Fibrocell Science Inc
Annual Report 2011

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, 2011OR ¨Transition Report Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934 Fibrocell Science, Inc.(Exact name of registrant as specified in its Charter.) Delaware 001-31564 87-0458888(State or other jurisdictionof incorporation) (CommissionFile Number) (I.R.S. EmployerIdentification No.)405 Eagleview BoulevardExton, Pennsylvania 19341(Address of principal executive offices, including zip code)(484) 713-6000(Issuer’s telephone number, including area code)Securities registered pursuant to Section 12(g) of the Act:Title of Each ClassCommon Stock, $.001 par value Indicate 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) filed all reports required to be filed by Section 13 or 15(d) of the Exchange Act during the preceding12 months (or for any shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past90 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 there is no disclosure of delinquent filers in response to Item 405 of Regulation S-K contained in this form, and no disclosurewill be contained, to the best of registrant’s knowledge, in definitive proxy or information statements incorporated by reference in Part III of this Form 10-K orany amendment to this Form 10-K. ¨Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, or a non-accelerated filer or a smaller reporting company.See the definitions of “large accelerated filer,” “accelerated filer” and “smaller reporting company” in Rule 12b-2 of the Exchange Act. (Check one): Large accelerated filer ¨ Accelerated filer ¨Non-accelerated filer ¨ (Do not check if a smaller reporting company) Smaller reporting company xIndicate by check mark whether the registrant is shell company (as defined in the Exchange Act Rule 12b-2) Yes ¨ No xThe aggregate market value of common stock held by non-affiliates of the registrant was $39.1 million as of June 30, 2011, the last business day of theregistrant’s most recently completed second fiscal quarter. Such aggregate market value was computed by reference to the closing price of the common stock asreported on the OTC Bulletin Board on June 30, 2011. For purposes of determining this amount only, the registrant has defined affiliates as including (a) theexecutive officers of the registrant as of June 30, 2011 and (b) all directors of the registrant as of June 30, 2011.Indicate by check mark whether the registrant has filed all documents and reports required to be filed by Section 12, 13 or 15(d) of the SecuritiesExchange Act of 1934 subsequent to the distribution of securities under a plan confirmed by a court. Yes x No ¨As of March 26, 2012, issuer had 96,078,253 shares issued and outstanding of common stock, par value $0.001.DOCUMENTS INCORPORATED BY REFERENCEPortions of the Proxy Statement for the 2011 Annual Meeting of Stockholders (the “Proxy Statement”), to be filed within 120 days of the end of the fiscalyear ended December 31, 2011, are incorporated by reference in Part III hereof. Except with respect to information specifically incorporated by reference in thisForm 10-K, the Proxy Statement is not deemed to be filed as part hereof. Table of ContentsTABLE OF CONTENTS Page PART I ITEM 1. BUSINESS 3 ITEM 1A. RISK FACTORS 15 ITEM 1B. UNRESOLVED STAFF COMMENTS 31 ITEM 2. PROPERTIES 31 ITEM 3. LEGAL PROCEEDINGS 31 ITEM 4. MINE SAFETY DISCLOSURE 31 PART II ITEM 5. MARKET FOR REGISTRANT’S COMMON EQUITY, RELATED STOCKHOLDER MATTERS AND ISSUER PURCHASESOF EQUITY SECURITIES 31 ITEM 6. SELECTED FINANCIAL DATA 33 ITEM 7. MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS 33 ITEM 8. FINANCIAL STATEMENTS AND SUPPLEMENTARY DATA 39 ITEM 9. CHANGES IN AND DISAGREEMENTS WITH ACCOUNTANTS ON ACCOUNTING AND FINANCIAL DISCLOSURE 39 ITEM 9A. CONTROLS AND PROCEDURES 39 ITEM 9B. OTHER INFORMATION 40 PART III ITEM 10. DIRECTORS, EXECUTIVE OFFICERS AND CORPORATE GOVERNANCE 40 ITEM 11. EXECUTIVE COMPENSATION 40 ITEM 12. SECURITY OWNERSHIP OF CERTAIN BENEFICIAL OWNERS AND MANAGEMENT AND RELATED STOCKHOLDERMATTERS 40 ITEM 13. CERTAIN RELATIONSHIPS AND RELATED TRANSACTIONS, AND DIRECTOR INDEPENDENCE 40 ITEM 14. PRINCIPAL ACCOUNTANT FEES AND SERVICES 41 PART IV ITEM 15. EXHIBITS AND FINANCIAL STATEMENT SCHEDULE 41 SIGNATURE PAGE 44 Table of ContentsPart 1This Annual Report on Form 10-K (including the section regarding Management’s Discussion and Analysis of Financial Condition and Results ofOperations) contains certain “forward-looking statements” within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E ofthe Securities Exchange Act of 1934, as amended, as well as information relating to Fibrocell Science, Inc. and its subsidiaries (referred to as “Fibrocell,”“Company,” “we,” or “our”) that is based on management’s exercise of business judgment and assumptions made by and information currently available tomanagement. Although forward-looking statements in this Annual Report on Form 10-K reflect the good faith judgment of our management, such statementscan only be based on facts and factors currently known by us. Consequently, forward-looking statements are inherently subject to risks and uncertainties andactual results and outcomes may differ materially from the results and outcomes discussed in or anticipated by the forward-looking statements. When used inthis document and other documents, releases and reports released by us, the words “anticipate,” “believe,” “estimate,” “expect,” “intend,” “the facts suggest”and words of similar import, are intended to identify any forward-looking statements. You should not place undue reliance on these forward-lookingstatements. These statements reflect our current view of future events and are subject to certain risks and uncertainties as noted below. Should one or more ofthese risks or uncertainties materialize, or should underlying assumptions prove incorrect, our actual results could differ materially from those anticipated inthese forward-looking statements. Actual events, transactions and results may materially differ from the anticipated events, transactions or results described insuch statements. Although we believe that our expectations are based on reasonable assumptions, we can give no assurance that our expectations willmaterialize. Many factors could cause actual results to differ materially from our forward looking statements including those set forth in Item 1A of this report.Other unknown, unidentified or unpredictable factors could materially and adversely impact our future results. We undertake no obligation and do not intendto update, revise or otherwise publicly release any revisions to our forward-looking statements to reflect events or circumstances after the date hereof or toreflect the occurrence of any unanticipated events. Several of these factors include, without limitation: • our ability to finance our business and continue in operations; • our ability to increase our manufacturing capacity and improve our manufacturing costs through the improvement of our manufacturing process,and our ability to validate any such improvements with the relevant regulatory agencies; • our ability to meet requisite regulations or receive regulatory approvals in the United States, Europe, Asia and the Americas, and our ability toretain any regulatory approvals that we may obtain; and the absence of adverse regulatory developments in the United States, Europe, Asia andthe Americas or any other country where we plan to conduct commercial operations; • whether our clinical human trials relating to the use of autologous cellular therapy applications, and such other indications as we may identify andpursue can be conducted within the timeframe that we expect, whether such trials will yield positive results, or whether additional applications forthe commercialization of autologous cellular therapy can be identified by us and advanced into human clinical trials; • our ability to develop autologous cellular therapies that have specific applications in cosmetic dermatology, and our ability to explore (and possiblydevelop) applications for periodontal disease, reconstructive dentistry, treatment of restrictive scars and burns and other health-related markets; • our ability to reduce our need for fetal bovine calf serum by improved use of less expensive media combinations and different media alternatives; • continued availability of supplies at satisfactory prices; • new entrance of competitive products or further penetration of existing products in our markets; 2Table of Contents • the effect on us from adverse publicity related to our products or the company itself; • any adverse claims relating to our intellectual property; • the adoption of new, or changes in, accounting principles; • our issuance of certain rights to our shareholders that may have anti-takeover effects; and • our dependence on physicians to correctly follow our established protocols for the safe administration of our product.We file reports with the Securities and Exchange Commission (“SEC” or “Commission”). We make available on our website(www.Fibrocellscience.com) free of charge our annual report on Form 10-K, quarterly reports on Form 10-Q, current reports on Form 8-K and amendments tothose reports as soon as reasonably practicable after we electronically file such materials with or furnish them to the SEC. Information appearing at our websiteis not a part of this Annual Report on Form 10-K. You can also read and copy any materials we file with the Commission at its Public Reference Room at 100F Street, NE, Washington, DC 20549. You can obtain additional information about the operation of the Public Reference Room by calling the Commission at1-800-SEC-0330. In addition, the Commission maintains an Internet site (www.sec.gov) that contains reports, proxy and information statements, and otherinformation regarding issuers that file electronically with the Commission, including Fibrocell Science.Our corporate headquarters is located at 405 Eagleview Boulevard, Exton, Pennsylvania 19341. Our phone number is (484) 713-6000. Our fiscal yearbegins on January 1, and ends on December 31, and any references herein to “Fiscal 2011” mean the year ended December 31, 2011, and references to other“Fiscal” years mean the year ending December 31, of the year indicated.We own or have rights to various copyrights, trademarks and trade names used in our business including but not limited to the following: FibrocellScience, Fibrocell Therapy, Fibrocell Science Process, Agera and Agera Rx, (LAVIV et al). This report also includes other trademarks, service marks andtrade names of other companies. Other trademarks and trade names appearing in this report are the property of the holder of such trademarks and trade names.We obtained statistical data, market data and other industry data and forecasts used in this Form 10-K from publicly available information. While webelieve that the statistical data, industry data, forecasts and market research are reliable, we have not independently verified the data, and we do not make anyrepresentation as to the accuracy of that information.Item 1. BusinessOverviewWe are a cellular aesthetic and therapeutic development stage biotechnology company focused on developing novel skin and tissue rejuvenation products.Our approved and clinical development product candidates are designed to improve the appearance of skin injured by the effects of aging, sun exposure, acneand burn scars with a patient’s own, or autologous, fibroblast cells produced by our proprietary Fibrocell process.We use our proprietary process to harvest autologous fibroblasts from a small skin punch biopsy from behind the ear with the use of a local anesthetic.We chose this location both because of limited exposure to the sun and to avoid creating a visible scar. The biopsy is then packed in a vial in a specialshipping container and shipped to our laboratory where the fibroblast cells are released from the biopsy and initiated into our cell culture process where thecells proliferate until they reach the required cell count. The fibroblasts are then harvested, cryopreserved, tested by quality control and released by qualityassurance prior to preparation of drug product. After wash and preparation of cells to formulate the drug product, additional quality testing is performed priorto release and distribution to the medical clinic. The number of cells and the frequency of injections may vary and will depend on the indication or applicationbeing studied. 3Table of ContentsOur lead product, LAVIV (United States adopted name, or USAN, is azficel-T), is the first and only personalized aesthetic cell therapy approved by theFood and Drug Administration (“FDA”) for the improvement of the appearance of moderate to severe nasolabial fold wrinkles in adults. LAVIV offers patientstheir own living fibroblast cells in a personalized therapy designed to improve the appearance of wrinkles. Our clinical development programs encompass bothaesthetic and therapeutic indications.We believe that because LAVIV and our product candidates are autologous, the risk of an immunological or allergic response is low. With regard to thetherapeutic markets, we believe that our product candidates may address an insufficiently met medical need for the treatment of each of restrictive burn scars,acne scars and vocal scarring. There are also numerous other potential areas of interest for our technology in the body. Certain of our product candidates arestill in clinical development and, as such, benefits we expect to see associated with our product candidates may not be validated in our clinical trials. Inaddition, disadvantages of our product candidates may become known in the future.Going ConcernWe emerged from Bankruptcy in September 2009 and continues to operate as a going concern. At December 31, 2011, we had cash and cashequivalents of approximately $10.8 million and working capital of $2.9 million.As of March 26, 2012, we had cash and cash equivalents of approximately $4.7 million and our accounts payable and accrued expenses wereapproximately $1.6 million. In addition, the Company has approximately $7.0 million of outstanding debt which is due in June 2012. Our current monthlycash run-rate is approximately $2.2 million. We will need to access the capital markets in the near future in order to fund future operations. There is noguarantee that any such required financing will be available on terms satisfactory to us or available at all. These matters create uncertainty relating to its abilityto continue as a going concern. The accompanying consolidated financial statements do not reflect any adjustments relating to the recoverability andclassification of assets or liabilities that might result from the outcome of these uncertainties.Through December 31, 2011, we have been primarily engaged in developing our initial product technology. In the course of our development activities,we have sustained losses and expects such losses to continue through at least 2012. During the year ended December 31, 2011, we financed our operationsprimarily through our existing cash received from external equity financings, but as discussed above we now require additional financing. There is substantialdoubt about our ability to continue as a going concern.Our ability to complete additional offerings is dependent on the state of the debt and/or equity markets at the time of any proposed offering, and suchmarket’s reception of us and the offering terms. Our ability to complete an offering is also dependent on the status of FDA regulatory milestones and ourclinical trials. There is no assurance that capital in any form would be available to us, and if available, on terms and conditions that are acceptable.As a result of the conditions discussed above, and in accordance with GAAP, there exists substantial doubt about our ability to continue as a goingconcern, and our ability to continue as a going concern is contingent, among other things, upon our ability to secure additional adequate financing or capital inthe near future. If we do not obtain additional funding, or do not anticipate additional funding, in the very near future, we will likely enter into bankruptcyand/or cease operations. Further, if we do raise additional cash resources in the near future, it may be raised in contemplation of or in connection withbankruptcy. If we enter into bankruptcy, it is likely that our common stock and common stock equivalents will become worthless and our creditors,including preferred stock, will receive significantly less than what is owed to them. 4Table of ContentsOur StrategyOur business strategy is focused on our unique autologous cellular platform. This strategy will be heavily dependent upon raising sufficient fundsand/or enter relevant strategic partnerships. Our key areas of focus are as follows: • Firstly, aesthetics and dermatology is our first focus. In June 2011, our lead product, LAVIV (United States adopted name, or USAN, is azficel-T), became the first and only personalized aesthetic cell therapy approved by the FDA for the improvement of the appearance of moderate to severenasolabial fold wrinkles in adults and we are currently in the process of launching the product in the United States. Other possible aestheticindications that we are considering pursuing include acne scarring, fine lines and wrinkles around the eyes and mouth, the décolletage and totalfacial treatment. We are developing a personalized topical cosmetic product consisting of a cream vehicle blended with the conditioned mediaextract from the cell culture of a customer’s own fibroblasts. The conditioned media used to promote fibroblast expansion contains protein extractsfrom the fibroblast cells produced in vitro. This media is collected from cell culture during routine feed and passage for use in formulation of thecosmetic product. Final formulation and distribution will be performed at Fibrocell’s Exton, PA manufacturing facility. At present, we areconducting characterization and safety testing in anticipation of launch in the third quarter, 2012. • Secondly, we plan to pursue in the future indications for burn scars and vocal scarring. Other potential areas of interest include wound healingand periodontal disease (recessive gum lines). • Thirdly, our long term vision is, in cooperation with UCLA, to biotransform autologous dermal fibroblasts to “factor free” IPSC cells capable ofdifferentiation into multiple cell types for toxicological, research use and therapeutic areas.Clinical Development ProgramsOur product development programs are focused on the aesthetic and therapeutic markets. These programs are supported by a number of clinical trialprograms at various stages of development.Our aesthetics development programs include product candidates to treat acne scarring and to provide full-face rejuvenation that includes theimprovement of fine lines, wrinkles, skin texture and appearance. Our therapeutic development programs are designed to treat restrictive burn scars and vocalscarring. All of our product candidates are non-surgical and minimally invasive. Although the discussions below may include estimates of when we expecttrials to be completed, the prediction of when a clinical trial will be completed is subject to a number of factors and uncertainties. Also, please refer to Part I,Item 1A of our Form 10-K for the year ended December 31, 2011, for a discussion of certain of our risk factors related to our clinical development programs,as well as other risk factors related to our business.Aesthetic Development ProgramsAcne Scars – Phase II Trial: In November 2007, we commenced an acne scar Phase II study. This study included approximately 95 subjects. Thisplacebo controlled trial was designed to evaluate the use of azficel-T to correct or improve the appearance of acne scars. Each subject served as their owncontrol, receiving azficel-T on one side of their face and placebo on the other. The subjects received three treatments two weeks apart. The follow-up andevaluation period was completed four months after each subject’s last injection. In March 2009, we disclosed certain trial data results, which includedstatistically significant efficacy results for the treatment of moderate to severe acne scars. Compilation of safety data and data related to the validation of thestudy photo guide assessment scale discussed below is ongoing and is also subject to additional financing.In connection with this acne scar program, we developed a photo guide for use in the evaluators’ assessment of acne study subjects. We had originallydesigned the acne scar clinical program as two randomized, double-blind, Phase III, placebo-controlled trials. However, our evaluator assessment scale andphoto guide have not previously been utilized in a clinical trial. In November 2007, the FDA recommended that we consider conducting a Phase II study inorder to address certain study issues, including additional validation related to our evaluator assessment scale. As such, we modified our clinical plans toinitiate a single Phase II trial. This Phase II study, was powered to demonstrate efficacy, and has allowed for a closer assessment of the evaluator assessmentscale and photo guide that is ongoing. We submitted on August 9, 2010, a clinical study report for its Phase II study of azficel-T for the treatment of moderateto severe acne scars to the FDA. We are currently in discussions with the FDA concerning the validation of the evaluator assessment scale and agreeing thepath forward for the acne program. These steps will be subject to obtaining sufficient financial resources. 