhibit 10.30 to the registrant’s Annual Report on Form 10-K filed on March 31,2009). 4.5 Registration Rights Agreement dated as of April 21, 2010 by and among Corcept Therapeutics Incorporated and the investors signatorythereto (incorporated by reference to Exhibit 4.2 to the registrant’s Current Report on Form 8-K filed on April 23, 2010). 67Table of ContentsExhibitNumber Description of Document 4.6 Registration Rights Agreement, dated as of March 29, 2012, by and among Corcept Therapeutics Incorporated and the investors signatorythereto (incorporated by reference to Exhibit 4.2 to the registrant’s Current Report on Form 8-K filed on March 29, 2012). 4.7 Form of Warrant issued in connection with the Securities Purchase Agreement by and among Corcept Therapeutics Incorporated and thepurchasers named therein, dated March 14, 2008 (incorporated by reference to Exhibit 4.4 to the registrant’s Annual Report on Form 10-Kfiled on March 31, 2008). 4.8 Form of Warrant issued in connection with Warrant Purchase Agreement dated as of March 25, 2012 by and among Corcept TherapeuticsIncorporated and the purchasers named therein (incorporated by reference to Exhibit 4.2 to the registrant’s Current Report on Form 8-Kfiled on March 29, 2012). 4.9 Warrant, dated March 25, 2008 issued to Kingsbridge Capital Limited (incorporated by reference to Exhibit 4.5 to the registrant’s AnnualReport on Form 10-K filed on March 31, 2008). 10.1 2000 Stock Option Plan (incorporated by reference to Exhibit 10.1 to the registrant’s Registration Statement on Form S-1 (RegistrationNo. 333-112676) filed on February 10, 2004). 10.2 License Agreement by and between The Board of Trustees of the Leland Stanford Junior University and Corcept TherapeuticsIncorporated, dated as of July 1, 1999 (incorporated by reference to Exhibit 10.6 to the registrant’s Registration Statement on Form S-1(Registration No. 333-112676) filed on February 10, 2004). 10.3# Memorandum of Understanding, Supply and Services Agreement, by and between Corcept Therapeutics Incorporated and ScinoPharmTaiwan, dated as of June 12, 2000 (incorporated by reference to Exhibit 10.9 to the registrant’s Registration Statement on Form S-1/A (FileNo. 333-112676) filed on March 19, 2004). 10.4 Master Services Agreement by and between Corcept Therapeutics Incorporated and PPD Development, LP, dated as of January 17, 2003(incorporated by reference to Exhibit 10.12 to the registrant’s Registration Statement on Form S-1/A (File No. 333-112676) filed on March19, 2004). 10.5# Manufacturing Agreement with Produits Chimiques Auxiliaires et de Synthese SA, dated November 8, 2006 (incorporated by reference toExhibit 10.15 to the registrant’s Annual Report on Form 10-K filed on April 2, 2007). 10.6 Form of Indemnification Agreement for directors and officers approved by the Board of Directors on September 24, 2007 (incorporated byreference to Exhibit 10.7 to the registrant’s Quarterly Report on Form 10-Q filed on November 14, 2007). 10.7 Securities Purchase Agreement by and among Corcept Therapeutics Incorporated and the purchasers named therein, dated March 14, 2008(incorporated by reference to Exhibit 10.24 to the registrant’s Annual Report on Form 10-K filed on March 31, 2008). 10.8 Common Stock Purchase Agreement by and between Kingsbridge Capital Limited and Corcept Therapeutics Incorporated dated as ofMarch 25, 2008 (incorporated by reference to Exhibit 10.26 to the registrant’s Annual Report on Form 10-K filed on March 31, 2008). 10.9# Master Service Agreement by and among Corcept Therapeutics Incorporated and ICON Clinical Research, L.P., signed on June 4, 2008(incorporated by reference to Exhibit 10.5 to the registrant’s Quarterly Report on Form 10-Q filed on August 14, 2008). 68††Table of ContentsExhibitNumber Description of Document 10.10 Amended and Restated Severance and Change in Control Agreement by and between Corcept Therapeutics Incorporated and Joseph K.Belanoff, M. D., dated September 19, 2008 (incorporated by reference to Exhibit 10.25 to the registrant’s Annual Report on Form 10-Kfiled on March 31, 2009). 10.11 Amended and Restated Severance and Change in Control Agreement by and between Corcept Therapeutics Incorporated and Robert L.Roe, M. D., dated September 19, 2008 (incorporated by reference to Exhibit 10.26 to the registrant’s Annual Report on Form 10-K filed onMarch 31, 2009). 10.12 Amended and Restated Severance and Change in Control Agreement by and between Corcept Therapeutics Incorporated and Anne M.LeDoux, dated September 19, 2008(incorporated by reference to Exhibit 10.27 to the registrant’s Annual Report on Form 10-K filed onMarch 31, 2009). 10.13 Amended and Restated Severance and Change in Control Agreement by and between Corcept Therapeutics Incorporated and James N.Wilson, dated September 19, 2008(incorporated by reference to Exhibit 10.28 to the registrant’s Annual Report on Form 10-K filed onMarch 31, 2009). 10.14 Securities Purchase Agreement by and among Corcept Therapeutics Incorporated and the purchasers named therein, dated October 12,2009 (incorporated by reference to Exhibit 10.1 to the registrant’s Quarterly Report on Form 10-Q filed on November 12, 2009). 10.15 Amended and Restated 2004 Equity Incentive Plan (incorporated by reference to the registrant’s Proxy Statement on Schedule 14A filedon May 7, 2009). 10.16 Form of Option Agreement for options granted pursuant to the Amended and Restated 2004 Equity Incentive Plan (incorporated byreference to Exhibit 10.25 to the registrant’s Annual Report on Form 10-K filed on March 15, 2011). 10.17 Development Agreement by and between Corcept Therapeutics Incorporated and Formulation Technologies L.L.C. d/b/a PharmaForm,dated as of December 14, 2006 (incorporated by reference to Exhibit 10.28 to the registrant’s Annual Report on Form 10-K filed on March15, 2011). 10.18 Master Services Agreement by and between Corcept Therapeutics Incorporated and United BioSource Corporation, dated as of June 29,2010 (incorporated by reference to Exhibit 10.29 to the registrant’s Annual Report on Form 10-K filed on March 15, 2011). 10.19 Employment offer letter to Steven Lo, dated August 9, 2010 (incorporated by reference to Exhibit 10.1 to the registrant’s Quarterly Reporton Form 10-Q filed on November 12, 2010). 10.20 Severance and Change in Control Agreement by and between Corcept Therapeutics Incorporated and Steven Lo, dated September 15,2010 (incorporated by reference to Exhibit 10.2 to the registrant’s Quarterly Report on Form 10-Q filed on November 12, 2010). 10.21 Severance and Change in Control Agreement by and between Corcept Therapeutics Incorporated and G. Charles Robb, dated September 1,2011 (incorporated by reference to Exhibit 10.2 to the registrant’s Quarterly Report on Form 10-Q filed on November 8, 2011). 10.22 Employment offer letter to G. Charles Robb dated August 12, 2011 (incorporated by reference to Exhibit 10.1 to the registrant’s QuarterlyReport on Form 10-Q filed on November 8, 2011). 10.23 Manufacturing and Supply Agreement with Formulation Technologies, LLC D/B/A PharmaForm, LLC, dated March 21, 2012(incorporated by reference to Exhibit 10.1 to the registrant’s Quarterly Report on Form 10-Q filed on May 10, 2012). 69††††††##††††#Table of ContentsExhibitNumber Description of Document 10.24 Warrant Purchase Agreement, dated as of March 25, 2012, by and among Corcept Therapeutics Incorporated and the purchasers namedtherein (incorporated by reference to Exhibit 10.1 to the registrant’s Current Report on Form 8-K filed on March 29, 2012). 10.25 Commercial Outsourcing Services Agreement with Integrated Commercialization Solutions, Inc., dated as of April 14, 2011 (incorporatedby reference to Exhibit 10.1 to the registrant’s Quarterly Report on Form 10-Q filed on August 9, 2012). 10.26 Amended and Restated Exclusive Pharmacy Product Purchase and Services Agreement with CuraScript, Inc., dated August 8, 2012(incorporated by reference to Exhibit 10.2 to the registrant’s Quarterly Report on Form 10-Q filed on August 9, 2012). 10.27 Amended and Restated Exclusive Wholesale Product Purchase Agreement with CuraScript SD Specialty Distribution, dated August 8,2012 (incorporated by reference to Exhibit 10.3 to the registrant’s Quarterly Report on Form 10-Q filed on August 9, 2012). 10.28† Corcept Therapeutics Incorporated 2012 Incentive Award Plan (incorporated by reference to Appendix A to the registrant’s DefinitiveProxy Statement on Schedule 14A filed with the SEC on May 21, 2012). 10.29 Form of 2012 Incentive Award Plan Stock Option Grant Notice and Agreement (incorporated by reference to Exhibit 4.5 to the registrant’sRegistration Statement on Form S-8 filed with the SEC on August 13, 2012). 10.30 Purchase and Sale Agreement with between Corcept Therapeutics Incorporated and Biopharma Secured Debt Fund II Sub, S.à r.l,, dated asof August 2, 2012 (incorporated by reference to Exhibit 10.4 to the registrant’s Quarterly Report on Form 10-Q filed on November 8,2012). 10.31 Amendment to Manufacturing Agreement with Produits Chimiques Auxiliaires et de Synthese SA, dated February 21, 2013. 23.1 Consent of Independent Registered Public Accounting Firm 24.1 Power of Attorney (See signature page) 31.1 Certification pursuant to Rule 13a-14(a) under the Securities Exchange Act of 1934 of Joseph K. Belanoff, M.D. 31.2 Certification pursuant to Rule 13a-14(a) under the Securities Exchange Act of 1934 of G. Charles Robb 32.1 Certification pursuant to 18 U.S.C. Section 1350 of Joseph K. Belanoff, M.D. 32.2 Certification pursuant to 18 U.S.C. Section 1350 of G. Charles Robb101* The following materials from the registrant’s Annual Report on Form 10-K for the year ended December 31, 2012, formatted in ExtensibleBusiness Reporting Language (XBRL): (i) Balance Sheets at December 31, 2012 and 2011, (ii) Statements of Comprehensive Loss for theYears Ended December 31, 2012, 2011 and 2010, (iii) Statements of Stockholders’ Equity for the Years Ended December 31, 2012, 2011and 2010, (iv) Statements of Cash Flows for the Years Ended December 31, 2012, 2011 and 2010, and (v) Notes to Financial Statements. #Confidential treatment granted †Management contract or compensatory plan or arrangement *Pursuant to Rule 406T of Regulation S-T, these XBRL data files are deemed furnished and not filed or a part of a registration statement or prospectusfor purposes of sections 11 or 12 of the Securities Act of 1933, as amended, are deemed not filed for purposes of section 18 of the Securities ExchangeAct of 1934, as amended, and otherwise is not subject to liability under these sections. 70###†#Table of ContentsSIGNATURESPursuant to the requirements of Section 13 or 15(d) of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on itsbehalf by the undersigned thereunto duly authorized. CORCEPT THERAPEUTICS INCORPORATEDBy: /s/ JOSEPH K. BELANOFF Joseph K. Belanoff, M.D.,Chief Executive OfficerDate: March 15, 2013POWER OF ATTORNEYKNOW ALL PERSONS BY THESE PRESENTS, that each person whose signature appears below hereby constitutes and appoints Joseph K. Belanoffand G. Charles Robb, and each of them acting individually, as his or her true and lawful attorneys-in-fact and agents, each with full power of substitution, forhim or her in any and all capacities, to sign any and all amendments to this report on Form 10-K and to file the same, with exhibits thereto and otherdocuments in connection therewith, with the Securities and Exchange Commission, granting unto said attorneys-in-fact and agents, with full power of each toact alone, full power and authority to do and perform each and every act and thing requisite and necessary to be done in connection therewith, as fully for allintents and purposes as he or she might or could do in person, hereby ratifying and confirming all that said attorneys-in-fact and agents, or his or theirsubstitute or substitutes, may lawfully do or cause to be done by virtue hereof.Pursuant to the requirements of the Exchange Act, this Annual Report on Form 10-K has been signed by the following persons on behalf of theregistrant and in the capacities and on the dates indicated: Signature Title Date/S/ JOSEPH K. BELANOFF Joseph K. Belanoff, M.D. Chief Executive Officer and Director (PrincipalExecutive Officer) March 15, 2013/S/ G. CHARLES ROBB G. Charles Robb Chief Financial Officer (Principal Financial Officer) March 15, 2013/S/ ANNE M. LEDOUX Anne M. LeDoux Vice President and Controller (Principal AccountingOfficer) March 15, 2013/S/ JAMES N. WILSON James N. Wilson Director and Chairman of the Board of Directors March 15, 2013/S/ G. LEONARD BAKER, JR. G. Leonard Baker, Jr. Director March 15, 2013/S/ DANIEL M. BRADBURY Daniel M. Bradbury Director March 15, 2013/S/ JOSEPH C. COOK, JR. Joseph C. Cook, Jr. Director March 15, 2013/S/ PATRICK G. ENRIGHT Patrick G. Enright Director March 15, 2013/S/ DAVID L. MAHONEY David L. Mahoney Director March 15, 2013/S/ JOSEPH L. TURNER Joseph L. Turner Director March 15, 2013 71Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDINDEX TO FINANCIAL STATEMENTS Page Report of Independent Registered Public Accounting Firm F-2 Audited Financial Statements Balance Sheets F-3 Statements of Comprehensive Loss F-4 Statement of Stockholders’ Equity F-5 Statements of Cash Flows F-6 Notes to Financial Statements F-7 F-1Table of ContentsREPORT OF INDEPENDENT REGISTERED PUBLIC ACCOUNTING FIRMThe Board of Directors and Stockholders of Corcept Therapeutics IncorporatedWe have audited the accompanying balance sheets of Corcept Therapeutics Incorporated as of December 31, 2012 and 2011, and the related statementsof comprehensive loss, stockholders’ equity and cash flows for