5Table of ContentsFull Face Rejuvenation—Phase II Open Label Trial: In March 2007, we commenced an open label (unblinded) trial of approximately 50 subjects.Injections of azficel-T began to be administered in July 2007. This trial was designed to further evaluate the safety and use of azficel-T to treat fine lines andwrinkles for the full face. Five investigators across the United States participated in this trial. The subjects received two series of injections approximately onemonth apart. In late December 2007, all 45 remaining subjects completed injections. The subjects were followed for twelve months following each subject’s lastinjection. Data results related to this trial were disclosed in August 2008, which included top line positive efficacy results related to this open label Phase IItrial.Additional safety data from this trial, collected through telephone calls placed to participating subjects twelve months from the date of their final studytreatment, were submitted to the FDA on November 1, 2009. No changes to the safety profile of azficel-T were identified during our review of this data.Facial cream: We are developing a personalized topical cosmetic product consisting of a cream vehicle blended with the conditioned media extract fromthe cell culture of a customer’s own fibroblasts. The conditioned media used to promote fibroblast expansion contains protein extracts from the fibroblast cellsproduced in vitro. This media is collected from cell culture during routine feed and passage for use in formulation of the cosmetic product. Final formulationand distribution will be performed at Fibrocell’s Exton, PA manufacturing facility. At present, we are conducting characterization and safety testing inanticipation of launch in the third quarter, 2012.Therapeutic Development ProgramsRestrictive Burn Scars—Phase II Trial: In January 2007, the Predecessor Company met with the FDA to discuss our clinical program for the use ofazficel-T for restrictive burn scar patients. This Phase II trial would evaluate the use of azficel-T to improve range of motion, function and flexibility, amongother parameters, in existing restrictive burn scars in approximately 20-30 patients. However, the Company delayed the screening and enrollment in this trialuntil such time as we raise sufficient additional financing and gather additional data regarding the burn scar market. The Company is currently finalizing aPhase II protocol for submission to the FDA. We expect this protocol to be finalized and submitted to the FDA in Q2 of 2012. The development of this programwill be subject to obtaining sufficient financial resources.Agera Skincare SystemsWe market and sell a skin care product line through our majority-owned subsidiary, Agera Laboratories, Inc., which was acquired in August 2006.Agera offers a complete line of skincare systems based on a wide array of proprietary formulations, trademarks and nano-peptide technology. These skincareproducts can be packaged to offer anti-aging, anti-pigmentary and acne treatment systems. Agera primarily markets its products in both the United States andEurope (primarily the United Kingdom).Our Target Market OpportunitiesAesthetic Market OpportunityLAVIV, is the first and only personalized aesthetic cell therapy approved by the FDA for the improvement of the appearance of moderate to severenasolabial fold wrinkles in adults and is, thus, directed primarily at the aesthetic market. Aesthetic procedures have traditionally been performed bydermatologists, plastic surgeons and other cosmetic surgeons. According to the American Society for Aesthetic Plastic Surgery, or ASAPS, the total market fornon-surgical cosmetic procedures was approximately $4.1 billion in 2010. We believe the aesthetic procedure market is driven by: • aging of the “baby boomer” population, which currently includes ages approximately 47 to 65; • the desire of many individuals to improve their appearance; 6Table of Contents • impact of managed care and reimbursement policies on physician economics, which has motivated physicians to establish or expand the menu ofelective, private-pay aesthetic procedures that they offer; and • broadening base of the practitioners performing cosmetic procedures beyond dermatologists and plastic surgeons to non-traditional providers.According to the ASAPS, 9.3 million surgical and non-surgical cosmetic procedures were performed in 2010, as compared to 10.0 million in 2009. Alsoaccording to the ASAPS, approximately 7.7 million and 8.5 million non-surgical procedures were performed in 2010 and 2009, respectively. We believe thatthe concept of non-surgical cosmetic procedures involving injectable materials has become more mainstream and accepted. According to the ASAPS, thefollowing table shows the top five non-surgical cosmetic procedures performed in 2010: Procedure Number Botulinum toxin type A 2,437,165 Hyaluronic acid 1,315,121 Laser hair removal 936,270 Laser skin resurfacing 562,706 Chemical peel 493,896 In 2010, procedures among the 35 to 50 year old age group made up approximately 44% of all cosmetic procedures. The 51 to 64 year old age groupmade up 28% of all cosmetic procedures in 2010, while the 19 to 34 year old age group made up 20% of cosmetic procedures in 2010. The Botulinum toxintype A injection was the most popular treatment of the nonsurgical procedures among the 35 to 50 year old age group.Therapeutic Market OpportunitiesIn addition to the aesthetic market, we believe there are opportunities for our Fibrocell Therapy to treat certain medical conditions such as acne scars,restrictive burn scars and tissue loss due to papillary recession. Presently, we are studying therapeutic applications of our technology for acne scars. We arenot aware of other autologous cell-based treatments for any of these therapeutic applications.Sales and MarketingIn June 2011, our lead product, LAVIV, became the first and only personalized aesthetic cell therapy approved by the FDA for the improvement of theappearance of moderate to severe nasolabial fold wrinkles in adults. We formally launched LAVIV in the United States in the fourth quarter of 2011. Ourstrategy is to launch LAVIV directly via our own sales force in the United States. As of the filing date of this 10-K, we have seven sales representativescovering the east and west coast and key metropolitan cities. We also have four customer service representatives in Exton, PA supporting our field salesrepresentatives. Our Agera skincare products are primarily sold directly to our established distributors and salons, with historically and recently very littlefocus on marketing efforts. We continue to attempt to identify additional third party distributors for our Agera product line.Intellectual PropertyWe believe that patents, trademarks, copyrights, proprietary formulations (related to our Agera skincare products) and other proprietary rights areimportant to our business. We also rely on trade secrets, know-how and continuing technological innovations to develop and maintain our competitive position.We seek to protect our intellectual property rights by a variety of means, including obtaining patents, maintaining trade secrets and proprietary know-how, andtechnological innovation to operate without infringing on the proprietary rights of others and to prevent others from infringing on our proprietary rights. Ourpolicy is to seek to protect our proprietary position by, among other methods, actively seeking patent protection in the United States and certain foreigncountries.As of December 31, 2011, we had 10 issued U.S. patents, 3 pending U.S. patent applications, 30 granted foreign patents and 3 pending internationalpatent applications. Our issued patents and patent applications primarily cover the method of using autologous cell fibroblasts for the repair of skin and softtissue defects and the use of autologous fibroblast cells for tissue regeneration. We are in the process of pursuing several other patent applications. 7Table of ContentsIn August 2006, we acquired 57% of the common stock of Agera Laboratories. Agera has a number of trade names, trademarks, exclusive proprietaryrights to product formulations and specified peptides that are used in the Agera skincare products.Our success depends in part on our ability to maintain our proprietary position through effective patent claims and their enforcement against ourcompetitors, and through the protection of our trade secrets. Although we believe our patents and patent applications provide a competitive advantage, thepatent positions of companies like ours are generally uncertain and involve complex legal and factual questions. We do not know whether any of our patentapplications or those patent applications which we have acquired will result in the issuance of any patents. Our issued patents, those that may be issued in thefuture or those acquired by us, may be challenged, invalidated or circumvented, and the rights granted under any issued patent may not provide us withproprietary protection or competitive advantages against competitors with similar technology. In particular, we do not know if competitors will be able to designvariations on our treatment methods to circumvent our current and anticipated patent claims. Furthermore, competitors may independently develop similartechnologies or duplicate any technology developed by us. Because of the extensive time required for the development, testing and regulatory review of apotential product, it is possible that, before any of our products can be commercialized or marketed, any related patent claim may expire or remain in force foronly a short period following commercialization, thereby reducing the advantage of the patent.We also rely upon trade secrets, confidentiality agreements, proprietary know-how and continuing technological innovation to remain competitive,especially where we do not believe patent protection is appropriate or obtainable. We continue to seek ways to protect our proprietary technology and tradesecrets, including entering into confidentiality or license agreements with our employees and consultants, and controlling access to and distribution of ourtechnologies and other proprietary information. While we use these and other reasonable security measures to protect our trade secrets, our employees orconsultants may unintentionally or willfully disclose our proprietary information to competitors.Our commercial success will depend in part on our ability to operate without infringing upon the patents and proprietary rights of third parties. It isuncertain whether the issuance of any third party patents would require us to alter our products or technology, obtain licenses or cease certain activities. Ourfailure to obtain a license to technology that we may require to discover, develop or commercialize our future products may have a material adverse impact onus. One or more third-party patents or patent applications may conflict with patent applications to which we have rights. Any such conflict may substantiallyreduce the coverage of any rights that may issue from the patent applications to which we have rights. If third parties prepare and file patent applications in theUnited States that also claim technology to which we have rights, we may have to participate in interference proceedings in the United States Patent andTrademark Office to determine priority of invention.We have collaborated and may collaborate in the future with other entities on research, development and commercialization activities. Disputes may ariseabout inventorship and corresponding rights in know-how and inventions resulting from the joint creation or use of intellectual property by us and oursubsidiaries, collaborators, partners, licensors and consultants. As a result, we may not be able to maintain our proprietary position.CompetitionThe pharmaceutical and dermal aesthetics industries are characterized by intense competition, rapid product development and technological change.Competition is intense among manufacturers of prescription pharmaceuticals and dermal injection products. Our core products are considered dermal injectionproducts.Now that our lead product, LAVIV, is approved by the FDA for the improvement of the appearance of moderate to severe nasolabial fold wrinkles inadults, we will compete with a variety of companies in the dermatology and plastic surgery markets, many of which offer substantially different treatmentsfor similar problems. These include silicone injections, laser procedures, facial surgical procedures, such as facelifts and eyelid surgeries, fat injections,dermabrasion, collagen, allogenic cell therapies, hyaluronic acid injections and Botulinum toxin injections, and other dermal fillers. Indirect competition comesfrom facial care treatment products. Items catering to the growing demand for therapeutic skin care products include facial scrubs, anti-aging treatments,tonics, astringents and skin-restoration formulas. However, we believe that LAVIV, a “first to market” autologous cellular technology, can complement othermodalities of treatment and represent a significant additional market opportunity. 8Table of ContentsMany of our competitors are large, well-established pharmaceutical, chemical, cosmetic or health care companies with considerably greater financial,marketing, sales and technical resources than those available to us. Additionally, many of our present and potential competitors have research anddevelopment capabilities that may allow them to develop new or improved products that may compete with our product lines. Our products could be renderedobsolete or made uneconomical by the development of new products to treat the conditions addressed by our products, technological advances affecting the costof production, or marketing or pricing actions by one or more of our competitors. Our facial aesthetics product may compete for a share of the existing marketwith numerous products and/or technologies that have become relatively accepted treatments recommended or prescribed by dermatologists and administeredby plastic surgeons and aesthetic dermatologists.Our ability to commercialize LAVIV and our other potential products and compete effectively will depend on, amongst other things, the following: • the effectiveness of our sales and marketing efforts; • the willingness of physicians to adopt an autologous cellular therapy; • the perception by physicians and other members of the health care community of the safety, efficacy and benefits of LAVIV or our other productscompared to those of competing products or therapies; • our ability to manufacture LAVIV and other products we may develop on a commercial scale, which will require us, in the short-term, to addpersonnel to our current manufacturing operation and, in the long-term, to build-out our current manufacturing facility; • the price of LAVIV and that of other products we may develop and commercialize relative to competing products; • our ability to advance our other product candidates through clinical trials and through the FDA approval process; • our ability to recruit, train, retain, manage and motivate our employees; and • our ability to sustain our commercial scale infrastructure, including our manufacturing facilities, development of a distribution network,information technology infrastructure and configure existing operational, manufacturing and financial systems and other operational and financialsystems necessary to support our increased scale as we grow our commercial organization.The field for therapeutic treatments or tissue regeneration for use in wound healing is rapidly evolving. A number of companies are either developing orselling therapies involving stem cells, human-based, animal-based or synthetic tissue products. If approved as a therapy for restrictive burn scars, vocalscarring or periodontal disease, our product candidates would or may compete with synthetic, human or animal derived cell or tissue products marketed bycompanies larger and better capitalized than us.The market for skincare products is quite competitive with low barriers to entry.Government RegulationOur Fibrocell Therapy technologies are subject to extensive government regulation, principally by the FDA and state and local authorities in the UnitedStates and by comparable agencies in foreign countries. Governmental authorities in the United States extensively regulate the pre-clinical and clinical testing,safety, efficacy, research, development, manufacturing, labeling, storage, record-keeping, advertising, promotion, import, export, marketing and distribution,among other things, of pharmaceutical products under various federal laws including the Federal Food, Drug and Cosmetic Act, or FFDCA, the Public HealthService Act, or PHSA, and under comparable laws by the states and in most foreign countries. 9Table of ContentsDomestic RegulationIn the United States, the FDA, under the Federal Food, Drug, and Cosmetic Act (“FFDCA”), the Public Health Service Act (“PHSA”), and other federalstatutes and regulations, subjects pharmaceutical and biologic products to rigorous review. If we do not comply with applicable requirements, we may befined, the government may refuse to approve our marketing applications or allow us to manufacture or market our products or product candidates, and wemay be criminally prosecuted. The FDA also has the authority to discontinue or suspend manufacture or distribution, require a product withdrawal or recallor revoke previously granted marketing authorizations if we fail to comply with regulatory standards or if we encounter problems during commercialoperations.FDA Approval ProcessTo obtain approval of a new product from the FDA, we must, among other requirements, submit data demonstrating the product’s safety and efficacyas well as detailed information on the manufacture and composition of the product candidate. In most cases, this entails extensive laboratory tests and pre-clinical and clinical trials. This testing and the preparation of necessary applications and processing of those applications by the FDA are expensive andtypically take many years to complete. The FDA may deny our applications or may not act quickly or favorably in reviewing these applications, and we mayencounter significant difficulties or costs in our efforts to obtain FDA approvals that could delay or preclude us from marketing any products we maydevelop. The FDA also may require post-marketing testing and surveillance to monitor the effects of approved products or place conditions on any approvalsthat could restrict the commercial applications of these products. Regulatory authorities may withdraw product approvals if we fail to comply with regulatorystandards or if we encounter problems following initial marketing. With respect to patented products or technologies, delays imposed by the governmentalapproval process may materially reduce the period during which we will have the exclusive right to exploit the products or technologies.The FDA does not apply a single regulatory scheme to human tissues and the products derived from human tissue. On a product-by-product basis, theFDA may regulate such products as drugs, biologics, or medical devices, in addition to regulating them as human cells, tissues, or cellular or tissue-basedproducts (“HCT/Ps”), depending on whether or not the particular product triggers any of an enumerated list of regulatory factors. A fundamental difference inthe treatment of products under these classifications is that the FDA generally permits HCT/Ps that do not trigger any of those regulatory factors to becommercially distributed without marketing approval. In contrast, products that trigger those factors, such as if they are more than minimally manipulatedwhen processed or manufactured, are regulated as drugs, biologics, or medical devices and require FDA approval. We have determined that our FibrocellTherapy (TM) triggers regulatory factors that make it a biologic, in addition to an HCT/P, and consequently, we must obtain approval from FDA beforemarketing Fibrocell Therapy (TM) and must also satisfy all regulatory requirements for HCT/Ps.The process required by the FDA before a new drug or biologic may be marketed in the United States generally involves the following: • completion of pre-clinical laboratory tests or trials and formulation studies; • submission to the FDA of an Investigational New Drug (“IND”) for a new drug or biologic, which must become effective before human clinicaltrials may begin; • performance of adequate and well-controlled human clinical trials to establish the safety and efficacy of the proposed drug or biologic for itsintended use; • detailed information on product characterization and manufacturing process; and • submission and approval of a New Drug Application, or NDA, for a drug, or a Biologics License Application, or BLA, for a biologic.Pre-clinical tests include laboratory evaluation of product chemistry formulation and stability, as well as animal and other studies to evaluate toxicity. Inview of the autologous nature of our product candidates and our prior clinical experience with our product candidates, we concluded that it was reasonablysafe to initiate clinical trials 10Table of Contentswithout pre-clinical studies and that the clinical trials would be adequate to further assess both the safety and efficacy of our product candidates. Under FDAregulations, the results of any pre-clinical testing, together with manufacturing information and analytical data, are submitted to the FDA as part of an INDapplication. The FDA requires a 30-day waiting period after the filing of each IND application before clinical trials may begin, in order to ensure that humanresearch subjects will not be exposed to unreasonable health risks. At any time during this 30-day period or at any time thereafter, the FDA may halt proposedor ongoing clinical trials, or may authorize trials only on specified terms. The IND application process may become extremely costly and substantially delaydevelopment of our products. Moreover, positive results of pre-clinical tests will not necessarily indicate positive results in clinical trials.The sponsor typically conducts human clinical trials in three sequential phases, which may overlap. These phases generally include the following: • Phase I: The product is usually first introduced into healthy humans or, on occasion, into patients, and is tested for safety, dosage tolerance,absorption, distribution, excretion and metabolism. • Phase II: The product is introduced into a limited subject population to: • assess its efficacy in specific, targeted indications; • assess dosage tolerance and optimal dosage; and • identify possible adverse effects and safety risks. • Phase III: These are commonly referred to as pivotal studies. If a product is found to have an acceptable safety profile and to be potentiallyeffective in Phase II clinical trials, new clinical trials will be initiated to further demonstrate clinical efficacy, optimal dosage and safety within anexpanded and diverse subject population at geographically-dispersed clinical study sites. • If the FDA does ultimately approve the product, it may require post-marketing testing, including potentially expensive Phase IV studies, toconfirm or further evaluate its safety and effectiveness.Before proceeding with a study, sponsors may seek a written agreement from the FDA regarding the design, size, and conduct of a clinical trial. This isknown as a Special Protocol Assessment, or SPA. Among other things, SPAs can cover clinical studies for pivotal trials whose data will form the primarybasis to establish a product’s efficacy. SPAs thus help establish up-front agreement with the FDA about the adequacy of a clinical trial design to support aregulatory approval, but the agreement is not binding if new circumstances arise. Even if the FDA agrees to an SPA, the agreement may be changed by thesponsor or the FDA on written agreement by both parties, or a senior FDA official determines that a substantial scientific issue essential to determining thesafety or effectiveness of the product was identified after the testing began. There is no guarantee that a study will ultimately be adequate to support anapproval even if the study is subject to an SPA. The FDA retains significant latitude and discretion in interpreting the terms of the SPA agreement and the dataand results from any study that is the subject of the SPA agreement.Clinical trials must meet requirements for Institutional Review Board, or IRB, oversight, patient informed consent and the FDA’s Good ClinicalPractices. Prior to commencement of each clinical trial, the sponsor must submit to the FDA a clinical plan, or protocol, accompanied by the approval of thecommittee responsible for overseeing clinical trials at the clinical trial sites. The FDA or the IRB at each institution at which a clinical trial is being performedmay order the temporary or permanent discontinuation of a clinical trial at any time if it believes that the clinical trial is not being conducted in accordancewith FDA requirements or presents an unacceptable risk to the clinical trial subjects. Data safety monitoring committees, who monitor certain studies to protectthe welfare of study subjects, may also require that a clinical study be discontinued or modified.The sponsor must submit to the FDA the results of the pre-clinical and clinical trials, together with, among other things, detailed information on themanufacturing and composition of the product, and proposed labeling, in the form of an NDA, or, in the case of a biologic, a BLA. The applicant must alsosubmit with the NDA or BLA a 11Table of Contentssubstantial user fee payment, unless a waiver or reduction applies. On February 17, 2009, the U.S. Small Business Administration issued a letter formallydetermining that we are a small business and therefore qualify for the Small Business Exception to the Prescription Drug and User fee Act of 1992(21 USC § 379h(b)(2)) related to our BLA submission for the nasolabial fold wrinkles indication. For fiscal year 2009, this fee was $1,247,200 forcompanies that did not receive an exception. The FDA has advised us it is regulating our Fibrocell Therapy as a biologic. Therefore, we expect to submit BLAsto obtain approval of our product candidates. In some cases, we may be able to expand the indications in an approved BLA through a Prior ApprovalSupplement. Each NDA or BLA submitted for FDA approval is usually reviewed for administrative completeness and reviewability within 45 to 60 daysfollowing submission of the application. If deemed complete, the FDA will “file” the NDA or BLA, thereby triggering substantive review of the application.The FDA can refuse to file any NDA or BLA that it deems incomplete or not properly reviewable. Once the submission has been accepted for filing, the FDAwill review the application and will usually respond to the applicant in accordance with performance goals the FDA has established for the review of NDAsand BLAs—six months from the receipt of the application for priority applications and ten months for regular applications. The review process is oftensignificantly extended by FDA requests for additional information, preclinical or clinical studies, clarification, or a risk evaluation and mitigation strategy, orREMS, or by changes to the application submitted by the applicant in the form of amendments.It is possible that our product candidates will not successfully proceed through this approval process or that the FDA will not approve them in anyspecific period of time, or at all. The FDA may deny or delay approval of applications that do not meet applicable regulatory criteria, or if the FDA determinesthat the clinical data do not adequately establish the safety and efficacy of the product. Satisfaction of FDA pre-market approval requirements for a newbiologic is a process that