each of the three years in the period ended December 31, 2012. These financial statements arethe responsibility of the Company’s management. Our responsibility is to express an opinion on these financial statements based on our audits.We conducted our audits in accordance with the standards of the Public Company Accounting Oversight Board (United States.) Those standardsrequire that we plan and perform the audit to obtain reasonable assurance about whether the financial statements are free of material misstatement. An auditincludes examining, on a test basis, evidence supporting the amounts and disclosures in the financial statements. An audit also includes assessing theaccounting principles used and significant estimates made by management, as well as evaluating the overall financial statement presentation. We believe thatour audits provide a reasonable basis for our opinion.In our opinion, the financial statements referred to above present fairly, in all material respects, the financial position of Corcept TherapeuticsIncorporated at December 31, 2012 and 2011, and the results of its operations and its cash flows for each of the three years in the period ended December 31,2012, in conformity with U.S. generally accepted accounting principles.We also have audited, in accordance with the standards of the Public Company Accounting Oversight Board (United States), Corcept TherapeuticsIncorporated’s internal control over financial reporting as of December 31, 2012, based on criteria established in Internal Control—Integrated Frameworkissued by the Committee of Sponsoring Organizations of the Treadway Commission and our report dated March 15, 2013 expressed an unqualified opinionthereon./s/ Ernst & Young LLPRedwood City, CaliforniaMarch 15, 2013 F-2Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDBALANCE SHEETS(in thousands, except per share amounts) December 31, 2012 2011 Assets Current assets: Cash and cash equivalents $93,032 $39,635 Trade receivables 557 — Inventory 853 — Prepaid expenses and other current assets 620 140 Total current assets 95,062 39,775 Strategic inventory 3,810 — Property and equipment, net of accumulated depreciation 150 26 Other assets 144 32 Total assets $99,166 $39,833 Liabilities and stockholders’ equity Current liabilities: Accounts payable $3,804 $3,611 Accrued clinical expenses 843 644 Accrued compensation 351 238 Other accrued liabilities 695 533 Long-term obligation—current portion 2,650 — Deferred revenue 16 — Total current liabilities 8,359 5,026 Long-term obligation, net of current portion 29,030 — Commitments Stockholders’ equity: Preferred stock, $0.001 par value, 10,000 shares authorized and no shares outstanding at December 31, 2012 or2011 — — Common stock, $0.001 par value, 280,000 and 140,000 shares authorized and 99,814 and 84,231 shares issuedand outstanding at December 31, 2012 and 2011, respectively 100 84 Additional paid-in capital 308,283 243,281 Accumulated deficit (246,606) (208,558) Total stockholders’ equity 61,777 34,807 Total liabilities and stockholders’ equity $99,166 $39,833 The accompanying notes are an integral part of these financial statements. F-3Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDSTATEMENTS OF COMPREHENSIVE LOSS(in thousands, except per share amounts) Year ended December 31, 2012 2011 2010 Product sales, net $3,307 $— $— Operating expenses: Cost of sales 91 — — Research and development 14,074 21,001 18,949 Selling, general and administrative 25,414 11,331 8,488 Total operating expenses 39,579 32,332 27,437 Loss from operations (36,272) (32,332) (27,437) Interest and other income — 3 1,496 Interest and other expense (1,776) (25) (25) Net loss and comprehensive loss $(38,048) $(32,354) $(25,966) Basic and diluted net loss per share $(0.41) $(0.39) $(0.38) Shares used in computing basic and diluted net loss per share 93,015 83,309 68,336 The accompanying notes are an integral part of these financial statements. F-4Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDSTATEMENT OF STOCKHOLDERS’ EQUITY(in thousands) Common Stock AdditionalPaid-in Capital NotesReceivablefromStockholders AccumulatedDeficit TotalStockholders’Equity Shares Amount Balance at December 31, 2009 62,475 $62 $172,369 $(101) $(150,238) $22,092 Sales of common stock under CEFF 519 1 1,609 — — 1,610 Issuance of common stock upon exercise of warrants andissuance of new warrants in private equity transaction 4,286 4 7,480 — — 7,484 Sale of common stock in public financing transaction 5,000 5 13,748 — — 13,753 Issuance of common stock upon exercise of options 124 — 151 — — 151 Stock-based compensation related to employee and directoroptions — — 1,947 — — 1,947 Stock-based compensation related to an option to a consultant — — 169 — — 169 Repayment of note receivable from stockholder — — — 4 — 4 Net loss and comprehensive loss (25,966) (25,966) Balance at December 31, 2010 72,404 72 197,473 (97) (176,204) 21,244 Sale of common stock in public financing transaction 11,500 12 41,771 — — 41,783 Issuance of common stock upon exercise of options 246 — 371 — — 371 Issuance of common stock upon exercise of warrants 81 — 231 — — 231 Stock-based compensation related to employee and directoroptions — — 3,016 — — 3,016 Stock-based compensation related to an option to a consultant — — 419 — — 419 Repayment of notes receivable from stockholders — — — 97 — 97 Net loss and comprehensive loss (32,354) (32,354) Balance at December 31, 2011 84,231 84 243,281 — (208,558) 34,807 Sale of common stock in public financing transaction 11,000 11 46,119 — — 46,130 Issuance of common stock upon exercise of warrants andissuance of new warrants in private equity transaction 4,202 4 12,815 — — 12,819 Issuance of common stock upon exercise of warrants 216 — 470 — — 470 Issuance of common stock upon exercise of options 165 1 288 — — 289 Stock-based compensation related to employee and directoroptions — — 5,102 — — 5,102 Stock-based compensation related to consultant options — — 208 — — 208 Net loss and comprehensive loss — — — (38,048) (38,048) Balance at December 31, 2012 99,814 $100 $308,283 $— $(246,606) $61,777 The accompanying notes are an integral part of these financial statements F-5Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDSTATEMENTS OF CASH FLOWS(in thousands) Year ended December 31, 2012 2011 2010 Operating activities Net loss $(38,048) $(32,354) $(25,966) Adjustments to reconcile net loss to net cash used in operations: Stock-based compensation 5,310 3,435 2,116 Accretion of interest expense 1,680 — — Amortization of debt financing costs 17 — — Depreciation and amortization of property and equipment 27 3 6 Changes in operating assets and liabilities: Trade receivables (557) — — Inventory (4,663) — — Prepaid expenses and other current assets (480) 278 135 Other assets 11 72 (23) Accounts payable 193 2.794 (453) Accrued clinical expenses 199 (171) 106 Accrued compensation and other liabilities 275 (1,457) 1,794 Deferred revenue 16 — — Net cash used in operating activities (36,020) (27,400) (22,285) Investing activities Purchases of property and equipment (151) (25) — Net cash used in investing activities (151) (25) — Financing activities Proceeds from issuance of common stock and warrants, including collection of stockholder notesreceivable, net of cash paid for issuance costs 59,708 42,482 23,002 Proceeds from issuance of long-term obligation, net of cash paid for issuance costs 29,860 — — Principal payments of obligations under capital leases — — (6) Net cash provided by financing activities 89,568 42,482 22,996 Net increase in cash and cash equivalents 53,397 15,057 711 Cash and cash equivalents at beginning of period 39,635 24,578 23,867 Cash and cash equivalents at end of period $93,032 $39,635 $24,578 The accompanying notes are an integral part of these financial statements F-6Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDNOTES TO FINANCIAL STATEMENTS1. Basis of Presentation and Summary of Significant Accounting PoliciesDescription of BusinessCorcept Therapeutics Incorporated was incorporated in the state of Delaware on May 13, 1998, and our facilities are located in Menlo Park, California.Corcept is a pharmaceutical company engaged in the discovery, development and commercialization of drugs for the treatment of severe metabolic andpsychiatric disorders. Since our inception in May 1998, we have been developing our lead product, Korlym™ , a potent glucocorticoid receptor II (GR-II)antagonist, which means that it blocks the activity of cortisol. On February 17, 2012, the United States Food and Drug Administration (FDA) approvedKorlym (mifepristone) 300 mg Tablets in the United States as a once-daily oral medication for treatment of hyperglycemia secondary to hypercortisolism inadult patients with endogenous Cushing’s syndrome who have type 2 diabetes mellitus or glucose intolerance and have failed surgery or are not candidatesfor surgery. We released Korlym for sale on April 10, 2012. We also have a clinical program for the use of mifepristone, the active ingredient in Korlym, forthe treatment of the psychotic features of psychotic depression. We are currently conducting a Phase 3 study for this indication. In addition, we havediscovered three series of novel selective GR-II antagonists and have moved a compound from one of these series, into clinical development. Unlessotherwise stated, all references in these financial statements to “we,” “us,” “our,” “Corcept,” the “Company,” “our company” and similar designations refer toCorcept Therapeutics Incorporated.We were considered to be in the development stage prior to the second quarter of 2012 when we recorded significant revenue from our plannedprincipal operations following commercialization of Korlym.Use of EstimatesThe preparation of financial statements in conformity with U.S. generally accepted accounting principles requires management to use assumptions andmake estimates to form judgments that affect the amounts reported in the financial statements and accompanying notes. Actual results could differ materiallyfrom those estimates.We evaluate our estimates and assumptions on an ongoing basis, including those related to our discounts for prompt payment of sales invoices,chargebacks and rebates, patient assistance, potential product returns, excess/obsolete inventories, allowances for doubtful accounts, accruals of clinical andpreclinical expenses, contingent liabilities, and the timing of payments with respect to our long-term capped royalty obligation, which determine its effectiveinterest rate. We base our estimates on relevant experience and on other specific assumptions that we believe are reasonable.We update our assumptions and estimates on a recurring basis as new information becomes available. Any changes in estimates are recorded in theperiod of the change.Cash and Cash EquivalentsWe invest our excess cash in bank deposits, money market accounts, corporate debt securities, and/or obligations of the U.S. government and U.S.government sponsored entities. We consider all highly liquid investments purchased with maturities of three months or less from the date of purchase to becash equivalents. Cash equivalents are carried at fair value, which approximates cost and, as of December 31, 2012 and 2011, all of our funds were invested incash and cash equivalents that consist of a money market fund maintained at a major U.S. financial institution. F-7Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDNOTES TO FINANCIAL STATEMENTS, Continued Credit Risks and ConcentrationsWe have a concentration of credit risk related to our cash and cash equivalents. We are exposed to credit risk in the event of default by the financialinstitutions holding these funds to the extent of the amount recorded on the balance sheet. We mitigate this risk by investing in a money market fund thatinvests primarily in short-term U.S. Treasury notes and bills. For the years ended December 31, 2012, 2011 and 2010, we experienced no loss or lack of accessto cash and cash equivalents in our operating or investment accounts.Beginning with the commercialization of Korlym in April 2012, we are also exposed to credit risk in regard to our trade receivables. We have only twocustomers — one specialty pharmacy and one specialty distributor, which are subsidiaries of the same corporate parent. We extend credit to these customersbased on their individual creditworthiness and that of their shared parent organization. We monitor our exposure and will record a reserve againstuncollectible trade receivables as necessary.We have a concentration of risk in regard to the manufacture of our product. As of December 31, 2012, we had one tablet manufacturer with anoperational facility — AAI Pharma, which was approved by the FDA in November 2012 for the manufacture of our commercial tablets. Our original tabletmanufacturer, PharmaForm, has temporarily suspended manufacturing operations for relocation to a new facility. We are currently in negotiations for acommercial manufacturing agreement with AAI Pharma. If PharmaForm is not able to qualify their new site or if AAI Pharma is unable to prepare Korlymtablets in the quantities and time frame required, we may not be able to manufacture our product in a timely manner. In addition, we have a single-sourcemanufacturer of mifepristone, the active pharmaceutical ingredient (API), in Korlym. In order to mitigate these risks related to the manufacture of our product,we placed strategic orders for additional quantities of mifepristone API during 2012 and had our original tablet manufacturer, PharmaForm, prepareadditional batches during the summer of 2012 before the closure of their qualified manufacturing site.Fair Value MeasurementsWe categorize financial instruments in a fair value hierarchy that prioritizes the information used to develop assumptions for measuring fair value. Thefair value hierarchy gives the highest priority to quoted prices in active markets for identical assets or liabilities (Level 1 input), then to quoted prices (innon-active markets or in active markets for similar assets or liabilities), inputs other than quoted prices that are observable for the asset or liability, and inputsthat are not directly observable, but that are corroborated by observable market data for the asset or liability (Level 2 input), then the lowest priority tounobservable inputs, for example, our own data about the assumptions that market participants would use in pricing an asset or liability (Level 3 input). Fairvalue is a market-based measurement, not an entity-specific measurement, and a fair value measurement should therefore be based on the assumptions thatmarket participants would use in pricing the asset or liability.No assets or liabilities in our financial statements are required to be reported at fair value other than our cash and cash equivalents and the obligationunder our Financing Agreement with Biopharma.Trade ReceivablesTrade receivables are recorded net of customer allowances for prompt payment and data services, doubtful accounts and sales returns. See thediscussion below under “Net Product Sales” regarding the methods for estimation of these allowances and sales returns. We determine our allowance fordoubtful accounts based on existing contractual payment terms, actual payment patterns of our customers and individual customer circumstances. To date,we have determined that an allowance for uncollectible trade receivables is not required. F-8Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDNOTES TO FINANCIAL STATEMENTS, Continued InventoryWe consider regulatory approval of product candidates to be uncertain, and product manufactured prior to regulatory approval may not be sold unlessregulatory approval is obtained. We expense the manufacturing costs for product candidates incurred prior to regulatory approval as research anddevelopment expense as we incur them. When regulatory approval of a product is obtained, we begin capitalizing manufacturing costs related to theapproved product into inventory, provided such product is produced by a facility the FDA has approved to manufacture Korlym.We value our inventories at the lower of cost or net realizable value. We determine the cost of inventory using the specific identification method,which approximates a first-in, first-out basis. We analyze our inventory levels quarterly and write down inventory that has become obsolete or has a cost basisin excess of its expected net realizable value, as well as any inventory quantities in excess of expected requirements. Any expired inventory is disposed ofand the related costs are recognized as cost of sales in the statement of comprehensive loss.Inventory amounts that are not expected to be consumed within twelve months following the balance sheet date are classified as strategic inventory, anoncurrent asset.Property and EquipmentWe state property and equipment at cost less accumulated depreciation. Property and equipment are depreciated using the straight-line method overthe estimated useful lives of the assets, ranging from three to five years.Long-term ObligationIn August 2012, we entered into a Purchase and Sale Agreement (Financing Agreement) with Biopharma Secured Debt Fund II Sub, S.à r.l (Biopharma),a private limited liability company organized under the laws of Luxembourg. Under the terms of the Financing Agreement, we received $30 million fromBiopharma and are obligated to make payments calculated as a percentage of (i) any licensing or other contingent payments arising from Korlym and anyother products containing mifepristone or any of our proprietary selective GR-II antagonists (Covered Products) and (ii) net Covered Product revenues earnedin the calendar quarter ending June 30, 2013 and thereafter (together, Korlym Receipts), until such time as we have paid Biopharma a total of $45 million.The accounting for the Financing Agreement requires us to make certain estimates and assumptions, including the timing of royalty payments due toBiopharma, the expected rate of return to Biopharma, the split between current and long-term portions of the obligation and the accretion of related interestexpense. Korlym has only been marketed since April 2012 and the magnitude and timing of Korlym revenue is difficult to predict. Therefore, these estimatesand assumptions are subject to significant variability and are likely to change as we gain experience marketing Korlym, which will result in changes in ourclassification of the current and long term portions of the amounts payable pursuant to the Financing Agreement, as well as the internal rate of return paid toBiopharma and the accretion of interest expense related to this obligation. Actual payment amounts will be based on Korlym Receipts over the term of theFinancing Agreement but in no event will the total amount paid to Biopharma exceed $45.0 million.The amount shown as the current portion of the obligation is an estimate of the total amount under the Financing Agreement that would be paid toBiopharma within twelve months following December 31, 2012. Under the Financing Agreement, our first payment to Biopharma will not be due untilJuly 2013. F-9Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDNOTES TO FINANCIAL STATEMENTS, Continued See Note 6, Long-term Obligation, for additional information regarding this agreement.Net Product SalesWe sell Korlym to a specialty pharmacy and a specialty distributor, which subsequently resell Korlym to patients and healthcare providers. Werecognize product revenues from sales of Korlym upon delivery to our customers as long as (i) there is persuasive evidence that an arrangement existsbetween ourselves and the customer, (ii) collectability is reasonably assured and (iii) the price is fixed or determinable. In order to conclude that the price isfixed or determinable, we must be able to (i) calculate gross product revenues from the sales to our customers and (ii) reasonably estimate net productrevenues.We calculate gross product revenues based on the price that we charge our customers. We estimate our net product revenues by deducting from ourgross product revenues (a) trade allowances, such as discounts for prompt payment and distributor fees, (b) estimated government rebates and chargebacks,(c) reserves for expected product returns and (d) estimated costs of our patient assistance program. We initially record estimates for these deductions at thetime we recognize the gross revenue. We update our estimates on a recurring basis as new information becomes available.Trade Allowances: We offer our customers a discount on Korlym sales for payment within 30 days. We also offer them a small discount for theprovision of data services. We expect our customers to earn these discounts and accordingly deduct them in full from gross product revenues and tradereceivables at the time we recognize such revenues.Rebates and Chargebacks: We contract with Medicaid and other government programs so that Korlym will be eligible for purchase by, or qualify forpartial or full reimbursement from, such government programs. We estimate the rebates and chargebacks that we are obligated to provide to governmentprograms and deduct these estimated amounts from our gross product sales at the time the revenues are recognized. We base our estimates of these rebates andchargebacks upon (i) the discount amounts applicable to government-funded programs and (ii) information obtained from our vendors regarding thepercentage of sales by our customers to patients who are covered by entities or programs that are eligible for such rebates and chargebacks.Allowances for Patient Assistance Program: We provide financial assistance to eligible patients whose insurance policies require them to pay highdeductibles and co-pays. We estimate the cost of assistance to be provided under this program by applying our actual experience regarding such assistance toour estimate of the percentage of our sales in the period that will be provided to patients covered by the program.Sales Returns: Our customers have the right to return Korlym beginning six months before the labeled expiration date and ending 12 months after thelabeled expiration date. This right of return is extended to our specialty distributor channel’s hospital customers who, generally, have the right to return onlyunopened bottles. The expiration date for the Korlym product sold in 2012 will not occur until late in 2013. We estimate the amount of Korlym that webelieve will be returned and deduct that estimated amount from gross revenue at the time we recognize such revenue. When estimating future returns, weanalyze quantitative and qualitative information including, but not limited to, actual return rates, the amount of product in the distribution channel, theexpected shelf life of such product, current and projected product demand, the introduction of competing products that may erode demand, and broadeconomic and industry-wide indicators. If we cannot reasonably estimate product returns with respect to a particular sale, we defer recognition of revenuefrom that sale until we can make a reasonable estimate. F-10Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDNOTES TO FINANCIAL STATEMENTS, Continued Cost of SalesCost of sales includes the cost of product (the cost to manufacture Korlym, which includes material, third-party manufacturing costs and indirectpersonnel and other overhead costs) based on units for which revenue is recognized in the current period, as well as costs of stability testing, logistics anddistribution of the product. We began capitalizing Korlym production costs as inventory following approval by the FDA on February 17, 2012. Prior toreceiving FDA approval for Korlym, we expensed all costs related to the manufacturing of the product as incurred; we classified these costs as research anddevelopment expense. A portion of the product manufactured prior to FDA approval is available for us to use commercially.Research and DevelopmentResearch and development expenses consist of costs incurred for research and development activities that we sponsor (see Note 2). These costs includedirect expenses, such as the cost of clinical trials, pre-clinical studies, manufacturing development, preparations for submissions to the FDA and efforts toprosecute and defend those submissions and the development of second-generation compounds, as well as research and development-related overheadexpenses. We also expense as incurred nonrefundable payments to third parties and our cost of acquiring technologies and materials used in research anddevelopment that have no alternative future use.We base our cost accruals for clinical trials, research and preclinical activities on estimates of work completed under service agreements, milestonesachieved, patient enrollment and past experience with similar contracts. Our estimates of work completed and associated cost accruals include ourassessments of information from third-party contract research organizations and the overall status of clinical trial and other development and administrativeactivities.Segment ReportingWe determine our operating segments based on the way we organize our business to make operating decisions and assess performance. We have onlyone operating segment, which concerns the discovery, development and commercialization of pharmaceutical products.Stock-Based CompensationStock-based compensation for employee and director optionsWe account for stock-based compensation related to option grants to employees and directors under the fair value method, based on the fair value-based measurement of the award at the grant date as determined utilizing the Black-Scholes option valuation model. For service-based awards, we recognizeexpense over the requisite service period. For options with performance-based vesting criteria, we begin to recognize expense when we believe there is a highdegree of probability (i.e., greater than 70%) of achieving the vesting criteria.Stock-based compensation expense related to non-employeesWe recognize the expense of options granted to non-employees based on the fair-value based measurement of the option grants at the time of vesting.For service-based awards, we recognize expense over the requisite service period. For options with performance-based vesting criteria, we recognize expensebased on the minimum number of shares that will vest over time as the criteria are met based on the Black-Scholes valuation of the vested shares.See Note 9 for a detailed discussion of stock-based compensation expense. F-11Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDNOTES TO FINANCIAL STATEMENTS, Continued Income TaxesWe determine deferred tax assets and liabilities based on the differences between the financial reporting and tax bases of assets and liabilities,measured using the enacted tax rates that will be in effect when the differences are expected to reverse. A valuation allowance is recorded when it is morelikely than not that the deferred tax asset will not be realized.No amounts have been recognized as interest or penalties on income tax related matters. The determination of an accounting policy as to theclassification of such costs has been deferred until such time as any such costs are incurred.2. Significant AgreementsCommercial AgreementsIn January 2012, we