may take a number of years and the actual time required may vary substantially based upon the type, complexity and novelty of theproduct or disease. The FDA reviews these applications and, when and if it decides that adequate data are available to show that the product is both safe andeffective and that other applicable requirements have been met, approves the drug or biologic for marketing. Government regulation may delay or preventmarketing of potential products for a considerable period of time and impose costly procedures upon our activities. Success in early stage clinical trials doesnot assure success in later stage clinical trials. Data obtained from clinical activities is not always conclusive and may be susceptible to varying interpretationsthat could delay, limit or prevent regulatory approval. Upon approval, a product candidate may be marketed only for those indications approved in the BLAor NDA and may be subject to labeling and promotional requirements or limitations, including warnings, precautions, contraindications and use limitations,which could materially impact profitability. Once approved, the FDA may withdraw the product approval if compliance with pre- and post-market regulatorystandards is not maintained or if safety, efficacy or other problems occur after the product reaches the marketplace.The FDA may, during its review of an NDA or BLA, ask for additional test data. If the FDA does ultimately approve the product, it may require post-marketing testing, including potentially expensive Phase IV studies, to confirm or otherwise further evaluate the safety and effectiveness of the product. TheFDA also may require, as a condition to approval or continued marketing of a drug a REMS, if deemed necessary to manage a known or potential serious riskassociated with the product. REMS can include additional educational materials for healthcare professionals and patients such as Medication Guides andPatient Package Inserts, a plan for communicating information to healthcare professionals, and restricted distribution of the product. In addition, the FDAmay, in some circumstances, impose restrictions on the use of the product, which may be difficult and expensive to administer and may require priorapproval of promotional materials. Following approval, FDA may require labeling changes or impose new post-approval study, risk management, ordistribution restriction requirements.Ongoing FDA RequirementsBefore approving an NDA or BLA, the FDA usually will inspect the facilities at which the product is manufactured and will not approve the productunless the manufacturing facilities are in compliance with the FDA’s current Good Manufacturing Practices, or cGMP, requirements which govern themanufacture, holding and distribution of a product. Manufacturers of human cellular or tissue-based biologics also must comply with the FDA’s Good TissuePractices, as applicable, and the general biological product standards. Following approval, the FDA periodically inspects drug and biologic manufacturingfacilities to ensure continued compliance with the cGMP requirements. Manufacturers must continue to expend time, money and effort in the areas ofproduction, quality control, record keeping and reporting to ensure compliance with those requirements. Failure to comply with these requirements subjects themanufacturer to possible legal or regulatory action, such as suspension of manufacturing, seizure of 12Table of Contentsproduct, voluntary recall of product, withdrawal of marketing approval or civil or criminal penalties. Adverse experiences with the product must be reported tothe FDA and could result in the imposition of marketing restrictions through labeling changes or market removal. Product approvals may be withdrawn ifcompliance with regulatory requirements is not maintained or if problems concerning safety or efficacy of the product occur following approval.The labeling, advertising, promotion, marketing and distribution of a drug or biologic product also must be in compliance with FDA and Federal TradeCommission (“FTC”) requirements which include, among others, standards and regulations for direct-to-consumer advertising, industry-sponsored scientificand educational activities, and promotional activities involving the internet. In general, all product promotion must be consistent with the FDA approval forsuch product, contain a balanced presentation of information on the product’s uses and benefits and important safety information and limitations on use, andotherwise not be false or misleading. The FDA and FTC have very broad enforcement authority, and failure to abide by these regulations can result inpenalties, including the issuance of a Warning Letter directing a company to correct deviations from regulatory standards and enforcement actions that caninclude seizures, injunctions and criminal prosecution.Manufacturers are also subject to various laws and regulations governing laboratory practices, the experimental use of animals and the use and disposalof hazardous or potentially hazardous substances in connection with their research. In each of the above areas, the FDA has broad regulatory and enforcementpowers, including the ability to levy fines and civil penalties, suspend or delay issuance of approvals, seize or recall products and deny or withdrawapprovals.Post-Marketing ObligationsThe Food and Drug Administration Amendments Act of 2007 expanded FDA authority over drug products after approval. All approved drug productsare subject to continuing regulation by the FDA, including record-keeping requirements, reporting of adverse experiences with the product, sampling anddistribution requirements, notifying the FDA and gaining its approval of certain manufacturing or labeling changes, complying with certain electronic recordsand signature requirements, submitting periodic reports to the FDA, maintaining and providing updated safety and efficacy information to the FDA, andcomplying with FDA promotion and advertising requirements. Failure to comply with the statutory and regulatory requirements can subject a manufacturer topossible legal or regulatory action, such as warning letters, suspension of manufacturing, seizure of product, injunctive action, criminal prosecution, or civilpenalties.The FDA may require post-marketing studies or clinical trials to develop additional information regarding the safety of a product. These studies or trialsmay involve continued testing of a product and development of data, including clinical data, about the product’s effects in various populations and any sideeffects associated with long-term use. The FDA may require post-marketing studies or trials to investigate known serious risks or signals of serious risks oridentify unexpected serious risks and may require periodic status reports if new safety information develops. Failure to conduct these studies in a timelymanner may result in substantial civil fines.Drug and biologics manufacturers and their subcontractors are required to register their establishments with the FDA and certain state agencies, and tolist their products with the FDA. The FDA periodically inspects manufacturing facilities in the United States and abroad in order to assure compliance withthe applicable cGMP regulations and other requirements. Facilities also are subject to inspections by other federal, foreign, state or local agencies. In complyingwith the cGMP regulations, manufacturers must continue to assure that the product meets applicable specifications, regulations and other post-marketingrequirements. We must ensure that any third-party manufacturers continue to ensure full compliance with all applicable regulations and requirements. Failureto comply with these requirements subjects the manufacturer to possible legal or regulatory action, such as suspension of manufacturing or recall or seizure ofproduct.Also, newly discovered or developed safety or efficacy data may require changes to a product’s approved labeling, including the addition of newwarnings and contraindications, additional pre-clinical or clinical studies, or even in some instances, revocation or withdrawal of the approval. Violations ofregulatory requirements at any stage, including after approval, may result in various adverse consequences, including the FDA’s withdrawal of an approvedproduct from the market, other voluntary or FDA-initiated action that could delay or restrict further marketing, and the imposition of civil fines and criminalpenalties against the manufacturer and BLA holder. In 13Table of Contentsaddition, later discovery of previously unknown problems may result in restrictions on the product, manufacturer or BLA holder, including withdrawal ofthe product from the market. Furthermore, new government requirements may be established that could delay or prevent regulatory approval of our productsunder development, or affect the conditions under which approved products are marketed.HIPAA RequirementsOther federal legislation may affect our ability to obtain certain health information in conjunction with our research activities. The Health InsurancePortability and Accountability Act of 1996, or HIPAA, mandates, among other things, the adoption of standards designed to safeguard the privacy andsecurity of individually identifiable health information. In relevant part, the U.S. Department of Health and Human Services, or HHS, has released two rulesto date mandating the use of new standards with respect to such health information. The first rule imposes new standards relating to the privacy ofindividually identifiable health information. These standards restrict the manner and circumstances under which covered entities may use and discloseprotected health information so as to protect the privacy of that information. The second rule released by HHS establishes minimum standards for the securityof electronic health information. While we do not believe we are directly regulated as a covered entity under HIPAA, the HIPAA standards impose requirementson covered entities conducting research activities regarding the use and disclosure of individually identifiable health information collected in the course ofconducting the research. As a result, unless they meet these HIPAA requirements, covered entities conducting clinical trials for us may not be able to share withus any results from clinical trials that include such health information.Other U.S. Regulatory RequirementsIn the United States, the research, manufacturing, distribution, sale, and promotion of drug and biological products are potentially subject to regulationby various federal, state and local authorities in addition to the FDA, including the Centers for Medicare and Medicaid Services (formerly the Health CareFinancing Administration), other divisions of the U.S. Department of Health and Human Services (e.g., the Office of Inspector General), the U.S. Departmentof Justice and individual U.S. Attorney offices within the Department of Justice, and state and local governments. For example, sales, marketing andscientific/educational grant programs must comply with the anti-fraud and abuse provisions of the Social Security Act, the False Claims Act, and similar statelaws, each as amended. Pricing and rebate programs must comply with the Medicaid rebate requirements of the Omnibus Budget Reconciliation Act of 1990and the Veterans Health Care Act of 1992, each as amended. If products are made available to authorized users of the Federal Supply Schedule of the GeneralServices Administration, additional laws and requirements apply. All of these activities are also potentially subject to federal and state consumer protection,unfair competition, and other laws.International RegulationThe regulation of our product candidates outside of the United States varies by country. Certain countries regulate human tissue products as apharmaceutical product, which would require us to make extensive filings and obtain regulatory approvals before selling our product candidates. Certain othercountries classify our product candidates as human tissue for transplantation but may restrict its import or sale. Other countries have no applicationregulations regarding the import or sale of products similar to our product candidates, creating uncertainty as to what standards we may be required to meet.ManufacturingWe currently have one operational manufacturing facility located in Exton, Pennsylvania. All component parts used in our Exton, Pennsylvaniamanufacturing process are readily available with short lead times, and all machinery is maintained and calibrated. We believe we have made improvements inour manufacturing processes, and we expect to continue such efforts in the future.We currently have limited manufacturing capacity, although we have sufficient manufacturing capacity to fill the orders for LAVIV we have receivedsince the launch of the product during the fourth quarter of 2011. To the extent we are successful in increasing the demand for LAVIV, we will need to addmanufacturing capacity, which will require us, in the short-term, to add personnel to our current manufacturing operation and, in the long-term, to build-outour current manufacturing facility. 14Table of ContentsOur Agera products are manufactured by a third-party contract manufacturer under a contract manufacturing agreement. The agreement is effectivethrough July 2014.Research and DevelopmentIn addition to our clinical development activities, our research and development activities include improving our manufacturing processes and reducingmanufacturing costs. We expense research and development costs as they are incurred. For the years ended December 31, 2011 and 2010, we incurred researchand development expenses of $7.2 million and $5.5 million, respectively.EmployeesAs of March 26, 2012, we employed 59 people on a full-time basis and one person on a part-time basis, all located in the United States, and oneemployee, our Chief Operating and Chief Financial Officer, who is based in Ireland and works in both Ireland and the United States. We also have 9 peopleworking on a contract basis in our manufacturing facility. We also employ one full-time and one part-time Agera employees. None of our employees are coveredby a collective bargaining agreement, and we consider our relationship with our employees to be good. We also employ consultants and temporary labor on anas needed basis to supplement existing staff.Segment InformationFinancial information concerning the Company’s business segments and geographic areas of operation is included in Note 15 in the Notes toConsolidated Financial Statements contained in this Form 10-K.Corporate HistoryOn August 10, 2001, our company, then known as American Financial Holding, Inc., acquired Isolagen Technologies through the merger of our wholly-owned subsidiary, Isolagen Acquisition Corp., and an affiliated entity, Gemini IX, Inc., with and into Isolagen Technologies. As a result of the merger,Isolagen Technologies became our wholly owned subsidiary. On November 13, 2001, we changed our name to Isolagen, Inc. On August 27, 2009, the UnitedStates Bankruptcy Court for the District of Delaware in Wilmington entered an order, or Confirmation Order, confirming the Joint First Amended Plan ofReorganization dated July 30, 2009, as supplemented by the Plan Supplement dated August 21, 2009, or the Plan, of Isolagen, Inc. and Isolagen’s whollyowned subsidiary, Isolagen Technologies, Inc. The effective date of the Plan was September 3, 2009. Isolagen, Inc. and Isolagen Technologies, Inc. weresubsequently renamed Fibrocell Science, Inc. and Fibrocell Technologies, Inc. respectively.Corporate WebsiteOur Internet website address is http://www.fibrocellscience.com. Our filings on Form 10-K, Form 10-Q, Form 3, Form 4, Form 5, Form 8-K and anyand all amendments thereto are available free of charge through this internet website as soon as reasonably practicable after they are filed or furnished to theSecurities and Exchange Commission, or the SEC. They are also available through the SEC at http://www.sec.gov/edgar/searchedgar/companysearch.html.The information contained in our website does not constitute part of this Form 10-K.Item 1A. Risk FactorsInvesting in our company involves a high degree of risk. Before investing in our company you should carefully consider the following risks,together with the financial and other information contained in this Form 10-K. If any of the following risks actually occurs, our business,prospects, financial condition and results of operations could be adversely affected. In that case, the trading price of our common stock wouldlikely decline and you may lose all or a part of your investment.We could fail to remain a going concern. We will need to raise substantial additional capital to fund our operations through commercialization ofour product candidates, and we do not have any commitments for that capital. 15Table of ContentsThere exists substantial doubt regarding our ability to continue as a going concern. As of December 31, 2011 we had cash and cash equivalents of $10.8million and working capital of $2.9 million.As of March 26, 2012, we had cash and cash equivalents of approximately $4.7 million and our accounts payable and accrued expenses wereapproximately $1.6 million. In addition, the Company has approximately $7.0 million of outstanding debt which is due in June 2012. Our current monthlycash run-rate is approximately $2.2 million. We will be required to raise additional cash resources in the near future in order to fund future operations, or wewill likely cease operations. There is no guarantee that any such required financing will be available on terms satisfactory to us or available at all. Thesematters create uncertainty relating to our ability to continue as a going concern.We will need additional capital to achieve commercialization of our product candidates, expansion of our manufacturing capacity, development of ourclinical development program and to execute our business strategy, and if we are unsuccessful in raising additional capital we will be unable to achievecommercialization of our product candidates or unable to fully execute our business strategy on a timely basis, if at all. If we raise additional capital throughthe issuance of debt securities, the debt securities may be secured and any interest payments would reduce the amount of cash available to operate and growour business. If we raise additional capital through the issuance of equity securities, such issuances will likely cause dilution to our stockholders, particularlyif we are required to do so during periods when our common stock is trading at low price levels. If we file for bankruptcy, it is likely that our common stockwill become worthless, given that there currently exists approximately $7.0 million of debt as of March 26, 2012, which has a priority over commonshareholders. In addition, our Series D Preferred Stock is senior to our common stock, and would be given a liquidation preference prior to the common stockin a bankruptcy event. Additionally, we do not know whether any financing, if obtained, will be adequate to meet our capital needs and to support our growth.If adequate capital cannot be obtained on satisfactory terms, we may terminate or delay our efforts related to regulatory approval of one or more of our productcandidates, curtail or delay the implementation of manufacturing process improvements or delay the expansion of our sales and marketing capabilities, any ofwhich could cause our business to fail.If we do not obtain additional funding, we will likely enter into bankruptcy and/or cease operations. Further, if we do raise additional cash resources inthe near future, it may be raised in contemplation of or in connection with bankruptcy. If we enter into bankruptcy, it is likely that our common stock andcommon stock equivalents will become worthless and our creditors will receive significantly less than what is owed to them.Our independent registered public accounting firm issued their report for our fiscal year ended December 31, 2011, which included an explanatoryparagraph for our uncertainty to continue as a going concern. If we became unable to continue as a going concern, we would have to liquidate our assets and wemay likely receive significantly less than the values at which they are carried on our consolidated financial statements. The inclusion of a going concernexplanatory paragraph in our independent registered public accounting firm’s audit opinion for the year ended December 31, 2011 may materially andadversely affect our stock price and our ability to raise new capital.We have significant risks relating to the commercialization of LAVIV including the following:LAVIV is our only FDA-approved product. If we fail to achieve and sustain commercial success for LAVIV, our business will suffer, our futureprospects may be harmed and our stock price would likely decline.On June 21, 2011, the FDA licensed our autologous cellular therapy product, LAVIV, as the first and only personalized aesthetic cell therapy, approvedby the FDA, for the improvement of the appearance of moderate to severe nasolabial fold wrinkles in adults. Prior to the launch of LAVIV in October 2011, wehad never sold or marketed an autologous cellular product in the U.S. Unless we can successfully commercialize another product candidate or acquire theright to market other approved products, we will continue to rely on LAVIV to generate substantially all of our revenue. Our ability to increase our revenues forLAVIV will depend on, and may be limited by, a number of factors, including the following: • acceptance of and ongoing satisfaction with LAVIV as the first in a new class of therapy in the United States; 16Table of Contents • our ability to develop and expand market share in the United States; • successfully expanding and sustaining our manufacturing capacity to meet demand; • whether physicians are willing to adopt LAVIV as part of their aesthetics treatment paradigm; • our ability to properly train a sufficient number of physicians to administer LAVIV, and whether or not the physicians correctly follow ourprotocols; and • the proper pricing of LAVIV relative to the market it serves.If for any reason we became unable to continue selling or manufacturing LAVIV, our business would be seriously harmed and could fail.If LAVIV were to become the subject of problems related to its efficacy, safety, or otherwise, our revenues from LAVIV could decrease.LAVIV, in addition to any other of our potential product candidates that may be approved by the FDA, will be subject to continual review by the FDA,and we cannot assure you that newly discovered or developed safety issues will not arise. With the use of any newly marketed drug by a wider patientpopulation, serious adverse events may occur from time to time that initially do not appear to relate to the drug itself. Any safety issues could cause us tosuspend or cease marketing of our approved products, cause us to modify how we market our approved products, subject us to substantial liabilities, andadversely affect our revenues and financial condition. In the event of a withdrawal of LAVIV from the market, our revenues would decline significantly andour business would be seriously harmed and could fail.Adoption of LAVIV for the treatment of the appearance of moderate to severe nasolabial fold wrinkles in adults may be slow or limited for avariety of reasons including competing therapies, perceived difficulties in the treatment process and cost. If LAVIV is not successful in gainingbroad acceptance as a treatment option for nasolabial fold wrinkles, our business would be harmed.The rate of adoption of LAVIV for nasolabial fold wrinkles will be dependent on several factors including educating and training physicians and theiroffices on the patient treatment process with LAVIV and autologous cellular therapy generally. As a first in class therapy, LAVIV utilizes a unique treatmentapproach, which can have associated challenges in practice for physicians. The logistics of the product, the injection technique required and the fact that theproduct constitutes a patient’s own cells represent different challenges for physicians. In addition, the tight manufacturing and injection timelines required fortreatment with LAVIV will require physicians to adjust practice mechanics, which may result in delay in market adoption of LAVIV as a preferred therapy.We are rapidly expanding our operations to support commercial launch of LAVIV, which has significantly increased our costs, and until weachieve economies of scale, we will incur negative margins on sales of LAVIV.We have and expect to continue to significantly increase our investment in commercial infrastructure. We will need to effectively manage the expansion ofour operations and facilities and continue to grow our infrastructure to commercialize LAVIV. We must effectively manage our supply chain, third-partyvendors and distribution network, all of which requires strict planning in order to meet production timelines for LAVIV. We continue to add manufacturing,quality control, quality assurance, marketing and sales personnel, and personnel in all other areas of our operations, which strains our existing managerial,operational, financial and other resources. As a result of the scaling of our manufacturing process and the limited orders we have received since the launch ofLAVIV in the fourth quarter of 2011, we are currently incurring negative margins on sales of LAVIV, and will continue to incur such margins until we are ableto generate significant sales volume. As discussed below, to accommodate increased sales, we will need to add manufacturing capacity, which will require us,in the short-term, to add personnel to our current manufacturing operation and, in the long-term, to build-out our current manufacturing facility. In pursuingexpansion, we must continue to monitor quality and effective controls, or we risk possible delays in approval of the facilities by the FDA for commercialmanufacturing. Any delay in readiness of our expanded Exton facility could result in the loss of revenue from potential sales of LAVIV, and adversely impactmarket acceptance for LAVIV. If we fail to manage the growth in our systems and personnel appropriately and successfully in order to achieve ourcommercialization plans for LAVIV, our revenues could suffer and our business could be harmed. 