signed a pharmacy purchase and service agreement with CuraScript, Inc. (CuraScript), and its affiliate Express Scripts SpecialtyDistribution Services, Inc., and, in February 2012, we signed a specialty distribution agreement with the same company. CuraScript was our sole customer ineach of these distribution channels for the initial launch of Korlym. The initial agreements are each for a one year term commencing on the launch date butmay be renewed for successive one-year terms upon written mutual agreement of the parties.In April 2011, we signed an agreement with Integrated Commercialization Solution (ICS) for the provision of warehousing and distribution of Korlymfor an initial term of three years that may be extended by mutual agreement. The majority of the costs under this agreement are variable and dependent on thevolume of material handled and transactions processed. Either party may terminate this agreement for non-performance upon 30 days written notice.In August 2010, we entered into an agreement with United Biosource Corporation (UBC) to assist us in developing our Risk Evaluation andMitigation Strategy (REMS), a plan for which we submitted to the FDA as part of our NDA for Korlym for the treatment of Cushing’s syndrome. In December2012, the FDA advised us that a REMS program was not necessary for our Cushing’s syndrome product. We decided to retain many parts of this program asour Support Program for Access and Reimbursement for Korlym (SPARK). The total commitment under the agreement, including amendments signed throughJune 2012 is $2.7 million, of which $1.6 million had been incurred through December 31, 2012, with the remainder to be incurred over the course of theagreement. The current agreement with UBC provides for services though March 31, 2015 and may be extended for additional periods at our request bywritten mutual agreement of the parties. Either party may terminate this agreement for non-performance upon 30 days written notice.Manufacturing Agreements Related to KorlymActive Pharmaceutical IngredientWe have an agreement with Produits Chimiques Auxiliaires et de Synthese SA (PCAS) for the manufacture of the active pharmaceutical ingredient(API) in Korlym, for our development and commercial needs that expires in June 2013. We intend to continue the relationship and are in the process ofnegotiations for a new agreement. The current agreement calls for us to purchase from PCAS at least 75 percent of our requirements until the termination ofthe agreement. If PCAS is unable to manufacture the product for a consecutive six-month period, we have the right to terminate the agreement withoutpenalty. F-12Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDNOTES TO FINANCIAL STATEMENTS, Continued We also have a memorandum of understanding with ScinoPharm Taiwan (ScinoPharm) whereby ScinoPharm agrees to manufacture API and we agree topurchase at least $1,000,000 of bulk mifepristone per year following the commercial launch of mifepristone for the treatment of psychotic depression. Noactivities are being performed to develop or qualify ScinoPharm’s manufacturing processes or facilities.Tablet ManufactureWe have entered into an agreement with another contract manufacturer, PharmaForm, L.L.C. (PharmaForm), for the production of Korlym tablets. Theagreement with PharmaForm was executed in March 2012 for an initial period of two years. The agreement will be automatically extended for additional oneyear periods unless one Party gives six months’ prior written notice that it does not want such an extension. The agreement with PharmaForm may beterminated by either party upon 180 days written notice; we may terminate projects initiated under this agreement with 30 days written notice. There are nominimum purchase amounts under this agreement.We are in negotiations for a commercial manufacturing agreement with AAI Pharma, our second tablet manufacturer whose facility was approved bythe FDA for manufacture of our commercial Korlym tablets in November 2012.See the discussion above in Note 1, Basis of Presentation and Summary of Significant Accounting Policies — Credit Risks and Concentrations, for afurther discussion of the business risks and mitigation measures taken in regard to tablet manufacture.Research and Development AgreementsIn October 1998, we entered into an agreement with The Board of Trustees of Leland Stanford Junior University (Stanford) in which Stanford grantedus an exclusive option to acquire an exclusive license for inventions and patents related to “Mifepristone for Psychotic Major Depression” and “Mifepristoneand Alzheimer’s Disease” owned by Stanford. (“Psychotic major depression” is referred to in this document as “psychotic depression”). In October 1999, weexercised our option to acquire an exclusive license to patents covering the use of glucocorticoid receptor antagonists for the treatment of psychoticdepression, early dementia, and cocaine-induced psychosis, as specified in the license agreement. This license agreement expires upon the expiration of therelated patents or upon notification by us to Stanford. In exchange for the license, we paid Stanford $47,000 and immediately issued 30,000 shares of ourcommon stock to Stanford. We are further required to pay Stanford $50,000 per year as a nonrefundable royalty payment. The annual royalty payments arecreditable against future royalties. We are also obligated to pay a $50,000 milestone upon filing of the first NDA by the FDA for mifepristone in one of theindications covered by the license and a $200,000 milestone upon FDA approval of the related drug. The milestone payments are also creditable againstfuture royalties. We have expensed the $47,000 payment made up front, the $50,000 annual nonrefundable royalty payments paid to date and the value ofthe common stock issued to Stanford as research and development costs.In 2003, we entered into a contract research agreement with Argenta Discovery Limited (Argenta) in which Argenta agreed to conduct research towardidentifying a novel small molecule glucocorticoid receptor antagonist for the treatment of psychotic depression, Alzheimer’s disease, and other metabolicand psychiatric disorders. We continued our relationship with Argenta through the end of 2011, requesting them to conduct research projects on a regularbasis. Under the agreements with Argenta, we may be obligated to make milestone payments upon the occurrence of certain events, including: (i) $5,000 forpatent filings related to products arising out of this agreement; (ii) $100,000 for each entry into a Phase 1 clinical trial of products arising out of thisagreement; and (iii) $500,000 in respect of each first national regulatory approval of each product arising from work performed under the F-13Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDNOTES TO FINANCIAL STATEMENTS, Continued agreement, provided that sales of the product by us or any future licensees reach $5,000,000. These obligations remain in force after the conclusion of workunder the agreement. In January 2012, we entered into a Master Services Agreement with Sygnature Discovery Limited, a contract research company locatedin the United Kingdom, which does not obligate us to any milestone payments.During 2008, we entered into agreements for services in connection with our ongoing Phase 3 trial of psychotic depression with ICON ClinicalResearch, L.P. (ICON) and MedAvante, Inc. (MedAvante) to manage the trial and conduct patient screening and evaluation services. The total commitmentunder these initial agreements was $21.1 million. In June 2009, we amended the agreements to reduce the commitments by $5.0 million in accordance withthe short-term reduction in the scope of activities under this trial. In December 2012, we further amended the agreements to reflect the increase in trialactivities toward our goal of concluding trial enrolment by the end of 2013, increasing the total commitments by $2.5 million. The total commitment underthese agreements, including amendments through 2012, is now estimated to be $18.6 million over the course of the trial. We expensed $10.4 million of thesecosts through December 31, 2012, with the remainder to be incurred over the course of the trial. Under the master services agreements with these vendors, theproject contracts may be terminated upon thirty to sixty days notice. If terminated early, we would be responsible for the costs incurred by the vendorsthrough the effective date of termination plus cancellation charges as stipulated in the agreements.3. Fair Value of Financial InstrumentsAs of December 31, 2012 and 2011, we had invested our financial assets in a money market fund that can be converted to cash at par on demand. Wemeasured these funds, which totaled $92.5 million and $39.0 million as of December 31, 2012 and 2011, respectively, at fair value, which approximates cost,as of the respective dates and classified them as Level 1 assets in the fair value hierarchy for financial assets.All cash equivalents and short-term investments held as of December 31, 2012 and 2011 were in active markets and valued based upon their quotedprices.4. Financial InstrumentsThe following tables present a summary of cash and cash equivalents. All amounts are in thousands. Cost UnrealizedGain UnrealizedLoss Fair Value December 31, 2012 Cash $579 $— $— $579 Money market fund 92,453 — — 92,453 $93,032 $— $— $93,032 Reported as: Cash and cash equivalents $93,032 $— $— $93,032 F-14Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDNOTES TO FINANCIAL STATEMENTS, Continued Cost UnrealizedGain UnrealizedLoss Fair Value December 31, 2011 Cash $659 $— $— $659 Money market fund 38,976 — — 38,976 $39,635 $— $— $39,635 Reported as: Cash and cash equivalents $39,635 $— $— $39,635 As of December 31, 2012 and 2011, all cash and cash equivalents were classified as available-for-sale securities. We did not invest in mortgage-backedsecurities or auction rate securities at any time during 2012 or 2011. We did not recognize any realized gains or losses on sales of available-for-saleinvestments for any period presented.5. Composition of Certain Balance Sheet ItemsInventoryThe following tables present the composition of inventory as of December 31, 2012. December 31,2012 (in thousands) Raw materials $3,478 Work in progress 1,165 Finished goods 20 Total inventory 4,663 Less strategic inventory classified as non-current (3,810) Total inventory classified as current $853 The finished goods inventory as of December 31, 2012 consists of tablets that were manufactured prior to FDA approval. The inventory value for thismaterial includes only the costs of bottling, packaging and labeling as the costs of raw materials and tablet manufacture were expensed prior to approval. Aswe had no product approved by the FDA as of December 31, 2011, we had no inventory on our balance sheet as of that date.In order to be prepared for potential demand for Korlym and because we had single-source manufacturers of both the API for Korlym and Korlymtablets prior to the approval by the FDA of our second tablet manufacturer in November 2012, we have invested in inventory of both of these materials.Inventory amounts that are not expected to be consumed within twelve months following the balance sheet date are referred to as “Strategic Inventory” andclassified as a noncurrent asset. F-15Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDNOTES TO FINANCIAL STATEMENTS, Continued Property and EquipmentProperty and equipment consists of the following: December 31, 2012 2011 (in thousands) Furniture and equipment $157 $67 Vehicles 41 — Software 15 9 Leasehold improvements 14 — 227 76 Less: accumulated depreciation (77) (50) $150 $26 Other Accrued LiabilitiesOther accrued liabilities consisted of the following: December 31, 2012 2011 (in thousands) Professional fees $311 $292 Commercialization costs 159 80 Government rebates 78 — Legal fees 31 46 Manufacturing costs 7 78 Other 109 37 $695 $533 6. Long-Term ObligationAs discussed in Note 1, Basis of Presentation and Summary of Significant Accounting Policies, Long-term Obligation, in August 2012, we enteredinto a Financing Agreement with Biopharma under which we received $30 million from Biopharma. In return, we are obligated to make payments, calculatedas a percentage of our net sales of Korlym, any future mifepristone-based products, our selective GR-II antagonists (together referred to as Covered Products)and any upfront, milestone or other contingent payments with respect to Covered Products. Biopharma’s right to receive payments will expire once it hasreceived cumulative payments of $45 million.Under the terms of the Financing Agreement, our payments are entirely variable, with no fixed minimums. If there are no net sales, upfront, milestone orother contingent payments in a period with respect to Covered Products, then no payment will be due for that period.We are obligated to make payments as follows: • 20 percent of our net product sales of Covered Products, beginning with the calendar quarter ending June 30, 2013, subject to quarterly paymentcaps of $2,250,000 during 2013, $3,000,000 during 2014, and $3,750,000 during 2015. There is no quarterly cap on payments with respect tonet product sales in 2016 and later. F-16Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDNOTES TO FINANCIAL STATEMENTS, Continued • 20 percent of payments received for upfront, milestone or other contingent fees under co-promotion and out-license agreements for CoveredProducts (without application of quarterly caps), provided however, that any amounts received under such agreements after the transaction’seffective date of August 2, 2012 but before June 30, 2013 would be deferred and made simultaneously with the payment for the calendar quarterending June 30, 2013. • The percentage used to calculate our payments to Biopharma would increase to 50 percent and any applicable payment caps would lapse if we(i) fail to provide Biopharma with certain information regarding our promotion and sales of Covered Products, (ii) do not devote a commerciallyreasonable amount of resources to the promotion and marketing of the Covered Products or (iii) violate the indebtedness covenant by incurringindebtedness greater than the sum of earnings before interest, taxes, depreciation and amortization, including such items as non-cash stock-basedcompensation, (EBITDA) for the four calendar quarters preceding such incurrence and, in each case, fail to cure within the applicable cure period. • Upon the occurrence of a Corcept change of control transaction or the licensing of Korlym to a third-party for promotion and sale in the UnitedStates, the entire $45 million, less any amounts already paid by us, would become due.To secure our obligations in connection with this Financing Agreement, we granted Biopharma a security interest in our rights in patents, trademarks,trade names, domain names, copyrights, know-how and regulatory approvals related to the Covered Products, all books and records relating to the foregoingand all proceeds of the foregoing (together, the Collateral). If we (i) fail to deliver a royalty payment when due and do not remedy that failure within 30 days,(ii) fail to maintain a first-priority perfected security interest in the Collateral in the United States and do not remedy that failure within five business days ofreceiving notice of such failure or (iii) become subject to an event of bankruptcy, then Biopharma may attempt to recover up to $45 million (after deductingany payments we have already made). In addition, pursuant to this agreement, we are not allowed to pay a dividend or other cash distribution, unless we willhave cash and cash equivalents in excess of $50 million after such payment.The cash payment of $30 million received from Biopharma was recorded as a long-term obligation at issuance. As discussed in Note 1, Basis ofPresentation and Summary of Significant Accounting Policies, Long-term Obligation, we have made an estimate of the timing of payments during the termof this agreement for purposes of calculating the expected rate of return to Biopharma, the accretion of related interest expense and the current portion of ourobligation. Interest expense of $1.7 million for the period from August 16, 2012, the date of funding of the Financing Agreement, through December 31,2012, is calculated using the effective interest method based on the internal interest rate to Biopharma that would result from this assumed payment stream.Korlym has only been marketed since April 2012 and the magnitude and timing of Korlym revenue is difficult to predict. Therefore, these estimates andassumptions are subject to significant variability and are likely to change as we gain experience marketing Korlym. The timing of payment amounts will bebased on actual Korlym Receipts recorded in the financial statements over the term of this agreement and may differ from these estimates. While changes inthe timing of Korlym revenue may affect the timing of recognition of interest expense and the split between the current and long-term portions of theobligation at any balance sheet date, the aggregate amount to be repaid to Biopharma is fixed.The carrying value of the long-term obligation at December 31, 2012, including accreted interest of $1.7 million, was $31.7 million. Under theFinancing Agreement, our first payment to Biopharma will not be due until July 2013. The long-term obligation, including accrued interest, is presented onthe balance sheet as of December 31, 2012 in two components; the Long-term obligation — current portion of $2,650,000, which equates to the estimatedamount due under the agreement to be paid within twelve months following that date, and the remaining $29,030,000, which is included in Long-termobligation, net of current portion. F-17Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDNOTES TO FINANCIAL STATEMENTS, Continued We capitalized $140,000 of issuance costs related to the Financing Agreement, which are being amortized over the estimated term of the obligation,based on the assumptions discussed above. At December 31, 2012, the unamortized issuance costs were $124,000, and are included in other assets on ourbalance sheet.The estimated fair value of the long-term obligation, as measured using Level 3 inputs, approximates the carrying amounts as presented on the balancesheet as of December 31, 2012.The following table provides a summary of the payment obligations under the Financing Agreement as of December 31, 2012, utilizing the paymentassumptions discussed above. (in thousands) Total repayment obligation $45,000 Less interest to be accreted in future periods (13,320) Less current portion, as of December 31, 2012 (2,650) Long-term obligation net of current portion, as of December 31, 2012 $29,030 7. Lease ObligationsAs of June 27, 2012, we signed an amendment to the lease for our office space that reflected an expansion of the space and extended our occupancythrough December 2013. At December 31, 2012, the remaining minimum rental payments under this operating lease were $428,000. The amended leaseprovides us with an option to extend the lease for one additional year.Rent expense amounted to $360,000, $285,000, and $250,000, for the years ended December 31, 2012, 2011 and 2010, respectively.8. Related Party TransactionsSee discussion below in Note 9, Preferred Stock and Stockholders’ Equity, under the captions Stockholder Notes Receivable and Common Stock,regarding the sale of securities in March 2012 to various investors, including members of our Board of Directors and related entities, and a Note Receivablefrom one of our officers.9. Preferred Stock and Stockholders’ EquityPreferred StockThe board of directors is authorized, subject to any limitations prescribed by law, without stockholder approval, to issue up to an aggregate of10,000,000 shares of preferred stock at $0.001 par value in one or more series and to fix the rights, preferences, privileges and restrictions granted to orimposed upon the preferred stock, including voting rights, dividend rights, conversion rights, redemption privileges and liquidation preferences. The rightsof the holders of common stock will be subject to the rights of holders of any preferred stock that may be issued in the future. F-18Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDNOTES TO FINANCIAL STATEMENTS, Continued As of December 31, 2012 and 2011, we had no outstanding shares of preferred stock.Common StockIncrease in number of authorized shares of common stockOn June 13, 2012, our stockholders approved an amendment to our Amended and Restated Certificate of Incorporation to increase the number ofauthorized shares of common stock from 140.0 million to 280.0 million shares at a par value of $0.001 per share. This amendment was filed with the DelawareSecretary of State on June 14, 2012 and became effective as of that date. Holders of common stock are entitled to one vote per share on all matters to be votedupon by our stockholders.Significant Stock transactionsThe following paragraphs describe significant transactions relating to the sale and issuance of common stock and the exercise and issuance of warrantsduring the years ended December 31, 2012, 2011 and 2010. Information regarding the issuance of common stock upon the exercise of stock options isdiscussed below under the caption, Stock Option Plans.Transactions during 2012On March 29, 2012, we issued approximately 4.2 million shares of our common stock upon the exercise of warrants that we had issued in a privateplacement transaction in April 2010 at an exercise price of $2.96 per share and sold new warrants to the same investors to purchase approximately 4.2 millionshares of common stock at an exercise price of $4.05 per share. The new warrants are exercisable through March 29, 2015. We generated net proceeds in thesetransactions of $12.8 million, after the deduction of issuance costs. Venture capital funds, trusts and other entities affiliated with members of our Board ofDirectors purchased approximately 40 percent of the securities sold in this transaction, with the remainder being purchased by other qualified investors.On July 6, 2012, we sold 11.0 million shares of our common stock in an underwritten public offering at a price to the public of $4.49 per share,generating net proceeds of $46.1 million after deducting expenses of the offering.During the year ended December 31, 2012, investors exercised additional warrants for the purchase of our common stock with exercise prices rangingfrom $1.66 to $2.96 per share. As a result, we issued an aggregate of approximately 216,000 shares of common stock and generated aggregate proceeds of$470,000.Transactions during 2011On January 26, 2011, we sold 11.5 million shares of our common stock in an underwritten public offering at a price to the public of $3.90 per share foraggregate net proceeds of $41.8 million after deducting the underwriter’s discount and commissions and other expenses of the offering. Longitude VenturePartners, L.P. purchased 750,000 (approximately 6.5%) of the shares sold in this transaction. Patrick Enright, who is a member of our board of directors, is amanaging member of Longitude Capital Partners, LLC, the general partner of Longitude Venture Partners, L.P.On July 13, 2011, we issued 80,991 shares of common stock to an investor upon the exercise of warrants that had been issued in our April 2010 warranttransaction and our March 2008 financing, for an average exercise price of $2.85 per share, receiving aggregate proceeds of $231,000. F-19Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDNOTES TO FINANCIAL STATEMENTS, Continued Transactions during 2010On April 21, 2010, we issued approximately 4.3 million shares of our common stock upon the exercise of warrants that had been issued in a privateplacement transaction in October 2009 at their exercise price of $1.66 per share and sold new warrants to the same investors to purchase a total ofapproximately 4.3 million shares of our common stock, which we refer to as the April 2010 Warrant Exchange. The warrants were originally exercisablethrough April 21, 2013 at an exercise price of $2.96 per share. The total net proceeds generated in this transaction were $7.5 million, after the deduction ofissuance costs. Approximately 40% of the securities sold in this transaction were purchased by venture capital funds, trusts and other entities affiliated withmembers of our Board of Directors, with the remainder being purchased by other qualified investors. As discussed above under the subcaption, Transactionsduring 2012, the warrants issued in this April 2010 transaction were exercised on March 29, 2012.On June 30, 2010, we sold 5.0 million shares of our common stock in an underwritten public offering at a price to the public of $3.00 per share foraggregate net proceeds of $13.8 million after deducting the underwriter’s discount and commissions and other expenses of the offering.During 2010, we also sold an aggregate of 518,639 shares of common stock to Kingsbridge Capital Limited (Kingsbridge) under the Committed EquityFinancing Facility (CEFF) at an average price of $3.13 per share, for net proceeds of $1.6 million. There were no underwriting discounts or commissions paidin connection with the CEFF sales and the transaction costs were immaterial.Committed Equity Financing FacilityEffective August 7, 2012, we terminated our CEFF with Kingsbridge. The termination of the CEFF has no effect on the warrant that was issued toKingsbridge for 330,000 shares of our common stock, which can be exercised at any time through September 25, 2013 for an exercise price of $3.525 pershare. Also, under the registration rights agreement issued in connection with the CEFF, we are required to continue to use commercially reasonable efforts tomaintain the effectiveness of the registration statement covering the shares sold under this agreement and to be issued upon the exercise of the warrant for aperiod of up to two years following the termination of the CEFF, subject to earlier termination on certain events. If we do not fulfill certain of our obligationsunder the registration rights agreement, we will be required to pay liquidated damages to Kingsbridge. No separate contingent obligation has been recordedas no liquidated damages have become probable of payment. In June 2008, the SEC declared effective our registration statement covering the resale of the330,000 shares issuable upon the exercise of the warrant.Registration Rights related to March 2008 FinancingIn March 2008, we sold approximately 8.9 million shares of our common stock and warrants to purchase approximately 4.5 million shares of ourcommon stock in a private placement (the March 2008 Financing). The registration rights agreement covering securities issued in the March 2008 Financingprovides that if we do not fulfill certain of our obligations under the registration rights agreement, we will be required to pay liquidated damages to theholders of the shares and warrants. We filed the registration statement covering the resale of the shares sold and shares underlying the warrants sold in thistransaction with the Securities and Exchange Commission (SEC) on April 11, 2008, and it was declared effective by the SEC on November 10, 2008. During2008, we