17Table of ContentsWe have significant risks relating to the manufacturing and regulation of LAVIV and our other product candidates, including the following:If we are able to increase orders for LAVIV, we will need to increase our manufacturing capacity, which will require significant expenditures andregulatory approval.We currently have limited manufacturing capacity, although we have sufficient manufacturing capacity to fill the orders for LAVIV we have receivedsince the launch of the product during the fourth quarter of 2011. To the extent we are successful in increasing the demand for LAVIV, we will need to addmanufacturing capacity, which will require us, in the short-term, to add personnel to our current manufacturing operation and, in the long-term, to build-outour current manufacturing facility. Increasing manufacturing capacity will require additional expenditures, for which we will require external financing. Inaddition, our ability to increase manufacturing capacity will be subject to additional FDA review.We are subject to significant regulation with respect to the manufacturing of our products.All of those involved in the preparation of a cellular therapy for clinical trials or commercial sale, including our existing supply contract manufacturersand clinical trial investigators, are subject to extensive regulation by the FDA. Components of a finished therapeutic product approved for commercial sale orused in late-stage clinical trials must be manufactured in accordance with current Good Manufacturing Practices. These regulations govern manufacturingprocesses and procedures and the implementation and operation of quality systems to control and assure the quality of investigational products and productsapproved for sale. Our facilities and quality systems and the facilities and quality systems of some or all of our third party contractors and suppliers mustpass inspection for compliance with the applicable regulations as a condition of FDA approval of our products. In addition, the FDA may, at any time, auditor inspect a manufacturing facility involved with the preparation of LAVIV or our other potential products or the associated quality systems for compliancewith the regulations applicable to the activities being conducted. The FDA also may, at any time following approval of a product for sale, audit ourmanufacturing facilities or those of our third party contractors. If any such inspection or audit identifies a failure to comply with applicable regulations or if aviolation of our product specifications or applicable regulation occurs independent of such an inspection or audit, we or the FDA may require remedialmeasures that may be costly and/or time consuming for us or a third party to implement and that may include the temporary or permanent suspension of aclinical trial or commercial sales, recalls, market withdrawals, seizures or the temporary or permanent closure of a facility. Any such remedial measuresimposed upon us or third parties with whom we contract could materially harm our business.Manufacturing difficulties, disruptions or delays could limit supply of our products and limit our product sales.Manufacturing biologic human therapeutic products is difficult, complex and highly regulated. We currently manufacture LAVIV at one facility in theU.S. and we also plan to manufacture our product candidates in the same facility. Our ability to adequately and timely manufacture and supply our productsis dependent on the uninterrupted and efficient operation of our sole facility and those of our third-party suppliers, which may be impacted by: • availability or contamination of raw materials and components used in the manufacturing process, particularly those for which we have no othersource or supplier; • capacity of our facility and those of our suppliers; • the performance of our information technology systems; • compliance with regulatory requirements; • inclement weather and natural disasters; • changes in forecasts of future demand for product components; 18Table of Contents • timing and actual number of production runs for product components; • potential facility contamination by microorganisms or viruses; • updating of manufacturing specifications; and • product quality success rates and yields.If the efficient manufacture and supply of our products is interrupted, we may experience delayed shipments or supply constraints. If we are at any timeunable to provide an uninterrupted supply of our products to patients, we may lose patients and physicians may elect to prescribe competing therapeuticsinstead of our products, which could materially and adversely affect our product sales and results of operations.Our manufacturing processes and those of our suppliers must undergo a potentially lengthy FDA approval process, as well as other regulatory approvalprocesses, and are subject to continued review by the FDA and other regulatory authorities. It is a multi-year process to build and license a new manufacturingfacility and it can take significant time to qualify and license a new supplier. In order to maintain supply, mitigate risks and to satisfy anticipated demand forLAVIV, we must successfully implement manufacturing projects on schedule, since we currently do not have sufficient manufacturing capacity to supplyLAVIV if orders for LAVIV significantly increase.If regulatory authorities determine that we or our suppliers or certain of our third-party service providers have violated regulations or if they restrict,suspend or revoke our prior approvals, they could prohibit us from manufacturing our products or conducting clinical trials or selling our marketed productsuntil we or the affected third-party service providers comply, or indefinitely. Because our third-party service providers are subject to FDA and foreignregulatory authorities, alternative qualified third-party service providers may not be available on a timely basis or at all. If we or our third-party serviceproviders cease or interrupt production or if our third-party service providers fail to supply materials, products or services to us, we may experience delayedshipments, and supply constraints for our products.We rely on a scheduling and product tracking system.We have developed a tracking system for the intake of physician orders for LAVIV, to track product delivery, and to store patient-related data we obtainfor purposes of manufacturing LAVIV. We rely on this system in order to maintain the chain of identity for each patient-specific dose of LAVIV, and to ensuretimely delivery of product prior to expiration. If our system was to fail or be compromised, we could lose traceability of patient cells potentially resulting inloss of revenue and our reputation could suffer. A loss of traceability could cause our business to be materially harmed and our results of operations would beadversely impacted.Our business, which depends on one facility, is vulnerable to natural disasters, telecommunication and information systems failures, terrorismand similar problems, and we are not fully insured for losses caused by all of these incidents.We currently conduct all our research, development and manufacturing operations in one facility located in Exton, Pennsylvania. As a result, all of thecommercial manufacturing of LAVIV for the U.S. market takes place at a single U.S. facility. If regulatory, manufacturing or other problems require us todiscontinue production at that facility, we will not be able to supply our product, which would adversely impact our business.Our Exton facility could be damaged by fire, floods, power loss, telecommunication and information systems failures or similar events. Our insurancepolicies have limited coverage levels for loss or damages in these events and may not adequately compensate us for any losses that may occur. In addition,terrorist acts or acts of war may cause harm to our employees or damage our Exton facility. The potential for future terrorist attacks, the national andinternational responses to terrorist attacks or perceived threats to national security, and other acts of war or hostility have created many economic and politicaluncertainties that could adversely affect our business and results of operations in ways that we cannot predict, and could cause our stock price to fluctuate ordecline. We are uninsured for these types of losses. 19Table of ContentsObtaining FDA and other regulatory approvals is complex, time consuming and expensive, and the outcomes are uncertain.The process of obtaining FDA and other regulatory approvals is time consuming, expensive and difficult. Clinical trials are required and the marketingand manufacturing of our product candidates are subject to rigorous testing procedures.The commencement and completion of clinical trials for any of our product candidates could be delayed or prevented by a variety of factors, including: • delays in obtaining regulatory approvals to commence a study; • delays in identifying and reaching agreement on acceptable terms with prospective clinical trial sites; • delays or failures in obtaining approval of our clinical trial protocol from an institutional review board, or IRB, to conduct a clinical trial at aprospective study site; • delays in the enrollment of subjects; • manufacturing difficulties; • failure of our clinical trials and clinical investigators to be in compliance with the FDA’s Good Clinical Practices, or GCP; • failure of our third-party contract research organizations, clinical site organizations and other clinical trial managers, to satisfy their contractualduties, comply with regulations or meet expected deadlines; • lack of efficacy during clinical trials; or • unforeseen safety issues.We do not know whether our clinical trials will need to be restructured or will be completed on schedule, if at all, or whether they will provide datanecessary to support necessary regulatory approval. Significant delays in clinical trials will impede our ability to commercialize our product candidates andgenerate revenue, and could significantly increase our development costs.We utilize bovine-sourced materials to manufacture LAVIV and our product candidates. Future FDA regulations, as well as currently proposedregulations, may require us to change the source of the bovine-sourced materials we use in our products or to cease using bovine-sourced materials. If we arerequired to use alternative materials in our products, and in the event that such alternative materials are available to us, or if we choose to change the materialsused in our products in the future, we would need to validate the new manufacturing process and run comparability trials with the reformulated product,which could delay our submission for regulatory approval.Even if marketing approval from the FDA is received for one or more of our product candidates, the FDA may impose post-marketing requirements,such as: • labeling and advertising requirements, restrictions or limitations, including the inclusion of warnings, precautions, contra-indications or uselimitations that could have a material impact on the future profitability of our product candidates; • testing and surveillance to further evaluate or monitor our future products and their continued compliance with regulatory standards andrequirements; 20Table of Contents • submitting products for inspection; or • imposing a risk evaluation and mitigation strategy, or REMS, to ensure that the benefits of the drug outweigh the risks.With respect to our LAVIV product, which was approved in June 2011, as part of our label the FDA required us to conduct a post-marketing study,which we expect to commence in mid-2012 and complete in 2014.Clinical trials may fail to demonstrate the safety or efficacy of our product candidates, which could prevent or significantly delay regulatoryapproval and prevent us from raising additional financing.Prior to receiving approval to commercialize any of our product candidates, we must demonstrate with substantial evidence from well-controlled clinicaltrials, and to the satisfaction of the FDA and other regulatory authorities in the United States and abroad, that our product candidates are both safe andeffective. We will need to demonstrate our product candidates’ efficacy and monitor their safety throughout the process. We previously completed a pivotalPhase III clinical trial related to our LAVIV. The success of prior pre-clinical or clinical trials does not ensure the success of these trials, which are beingconducted in populations with different racial and ethnic demographics than our previous trials. If our current trials or any future clinical trials areunsuccessful, our business and reputation would be harmed and the price at which our stock trades could be adversely affected.All of our product candidates are subject to the risks of failure inherent in the development of biotherapeutic products. The results of early-stage clinicaltrials of our product candidates do not necessarily predict the results of later-stage clinical trials. Product candidates in later-stage clinical trials may fail todemonstrate desired safety and efficacy traits despite having successfully progressed through initial clinical testing. Even if we believe the data collected fromclinical trials of our product candidates is promising, this data may not be sufficient to support approval by the FDA or any other U.S. or foreign regulatoryapproval. Pre-clinical and clinical data can be interpreted in different ways. Accordingly, FDA officials could reach different conclusions in assessing suchdata than we do, which could delay, limit or prevent regulatory approval. In addition, the FDA, other regulatory authorities, our Institutional Review Boards orwe, may suspend or terminate clinical trials at any time.Unlike our Phase III nasolabial fold wrinkles trial, our Phase II Acne Scar trial is not subject to a SPA with the FDA. In addition, we have developed aphoto guide for use in the evaluators’ assessment of acne study subjects. Our evaluator assessment scale and photo guide have not been previously used in aclinical trial. To obtain FDA approval with respect to the acne scar indication, we will require FDA concurrence with the use of our evaluator assessment scaleand photo guide.Any failure or delay in completing clinical trials for our product candidates, or in receiving regulatory approval for the sale of any product candidates,has the potential to materially harm our business, and may prevent us from raising necessary, additional financing that we may need in the future.Other significant risk factors include the following:Since our emergence from bankruptcy we have completed numerous equity financings of convertible securities, and it is likely that we will makeadditional equity financings in the future, which may materially and adversely affect the price of our common stock. We have a significantnumber of convertible securities that may result in significant dilution to our common stockholders.Sales of substantial amounts of shares of our common stock in the public market, or the perception that those sales may occur, could cause the marketprice of our common stock to decline. We have used and it is likely that we will continue to use our common stock or securities convertible into orexchangeable for our common stock to fund our working capital needs or to acquire technology, product rights or businesses, or for other purposes. If we issueadditional equity securities, particularly during times when our common stock is trading at relatively low price levels, the price of our common stock may bematerially and adversely affected. 21Table of ContentsSince our emergence from bankruptcy we have completed numerous equity financings of convertible preferred stock and warrants. The conversion orexercise of the preferred stock or warrants, as applicable, into common stock and the sale of such common stock into the market may cause the price of ourcommon stock to fall. Even if such sales do not occur, the market may anticipate such sales in the future, which may cause the price of our common stock tofall.Furthermore, our outstanding preferred stock has a mandatory conversion feature that we may trigger if the price of our common stock trades above$1.00 per share for a period of 20 days. As of March 26, 2012, if such price occurs and if we trigger the mandatory conversion feature, we would be requiredto issue in excess of 6 million shares of common stock. The issuance of these shares or the sale of these shares may materially reduce the price of our commonstock.We have a significant number of warrants and convertible preferred stock outstanding that contain anti-dilution and price-protection provisionsthat may result in the reduction of their exercise prices or conversion prices in the future.Since October 2009, we have completed several offerings of convertible preferred stock and warrants. Many of these securities contain anti-dilutionprovisions, which provisions require the lowering of the conversion price or exercise price, as applicable, to the purchase price of future offerings.Furthermore, with respect to certain of the warrants issued in these offerings, if we complete an offering below the exercise price of such warrants, the numberof shares issuable under the warrants will be proportionately increased such that the aggregate exercise price payable after taking into account the decrease inthe exercise price, shall be equal to the aggregate exercise price prior to such adjustment. The conversion and exercise price of our convertible preferred stockand warrants has been lowered in the past (with proportional increases in the number of shares underlying the warrants as described in the preceding sentence)due to the completion of subsequent financings. If in the future we issue securities for less than the conversion or exercise price of the securities we issued inthese prior financings, we may be required to further reduce the relevant conversion or exercise prices, and the number of shares underlying the warrants maybe increased.During the term that the warrants and preferred stock are outstanding, the holders of those securities are given the opportunity to profit from a rise in themarket price of our common stock. In addition, certain of the warrants are not redeemable by us. We may find it more difficult to raise additional equitycapital while these warrants or preferred stock are outstanding. At any time during which these warrants are likely to be exercised, we may be able to obtainadditional equity capital on more favorable terms from other sources.We have yet to be profitable, we expect losses to increase from current levels and we will continue to experience significant negative cash flow aswe expand our operations, which may limit or delay our ability to become profitable.We have incurred losses since our inception, have never generated significant revenue from commercial sales of our products, and have never beenprofitable. We are focused on the commercialization of LAVIV and product development, and we have expended significant resources on the launch of LAVIV,our clinical trials, personnel and research and development. We expect these costs to continue to rise in the future. We expect to continue to experience increasingoperating losses and negative cash flow as we expand our operations.We expect to continue to incur significant additional costs and expenses related to: • the commercialization of LAVIV; • expansion of laboratory and manufacturing operations, including the hiring of manufacturing and quality control and assurance personnel; • FDA clinical trials and regulatory approvals; 22Table of Contents • research and development; • brand development; • personnel costs; • development of relationships with strategic business partners, including physicians who might use our future products; and • interest expense and amortization of issuance costs related to our outstanding note payables.If our product candidates fail in clinical trials or do not gain regulatory approval, if our product candidates do not achieve market acceptance, or if wedo not succeed in effectively and efficiently implementing manufacturing process and technology improvements to make our product commercially viable, wewill not be profitable. If we fail to become and remain profitable, or if we are unable to fund our continuing losses, our business may fail.We will continue to experience operating losses and significant negative cash flow until we begin to generate significant revenue from LAVIV, which willrequire a significant increase in our manufacturing capacity.If physicians do not follow our established protocols, the efficacy and safety of our product candidates may be adversely affected.We are dependent on physicians to follow our established protocols both as to the administration and the handling of our product candidates inconnection with our clinical trials, and we continue to be dependent on physicians to follow such protocols after our product candidates are commercialized.The treatment protocol requires each physician to verify the patient’s name and date of birth with the patient and the patient records immediately prior toinjection. In the event more than one patient’s cells are delivered to a physician or we deliver the wrong patient’s cells to the physician, which has occurred inthe past, it is the physician’s obligation to follow the treatment protocol and assure that the patient is treated with the correct cells. If the physicians do notfollow our protocol, the efficacy and safety of our product candidates may be adversely affected.As a result of our limited operating history, we may not be able to correctly estimate our future operating expenses, which could lead to cashshortfalls.We have a limited operating history and our primary business activities consist of commercializing our LAVIV product and conducting clinical trials.As such, our historical financial data is of limited value in estimating future operating expenses. Our budgeted expense levels are based in part on ourexpectations concerning the costs commercializing our LAVIV product and of our clinical trials, which depend on the success of such trials and our ability toeffectively and efficiently conduct such trials, and expectations related to our efforts to achieve FDA approval with respect to our product candidates. Inaddition, our budgeted expense levels are based in part on our expectations of future revenue that we may receive from our Agera product line, and the size offuture revenue depends on the choices and demand of individuals. Our limited operating history and clinical trial experience make these costs and revenuesdifficult to forecast accurately. We may be unable to adjust our operations in a timely manner to compensate for any unexpected increase in costs or shortfall inrevenue. Further, our fixed manufacturing costs and business development and marketing expenses will increase significantly as we expand our operations.Accordingly, a significant increase in costs or shortfall in revenue could have an immediate