recorded $1.3 million in liquidated damages to other non-operating expense because of the delay in the effectiveness of the registration statement,which represented approximately 5% of the purchase price. No separate contingent obligation has been recorded since that time as no additional liquidateddamages have become probable of payment. F-20Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDNOTES TO FINANCIAL STATEMENTS, Continued No dividends have been declared or paid by us.Shares of common stock reserved for future issuance as of December 31, 2012 are as follows: (in thousands) Common stock: Exercise of outstanding options 11,626 Exercise of warrants 8,904 Shares available for grant under stock option plans 4,055 24,585 On January 30, 2013, our Board of Directors authorized an increase of 3,992,570 shares in the number of shares available under the 2012 Plan, whichwas equivalent to 4% of the shares of our common stock outstanding as of December 31, 2012, pursuant to the terms of the 2012 Plan.Stock Option PlansWe have three stock option plans—the 2000 Stock Option Plan (the 2000 Plan), the 2004 Equity Incentive Plan (the 2004 Plan) and the 2012Incentive Award Plan (the 2012 Plan). As of December 31, 2012, all option grants under the 2000 Plan were fully vested and grants covering approximately214,000 shares remained outstanding with contractual lives expiring through March 2014.In 2004, our board of directors and stockholders approved the 2004 Plan, which became effective upon the completion of our Initial Public Offering(IPO), after which time, no additional options have been or will be issued under the 2000 Plan. Under the 2004 Plan, options, stock purchase and stockappreciation rights and restricted stock awards can be issued to our employees, officers, directors and consultants. The 2004 Plan provided that the exerciseprice for incentive stock options will be no less than 100% of the fair value of the Company’s common stock, as of the date of grant. Options granted underthe 2004 Plan vest over periods ranging from one to five years. The vesting period of the options is generally equivalent to the requisite service period. InNovember 2011, our Board of Directors authorized an increase in the shares available for issuance under the 2004 Plan equal to 4 percent of the shares of ourcommon stock outstanding as of December 31, 2011, pursuant to the terms of the 2004 Plan. Accordingly, as of January 1, 2012, the shares available forissuance under the 2004 Plan increased by a total of 3,369,249 shares.In February 2012, our Board of Directors and stockholders approved the 2012 Plan, which became effective upon its approval at our Annual Meetingof Stockholders on June 13, 2012. As of the effective date of the 2012 Plan, approximately 5.3 million shares that remained available for issuance of newgrants under the 2004 Plan were transferred to the 2012 Plan. After that date, no additional options were or will be issued under the 2004 Plan. Vested optionsunder the 2000 Plan and the 2004 Plan that are not exercised within the remaining contractual life and any options under the 2004 Plan that do not vestbecause of terminations after the effective date of the 2012 Plan will be added to the pool of shares available for future grants under the 2012 Plan.Under the 2012 Plan, we can issue options, stock purchase and stock appreciation rights and restricted stock awards to our employees, officers,directors and consultants. The 2012 Plan provides that the exercise price for incentive stock options will be no less than 100 percent of the fair value of ourcommon stock, as of the date of grant. Options granted under the 2012 Plan are expected to vest over periods ranging from one to four years. We expect thevesting period of the options that we grant under the 2012 Plan to be generally equivalent to the requisite service period.Upon exercise of options, new shares are issued. F-21Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDNOTES TO FINANCIAL STATEMENTS, Continued As of December 31, 2012, 4,054,507 shares remained available for future grants under the 2012 Plan. See discussion above under Common Stockregarding an additional increase to the shares available for grant under the 2012 Plan that was authorized by the Board of Directors in January 2013.Option activity during 2010, 2011 and 2012The following table summarizes all stock plan activity: Outstanding Options SharesAvailableFor FutureGrant SharesSubject toOptionsOutstanding Weighted-AverageExercisePrice WeightedAverageRemainingContractualLife AggregateIntrinsicValue (in thousands) (in thousands) (in years) (in thousands) Balance at December 31, 2009 201 7,347 $2.28 Increase in shares authorized for grant 2,499 — — Shares granted (838) 838 $3.40 Shares exercised — (124) $1.22 Shares cancelled and forfeited under 2000 Plan — (13) $15.00 Shares cancelled and forfeited under 2004 Plan 87 (87) $2.26 Balance at December 31, 2010 1,949 7,961 $2.40 Increase in shares authorized for grant 2,896 — — Shares granted (2,825) 2,825 $3.97 Shares exercised — (246) $1.51 Shares cancelled and forfeited under 2000 Plan — (1) $0.10 Shares cancelled and forfeited under 2004 Plan 231 (231) $1.72 Balance at December 31, 2011 2,251 10,308 $2.86 Increase in shares authorized for grant 3,369 — — Shares granted (1,695) 1,695 $3.26 Shares exercised — (165) $1.91 Shares expired under 2000 Plan 11 (93) $7.00 Shares cancelled and forfeited under 2004 and2012 Plans 119 (119) $3.26 Balance at December 31, 2012 4,055 11,626 $2.90 6.6 $711 Options exercisable at December 31, 2012 8,198 $2.66 4.3 $696 Options fully vested and expected to vest atDecember 31, 2012 11,626 $2.90 6.6 $711 All stock option grants vest solely based upon continuing service, with the exception of the following awards with performance-based vesting criteria:1) an award to a consultant of 50,000 shares that vested in its entirety on the filing by the FDA of our NDA for Korlym in June 2011, 2) awards to Joseph K.Belanoff, our Chief Executive Officer, and Robert L. Roe, our President, of 500,000 shares and 350,000 shares, respectively, F-22Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDNOTES TO FINANCIAL STATEMENTS, Continued that vested in their entirety upon the receipt of approval of the Korlym NDA in February 2012, and 3) an award to a consultant for 10,000 shares that vestedupon issuance in December 2012 due to the completion of the required services.The total intrinsic value of options exercised during the years ended December 31, 2012, 2011 and 2010 was $303,000, $702,000 and $250,000,respectively, based on the difference between the closing price of our common stock on the date of exercise of the options and the exercise price.The total grant date fair value of options to employees and directors that vested during the years ended December 31, 2012, 2011 and 2010 was $5.0million, $2.8 million and $1.9 million, respectively.The following is a summary of options outstanding and options exercisable at December 31, 2012. Exercise PricesOf Options Options Outstanding Options Exercisable NumberofShares WeightedAverageRemainingContractualLife WeightedAverageExercisePrice AggregateIntrinsicValue Numberof Shares WeightedAverageExercisePrice AggregateIntrinsicValue (in thousands) (in years) (in thousands) (in thousands) (in thousands) $0.96 - $ 1.25 2,363 6.2 $1.13 $711 2,302 $1.13 $696 $1.26 - $ 3.50 4,718 6.4 $2.12 — 3,308 $1.93 — $3.51 - $ 5.00 4,111 7.5 $4.23 — 2,154 $4.27 — $5.01 - $ 14.50 434 1.3 $8.29 — 434 $8.29 — 11,626 6.6 $2.90 $711 8,198 $2.66 $696 The aggregate intrinsic value in the table above represents the total pre-tax intrinsic value that option holders would have received had all optionholders exercised their options on December 31, 2012. The aggregate intrinsic value is the difference between our closing stock price on December 31, 2012and the exercise price, multiplied by the number of in-the-money options.Stock-Based Compensation related to Employee and Director OptionsAssumptions used in determining fair value-based measurements for options to employees and directorsThe following table summarizes the weighted-average assumptions and resultant fair value-based measurements for options granted to employees anddirectors. Year Ended December 31, 2012 2011 2010 Weighted-average assumptions for stock options granted: Risk-free interest rate 1.06% 2.65% 1.83% Expected term 6.7 years 8.9 years 5.9 years Expected volatility of stock price 86.6% 90.0% 96.3% Dividend rate 0% 0% 0% Weighted average grant date fair value-based measurement $2.41 $3.29 $2.68 F-23Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDNOTES TO FINANCIAL STATEMENTS, Continued For options granted from January 1, 2006 through September 2009, the expected term used in determining the fair value was based on the “simplified”method prescribed by the SEC, and considers the weighted-average of the vesting period and contractual life of the options. For options granted sinceSeptember 2009, the expected term has been based on a formula that considers the expected service period and expected post-vesting termination behaviordifferentiated by whether the grantee is an employee, an officer or a director.The expected volatility of our stock used in determining the fair value-based measurement of option grants to employees, officers and directors isbased on a weighted-average combination of the volatility of our own stock price and that of a group of peer companies for those grants with expected termslonger than the period of time that we have been a public company. For stock options granted to employees with expected terms of less than the period oftime that we have been a public company, the volatility is based on historical data of the price for our common stock for periods of time equivalent to theexpected term of these grants.Since we have a limited employee base and have experienced minimal turnover, we do not apply a forfeiture rate. When an employee terminates, wewill record a change in accounting estimate that represents the difference between the expense recorded in the financial statements and the expense thatwould have been recorded based upon the rights to options that vested during the individual’s service as an employee.Summary of compensation expense related to options to employees and directorsWe recognized compensation expense of $5.1 million, $3.0 million and $1.9 million, related to options to employees and directors during the yearsended December 31, 2012, 2011 and 2010, respectively. The data for the year ended December 31, 2012 includes $1.3 million of expense related toperformance-based option awards to officers that vested upon the FDA approval of Korlym in February 2012, which is classified as selling, general andadministrative expense.As of December 31, 2012, we had $8.9 million of unrecognized compensation expense for employee and director options outstanding as of that date,which had a remaining weighted-average vesting period of 2.7 years.Stock Options to ConsultantsWe expense stock-based compensation related to service-based option grants to non-employees on a straight line basis over the vesting period of theoptions, which approximates the period over which the related services are rendered, based on the fair value-based measurement of the options using theBlack-Scholes option pricing model. The assumptions used in these calculations are similar to those used for the determination of fair value-basedmeasurement for options granted to employees and directors, with the exception that, for non-employee options, the remaining contractual term is utilized asthe expected term of the option and the fair value-based measurement related to unvested non-employee options is re-measured quarterly, based on the thencurrent stock price as reflected on the NASDAQ Capital Market. For options with performance-based vesting criteria, we recognize expense based on theminimum number of shares that will vest over time as the criteria are met based on the Black-Scholes valuation of the vested shares.We recorded charges to expense for stock options granted to consultants of $208,000, $419,000, and $169,000 for the years ended December 31, 2012,2011 and 2010, respectively.As of December 31, 2012, all options that had been granted to consultants were fully vested. F-24Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDNOTES TO FINANCIAL STATEMENTS, Continued Summary of Stock-based Compensation ExpenseThe following table presents a summary of non-cash stock-based compensation by financial statement classification. Year ended December 31, 2012 2011 2010 (in thousands) Research and development expense $546 $547 $220 Selling, general and administrative expense 4,764 2,888 1,896 Total $5,310 $3,435 $2,116 Stockholder Notes ReceivableIn 2001, we recorded notes receivable from stockholders in the aggregate amount of $438,165 in connection with the exercise of options issued underthe 2000 Plan to purchase 585,000 shares of common stock. The notes were secured by the related shares of common stock and were full recourse notes, withinterest compounded annually at the rate of 6.5% per year. As of December 31, 2011, all amounts of principal and interest related to these notes had beenpaid.WarrantsOutstanding warrants at December 31, 2012 were as follows: Number of shares Exercise Price Expiration Date March 2008 Financing 4,371,478 $2.77 3/25/15 Kingsbridge CEFF 330,000 $3.525 9/25/13 March 2012 Warrant Exchange 4,202,443 $4.05 3/29/15 Total warrants outstanding 8,903,921 10. Other IncomeIn June 2010, we received a payment of $750,000 in connection with the favorable settlement of a lawsuit. This is the full