and material adverse effect on our business, results of operationsand financial condition.Our operating results may fluctuate significantly in the future, which may cause our results to fall below the expectations of securities analysts,stockholders and investors.Our operating results may fluctuate significantly in the future as a result of a variety of factors, many of which are outside of our control. These factorsinclude, but are not limited to: • the level of demand and profitability of LAVIV; 23Table of Contents • the timely and successful implementation of improved manufacturing processes; • our ability to attract and retain personnel with the necessary strategic, technical and creative skills required for effective operations; • the amount and timing of expenditures by practitioners and their patients; • introduction of new technologies; • product liability litigation, class action and derivative action litigation, or other litigation; • the amount and timing of capital expenditures and other costs relating to the expansion of our operations; • the state of the debt and/or equity markets at the time of any proposed offering we choose to initiate; • our ability to successfully integrate new acquisitions into our operations; • government regulation and legal developments regarding LAVIV and our product candidates in the United States and in the foreign countries inwhich we may operate in the future; and • general economic conditions.As a strategic response to changes in the competitive environment, we may from time to time make pricing, service, technology or marketing decisionsor business or technology acquisitions that could have a material adverse effect on our operating results. Due to any of these factors, our operating results mayfall below the expectations of securities analysts, stockholders and investors in any future period, which may cause our stock price to decline.We may be liable for product liability claims not covered by insurance.Physicians who used our facial aesthetic product in the past, or who may use any of our future products, and patients who have been treated by ourfacial aesthetic product in the past, or who may use any of our future products, may bring product liability claims against us. While we have taken, andcontinue to take, what we believe are appropriate precautions, we may be unable to avoid significant liability exposure. We currently keep in force productliability insurance, although such insurance may not be adequate to fully cover any potential claims or may lapse in accordance with its terms prior to theassertion of claims. We may be unable to obtain product liability insurance in the future, or we may be unable to do so on acceptable terms. Any insurance weobtain or have obtained in the past may not provide adequate coverage against any asserted claims. In addition, regardless of merit or eventual outcome,product liability claims may result in: • diversion of management’s time and attention; • expenditure of large amounts of cash on legal fees, expenses and payment of damages; • decreased demand for our products or any of our future products and services; or • injury to our reputation.If we are the subject of any future product liability claims, our business could be adversely affected, and if these claims are in excess of insurancecoverage, if any, that we may possess, our financial position will suffer.Our failure to comply with extensive governmental regulation may significantly affect our operating results.Even if we obtain regulatory approval for some or all of our product candidates, we will continue to be subject to extensive ongoing requirements by theFDA, as well as by a number of foreign, national, state and local 24Table of Contentsagencies. These regulations will impact many aspects of our operations, including testing, research and development, manufacturing, safety, efficacy,labeling, storage, quality control, adverse event reporting, import and export, record keeping, approval, distribution, advertising and promotion of our futureproducts. We must also submit new or supplemental applications and obtain FDA approval for certain changes to an approved product, product labeling ormanufacturing process. Application holders must also submit advertising and other promotional material to the FDA and report on ongoing clinical trials. TheFDA enforces post-marketing regulatory requirements, including the cGMP requirements, through periodic unannounced inspections. We do not knowwhether we will pass any future FDA inspections. Failure to pass an inspection could disrupt, delay or shut down our manufacturing operations. Failure tocomply with applicable regulatory requirements could, among other things, result in: • administrative or judicial enforcement actions; • changes to advertising; • failure to obtain marketing approvals for our product candidates; • revocation or suspension of regulatory approvals of products; • product seizures or recalls; • court-ordered injunctions; • import detentions; • delay, interruption or suspension of product manufacturing, distribution, marketing and sales; or • civil or criminal sanctions.The discovery of previously unknown problems with our future products may result in restrictions of the products, including withdrawal from themarket. In addition, the FDA may revisit and change its prior determinations with regard to the safety or efficacy of our future products. If the FDA’s positionchanges, we may be required to change our labeling or cease to manufacture and market our future products. Even prior to any formal regulatory action, wecould voluntarily decide to cease the distribution and sale or recall any of our future products if concerns about their safety or efficacy develop.In their regulation of advertising and other promotion, the FDA and the FTC may issue correspondence alleging that some advertising or promotionalpractices are false, misleading or deceptive. The FDA and FTC are authorized to impose a wide array of sanctions on companies for such advertising andpromotion practices, which could result in any of the following: • incurring substantial expenses, including fines, penalties, legal fees and costs to comply with the FDA’s requirements; • changes in the methods of marketing and selling products; • taking FDA mandated corrective action, which may include placing advertisements or sending letters to physicians rescinding previousadvertisements or promotions; or • disruption in the distribution of products and loss of sales until compliance with the FDA’s position is obtained. 25Table of ContentsImproper promotional activities may also lead to investigations by federal or state prosecutors, and result in criminal and civil penalties. If we becomesubject to any of the above requirements, it could be damaging to our reputation and restrict our ability to sell or market our future products, and our businesscondition could be adversely affected. We may also incur significant expenses in defending ourselves.Physicians may prescribe pharmaceutical or biologic products for uses that are not described in a product’s labeling or differ from those tested by usand approved by the FDA. While such “off-label” uses are common and the FDA does not regulate physicians’ choice of treatments, the FDA does restrict amanufacturer’s communications on the subject of off-label use. Companies cannot promote FDA-approved pharmaceutical or biologic products for off-labeluses, but under certain limited circumstances they may disseminate to practitioners’ articles published in peer-reviewed journals. To the extent allowed by theFDA, we intend to disseminate peer-reviewed articles on our future products to practitioners. If, however, our activities fail to comply with the FDA’sregulations or guidelines, we may be subject to warnings from, or enforcement action by, the FDA or other regulatory or law enforcement authorities.Our sales, marketing, and scientific/educational grant programs, if any in the future, must also comply with applicable requirements of the anti-fraudand abuse provisions of the Social Security Act, the False Claims Act, the federal anti-kickback law, and similar state laws, each as amended. Pricing andrebate programs must comply with the Medicaid rebate requirements of the Omnibus Budget Reconciliation Act of 1990 and the Veteran’s Health Care Act of1992, each as amended. If products are made available to authorized users of the Federal Supply Schedule of the General Services Administration, additionallaws and requirements apply. All of these activities are also potentially subject to federal and state consumer protection and unfair competition laws. Thedistribution of product samples to physicians must comply with the requirements of the Prescription Drug Marketing Act.Depending on the circumstances, failure to meet post-approval requirements can result in criminal prosecution, fines or other penalties, injunctions,recall or seizure of products, total or partial suspension of production, denial or withdrawal of pre-marketing product approvals, or refusal to allow us to enterinto supply contracts, including government contracts. Any government investigation of alleged violations of law could require us to expend significant timeand resources in response, and could generate negative publicity.Our competitors in the pharmaceutical, medical device and biotechnology industries may have superior products, manufacturing capabilities,financial resources or marketing position.The human healthcare products and services industry is extremely competitive. Our competitors include major pharmaceutical, medical device andbiotechnology companies. Most of these competitors have more extensive research and development, marketing and production capabilities and greaterfinancial resources than we do. Our future success will depend on our ability to develop and market effectively our products against those of our competitors.If our products cannot compete effectively in the marketplace, our results of operations and financial position will suffer.We are dependent on our key manufacturing, quality and other management personnel, and the loss of any of these individuals could harm ourbusiness.We are dependent on the efforts of our key management and manufacturing and quality staff. The loss of any of these individuals, or our inability torecruit and train additional key personnel in a timely manner, could materially and adversely affect our business and our future prospects. A loss of one ormore of our current officers or key personnel could severely and negatively impact our operations. We have employment agreements with most of our keymanagement personnel, but some of these people are employed “at-will,” and any of them may elect to pursue other opportunities at any time. We have nopresent intention of obtaining key man life insurance on any of our executive officers or key management personnel.We may need to attract, train and retain additional highly qualified senior executives and manufacturing and quality personnel in the future.In the future, we may need to seek additional senior executives, as well as manufacturing and quality staff members. There is a high demand for highlytrained executive, manufacturing and quality personnel in our industry. We do not know whether we will be able to attract, train and retain highly qualifiedmanufacturing and quality personnel in the future, which could have a material adverse effect on our business, financial condition and results of operations. 26Table of ContentsIf we are unable to adequately protect our intellectual property and proprietary technology, the value of our technology and future products willbe adversely affected, and if we are unable to enforce our intellectual property against unauthorized use by third parties our business may bematerially harmed.Our long-term success largely depends on our future ability to market technologically competitive products. Our ability to achieve commercial successwill depend in part on obtaining and maintaining patent protection and trade secret protection of our technology and future products, as well as successfullydefending these patents against third party challenges. In order to do so we must: • obtain and protect commercially valuable patents or the rights to patents both domestically and abroad; • operate without infringing upon the proprietary rights of others; and • prevent others from successfully challenging or infringing our proprietary rights.As of December 31, 2011, we had 10 issued U.S. patents, 3 pending U.S. patent applications, 30 granted foreign patents and 3 pending internationalpatent applications. However, we may not be able to obtain additional patents relating to our technology or otherwise protect our proprietary rights. If we fail toobtain or maintain patents from our pending and future applications, we may not be able to prevent third parties from using our proprietary technology. Wewill be able to protect our proprietary rights from unauthorized use only to the extent that these rights are covered by valid and enforceable patents that wecontrol or are effectively maintained by us as trade secrets. Furthermore, the degree of future protection of our proprietary rights is uncertain because legalmeans afford only limited protection and may not adequately protect our rights or permit us to gain or keep a competitive advantage.The patent situation of companies in the markets in which we compete is highly uncertain and involves complex legal and factual questions for whichimportant legal principles remain unresolved. No consistent policy regarding the breadth of claims allowed in such companies’ patents has emerged to date inthe United States. The laws of other countries do not protect intellectual property rights to the same extent as the laws of the United States, and manycompanies have encountered significant problems in protecting and defending such rights in foreign jurisdictions. The legal systems of certain countries,particularly certain developing countries, do not favor the enforcement of patents and other intellectual property protection, particularly those relating tobiotechnology and/or pharmaceuticals, which could make it difficult for us to stop the infringement of our patents in foreign countries in which we holdpatents. Proceedings to enforce our patent rights in the United States or in foreign jurisdictions would likely result in substantial cost and divert our efforts andattention from other aspects of our business. Changes in either the patent laws or in interpretations of patent laws in the United States or other countries maydiminish the value of our intellectual property. Accordingly, we cannot predict the breadth of claims that may be allowed or enforced in our patents or in third-party patents.Other risks and uncertainties that we face with respect to our patents and other proprietary rights include the following: • the inventors of the inventions covered by each of our pending patent applications might not have been the first to make such inventions; • we might not have been the first to file patent applications for these inventions or similar technology; • the future and pending applications we will file or have filed, or to which we will or do have exclusive rights, may not result in issued patents ormay take longer than we expect to result in issued patents; • the claims of any patents that are issued may not provide meaningful protection; 27Table of Contents • our issued patents may not provide a basis for commercially viable products or may not be valid or enforceable; • we might not be able to develop additional proprietary technologies that are patentable; • the patents licensed or issued to us may not provide a competitive advantage; • patents issued to other companies, universities or research institutions may harm our ability to do business; • other individual companies, universities or research institutions may independently develop or have developed similar or alternative technologiesor duplicate our technologies and commercialize discoveries that we attempt to patent; • other companies, universities or research institutions may design around technologies we have licensed, patented or developed; and • many of our patent claims are method, rather than composition of matter, claims; generally composition of matter claims are easier to enforce andare more difficult to circumvent.Our business may be harmed and we may incur substantial costs as a result of litigation or other proceedings relating to patent and otherintellectual property rights.A third party may assert that we, one of our subsidiaries or one of our strategic collaborators has infringed his, her or its patents and proprietary rightsor challenge the validity or enforceability of our patents and proprietary rights. Likewise, we may need to resort to litigation to enforce our patent rights or todetermine the scope and validity of a third party’s proprietary rights.We cannot be sure that other parties have not filed for or obtained relevant patents that could affect our ability to obtain patents or operate our business.Even if we have previously filed patent applications or obtain issued patents, others may file their own patent applications for our inventions and technology,or improvements to our inventions and technology. We have become aware of published patent applications filed after the issuance of our patents that, shouldthe owners pursue and obtain patent claims to our inventions and technology could require us to challenge such patent claims. Others may challenge our patentor other intellectual property rights or sue us for infringement. In all such cases, we may commence legal proceedings to resolve our patent or other intellectualproperty disputes or defend against charges of infringement or misappropriation. An adverse determination in any litigation or administrative proceeding towhich we may become a party could subject us to significant liabilities, result in our patents being deemed invalid, unenforceable or revoked, or drawn into aninterference, require us to license disputed rights from others, if available, or to cease using the disputed technology. In addition, our involvement in any ofthese proceedings may cause us to incur substantial costs and result in diversion of management and technical personnel. Furthermore, parties making claimsagainst us may be able to obtain injunctive or other equitable relief that could effectively block our ability to develop, commercialize and sell products, andcould result in the award of substantial damages against us.The outcome of these proceedings is uncertain and could significantly harm our business. If we do not prevail in this type of litigation, we or ourstrategic collaborators may be required to: • pay monetary damages; • expend time and funding to redesign our Fibrocell Therapy so that it does not infringe others’ patents while still allowing us to compete in themarket with a substantially similar product; • obtain a license, if possible, in order to continue manufacturing or marketing the affected products or services, and pay license fees and royalties,which may be non-exclusive. This license may be non-exclusive, giving our competitors access to the same intellectual property, or the patentowner may require that we grant a cross-license to our patented technology; or 28Table of Contents • stop research and commercial activities relating to the affected products or services if a license is not available on acceptable terms, if at all.Any of these events could materially adversely affect our business strategy and the value of our business.In addition, the defense and prosecution of intellectual property suits, interferences, oppositions and related legal and administrative proceedings in theUnited States and elsewhere, even if resolved in our favor, could be expensive and time consuming and could divert financial and managerial resources. Someof our competitors may be able to sustain the costs of complex patent litigation more effectively than we can because they have substantially greater financialresources.We have not declared any dividends on our common stock to date, and we have no intention of declaring dividends in the foreseeable future.The decision to pay cash dividends on our common stock rests with our Board of Directors and will depend on our earnings, unencumbered cash,capital requirements and financial condition. We do not anticipate declaring any dividends in the foreseeable future, as we intend to use any excess cash tofund our operations. Investors in our common stock should not expect to receive dividend income on their investment, and investors will be dependent on theappreciation of our common stock to earn a return on their investment.Provisions in our charter documents could prevent or delay stockholders’ attempts to replace or remove current management.Our charter documents provide for staggered terms for the members of our Board of Directors. Our Board of Directors is divided into three staggeredclasses, and each director serves a term of three years. At stockholders’ meetings, only those directors comprising one of the three classes will have completedtheir term and be subject to re-election or replacement.In addition, our Board of Directors is authorized to issue “blank check” preferred stock, with designations, rights and preferences as they maydetermine. Accordingly, our Board of Directors has in the past and may in the future, without stockholder approval, issue shares of preferred stock withdividend, liquidation, conversion, voting or other rights that could adversely affect the voting power or other rights of the holders of our common stock. Thistype of preferred stock could also be issued to discourage, delay or prevent a change in our control.The use of a staggered Board of Directors, the ability to issue “blank check” preferred stock, and the adoption of stockholder rights plans are traditionalanti-takeover measures. These provisions in our charter documents make it difficult for a majority stockholder to gain control of the Board of Directors and ofour company. These provisions may be beneficial to our management and our Board of Directors in a hostile tender offer and may have an adverse impact onstockholders who may want to participate in such a tender offer, or who may want to replace some or all of the members of our Board of Directors.Provisions in our bylaws provide for indemnification of officers and directors, which could require us to direct funds away from our business andfuture products.Our bylaws provide for the indemnification of our officers and directors. We have in the past and may in the future be required to advance costsincurred by an officer or director and to pay judgments, fines and expenses incurred by an officer or director, including reasonable attorneys’ fees, as a resultof actions or proceedings in which our officers and directors are involved by reason of being or having been an officer or director of our company. Funds paidin satisfaction of judgments, fines and expenses may be funds we need for the operation of our business and the development of our product candidates,thereby affecting our ability to attain profitability. 29Table of ContentsBecause our consolidated financial statements for the year ended December 31, 2009 reflect fresh-start accounting adjustments made onemergence from bankruptcy and because of the effects of the transactions that became effective pursuant to the Plan, financial information inour current and future financial statements will not be comparable to our financial information from prior periods.In connection with our emergence from bankruptcy, we adopted fresh-start accounting as of September 1, 2009 in accordance with ASC 852-10. Theadoption of fresh-start accounting resulted in our becoming a new entity for financial reporting purposes. As required by fresh-start accounting, our assets andliabilities have been preliminarily adjusted to fair value, and certain assets and liabilities not previously recognized in our financial statements have beenrecognized. In addition to fresh-start accounting, our financial statements reflect all effects of the transactions implemented by the Plan. Accordingly, thefinancial statements prior to September 1, 2009 are not comparable with the financial statements for periods on or after September 1, 2009. Furthermore, theestimates and assumptions used to implement fresh-start accounting are inherently subject to significant uncertainties and contingencies beyond our control.Accordingly, we cannot provide assurance that the estimates, assumptions, and values reflected in the valuations will be realized, and actual results couldvary materially.Future sales of our common stock may depress our stock price.The market price of our common stock could decline as a result of sales of substantial amounts of our common stock in the public market, or as aresult of the perception that these sales could occur, which could occur if we issue a large number of shares of common stock (or securities convertible into ourcommon stock) in connection with a future financing, as our common stock is trading at low levels. These factors could make it more difficult for us to raisefunds through future offerings of common stock or other equity securities. As of March 26, 2012, there were 96,078,253 shares of common stock issuedand outstanding. All of our outstanding shares are freely transferable without restriction or further registration under the Securities Act. In addition to ourcommon stock outstanding, as of such date, we had preferred stock outstanding that was convertible into a total of 6,882,000 shares of common stock andwarrants outstanding that were exercisable for a total of 49,135,602 shares of common stock.There is a limited, volatile and sporadic public trading market for our common stock.There is a limited, volatile and sporadic public trading market for our common stock. Without an active trading market, there can be no assurance ofany liquidity or resale value of our common stock, and stockholders may be required to hold shares of our common stock for an indefinite period of time.Provisions of the warrants issued in connection with certain of our prior financings provide for preferential treatment to the holders of thewarrants and could impede a sale of the Company.The warrants we issued in connection with certain of our prior financings gives each holder the option to receive a cash payment based on a Black-Scholes valuation upon our change of control or upon our failure to be listed on any trading market. We are required, at the warrant holder’s option, exercisableat any time concurrently with, or within 30 days after, the announcement of a fundamental transaction, to redeem all or any portion of these warrants from thewarrant holder by paying to the holder an amount of cash equal to the Black-Scholes value of the remaining unexercised portion of the warrant on or prior tothe date of the consummation of such fundamental transaction.We depend on a third-party manufacturer for our Agera product line, the loss or unavailability of which would require us to find a substitutemanufacturer, if available, resulting in delays in production and additional expenses.Our Agera skin care product line is manufactured by a third party. We are dependent on this third party to manufacture Agera’s products, and themanufacturer is responsible for supplying the formula ingredients for the Agera product lines. If for any reason the manufacturer discontinues production ofAgera’s products at a time when we have a low volume of inventory on hand or are experiencing a high demand for the products, significant delays inproduction of the products and interruption of product sales may result as we seek to establish a relationship and commence production with a newmanufacturer, which would negatively impact our results of operation. 30Table of ContentsThe large majority of our revenue, which relates to the Agera business segment, is to one international customer.Our revenues, which relate solely to the Agera business segment, are highly concentrated in one large, international customer. This large customerrepresented 65% and 72% of 2011 and 2010 consolidated revenues, respectively. Further, this large customer represented 85% and 88% of consolidatedaccounts receivable, net, at December 31, 2011 and December 31, 2010, respectively. A reduction of revenue related to this large customer, due to competitorproduct alternatives, pricing pressures, the financial health of the large customer, or otherwise, would have a significant, negative impact on the business ofAgera, and the related value thereof.Item 1B. Unresolved Staff CommentsNone.Item 2. PropertiesOur corporate headquarters and manufacturing operations are located in one location, Exton, Pennsylvania. The Exton, Pennsylvania location is leasedand consists of approximately 86,500 square feet. The lease is noncancelable through March 31, 2013. Subsequent to December 31, 2011, we renegotiated thelease and extended it for a period of ten years until March 31, 2023.Item 3. Legal ProceedingsNone.Item 4. Mine Safety DisclosureN/A.Part IIItem 5. Market for Registrant’s Common Equity, Related Stockholder Matters and Issuer Purchases of Equity SecuritiesMarket InformationOur common stock has traded on the OTCBB since October 21, 2009 under the symbol “FCSC.” Currently, there is only a limited, sporadic andvolatile market for our stock on the OTCBB. The following table sets forth, for the period indicated, the high and low sales prices of our common stock onthe OTCBB. These prices represent prices between inter-dealer prices, without retail markup, markdown, or commission, and may not represent actualtransactions. High Low Year Ended December 31, 2011 First Quarter $0.90 $0.52 Second Quarter $1.36 $0.72 Third Quarter $0.86 $0.45 Fourth Quarter $0.56 $0.39 Year Ended December 31, 2010 First Quarter $1.13 $0.80 Second Quarter $1.04 $0.65 Third Quarter $0.85 $0.53 Fourth Quarter $0.60 $0.40 The closing price of our common stock on March 26, 2012 was $0.47 as reported on the OTCBB. 31Table of ContentsHolders of RecordAs of March 26, 2012, there were 96,078,253 shares of our common stock outstanding and held by 244 stockholders of record. As of March 26,2012, there were 3,250 shares issued and no shares outstanding for Series A preferred stock, 4,640 shares issued and no shares outstanding for Series Bpreferred stock and 7,779 shares issued and 3,441 shares outstanding for Series D preferred stock.DividendsWe have never paid any cash dividends on our common stock and our board of directors does not intend to do so in the foreseeable future. Thedeclaration and payment of dividends in the future, of which there can be no assurance, will be determined by the board of directors in light of conditions thenexisting, including earnings, financial condition, capital requirements and other factors.Holders of our Series D Preferred Stock are entitled to receive cumulative dividends at the rate per share (as a percentage of the stated value per share) of6% per annum (subject to increase in certain circumstances), payable quarterly in arrears. The dividends are payable in cash, or at our option, in dulyauthorized, validly issued, fully paid and non-assessable shares of common stock equal to 110% of the cash dividend amount payable on the dividendpayment date, or a combination thereof; provided that we may not pay the dividends in shares of common stock unless we meet certain conditions describedin the Certificate of Designation, including that the resale of the shares has been registered under the Securities Act. If we pay the dividend in shares ofcommon stock, the common stock will be valued for such purpose at 80% of the average of the volume weighted average price for the 10 consecutive tradingdays ending on the trading day that is immediately prior to the dividend payment date. Cash payments for Series A dividends were approximately $0.1 millionfor 2010 and cash payments for Series A, Series B and Series D dividends were approximately $0.6 million for 2011.Penny StockThe SEC has adopted rules that regulate broker-dealer practices in connection with transactions in penny stocks. Our stock is currently a “pennystock.” Penny stocks are generally equity securities with a price of less than $5.00, other than securities registered on certain national securities exchanges.The penny stock rules require a broker-dealer, prior to a transaction in a penny stock not otherwise exempt from those rules, deliver a standardized riskdisclosure document prepared by the SEC, which: (a) contains a description of the nature and level of risk in the market for penny stocks in both publicofferings and secondary trading; (b) contains a description of the broker’s or dealer’s duties to the customer and of the rights and remedies available to thecustomer with respect to a violation to such duties or other requirements of securities’ laws; (c) contains a brief, clear, narrative description of a dealer market,including bid and ask prices for penny stocks and significance of the spread between the bid and ask price; (d) contains a toll-free telephone number forinquiries on disciplinary actions; (e) defines significant terms in the disclosure document or in the conduct of trading in penny stocks; and (f) contains suchother information and is in such form as the SEC shall require by rule or regulation. The broker-dealer also must provide to the customer, prior to effectingany transaction in a penny stock, (a) bid and offer quotations for the penny stock; (b) the compensation of the broker-dealer and its salesperson in thetransaction; (c) the number of shares to which such bid and ask prices apply, or other comparable information relating to the depth and liquidity of themarket for such stock; and (d) monthly account statements showing the market value of each penny stock held in the customer’s account. In addition, thepenny stock rules require that prior to a transaction in a penny stock not otherwise exempt from those rules, the broker-dealer must make a special writtendetermination that the penny stock is a suitable investment for the purchaser and receive the purchaser’s written acknowledgment of the receipt of a riskdisclosure statement, a written agreement to transactions involving penny stocks, and a signed and dated copy of a written suitably statement.These disclosure requirements may have the effect of reducing the trading activity in the secondary market for our stock if it becomes subject to thesepenny stock rules. 32Table of ContentsRecent Sales of Unregistered SecuritiesAll information regarding the financings we completed during 2011 have been previously disclosed in current reports we have filed on Form 8-K.Purchases of Equity Securities.We did not repurchase any of our equity securities during the twelve months ended 2011.Item 6. Selected Financial DataWe are a smaller reporting company, and are not required to report this information.Item 7. Management’s Discussion and Analysis of Financial Condition and Results of OperationsGeneralWe are a cellular aesthetic and therapeutic development stage biotechnology company focused on developing novel skin and tissue rejuvenation products.Our clinical development product candidates are designed to improve the appearance of skin injured by the effects of aging, sun exposure, acne and burnscars with a patient’s own, or autologous, fibroblast cells produced by our proprietary Fibrocell process. Our clinical development programs encompass bothaesthetic and therapeutic indications.Our lead product, LAVIV, is the first and only personalized aesthetic cell therapy approved by the FDA for the improvement of the appearance ofmoderate to severe nasolabial fold wrinkles in adults.During 2009 we completed a Phase II study for the treatment of acne scars. We announced on November 3, 2011, that the first scientific presentation ofdata demonstrating the efficacy of LAVIV (azficel-T) in treating moderate-to-severe depressed acne scars was presented at the American Society forDermatologic Surgery (ASDS) annual meeting in Washington, D.C. During 2008 we completed our open-label Phase II study related to full face rejuvenation.We also develop and market an advanced skin care product line through our Agera subsidiary, in which we acquired a 57% interest in August 2006.Exit from BankruptcyOn August 27, 2009, the United States Bankruptcy Court for the District of Delaware in Wilmington entered an order, or Confirmation Order,confirming the Joint First Amended Plan of Reorganization dated July 30, 2009, as supplemented by the Plan Supplement dated August 21, 2009, or the Plan,of Isolagen, Inc. and Isolagen’s wholly owned subsidiary, Isolagen Technologies, Inc. The effective date of the Plan was September 3, 2009. Isolagen, Inc. andIsolagen Technologies, Inc. were subsequently renamed Fibrocell Science, Inc. and Fibrocell Technologies, Inc., respectively. Fibrocell now operates outside ofthe restraints of the bankruptcy process, free of the debts and liabilities discharged by the Plan.Going ConcernThe Company emerged from Bankruptcy in September 2009 and continues to operate as a going concern. At December 31, 2011, the Company hadcash and cash equivalents of approximately $10.8 million and working capital of $2.9 million.As of March 26, 2012, the Company had cash and cash equivalents of approximately $4.7 million and our accounts payable and accrued expenseswere approximately $1.6 million. In addition, the Company has approximately $7.0 million of outstanding debt which is due in June 2012. The Company’scurrent monthly cash run-rate is approximately $2.2 million. The Company will need to access the capital markets in the near future in order to fund futureoperations. There is no guarantee that any such required financing will be available on terms satisfactory to the Company or available at all. These matterscreate uncertainty relating to its ability to continue as a going concern. The accompanying consolidated financial statements do not reflect any adjustmentsrelating to the recoverability and classification of assets or liabilities that might result from the outcome of these uncertainties. 33Table of ContentsFurther, if the Company raises additional cash resources in the near future, it may be raised in contemplation of or in connection with bankruptcy. Inthe event of a bankruptcy, it is likely that its common stock and common stock equivalents will become worthless and our creditors will receive significantlyless than what is owed to them.Through December 31, 2011, the Company has been primarily engaged in developing its initial product technology. In the course of its developmentactivities, the Company has sustained losses and expects such losses to continue through at least 2012. During the year ended December 31, 2011, theCompany financed its operations primarily through its existing cash received from external equity financings, but as discussed above it now requiresadditional financing. There is substantial doubt about the Company’s ability to continue as a going concern.The Company’s ability to complete additional offerings is dependent on the state of the debt and/or equity markets at the time of any proposed offering,and such market’s reception of the Company and the offering terms. The Company’s ability to complete an offering is also dependent on the status of its Foodand Drug Administration (“FDA”) regulatory milestones and its clinical trials. There is no assurance that capital in any form would be available to theCompany, and if available, on terms and conditions that are acceptable.As a result of the conditions discussed above, and in accordance with Generally Accepted Accounting Principles (“GAAP”), there exists substantialdoubt about the Company’s ability to continue as a going concern, and its ability to continue as a going concern is contingent, among other things, upon itsability to secure additional adequate financing or capital in the near future. If the Company does not obtain additional funding, or does not anticipate additionalfunding, in the near future, it will likely enter into bankruptcy and/or cease operations. Further, if it does raise additional cash resources in the near future, itmay be raised in contemplation of or in connection with bankruptcy. If the Company enters into bankruptcy, it is likely that its common stock and commonstock equivalents will become worthless and its creditors, including preferred stock, will receive significantly less than what is owed to them.Critical Accounting PoliciesThe following discussion and analysis of financial condition and results of operations are based upon our consolidated financial statements, whichhave been prepared in conformity with GAAP. However, certain accounting policies and estimates are particularly important to the understanding of ourfinancial position and results of operations and require the application of significant judgment by our management or can be materially affected by changesfrom period to period in economic factors or conditions that are outside of the control of management. As a result they are subject to an inherent degree ofuncertainty. In applying these policies, our management uses their judgment to determine the appropriate assumptions to be used in the determination of certainestimates. Those estimates are based on our historical operations, our future business plans and projected financial results, the terms of existing contracts, ourobservance of trends in the industry, information provided by our customers and information available from other outside sources, as appropriate. Thefollowing discusses our critical accounting policies and estimates.Intangible Assets: Intangible assets are research and development assets related to the Company’s primary study that was recognized upon emergencefrom bankruptcy. This value is related to research and development assets that are not subject to amortization.Intangibles are tested for recoverability whenever events or changes in circumstances indicate the carrying amount may not be recoverable. Theimpairment test consists of a comparison of the fair value of the intangible asset to its carrying amount. If the carrying amount exceeds the fair value, animpairment loss is recognized equal in amount to that excess.Income Taxes: An asset and liability approach is used for financial accounting and reporting for income taxes. Deferred income taxes arise fromtemporary differences between income tax and financial reporting and principally relate to recognition of revenue and expenses in different periods for financialand tax accounting purposes and are measured using currently enacted tax rates and laws. In addition, a deferred tax asset can be generated by net operatingloss (“NOLs”) carryover. If it is more likely than not that some portion or all of a deferred tax asset will not be realized, a valuation allowance is recognized. 34Table of ContentsWarrant Liability: We account for our warrants in accordance with U.S. GAAP. The warrants are measured at fair value and liability-classified underAccounting Standards Codification (“ASC”) 815, Derivatives and Hedging, (“ASC 815”) because the warrants contain “down-round protection” andtherefore, do not meet the scope exception for treatment as a derivative under ASC 815. Since “down-round protection” is not an input into the calculation ofthe fair value of the warrants, the warrants cannot be considered indexed to the Company’s own stock which is a requirement for the scope exception asoutlined under ASC 815. Effective December 31, 2011, we calculated the fair value of the warrants using the Monte Carlo simulation valuation method due tothe changes in the product status with the approval of LAVIV. Prior to December 31, 2011, the Black-Scholes option-pricing model was utilized due to theassumptions present prior to the approval of LAVIV. The fair value is affected by changes in inputs to that model including our stock price, expected stockprice volatility, the contractual term, and the risk-free interest rate. We will continue to classify the fair value of the warrants as a liability until the warrants areexercised, expire or are amended in a way that would no longer require these warrants to be classified as a liability.Preferred Stock and Derivative Liability: The preferred stock has been classified within the mezzanine section between liabilities and equity in itsconsolidated balance sheets in accordance with ASC 480, Distinguishing Liabilities from Equity (“ASC 480”) because any holder of Series A, B or DPreferred may require the Company to redeem all of its Series A, B or D Preferred in the event of a triggering event which is outside of the control of theCompany.The embedded conversion option for the Series A Preferred, Series B Preferred and Series D Preferred has been recorded as a derivative liability underASC 815 in the Company’s consolidated balance sheet as of December 31, 2011 and December 31, 2010, and will be re-measured on the Company’sreporting dates. The fair value of the derivative liability is determined using the Black-Scholes option pricing model and is affected by changes in inputs tothat model including our stock price, expected stock price volatility, the contractual term, and the risk-free interest rate. The Company will continue to classifythe fair value of the embedded conversion option as a liability until the preferred stock is converted into common stock.Stock-Based Compensation: We account for stock-based awards to employees using the fair value based method to determine compensation for allarrangements where shares of stock or equity instruments are issued for compensation. In addition, the Company accounts for stock-based compensation tononemployees in accordance with the accounting guidance for equity instruments that are issued to other than employees. We use a Black-Scholes option-pricing model to determine the fair value of each option grant as of the date of grant for expense incurred. The Black-Scholes model requires inputs for risk-free interest rate, dividend yield, volatility and expected lives of the options. Expected volatility is based on historical volatility of our competitor’s stock sincethe Predecessor Company ceased trading as part of the bankruptcy and emerged as a new entity. The risk-free rate for periods within the contractual life of theoption is based on the U.S. Treasury yield curve in effect at the time of the grant. The expected lives for options granted represents the period of time thatoptions granted are expected to be outstanding and is derived from the contractual terms of the options granted. We estimate future forfeitures of options basedupon expected forfeiture rates.Research and Development Expenses: Research and development costs are expensed as incurred and include salaries and benefits, costs paid to third-party contractors to perform research, conduct clinical trials, develop and manufacture drug materials and delivery devices, and a portion of facilities cost.Clinical trial costs are a significant component of research and development expenses and include costs associated with third-party contractors. Invoicing fromthird-party contractors for services performed can lag several months. We accrue the costs of services rendered in connection with third-party contractoractivities based on our estimate of management fees, site management and monitoring costs and data management costs. Actual clinical trial costs may differfrom estimated clinical trial costs and are adjusted for in the period in which they become known.Basis of PresentationAs of September 1, 2009, the Company adopted fresh-start accounting in accordance with ASC 852-10, Reorganizations. The Company selectedSeptember 1, 2009, as the date to effectively apply fresh-start accounting based on the absence of any material contingencies at the August 27, 2009confirmation hearing and the immaterial impact of transactions between August 27, 2009 and September 1, 2009. The adoption of fresh-start accountingresulted in the Company becoming a new entity for financial reporting purposes. 