amount due to us insettlement of this matter.In November 2010, we received grants totaling $733,438 from the United States Treasury’s Therapeutic Discovery Project Grant program. Thisrepresented the maximum available grant of $244,479 for each of our three clinical programs. F-25Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDNOTES TO FINANCIAL STATEMENTS, Continued 11. Net Loss Per ShareBasic and diluted net loss per share is computed by dividing the net loss by the weighted-average number of common shares outstanding during theperiod. The computation of net loss per share for each period, including the number of weighted-average shares outstanding, is shown on the face of thestatements of comprehensive loss.We have excluded the impact of common stock equivalents relating to shares underlying outstanding stock option grants and warrants from thecalculation of diluted net loss per common share because all such securities are antidilutive for all periods presented.The following table presents information on securities outstanding as of the end of each period that could potentially dilute the per share data in thefuture. December 31, 2012 2011 2010 (in thousands) Stock options outstanding 11,626 10,308 7,961 Warrants outstanding 8,904 9,119 9,200 Total 20,530 19,427 17,161 12. Income TaxesDeferred income taxes reflect the net tax effects of temporary differences between the carrying amounts of assets and liabilities for financial reportingpurposes and the amounts used for income tax purposes. Significant components of our deferred tax assets are as follows: December 31, 2012 2011 (in thousands) Deferred tax assets: Federal and state net operating losses $45,954 $45,796 Capitalized research and patent costs 22,631 24,318 Biopharma Financing Agreement 12,108 — Stock-based compensation costs 4,320 3,056 Research credits 19,236 17,078 Total deferred tax assets 104,249 90,248 Valuation allowance (104,249) (90,248) Net deferred tax assets $— $— F-26Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDNOTES TO FINANCIAL STATEMENTS, Continued Realization of deferred tax assets is dependent upon future earnings, if any, the timing and amount of which are uncertain. Accordingly, the netdeferred tax assets have been fully offset by a valuation allowance. The valuation allowance increased by $14.0 million, $16.0 million and $13.5 million forthe years ended December 31, 2012, 2011 and 2010, respectively.At December 31, 2012 we had net operating loss carryforwards available to offset any future taxable income that we may generate for federal incometax purposes of $116.2 million, which expire in the years 2019 through 2032, and California net operating loss carryforwards of $110.6 million, which expirein the years 2013 through 2032. We also had federal and California research and development tax credits of $17.9 million and $2.0 million, respectively. Thefederal research credits will expire in the years 2019 through 2032 and the California research credits have no expiration date. Our deferred tax assets havebeen offset by a full valuation allowance as the realization of such assets is uncertain. Utilization of our net operating losses and tax credit carryforwards maybe subject to substantial annual limitation due to the ownership change limitations provided by the Internal Revenue Code and similar state provisions. Suchlimitations could result in the expiration of the net operating losses and tax credit carryforwards before utilization.All tax years from inception remain open to examination by the Internal Revenue Service and the California Franchise Tax Board until such time as thenet operating losses and research credits are either fully utilized or expire.The following table presents a reconciliation from the statutory federal income tax rate to the effective rate. Year ended December 31, 2012 2011 2010 (in thousands) U.S. federal taxes (benefit) at statutory rate $(12,936) $(11,000) $(8,828) Unutilized, net operating loss 11,663 8,588 7,208 Non-deductible offset of Orphan Drug Credit 827 2,119 1,671 Non-deductible stock based compensation 404 280 189 Research & development grants under Section 48D — — (249) Other 42 13 9 Total $— $— $— 13. CommitmentsWe have entered into a number of agreements to conduct clinical trials and pre-clinical studies for further development of our lead product, Korlym,and our proprietary, selective GR-II antagonists. See the discussion in Note 2, Significant Agreements for further discussion regarding the commitmentsunder these agreements.In the ordinary course of our business, we make certain indemnities, commitments and guarantees under which we may be required to make paymentsin relation to certain transactions. These include indemnities of clinical investigators and contract research organizations involved in the development of ourclinical stage product candidates, indemnities of contract manufacturers and indemnities to our directors and officers to the maximum extent permitted underthe laws of the State of Delaware. The duration of these indemnities, commitments and guarantees varies, and in certain cases, is indefinite. The majority ofthese indemnities, commitments and guarantees do not provide for any limitation of the maximum potential future payments that we could be obligated tomake. We have not recorded any liability for these indemnities, commitments and F-27Table of ContentsCORCEPT THERAPEUTICS INCORPORATEDNOTES TO FINANCIAL STATEMENTS, Continued guarantees in the accompanying balance sheets. However, we would accrue for losses for any known contingent liability, including those that may arise fromindemnification provisions, when future payment is probable. No such losses have been recorded to date.14. Quarterly Financial Data (Unaudited)The following table is in thousands, except per share amounts: Quarter Ended March 31 June 30 September 30 December 31 2012 Product sales, net $— $875 $1,055 $1,377 Gross profit on product sales — 827 1,031 1,358 Net loss (11,034) (7,597) (8,293) (11,124) Basic and diluted net loss per share (0.13) (0.09) (0.08) (0.11) 2011 Net loss (7,101) (8,882) (6,435) (9,936) Basic and diluted net loss per share (0.09) (0.11) (0.08) (0.12) The table above does not reflect data for product sales and gross profit during any quarters of 2011 or for the quarter ended March 31, 2012 as webegan commercial sales of our first product in April 2012. F-28Table of ContentsExhibit Index ExhibitNumber Description of Document 3.1 Amended and Restated Certificate of Incorporation, as amended (incorporated by reference to Exhibit 3.1 to the registrant’s QuarterlyReport on Form 10-Q filed on August 9. 2012). 3.2 Amended and Restated Bylaws (incorporated by reference to Exhibit 3.1 to the registrant’s Current Report on Form 8-K filed on September27, 2007). 4.1 Specimen Common Stock Certificate (incorporated by reference to Exhibit 4.1 to the registrant’s Registration Statement on Form S-1(Registration No. 333-112676) filed on February 10, 2004). 4.2 Registration Rights Agreement by and among Corcept Therapeutics Incorporated and the investors signatory thereto, dated March 14,2008 (incorporated by reference to Exhibit 10.25 to the registrant’s Annual Report on Form 10-K filed on March 31, 2008). 4.3 Registration Rights Agreement by and between Corcept Therapeutics Incorporated and Kingsbridge Capital Limited, dated as of March25, 2008 (incorporated by reference to Exhibit 10.27 to the registrant’s Annual Report on Form 10-K filed on March 31, 2008). 4.4 Amendment to Registration Rights Agreement by and among Corcept Therapeutics Incorporated and the investors signatory thereto, datedNovember 11, 2008 (incorporated by reference to Exhibit 10.30 to the registrant’s Annual Report on Form 10-K filed on March 31, 2009). 4.5 Registration Rights Agreement dated as of April 21, 2010 by and among Corcept Therapeutics Incorporated and the investors signatorythereto (incorporated by reference to Exhibit 4.2 to the registrant’s Current Report on Form 8-K filed on April 23, 2010). 4.6 Registration Rights Agreement, dated as of March 29, 2012, by and among Corcept Therapeutics Incorporated and the investors signatorythereto (incorporated by reference to Exhibit 4.2 to the registrant’s Current Report on Form 8-K filed on March 29, 2012). 4.7 Form of Warrant issued in connection with the Securities Purchase Agreement by and among Corcept Therapeutics Incorporated and thepurchasers named therein, dated March 14, 2008 (incorporated by reference to Exhibit 4.4 to the registrant’s Annual Report on Form 10-Kfiled on March 31, 2008). 4.8 Form of Warrant issued in connection with Warrant Purchase Agreement dated as of March 25, 2012 by and among Corcept TherapeuticsIncorporated and the purchasers named therein (incorporated by reference to Exhibit 4.2 to the registrant’s Current Report on Form 8-Kfiled on March 29, 2012). 4.9 Warrant, dated March 25, 2008 issued to Kingsbridge Capital Limited (incorporated by reference to Exhibit 4.5 to the registrant’s AnnualReport on Form 10-K filed on March 31, 2008). 10.1 2000 Stock Option Plan (incorporated by reference to Exhibit 10.1 to the registrant’s Registration Statement on Form S-1 (RegistrationNo. 333-112676) filed on February 10, 2004). 10.2 License Agreement by and between The Board of Trustees of the Leland Stanford Junior University and Corcept TherapeuticsIncorporated, dated as of July 1, 1999 (incorporated by reference to Exhibit 10.6 to the registrant’s Registration Statement on Form S-1(Registration No. 333-112676) filed on February 10, 2004). 10.3# Memorandum of Understanding, Supply and Services Agreement, by and between Corcept Therapeutics Incorporated and ScinoPharmTaiwan, dated as of June 12, 2000 (incorporated by reference to Exhibit 10.9 to the registrant’s Registration Statement on Form S-1/A (FileNo. 333-112676) filed on March 19, 2004). 10.4 Master Services Agreement by and between Corcept Therapeutics Incorporated and PPD Development, LP, dated as of January 17, 2003(incorporated by reference to Exhibit 10.12 to the registrant’s Registration Statement on Form S-1/A (File No. 333-112676) filed on March19, 2004).†Table of ContentsExhibitNumber Description of Document 10.5# Manufacturing Agreement with Produits Chimiques Auxiliaires et de Synthese SA, dated November 8, 2006 (incorporated by reference toExhibit 10.15 to the registrant’s Annual Report on Form 10-K filed on April 2, 2007). 10.6 Form of Indemnification Agreement for directors and officers approved by the Board of Directors on September 24, 2007 (incorporated byreference to Exhibit 10.7 to the registrant’s Quarterly Report on Form 10-Q filed on November 14, 2007). 10.7 Securities Purchase Agreement by and among Corcept Therapeutics Incorporated and the purchasers named therein, dated March 14, 2008(incorporated by reference to Exhibit 10.24 to the registrant’s Annual Report on Form 10-K filed on March 31, 2008). 10.8 Common Stock Purchase Agreement by and between Kingsbridge Capital Limited and Corcept Therapeutics Incorporated dated as ofMarch 25, 2008 (incorporated by reference to Exhibit 10.26 to the registrant’s Annual Report on Form 10-K filed on March 31, 2008). 10.9# Master Service Agreement by and among Corcept Therapeutics Incorporated and ICON Clinical Research, L.P., signed on June 4, 2008(incorporated by reference to Exhibit 10.5 to the registrant’s Quarterly Report on Form 10-Q filed on August 14, 2008). 10.10 Amended and Restated Severance and Change in Control Agreement by and between Corcept Therapeutics Incorporated and Joseph K.Belanoff, M. D., dated September 19, 2008 (incorporated by reference to Exhibit 10.25 to the registrant’s Annual Report on Form 10-Kfiled on March 31, 2009). 10.11 Amended and Restated Severance and Change in Control Agreement by and between Corcept Therapeutics Incorporated and Robert L.Roe, M. D., dated September 19, 2008 (incorporated by reference to Exhibit 10.26 to the registrant’s Annual Report on Form 10-K filed onMarch 31, 2009). 10.12 Amended and Restated Severance and Change in Control Agreement by and between Corcept Therapeutics Incorporated and Anne M.LeDoux, dated September 19, 2008(incorporated by reference to Exhibit 10.27 to the registrant’s Annual Report on Form 10-K filed onMarch 31, 2009). 10.13 Amended and Restated Severance and Change in Control Agreement by and between Corcept Therapeutics Incorporated and James N.Wilson, dated September 19, 2008(incorporated by reference to Exhibit 10.28 to the registrant’s Annual Report on Form 10-K filed onMarch 31, 2009). 10.14 Securities Purchase Agreement by and among Corcept Therapeutics Incorporated and the purchasers named therein, dated October 12,2009 (incorporated by reference to Exhibit 10.1 to the registrant’s Quarterly Report on Form 10-Q filed on November 12, 2009). 10.15 Amended and Restated 2004 Equity Incentive Plan (incorporated by reference to the registrant’s Proxy Statement on Schedule 14A filedon May 7, 2009). 10.16 Form of Option Agreement for options granted pursuant to the Amended and Restated 2004 Equity Incentive Plan (incorporated byreference to Exhibit 10.25 to the registrant’s Annual Report on Form 10-K filed on March 15, 2011). 10.17 Development Agreement by and between Corcept Therapeutics Incorporated and Formulation Technologies L.L.C. d/b/a PharmaForm,dated as of December 14, 2006 (incorporated by reference to Exhibit 10.28 to the registrant’s Annual Report on Form 10-K filed on March15, 2011). 10.18 Master Services Agreement by and between Corcept Therapeutics Incorporated and United BioSource Corporation, dated as of June 29,2010 (incorporated by reference to Exhibit 10.29 to the registrant’s Annual Report on Form 10-K filed on March 15, 2011). 