35Table of ContentsAccordingly, the financial statements prior to September 1, 2009 are not comparable with the financial statements for periods on or after September 1,2009. References to “Successor” or “Successor Company” refer to the Company on or after September 1, 2009, after giving effect to the cancellation ofIsolagen, Inc. common stock issued prior to the Effective Date, the issuance of new Fibrocell Science, Inc. common stock in accordance with the Plan, and theapplication of fresh-start accounting. References to “Predecessor” or “Predecessor Company” refer to the Company prior to September 1, 2009.The following discussion should be read in conjunction with the Consolidated Financial Statements and the accompanying Notes to the ConsolidatedFinancial Statements included in this 10-K.Results of OperationsComparison of Years Ending December 31, 2011 and 2010Revenue and Cost of Sales. Revenue and cost of sales for the years ended December 31, 2011 and 2010 were comprised of the following: Year endedDecember 31, Increase(Decrease) 2011 2010 $000s % (in thousands) Total revenue $812 $936 $(124) (13.2)% Cost of sales 464 502 (38) (7.5)% Gross profit $348 $434 $(86) (19.8)% Revenue decreased $0.1 million to $0.8 million for the year ended December 31, 2011 as compared to $0.9 million for the year ended December 31,2010. Our revenue is from the operations of Agera which markets and sells a complete line of advanced skin care systems based on a wide array of proprietaryformulations, trademarks and nano-peptide technology.Costs of sales remained constant at $0.5 million for the year ended December 31, 2011 and for the year ended December 31, 2010. As a percentage ofrevenue, Agera’s cost of sales was approximately 57% for the year ended December 31, 2011 and 54% for the year ended December 31, 2010. Cost of sales asa percentage of revenue in 2011 has increased as compared to 2010 primarily due to component costs (containers, cartons and labels).Selling, General and Administrative Expense. Selling, general and administrative expense for the year ended December 31, 2011 and 2010 was comprised ofthe following: Year EndedDecember 31, Increase(Decrease) 2011 2010 $000s % (in thousands) Compensation and related expense $4,687 $2,501 $2,186 87% External services – consulting 693 942 (249) (26)% Marketing expense 3,820 157 3,663 2,339% License fees 805 17 788 4,681% Facilities and related expense and other 3,206 2,899 307 11% Total selling, general and administrative expense $13,211 $6,516 $6,695 103% Selling, general and administrative expenses increased by approximately $6.7 million, or 103%, to $13.2 million for the year ended December 31, 2011as compared to $6.5 million for the year ended December 31, 2010. The increase primarily consists of an increase in stock compensation expense of $1.8million, an increase in salaries of $0.4 million, an increase in marketing expense of $3.7 million in preparation of the launch of LAVIV and an increase inlicense fees of $0.8 million for FDA product and establishment fees. Consulting fees decreased $0.2 million due to the hiring of key personnel offset by anincrease in office expense. 36Table of ContentsResearch and Development Expense. Research and development expense for the year ended December 31, 2011 and 2010 was comprised of the following: Year EndedDecember 31, Increase(Decrease) 2011 2010 $000s % (in thousands) Compensation and related expense $2,108 $1,600 $508 32%External services – consulting 1,927 2,129 (202) (10)%Lab costs and related expense 1,620 879 741 84%Facilities and related expense 1,516 878 638 73% Total research and development expense $7,171 $5,486 $1,685 31%Research and development expense increased $1.7 million to $7.2 million for the year ended December 31, 2011 as compared to $5.5 million for theyear ended December 31, 2010. The increase is primarily due to an increase of $0.4 million in compensation and related expense, an increase of $0.1 millionfor stock compensation expense, an increase of $0.7 million for lab costs and $0.6 million for contract labor as the Company prepares for the launch andproduction of the product LAVIV, offset by $0.1 million decrease for consulting fees. Research and development costs are composed primarily of quality andmanufacturing costs in connection with LAVIV which was recently approved by the FDA. As we begin selling LAVIV these costs will appear as cost of goodssold on the statements of operations. There are also other costs related to other potential indications for our Fibrocell Therapy, such as acne scars and burnscars. Also, research and development expense includes costs to develop manufacturing, cell collection and logistical process improvements. Research anddevelopment costs primarily include personnel and laboratory costs related to these FDA trials and certain consulting costs. The total inception (December 28,1995) to date cost of research and development as of August 31, 2009 for the Predecessor Company was $56.3 million and total inception (September 1,2009) to date cost of research and development as of December 31, 2011, for the Successor Company was $14.5 million.Other income (expense). In November 2010, we received one grant totaling $0.2 million under the Qualified Therapeutic Discovery Project Grants Program.The Qualified Therapeutic Discovery Project Grants Program was included in the healthcare reform legislation, and established a one-time pool of $1 billionfor grants to small biotechnology companies developing novel therapeutics which show potential to: (a) result in new therapies that either treat areas of unmetmedical need, or prevent, detect, or treat chronic or acute diseases and conditions; (b) reduce long-term health care costs in the United States; or(c) significantly advance the goal of curing cancer within a the 30-year period. There are no matching funding requirements or other requirements necessary toreceive the funding.Interest expense. Interest expense remained relatively constant at $1.1 million for the years ended December 31, 2011 and 2010. Our interest expense for theyears ended December 31, 2011 and 2010 is related to the 12.5% notes we issued in connection with our bankruptcy plan.Change in Revaluation of Warrant and Derivative Liability. During the years ended December 31, 2011 and 2010, we recorded non-cash expense of $4.8million and $0.5 million for warrant expense, respectively, in our statements of operations due to an increase in the fair value of the warrant liability. Thisincrease in fair value was primarily due to a change in the valuation method from the Black Scholes model to the Monte Carlo simulation model. In addition,the number of shares underlying the warrants increased in 2011 due to the issuance of our Series D preferred stock, which triggered the anti-dilution protectionin the warrants resulting in the lowering of the exercise price of the warrants and the increase in the number of shares underlying such warrants. During theyear ended December 31, 2011, we recorded non-cash expense of $5.5 million for derivative revaluation expense in our statements of operations due to thechange in the fair value of the derivative liability related to the Series A, B and D preferred stock financings.Net Loss attributable to common shareholders. Net loss, excluding reorganization items, increased $18.5 million to $31.4 million for the year endedDecember 31, 2011, as compared to $12.9 million for the year ended December 31, 2010. The increase in expense is due to preparation for the launch andproduction of LAVIV. 37Table of ContentsLiquidity and Capital ResourcesThe following table summarizes our cash flows from operating, investing and financing activities for the two years ended December 31, 2011 and 2010: Year Ended December 31, 2011 2010 (in thousands) Statement of Cash Flows Data: Total cash provided by (used in): Operating activities $(16,837) $(9,266) Investing activities (1,570) (30) Financing activities 28,336 8,795 Operating Activities. Cash used in operating activities during the year ended December 31, 2011 amounted to $16.8 million, an increase of $7.5 million overthe year ended December 31, 2010. The increase in our cash used in operating activities over the prior year is primarily due to an increase in net losses(adjusted for non-cash items) of $6.6 million, in addition to operating cash outflows from changes in operating assets and liabilities.Investing Activities. Cash used in investing activities during the year ended December 31, 2011 amounted to $1.6 million due to the purchase of propertyand equipment for the lab facility in Exton, Pennsylvania in preparation of the launch of LAVIV.Financing Activities. There was $28.3 million cash proceeds received from financing activities during the year ended December 31, 2011, as compared to$8.8 million received from financing activities during the year ended December 31, 2010. During the years ended December 31, 2011 and 2010, we raisedcash of $30.4 million and $9.0 million, respectively, from the issuance of common stock, preferred stock and warrants, offset primarily by principal debtpayments of $1.3 million in 2011 and dividend payments of $0.6 million and $0.1 million in 2011 and 2010, respectively.Working CapitalAs of December 31, 2011, we had cash and cash equivalents of $10.8 million and working capital of $2.9 million. As of March 26, 2012, theCompany had cash and cash equivalents of approximately $4.7 million and our accounts payable and accrued expenses were approximately $1.6 million. Inaddition, the Company has approximately $7.0 million of outstanding debt which is due in June 2012. The Company’s current monthly cash run-rate isapproximately $2.2 million. The Company will need to access the capital markets in the near future in order to fund future operations. There is no guaranteethat any such required financing will be available on terms satisfactory to the Company or available at all. These matters create uncertainty relating to itsability to continue as a going concern. The accompanying consolidated financial statements do not reflect any adjustments relating to the recoverability andclassification of assets or liabilities that might result from the outcome of these uncertainties.Factors Affecting Our Capital ResourcesInflation did not have a significant impact on the Company’s results during the year ended December 31, 2011.Off-Balance Sheet TransactionsWe do not engage in material off-balance sheet transactions. 38Table of ContentsContractual ObligationsThe following table summarizes our contractual obligations as of December 31, 2011 (in thousands): Payments due by period Total 2012 2013 and2014 2015 and2016 2017 andthereafter Contractual Obligations Debt obligation $6,731 $6,731 $— $— $— Operating lease obligations 14,205 884 2,152 2,465 8,704 Total $20,936 $7,615 $2,152 $2,465 $8,704 Operating lease obligations are stated based on renewed lease agreement for the office, warehouse and laboratory facilities executed in February 2012.Item 8. Financial Statements and Supplementary DataThe financial statements, including the notes thereto and report of the independent registered public accounting firm thereon are included in this report asset forth in the “Index to Financial Statements.” See F-1 for Index to Consolidated Financial Statements.Item 9. Changes in and Disagreements with Accountants on Accounting and Financial Disclosure.N/A.Item 9A. Controls and ProceduresEvaluation of Disclosure Controls and ProceduresOur management, including our principal executive officer and principal financial officer, evaluated the disclosure controls and procedures related to therecording, processing, summarization and reporting of information in the periodic reports that the Company files with the SEC. These disclosure controls andprocedures have been designed to ensure that (a) material information relating to the Company, including its consolidated subsidiaries, is made known tomanagement, including these officers, by other employees of the Company, and (b) this information is recorded, processed, summarized, evaluated andreported, as applicable, within the time periods specified in the SEC’s rules and forms. As of December 31, 2011, the officers (the principal executive officerand principal financial officer) concluded that the Company’s disclosure controls and procedures were effective.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 in ExchangeAct Rules 13a-15(f) and 15d-15(f). Under the supervision and with the participation of our management, including our principal executive officer andprincipal financial officer, we conducted an evaluation of the effectiveness of our internal control over financial reporting based on the framework in InternalControl — Integrated Framework issued by the Committee of Sponsoring Organizations of the Treadway Commission.Our internal control over financial reporting is a process designed to provide reasonable assurance regarding the reliability of financial reporting and thepreparation of financial statements for external purposes in accordance with generally accepted accounting principles in the United States of America. Ourinternal control over financial reporting includes those policies and procedures that (i) pertain to the maintenance of records that, in reasonable detail,accurately and fairly reflect the transactions and dispositions of the assets of the company; (ii) 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 (iii) 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. 39(1)(1)Table of ContentsBecause of its inherent limitations, internal control over financial reporting may not prevent or detect misstatements. Also, projections of any evaluationof effectiveness to future periods are subject to the risk that controls may become inadequate because of changes in conditions, or that the degree of compliancewith the policies or procedures may deteriorate.Based on our evaluation under the framework in Internal Control — Integrated Framework, our management concluded that our internal control overfinancial reporting was effective as of December 31, 2011. This annual report does not include an attestation report of our registered public accounting firmregarding internal control over financial reporting. As we are a smaller reporting company, management’s report is not subject to attestation by our registeredpublic accounting firm pursuant to Section 404(c) of the Sarbanes-Oxley Act of 2002 that permits us to provide only management’s report in this annualreport.Changes in Internal ControlsThere was no change in our internal control over financial reporting that occurred during the fourth fiscal quarter that has materially affected, or isreasonably likely to materially affect, our internal control over financial reporting.Item 9B. Other InformationNone.Part IIIItem 10. Directors, Executive Officers and Corporate GovernanceThe information required by this Item 10 will be included in the Company’s Proxy Statement for the 2012 Annual Meeting of Stockholders which willbe filed with the Securities and Exchange Commission no later than April 29, 2012 and is incorporated into this Item 10 by reference.Code of Ethics. We have adopted a written code of ethics that applies to our principal executive officer, principal financial officer, principal accountingofficer or controller and any persons performing similar functions. The code of ethics is on our website at www.fibrocellscience.com. We intend to disclose anyfuture amendments to, or waivers from, the code of ethics within four business days of the waiver or amendment through a website posting or by filing aCurrent Report on Form 8-K with the SEC.Item 11. Executive CompensationThe information required under this Item 11 is incorporated herein by reference to the Company’s definitive proxy statement pursuant to Regulation14A, which proxy statement will be filed with the Securities and Exchange Commission not later than 120 days after the close of the Company’s fiscal yearended December 31, 2011.Item 12. Security Ownership of Certain Beneficial Owners and Management and Related Stockholder MattersThe information required under this Item 12 is incorporated herein by reference to the Company’s definitive proxy statement pursuant to Regulation14A, which proxy statement will be filed with the Securities and Exchange Commission not later than 120 days after the close of the Company’s fiscal yearended December 31, 2011.Item 13. Certain Relationships and Related Transactions, and Director IndependenceThe information required under this Item 13 is incorporated herein by reference to the Company’s definitive proxy statement pursuant to Regulation 14A,which proxy statement will be filed with the Securities and Exchange Commission not later than 120 days after the close of the Company’s fiscal year endedDecember 31, 2011. 40Table of ContentsItem 14. Principal Accountant Fees and ServicesThe information required under this Item 14 is incorporated herein by reference to the Company’s definitive proxy statement pursuant to Regulation 14A,which proxy statement will be filed with the Securities and Exchange Commission not later than 120 days after the close of the Company’s fiscal year endedDecember 31, 2011.Part IVItem 15. Exhibits and Financial Statement Schedule(a)(1) Financial Statements. • Report of Independent Registered Public Accounting Firm • Consolidated Balance Sheets as of December 31, 2011 and 2010 • Consolidated Statements of Operations for the years ended December 31, 2011 and 2010 (Successor Company), from inception (September 1,2009) to December 31, 2011 (Successor Company) and from inception to August 31, 2009 (Predecessor Company) • Consolidated Statements of Shareholders’ Deficit and Comprehensive Income (Loss) from inception to August 31, 2009 (Predecessor Company)and from inception (September 1, 2009) to December 31, 2011 (Successor Company) • Consolidated Statements of Cash Flows for the years ended December 31, 2011 and 2010, from inception (September 1, 2009) to December 31,2011 (Successor Company) and cumulative period from inception (December 28, 1995) to August 31, 2009 (Predecessor Company) • Notes to Consolidated Financial Statements(a)(2) Financial Statement Schedule.All schedules are omitted because of the absence of conditions under which they are required or because the required information is presented in theFinancial Statements or Notes thereto.(a)(3) The exhibits listed under Item 15(b) are filed or incorporated by reference herein. 41Table of Contents(b) Exhibits.The following exhibits are filed as part of this annual report:EXHIBIT NO. IDENTIFICATION OF EXHIBIT EXHIBITNO. IDENTIFICATION OF EXHIBIT 2.1 Debtors’ First Amended Joint Plan of Reorganization dated July 30, 2009 and Disclosure Statement (filed as Exhibit 10.2 to the Company’sForm 10-Q for quarter ended June 30, 2009, filed on August 12, 2009 and as Exhibit 99.1 to our Form 8-K filed September 2, 2009) 3.1 Amended and Restated Certificate of Incorporation (incorporated by reference to Exhibit 3.1 to our Form 8-K filed September 2, 2009) 3.2 Amended and Restated Bylaws (incorporated by reference to Exhibit 3.2 to our Form 8-K filed September 2, 2009) 3.3 Certificate of Designation of Preferences, Rights and Limitations of Series A 6% Convertible Preferred Stock (incorporated by reference toExhibit 3.1 to our Form 8-K filed October 14, 2009) 3.4 Certificate of Designation of Preferences, Rights and Limitations of Series B Convertible Preferred Stock, dated July 16, 2010. (incorporatedby reference to Exhibit 3.1 to our Form 8-K filed July 20, 2010). 3.5 Amended and Restated Certificate of Designation of Preferences, Rights and Limitations of Series D Convertible Preferred Stock. (incorporatedby reference to Exhibit 3.2 to our Form 8-K filed December 8, 2010). 4.1 Form of Common Stock Certificate (incorporated by reference to Exhibit 4.1 to our Form 10-Q filed November 23, 2009) 4.2 Form of Class A/B Common Stock Purchase Warrant issued in October 2009 offering (incorporated by reference to Exhibit 4.1 to our Form 8-K filed October 14, 2009) 4.3 Form of 12.5% Promissory Note (incorporated by reference to Exhibit 10.1 to our Form 8-K filed September 10, 2009) 4.4 Form of Placement Agent Warrant issued in November 2009 offering (incorporated by reference to Exhibit 4.2 to our Form 10-Q filedNovember 23, 2009) 4.5 Common Stock Purchase Warrant issued in March 2010 offering (incorporated by reference to Exhibit 4.1 to our Form 8-K filed March 3,2010) 4.6 Form of Common Stock Purchase Warrant issued in July 2010 Series B preferred stock offering (incorporated by reference to Exhibit 4.1 toour Form 8-K filed July 20, 2010) 4.7 Form of Placement Agent Warrant issued in July 2010 Series B preferred stock offering (incorporated by reference to Exhibit 4.2 to our Form8-K filed July 20, 2010) 4.8 Form of Common Stock Purchase Warrant used for Series B preferred stock offering (incorporated by reference to Exhibit 4.1 of the Form 8-K filed October 22, 2010). 4.9 Form of Common Stock Purchase Warrant used for the Series D preferred stock offering (incorporated by reference to Exhibit 4.1 of theForm 8-K filed February 15, 2011). 4.10 Common Stock Purchase Warrant issued in August 2011 offering (incorporated by reference to Exhibit 4.1 to our Form 8-K filed August 4,2011) 10.1 Securities Purchase Agreement dated October 13, 2009 between the Company and the Series A Preferred Stock Purchasers (incorporated byreference to Exhibit 10.1 to our Form 8-K filed October 14, 2009) 10.2 Amended and Restated Employment Agreement between the Company and Declan Daly dated August 24, 2010 (incorporated by reference toExhibit 10.1 to our Form 8-K filed August 27, 2010) 10.3 Consulting Agreement between the Company and Robert Langer (incorporated by reference to Exhibit 10.2 to our Form 10-Q filed November23, 2009) 10.4 2009 Equity Incentive Plan, as amended (incorporated by reference to Exhibit 4.5 to our Form S-8 filed March 3, 2011) 10.5 Lease Agreement between Isolagen, Inc and The Hankin Group dated April 7, 2005 (previously filed as an exhibit to the company’s Form 8-K, filed on April 12, 2005) 42Table of Contents 10.6 Purchase Option Agreement between Isolagen, Inc and 405 Eagleview Associates dated April 7, 2005 (previously filed as an exhibit to thecompany’s Form 8-K, filed on April 12, 2005) 10.7 Intellectual Property Purchase Agreement between Isolagen Technologies, Inc., Gregory M. Keller, and PacGen Partners (previously filed as anexhibit to the company’s amended Form S-1, as filed on October 24, 2003) 10.8 Employment Agreement between the Company and David Pernock (incorporated by reference to Exhibit 10.1 to our Form 8-K filed February1, 2010) 10.9 Securities Purchase Agreement dated March 2, 2010 (incorporated by reference to Exhibit 10.1 to our Form 8-K filed March 3, 2010) 10.10 Registration Rights Agreement dated March 2, 2010 (incorporated by reference to Exhibit 10.2 to our Form 8-K filed March 3, 2010) 10.11 Registration Rights Agreement between the Company and the Series A Preferred Stock Purchasers, dated October 13, 2009 (incorporated byreference to Exhibit 10.2 to our Form 8-K filed October 14, 2009) 10.12 Securities Purchase Agreement between the Company and Series B Preferred Stock Purchasers (incorporated by reference to Exhibit 10.1 to ourForm 8-K filed July 20, 2010) 10.13 Form of Registration Rights Agreement between the Company and Series B Preferred Stock Purchasers (incorporated by reference toExhibit 10.2 to our Form 8-K filed July 20, 2010) 10.14 Form of Securities Purchase Agreement between the Company and Series B Preferred Stock Purchasers (incorporated by reference toExhibit 4.1 of the Form 8-K filed October 22, 2010). 10.15 Securities Purchase Agreement dated August 3, 2011 (incorporated by reference to Exhibit 10.1 to our Form 8-K filed August 4, 2011) 10.16 Registration Rights Agreement dated August 3, 2011 (incorporated by reference to Exhibit 10.2 to our Form 8-K filed August 4, 2011)*10.17 Amendment to Lease Agreement between Fibrocell Science, Inc. and The Hankin Group dated February 17, 2012 21 List of Subsidiaries (previously filed as an exhibit to the company’s Annual Report on Form 10-K for the fiscal year ended December 31,2006)*23.1 Consent of BDO USA, LLP*31.1 Certification pursuant to Rule 13a-14(a) and 15d-14(a), required under Section 302 of the Sarbanes-Oxley Act of 2002*31.2 Certification pursuant to Rule 13a-14(a) and 15d-14(a), required under Section 302 of the Sarbanes-Oxley Act of 2002*32.1 Certification pursuant to 18 U.S.C. Section 1350 as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002*32.2 Certification pursuant to 18 U.S.C. Section 1350 as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002101.INS XBRL Instance Document.101.SCH XBRL Taxonomy Extension Schema Document.101.CAL XBRL Taxonomy Extension Calculation Linkbase Document.101.LAB XBRL Taxonomy Extension Label Linkbase Document.101.PRE XBRL Taxonomy Extension Presentation Linkbase Document.101.DEF XBRL Taxonomy Extension Definition Linkbase Document. *Filed herewith. 43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. FIBROCELL SCIENCE, INC.By: /s/ David PernockDavid PernockChief Executive OfficerDate: March 30, 2012Pursuant to the requirements of the Securities Exchange Act of 1934, this report has been signed below by the following persons on behalf of theRegistrant and in the capacities and on the date indicated. Signature Title Date/s/ David PernockDavid Pernock Chief Executive Officer and Chairman of the Board of Directors March 30, 2012/s/ Declan DalyDeclan Daly Chief Financial Officer, Chief Operating Officer and Director March 30, 2012/s/ Kelvin MooreKelvin Moore Director March 30, 2012/s/ Dr. Robert LangerDr. Robert Langer Director March 30, 2012/s/ Marc MazurMarc Mazur Director March 30, 2012/s/ Dr. George KorkosDr. George Korkos Director March 30, 2012 44Table of ContentsFibrocell Science, Inc.