10.19 Employment offer letter to Steven Lo, dated August 9, 2010 (incorporated by reference to Exhibit 10.1 to the registrant’s Quarterly Reporton Form 10-Q filed on November 12, 2010).†††††††##†Table of ContentsExhibitNumber Description of Document 10.20 Severance and Change in Control Agreement by and between Corcept Therapeutics Incorporated and Steven Lo, dated September 15,2010 (incorporated by reference to Exhibit 10.2 to the registrant’s Quarterly Report on Form 10-Q filed on November 12, 2010). 10.21 Severance and Change in Control Agreement by and between Corcept Therapeutics Incorporated and G. Charles Robb, dated September 1,2011 (incorporated by reference to Exhibit 10.2 to the registrant’s Quarterly Report on Form 10-Q filed on November 8, 2011). 10.22 Employment offer letter to G. Charles Robb dated August 12, 2011 (incorporated by reference to Exhibit 10.1 to the registrant’s QuarterlyReport on Form 10-Q filed on November 8, 2011). 10.23 Manufacturing and Supply Agreement with Formulation Technologies, LLC D/B/A PharmaForm, LLC, dated March 21, 2012(incorporated by reference to Exhibit 10.1 to the registrant’s Quarterly Report on Form 10-Q filed on May 10, 2012). 10.24 Warrant Purchase Agreement, dated as of March 25, 2012, by and among Corcept Therapeutics Incorporated and the purchasers namedtherein (incorporated by reference to Exhibit 10.1 to the registrant’s Current Report on Form 8-K filed on March 29, 2012). 10.25 Commercial Outsourcing Services Agreement with Integrated Commercialization Solutions, Inc., dated as of April 14, 2011 (incorporatedby reference to Exhibit 10.1 to the registrant’s Quarterly Report on Form 10-Q filed on August 9, 2012). 10.26 Amended and Restated Exclusive Pharmacy Product Purchase and Services Agreement with CuraScript, Inc., dated August 8, 2012(incorporated by reference to Exhibit 10.2 to the registrant’s Quarterly Report on Form 10-Q filed on August 9, 2012). 10.27 Amended and Restated Exclusive Wholesale Product Purchase Agreement with CuraScript SD Specialty Distribution, dated August 8,2012 (incorporated by reference to Exhibit 10.3 to the registrant’s Quarterly Report on Form 10-Q filed on August 9, 2012). 10.28 Corcept Therapeutics Incorporated 2012 Incentive Award Plan (incorporated by reference to Appendix A to the registrant’s DefinitiveProxy Statement on Schedule 14A filed with the SEC on May 21, 2012). 10.29 Form of 2012 Incentive Award Plan Stock Option Grant Notice and Agreement (incorporated by reference to Exhibit 4.5 to the registrant’sRegistration Statement on Form S-8 filed with the SEC on August 13, 2012). 10.30 Purchase and Sale Agreement with between Corcept Therapeutics Incorporated and Biopharma Secured Debt Fund II Sub, S.à r.l,, dated asof August 2, 2012 (incorporated by reference to Exhibit 10.4 to the registrant’s Quarterly Report on Form 10-Q filed on November 8,2012). 10.31 Amendment to Manufacturing Agreement with Produits Chimiques Auxiliaires et de Synthese SA, dated February 21, 2013. 23.1 Consent of Independent Registered Public Accounting Firm 24.1 Power of Attorney (See signature page) 31.1 Certification pursuant to Rule 13a-14(a) under the Securities Exchange Act of 1934 of Joseph K. Belanoff, M.D. 31.2 Certification pursuant to Rule 13a-14(a) under the Securities Exchange Act of 1934 of G. Charles Robb 32.1 Certification pursuant to 18 U.S.C. Section 1350 of Joseph K. Belanoff, M.D. 32.2 Certification pursuant to 18 U.S.C. Section 1350 of G. Charles Robb†††####††#Table of ContentsExhibitNumber Description of Document101* The following materials from the registrant’s Annual Report on Form 10-K for the year ended December 31, 2012, formatted inExtensible Business Reporting Language (XBRL): (i) Balance Sheets at December 31, 2012 and 2011, (ii) Statements ofComprehensive Loss for the Years Ended December 31, 2012, 2011 and 2010, (iii) Statements of Stockholders’ Equity for the YearsEnded December 31, 2012, 2011 and 2010, (iv) Statements of Cash Flows for the Years Ended December 31, 2012, 2011 and 2010,and (v) Notes to Financial Statements. #Confidential treatment granted †Management contract or compensatory plan or arrangement *Pursuant to Rule 406T of Regulation S-T, these XBRL data files are deemed furnished and not filed or a part of a registration statement or prospectusfor purposes of sections 11 or 12 of the Securities Act of 1933, as amended, are deemed not filed for purposes of section 18 of the Securities ExchangeAct of 1934, as amended, and otherwise is not subject to liability under these sections.Exhibit 10.31Corcept Therapeutics Incorporated149 Commonwealth DriveMenlo Park, CA 94025February 21, 2013Produits Chimiques Auxiliaires et de Synthese SA (“PCAS”)23 Rue Bossuet91161 Longjumeau CedexFranceAttn. Don LaFerle Re:Extension of Manufacturing and Supply AgreementDear Don,On behalf of Corcept Therapeutics Inc. (“Corcept”), I propose amending the Manufacturing and Supply Agreement between Corcept and PCAS datedNovember 3, 2006 (the “Agreement”) as follows:The language of Section 9.1 (Term) of the Agreement will be deleted in its entirety and replaced with the following text: “This Agreement shall becomeeffective on November 3, 2006 and shall terminate on June 30, 2013.”Our purpose in proposing this change is to make sure we have an effective contract in place during the next few months while we work the details of asuccessor agreement.If this amendment to the Agreement is acceptable to PCAS, please sign and date in the space provided and return a copy to me. Please let me know if youhave questions.Sincerely,/s/ Charles Robb, CFOCharles RobbChief Financial OfficerCorcept Therapeutics Inc.Approved: /s/ Charles Robb, CFO /s/ Didier CombisSignature SignatureCharles Robb, CFO Didier CombisPrint Name & Title Director, Custom Synthesis and PharmaChemicals Print Name & Title2/20/13 2/23/13Date DateExhibit 23.1Consent of Independent Registered Public Accounting FirmWe consent to the incorporation by reference in the following Registration Statements:(1) Registration Statement (Form S-8 No. 333-116127) pertaining to the 2000 Stock Option Plan and the Amended and Restated 2004 Equity Incentive Planof Corcept Therapeutics Incorporated,(2) Registration Statements (Form S-8 Nos. 333-150199, 333-158406, 333-164531, 333-172841 and 333-180073) pertaining to the Amended and Restated2004 Equity Incentive Plan of Corcept Therapeutics Incorporated,(3) Registration Statement (Form S-8 No. 333-183284) pertaining to the 2012 Incentive Award Plan of Corcept Therapeutics Incorporated, and(4) Registration Statements (Form S-3 Nos. 333-149087, 333-150204, 333-163140, 333-167211, 333-168928, 333-141881, 333-150232, 333-150259, 333-174073 and 333-181672) of Corcept Therapeutics Incorporated and in the related Prospectuses;of our reports dated March 15, 2013, with respect to the financial statements of Corcept Therapeutics Incorporated and the effectiveness of internal controlover financial reporting of Corcept Therapeutics Incorporated included in this Annual Report (Form 10-K) of Corcept Therapeutics Incorporated for the yearended December 31, 2012./s/ Ernst & Young LLPRedwood City, CaliforniaMarch 15, 2013Exhibit 31.1CERTIFICATIONI, Joseph K. Belanoff, M.D., certify that: 1.I have reviewed this Annual Report on Form 10-K for the period ended December 31, 2012 of Corcept Therapeutics Incorporated; 2.Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make thestatements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by thisreport; 3.Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects thefinancial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report; 4.The registrant’s other certifying officer(s) and I are responsible for establishing and maintaining disclosure controls and procedures (as defined inExchange Act Rules 13a-15(e) and 15d-15(e) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f))for the registrant and have: (a)Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, toensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others within thoseentities, particularly during the period in which this report is being prepared; (b)Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under oursupervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements forexternal purposes in accordance with generally accepted accounting principles; (c)Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about theeffectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and (d)Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recentfiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materiallyaffect, the registrant’s internal control over financial reporting; and 5.The registrant’s other certifying officer(s) and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to theregistrant’s auditors and the audit committee of the registrant’s board of directors (or persons performing the equivalent functions): (a)All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are reasonablylikely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and (b)Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal controlover financial reporting. /s/ Joseph K. BelanoffJoseph K. Belanoff, M.D.Chief Executive OfficerMarch 15, 2013Exhibit 31.2CERTIFICATIONI, G. Charles Robb, certify that: 1.I have reviewed this Annual Report on Form 10-K for the period ended December 31, 2012 of Corcept Therapeutics Incorporated; 2.Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make thestatements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by thisreport; 3.Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects thefinancial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report; 4.The registrant’s other certifying officer(s) and I are responsible for establishing and maintaining disclosure controls and procedures (as defined inExchange Act Rules 13a-15(e) and 15d-15(e) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f))for the registrant and have: (a)Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, toensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others within thoseentities, particularly during the period in which this report is being prepared; (b)Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under oursupervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements forexternal purposes in accordance with generally accepted accounting principles; (c)Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about theeffectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and (d)Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recentfiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materiallyaffect, the registrant’s internal control over financial reporting; and 5.The registrant’s other certifying officer(s) and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to theregistrant’s auditors and the audit committee of the registrant’s board of directors (or persons performing the equivalent functions): (a)All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are reasonablylikely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and (b)Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal controlover financial reporting. /s/ G. Charles RobbG. Charles RobbChief Financial OfficerMarch 15, 2013Exhibit 32.1Corcept Therapeutics IncorporatedCERTIFICATION PURSUANT TO18 U.S.C. SECTION 1350,AS ADOPTED PURSUANT TOSECTION 906 OF THE SARBANES-OXLEY ACT OF 2002In connection with the Annual Report of Corcept Therapeutics Incorporated (the “Company”) on Form 10-K for the period ended December 31, 2012,as filed with the Securities and Exchange Commission on the date hereof (the “Report”), I, Joseph K. Belanoff, M.D., Chief Executive Officer of theCompany, certify, pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002, that: (1)The Report fully complies with the requirements of Section 13(a) or 15(d) of the Securities Exchange Act of 1934; and (2)The information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of theCompany. /s/ Joseph K. BelanoffJoseph K. Belanoff, M.D.Chief Executive OfficerMarch 15, 2013This certification is not deemed filed with the Securities and Exchange Commission and is not to be incorporated by reference into any filing ofCorcept Therapeutics Incorporated under the Securities Act of 1933, as amended, or the Securities Exchange Act of 1934, as amended, irrespective of anygeneral incorporation language contained in such filing.Exhibit 32.2Corcept Therapeutics IncorporatedCERTIFICATION PURSUANT TO18 U.S.C. SECTION 1350,AS ADOPTED PURSUANT TOSECTION 906 OF THE SARBANES-OXLEY ACT OF 2002In connection with the Annual Report of Corcept Therapeutics Incorporated (the “Company”) on Form 10-K for the period ended December 31, 2012,as filed with the Securities and Exchange Commission on the date hereof (the “Report”), I, G. Charles Robb, Chief Financial Officer of the Company, certify,pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002, that: (1)The Report fully complies with the requirements of Section 13(a) or 15(d) of the Securities Exchange Act of 1934; and (2)The information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of theCompany. /s/ G. Charles RobbG. Charles RobbChief Financial OfficerMarch 15, 2013This certification is not deemed filed with the Securities and Exchange Commission and is not to be incorporated by reference into any filing ofCorcept Therapeutics Incorporated under the Securities Act of 1933, as amended, or the Securities Exchange Act of 1934, as amended, irrespective of anygeneral incorporation language contained in such filing.

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