(A Development Stage Company)Index to Consolidated Financial Statements PAGE Report of Independent Registered Public Accounting Firm F-2 Consolidated Balance Sheets as of December 31, 2011 and 2010 F-3 Consolidated Statements of Operations for the years ended December 31, 2011 and 2010 (Successor Company), from inception (September 1,2009) to December 31, 2011 (Successor Company) and from inception to August 31, 2009 (Predecessor Company) F-4 Consolidated Statements of Shareholders’ Deficit and Comprehensive Income (Loss) From Inception (December 28, 1995) to August 31, 2009(Predecessor Company) and from inception (September 1, 2009) to year ended December 31, 2011 (Successor Company) F-5 Consolidated Statements of Cash Flows for the years ended December 31, 2011 and 2010 (Successor Company), cumulative period from inception(September 1, 2009) to December 31, 2011 (Successor Company) and cumulative period from inception (December 28, 1995) to August 31,2009 (Predecessor Company) F-18 Notes to Consolidated Financial Statements F-19 F1Table of ContentsREPORT OF INDEPENDENT REGISTERED PUBLIC ACCOUNTING FIRMTo the Board of Directors and Shareholders of Fibrocell Science, Inc. (a development stage company)Exton, PennsylvaniaWe have audited the accompanying consolidated balance sheets of Fibrocell Science, Inc. (in the development stage) as of December 31, 2011 and 2010 and therelated consolidated statements of operations, shareholders’ equity (deficit) and comprehensive loss, and cash flows for the years ended December 31, 2011and 2010 (“Successor”), and for the period from the Successor’s inception of operations (September 1, 2009) through December 31, 2011 and for the periodfrom the Predecessor’s inception of operations (December 28, 1995) through August 31, 2009. We have also audited the statements of shareholders’ equity(deficit) for the period from December 28, 1995 (Predecessor’s inception) through August 31, 2009 and for the period from the Successor’s inception ofoperations (September 1, 2009) through December 31, 2011. These consolidated financial statements are the 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 standards require thatwe plan and perform the audit to obtain reasonable assurance about whether the financial statements are free of material misstatement. The Company is notrequired to have, nor were we engaged to perform an audit of its internal control over financial reporting. Our audits included consideration of internal controlover financial reporting as a basis for designing audit procedures that are appropriate in the circumstances, but not for the purpose of expressing an opinion onthe effectiveness of the Company’s internal control over financial reporting. Accordingly, we express no opinion. An audit also includes examining, on a testbasis, evidence supporting the amounts and disclosures in the financial statements, assessing the accounting principles used and significant estimates madeby management, as well as evaluating the overall financial statement presentation. We believe that our audits provide a reasonable basis for our opinion.In our opinion, the consolidated financial statements referred to above present fairly, in all material respects, the financial position of Fibrocell Science, Inc. atDecember 31, 2011 and 2010, and the results of its operations and its cash flows for the years then ended (“Successor”), and for the period from theSuccessor’s inception of operations (September 1, 2009) through December 31, 2011 and for the period from the Predecessor’s inception of operations(December 31, 1995) through August 31, 2009 and the statements of shareholders’ equity (deficit) for the period from December 28, 1995 (Predecessor’sinception) to August 31, 2009 and for the period from the Successor’s inception of operations (September 1, 2009) through December 31, 2011, in conformitywith accounting principles generally accepted in the United States of America.The accompanying financial statements have been prepared assuming that the Company will continue as a going concern. As discussed in Note 3 to thefinancial statements, the Company has suffered recurring losses from operations, has a net capital deficit, and has limited cash resources that raisesubstantial doubt about its ability to continue as a going concern. Management’s plan in regard to these matters is also described in Note 3. The financialstatements do not include any adjustments that might result from the outcome of this uncertainty./s/ BDO USA, LLPHouston, TexasMarch 30, 2012 F2Table of ContentsFibrocell Science, Inc.(A Development Stage Company)Consolidated Balance Sheets December 31,2011 December 31,2010 Assets Current assets: Cash and cash equivalents $10,798,995 $867,738 Accounts receivable, net 215,714 229,891 Inventory, net 266,348 258,939 Prepaid expenses and other current assets 1,217,596 559,082 Total current assets 12,498,653 1,915,650 Property and equipment, net of accumulated depreciation of $165,841 and $8,085, respectively 1,433,938 21,589 Intangible assets and other assets 6,340,906 6,340,906 Total assets $20,273,497 $8,278,145 Liabilities, Redeemable Preferred Stock, Shareholders’ Deficit and Noncontrolling Interest Current liabilities: Current debt $6,730,861 $56,911 Accounts payable 1,899,045 1,096,125 Accrued expenses 926,141 789,482 Deferred revenue 55,400 — Total current liabilities 9,611,447 1,942,518 Long-term debt — 7,290,881 Deferred tax liability 2,500,000 2,500,000 Warrant liability 13,087,000 8,171,518 Derivative liability 533,549 2,120,360 Other long-term liabilities 142,002 255,606 Total liabilities 25,873,998 22,280,883 Commitments Preferred stock series A, $0.001 par value; 9,000 shares authorized; 3,250 shares issued; 0 and 2,886 sharesoutstanding, respectively — 1,280,150 Preferred stock series B, $0.001 par value; 9,000 shares authorized; 4,640 shares issued; 0 and 4,640 sharesoutstanding, respectively — — Preferred stock series B, $0.001 par value; subscription receivable — (210,000) Preferred stock series D, $0.001 par value; 8,000 shares authorized; 7,779 and 1,645 shares issued, respectively,and 3,641 and 1,645 shares outstanding, respectively — — Fibrocell Science, Inc. shareholders’ deficit: Common stock, $0.001 par value; 250,000,000 shares authorized; 95,678,255 and 20,375,500 issued andoutstanding, respectively 95,678 20,376 Common stock-subscription receivable (550,020) — Additional paid-in capital 43,734,339 2,437,893 Accumulated deficit during development stage (49,349,080) (17,981,530) Total Fibrocell Science, Inc. shareholders’ deficit (6,069,083) (15,523,261) Noncontrolling interest 468,582 450,373 Total deficit and noncontrolling interest (5,600,501) (15,072,888) Total liabilities, preferred stock, shareholders’ deficit and noncontrolling interest $20,273,497 $8,278,145 The accompanying notes are an integral part of these consolidated financial statements. F3Table of ContentsFibrocell Science, Inc.(A Development Stage Company)Consolidated Statements of Operations Successor Successor Successor Predecessor For the year endedDecember 31, 2011 For the year endedDecember 31, 2010 Cumulative periodfrom September 1,2009 (date ofinception) toDecember 31, 2011 Cumulative periodfrom December 28,1995 (date ofinception) toAugust 31, 2009 Revenue Product sales $812,235 $936,369 $2,078,545 $4,818,994 License fees — — — 260,000 Total revenue 812,235 936,369 2,078,545 5,078,994 Cost of sales 463,874 502,648 1,148,570 2,279,335 Gross profit 348,361 433,721 929,975 2,799,659 Selling, general and administrative expenses 13,211,486 6,515,581 22,435,423 84,805,520 Research and development expenses 7,170,520 5,486,319 14,480,035 56,269,869 Operating loss (20,033,645) (11,568,179) (35,985,483) (138,275,730) Other income (expense) Interest income — — 1 6,989,539 Reorganization items, net — 3,303 (69,174) 73,538,984 Other income — 244,479 244,479 316,338 Warrant expense (4,762,694) (465,232) (5,547,010) — Derivative revaluation expense (5,451,518) — (5,451,518) — Interest expense (1,061,862) (1,045,199) (2,354,235) (18,790,218) Loss from continuing operations before income taxes (31,309,719) (12,830,828) (49,162,940) (76,221,087) Income tax benefit — — — 190,754 Loss from continuing operations (31,309,719) (12,830,828) (49,162,940) (76,030,333) Loss from discontinued operations (39,622) (48,805) (100,540) (41,091,311) Net loss (31,349,341) (12,879,633) (49,263,480) (117,121,644) Deemed dividend associated with beneficial conversion — — — (11,423,824) Preferred stock dividends — — — (1,589,861) Net (income) loss attributable to noncontrolling interest (18,209) (51,898) (85,600) 1,799,523 Net loss attributable to Fibrocell Science, Inc. commonshareholders. $(31,367,550) $(12,931,531) $(49,349,080) $(128,335,806) Per share information: Loss from continuing operations-basic and diluted $(0.57) $(0.68) $(1.46) $(4.30) Loss from discontinued operations-basic and diluted — — — (2.32) Income attributable to noncontrolling interest — — — 0.10 Deemed dividend associated with beneficial conversion ofpreferred stock — — — (0.65) Preferred stock dividends — — — (0.09) Net loss attributable to common shareholders per common share—basic and diluted $(0.57) $(0.68) $(1.46) $(7.26) Weighted average number of basic and diluted common sharesoutstanding 54,857,520 18,757,756 33,664,124 17,678,219 The accompanying notes are an integral part of these consolidated financial statements. F4Table of ContentsFibrocell Science, Inc.(A Development Stage Company)Consolidated Statements of Shareholders’ Equity (Deficit) and Comprehensive Income (Loss) Series APreferred Stock Series BPreferred Stock Common Stock AdditionalPaid-InCapital Treasury Stock AccumulatedOtherComprehensiveIncome AccumulatedDeficit DuringDevelopmentStage TotalShareholders’ Equity(Deficit) Number ofShares Amount Number ofShares Amount NumberofShares Amount Number ofShares Amount Issuance of common stock for cash on12/28/95 — $— — $— 2,285,291 $2,285 $(1,465) — $— $— $— $820 Issuance of common stock for cash on11/7/96 — — — — 11,149 11 49,989 — — — — 50,000 Issuance of common stock for cash on11/29/96 — — — — 2,230 2 9,998 — — — — 10,000 Issuance of common stock for cash on12/19/96 — — — — 6,690 7 29,993 — — — — 30,000 Issuance of common stock for cash on12/26/96 — — — — 11,148 11 49,989 — — — — 50,000 Net loss — — — — — — — — — — (270,468) (270,468) Balance, 12/31/96 (Predecessor) — $— — $— 2,316,508 $2,316 $138,504 — $— $— $(270,468) $(129,648) Issuance of common stock for cash on12/27/97 — — — — 21,182 21 94,979 — — — — 95,000 Issuance of common stock for serviceson 9/1/97 — — — — 11,148 11 36,249 — — — — 36,260 Issuance of common stock for serviceson 12/28/97 — — — — 287,193 287 9,968 — — — — 10,255 Net loss — — — — — — — — — — (52,550) (52,550) Balance, 12/31/97(Predecessor) — $— — $— 2,636,031 $2,635 $279,700 — $— $— $(323,018) $(40,683) The accompanying notes are an integral part of these consolidated financial statements. F5Table of Contents Series APreferred Stock Series BPreferred Stock Common Stock AdditionalPaid-InCapital Treasury Stock AccumulatedOtherComprehensiveIncome AccumulatedDeficit DuringDevelopmentStage TotalShareholders’ Equity(Deficit) Number ofShares Amount Number ofShares Amount Number ofShares Amount Number ofShares Amount Issuance of common stock for cashon 8/23/98 — $— — $— 4,459 $4 $20,063 — $— $— $— $20,067 Repurchase of common stock on9/29/98 — — — — — — — 2,400 (50,280) — — (50,280) Net loss — — — — — — — — — — (195,675) (195,675) Balance, 12/31/98 (Predecessor) — $— — $— 2,640,490 $2,639 $299,763 2,400 $(50,280) $— $(518,693) $(266,571) Issuance of common stockfor cash on 9/10/99 — — — — 52,506 53 149,947 — — — — 150,000 Net loss — — — — — — — — — — (1,306,778) (1,306,778) Balance, 12/31/99 (Predecessor) — $— — $— 2,692,996 $2,692 $449,710 2,400 $(50,280) $— $(1,825,471) $(1,423,349) Issuance of common stockfor cash on 1/18/00 — — — — 53,583 54 1,869 — — — — 1,923 Issuance of common stockfor services on 3/1/00 — — — — 68,698 69 (44) — — — — 25 Issuance of common stockfor services on 4/4/00 — — — — 27,768 28 (18) — — — — 10 Net loss — — — — — — — — — — (807,076) (807,076) Balance, 12/31/00 (Predecessor) — $— — $— 2,843,045 $2,843 $451,517 2,400 $(50,280) $— $(2,632,547) $(2,228,467) The accompanying notes are an integral part of these consolidated financial statements. F6Table of Contents Series APreferred Stock Series BPreferred Stock Common Stock AdditionalPaid-InCapital Treasury Stock AccumulatedOtherComprehensiveIncome AccumulatedDeficit DuringDevelopmentStage TotalShareholders’ Equity(Deficit) Number ofShares Amount Number ofShares Amount Number ofShares Amount Number ofShares Amount Issuance of common stockfor services on 7/1/01 — $— — $— 156,960 $157 $(101) — $— $— $— $56 Issuance of common stockfor services on 7/1/01 — — — — 125,000 125 (80) — — — — 45 Issuance of common stockfor capitalization ofaccrued salaries on8/10/01 — — — — 70,000 70 328,055 — — — — 328,125 Issuance of common stockfor conversion ofconvertible debt on8/10/01 — — — — 1,750,000 1,750 1,609,596 — — — — 1,611,346 Issuance of common stockfor conversion ofconvertible shareholdernotes payable on8/10/01 — — — — 208,972 209 135,458 — — — — 135,667 Issuance of common stockfor bridge financing on8/10/01 — — — — 300,000 300 (192) — — — — 108 Retirement of treasury stockon 8/10/01 — — — — — — (50,280) (2,400) 50,280 — — — Issuance of common stockfor net assets of Geminion 8/10/01 — — — — 3,942,400 3,942 (3,942) — — — — — Issuance of common stockfor net assets of AFH on8/10/01 — — — — 3,899,547 3,900 (3,900) — — — — — Issuance of common stockfor cash on 8/10/01 — — — — 1,346,669 1,347 2,018,653 — — — — 2,020,000 Transaction and fundraising expenses on8/10/01 — — — — — — (48,547) — — — — (48,547) Issuance of common stockfor services on 8/10/01 — — — — 60,000 60 — — — — — 60 Issuance of common stockfor cash on 8/28/01 — — — — 26,667 27 39,973 — — — — 40,000 Issuance of common stockfor services on 9/30/01 — — — — 314,370 314 471,241 — — — — 471,555 The accompanying notes are an integral part of these consolidated financial statements. F7Table of Contents Series APreferred Stock Series BPreferred Stock Common Stock AdditionalPaid-InCapital Treasury Stock AccumulatedOtherComprehensiveIncome AccumulatedDeficit DuringDevelopmentStage TotalShareholders’ Equity(Deficit) Number ofShares Amount Number ofShares Amount Number ofShares Amount Number ofShares Amount Uncompensated contribution ofservices—3rd quarter — $— — $— — $— $55,556 — $— $— $— $55,556 Issuance of common stock forservices on 11/1/01 — — — — 145,933 146 218,754 — — — — 218,900 Uncompensated contribution ofservices—4th quarter — — — — — — 100,000 — — — — 100,000 Net loss — — — — — — — — — — (1,652,004) (1,652,004) Balance, 12/31/01 (Predecessor) — $— — $— 15,189,563 $15,190 $5,321,761 — $— $— $(4,284,551) $1,052,400 Uncompensated contribution ofservices—1st quarter — — — — — — 100,000 — — — — 100,000 Issuance of preferred stock for cashon 4/26/02 905,000 905 — — — — 2,817,331 — — — — 2,818,236 Issuance of preferred stock for cashon 5/16/02 890,250 890 — — — — 2,772,239 — — — — 2,773,129 Issuance of preferred stock for cashon 5/31/02 795,000 795 — — — — 2,473,380 — — — — 2,474,175 Issuance of preferred stock for cashon 6/28/02 229,642 230 — — — — 712,991 — — — — 713,221 Uncompensated contribution ofservices—2nd quarter — — — — — — 100,000 — — — — 100,000 Issuance of preferred stock for cashon 7/15/02 75,108 75 — — — — 233,886 — — — — 233,961 Issuance of common stock for cashon 8/1/02 — — — — 38,400 38 57,562 — — — — 57,600 Issuance of warrants for services on9/06/02 — — — — — — 103,388 — — — — 103,388 Uncompensated contribution ofservices—3rd quarter — — — — — — 100,000 — — — — 100,000 Uncompensated contribution ofservices—4th quarter — — — — — — 100,000 — — — — 100,000 Issuance of preferred stock fordividends 143,507 144 — — — — 502,517 — — — (502,661) — Deemed dividend associated withbeneficial conversion of preferredstock — — — — — — 10,178,944 — — — (10,178,944) — Comprehensive income: Net loss — — — — — — — — — — (5,433,055) (5,433,055) Other comprehensive income, foreigncurrency translation adjustment — — — — — — — — — 13,875 — 13,875 Comprehensive loss — — — — — — — — — — — (5,419,180) Balance, 12/31/02 (Predecessor) 3,038,507 $3,039 — $— 15,227,963 $15,228 $25,573,999 — $— $13,875 $(20,399,211) $5,206,930 The accompanying notes are an integral part of these consolidated financial statements. F8Table of Contents Series APreferred Stock Series BPreferred Stock Common Stock AdditionalPaid-InCapital Treasury Stock AccumulatedOtherComprehensiveIncome AccumulatedDeficitDuringDevelopmentStage TotalShareholders’Equity(Deficit) Number ofShares Amount Number ofShares Amount Number ofShares Amount Number ofShares Amount Issuance of common stock for cash on1/7/03 — $— — $— 61,600 $62 $92,338 — $— $— $— $92,400 Issuance of common stock for patentpending acquisition on 3/31/03 — — — — 100,000 100 539,900 — — — — 540,000 Cancellation of common stock on 3/31/03 — — — — (79,382) (79) (119,380) — — — — (119,459) Uncompensated contribution of services—1st quarter — — — — — — 100,000 — — — — 100,000 Issuance of preferred stock for cash on5/9/03 — — 110,250 110 — — 2,773,218 — — — — 2,773,328 Issuance of preferred stock for cash on5/16/03 — — 45,500 46 — — 1,145,704 — — — — 1,145,750 Conversion of preferred stock into commonstock—2nd qtr (70,954) (72) — — 147,062 147 40,626 — — — — 40,701 Conversion of warrants into common stock—2nd qtr — — — — 114,598 114 (114) — — — — — Uncompensated contribution of services—2nd quarter — — — — — — 100,000 — — — — 100,000 Issuance of preferred stock dividends — — — — — — — — — — (1,087,200) (1,087,200) Deemed dividend associated with beneficialconversion of preferred stock — — — — — — 1,244,880 — — — (1,244,880) — Issuance of common stock for cash—3qtr — — — — 202,500 202 309,798 — — — — 310,000 Issuance of common stock for cash on8/27/03 — — — — 3,359,331 3,359 18,452,202 — — — — 18,455,561 Conversion of preferred stock into commonstock—3 qtr (2,967,553) (2,967) (155,750) (156) 7,188,793 7,189 (82,875) — — — — (78,809) Conversion of warrants into common stock—3 qtr — — — — 212,834 213 (213) — — — — — Compensation expense on warrants issuedto non-employees — — — — — — 412,812 — — — — 412,812 Issuance of common stock for cash—4qtr — — — — 136,500 137 279,363 — — — — 279,500 Conversion of warrants into common stock—4 qtr — — — — 393 — — — — — — — Comprehensive income: Net loss — — — — — — — — — — (11,268,294) (11,268,294) Other comprehensive income, foreigncurrency translation adjustment — — — — — — — — — 360,505 — 360,505 Comprehensive loss — — — — — — — — — — — (10,907,789) Balance, 12/31/03 (Predecessor) — $— — $— 26,672,192 $26,672 $50,862,258 — $— $374,380 $(33,999,585) $17,263,725 The accompanying notes are an integral part of these consolidated financial statements. F9rdrdrdththTable of Contents Series APreferred Stock Series BPreferred Stock Common Stock AdditionalPaid-InCapital Treasury Stock AccumulatedOtherComprehensiveIncome AccumulatedDeficitDuringDevelopmentStage TotalShareholders’Equity(Deficit) Number ofShares Amount Number ofShares Amount Number ofShares Amount Number ofShares Amount Conversion of warrants into commonstock—1 qtr — $— — $— 78,526 $79 $(79) — $— $— $— $— Issuance of common stock for cash inconnection with exercise of stockoptions—1 qtr — — — — 15,000 15 94,985 — — — — 95,000 Issuance of common stock for cash inconnection with exercise of warrants—1 qtr — — — — 4,000 4 7,716 — — — — 7,720 Compensation expense on options andwarrants issued to non-employeesand directors—1 qtr — — — — — — 1,410,498 — — — — 1,410,498 Issuance of common stock in connectionwith exercise of warrants—2 qtr — — — — 51,828 52 (52) — — — — — Issuance of common stock for cash—2qtr — — — — 7,200,000 7,200 56,810,234 — — — — 56,817,434 Compensation expense on options andwarrants issued to non-employeesand directors—2 qtr — — — — — — 143,462 — — — — 143,462 Issuance of common stock in connectionwith exercise of warrants—3 qtr — — — — 7,431 7 (7) — — — — — Issuance of common stock for cash inconnection with exercise of stockoptions—3 qtr — — — — 110,000 110 189,890 — — — — 190,000 Issuance of common stock for cash inconnection with exercise of warrants—3 qtr — — — — 28,270 28 59,667 — — — — 59,695 Compensation expense on options andwarrants issued to non-employeesand directors—3 qtr — — — — — — 229,133 — — — — 229,133 Issuance of common stock in connectionwith exercise of warrants—4 qtr — — — — 27,652 28 (28) — — — — — Compensation expense on options andwarrants issued to non-employees,employees, and directors—4 qtr — — — — — — 127,497 — — — — 127,497 Purchase of treasury stock—4 qtr — — — — — — — 4,000,000 (25,974,000) — — (25,974,000) Comprehensive income: Net loss — — — — — — — — — — (21,474,469) (21,474,469) Other comprehensive income, foreigncurrency translation adjustment — — — — — — — — — 79,725 — 79,725 Other comprehensive income, netunrealized gain on available- for-saleinvestments — — — — — — — — — 10,005 — 10,005 Comprehensive loss — — — — — — — — — — — (21,384,739) Balance, 12/31/04 (Predecessor) — $— — $— 34,194,899 $34,195 $109,935,174 4,000,000 $(25,974,000) $464,110 $(55,474,054) $28,985,425 The accompanying notes are an integral part of these consolidated financial statements. F10ststststndndndrdrdrdrdthththTable of Contents Series APreferred Stock Series BPreferred Stock Common Stock AdditionalPaid-InCapital Treasury Stock AccumulatedOtherComprehensiveIncome (Loss) AccumulatedDeficitDuringDevelopmentStage TotalShareholders’Equity(Deficit) Number ofShares Amount Number ofShares Amount Number ofShares Amount Number ofShares Amount Issuance of common stock for cash inconnection with exercise of stockoptions—1 qtr — $— — $— 25,000 $25 $74,975 — $— $— $— $75,000 Compensation expense on options andwarrants issued to non-employees—1 qtr — — — — — — 33,565 — — — — 33,565 Conversion of warrants into commonstock—2 qtr — — — — 27,785 28 (28) — — — — — Compensation expense on options andwarrants issued to non-employees—2 qtr — — — — — — (61,762) — — — — (61,762) Compensation expense on options andwarrants issued to non-employees—3 qtr — — — — — — (137,187) — — — — (137,187) Conversion of warrants into commonstock—3qtr — — — — 12,605 12 (12) — — — — — Compensation expense on options andwarrants issued to non-employees—4 qtr — — — — — — 18,844 — — — — 18,844 Compensation expense on acceleration ofoptions—4 qtr — — — — — — 14,950 — — — — 14,950 Compensation expense on restrictedstock award issued to employee—4 qtr — — — — — — 606 — — — — 606 Conversion of predecessor companyshares — — — — 94 — — — — — — — Comprehensive loss: Net loss — — — — — — — — — — (35,777,584) (35,777,584) Other comprehensive loss, foreigncurrency translation adjustment — — — — — — — — — (1,372,600) — (1,372,600) Foreign exchange gain on substantialliquidation of foreign entity 133,851 133,851 Other comprehensive loss, net unrealizedgain on available-for-saleinvestments — — — — — — — — — (10,005) — (10,005) Comprehensive loss — — — — — — — — — — — (37,026,338) Balance, 12/31/05 (Predecessor) — $— — $— 34,260,383 $34,260 $109,879,125 4,000,000 $(25,974,000) $(784,644) $(91,251,638) $(8,096,897) The accompanying notes are an integral part of these consolidated financial statements. F11ststndndrdrd thththTable of Contents Series APreferred Stock Series BPreferred Stock Common Stock AdditionalPaid-InCapital Treasury Stock AccumulatedOtherComprehensiveIncome AccumulatedDeficitDuringDevelopmentStage TotalShareholders’Equity(Deficit) Number ofShares Amount Number ofShares Amount Number ofShares Amount Number ofShares Amount NoncontrollingInterest Compensation expense onoptions and warrantsissued to non-employees—1 qtr — $— — $— — $— $42,810 — $— $— $— $— $42,810 Compensation expense onoption awards issuedto employees anddirectors—1 qtr — — — — — — 46,336 — — — — — 46,336 Compensation expense onrestricted stock issuedto employees—1 qtr — — — — 128,750 129 23,368 — — — — — 23,497 Compensation expense onoptions and warrantsissued to non-employees—2 qtr — — — — — — 96,177 — — — — — 96,177 Compensation expense onoption awards issuedto employees anddirectors—2 qtr — — — — — — 407,012 — — — — — 407,012 Compensation expense onrestricted stock toemployees—2 qtr — — — — — — 4,210 — — — — — 4,210 Cancellation of unvestedrestricted stock—2qtr — — — — (97,400) (97) 97 — — — — — — Issuance of commonstock for cash inconnection withexercise of stockoptions—2 qtr — — — — 10,000 10 16,490 — — — — — 16,500 Compensation expense onoptions and warrantsissued to non-employees—3 qtr — — — — — — 25,627 — — — — — 25,627 Compensation expense onoption awards issuedto employees anddirectors—3 qtr — — — — — — 389,458 — — — — — 389,458 Compensation expense onrestricted stock toemployees—3 qtr — — — — — — 3,605 — — — — — 3,605 Issuance of commonstock for cash inconnection withexercise of stockoptions—3 qtr — — — — 76,000 76 156,824 — — — — — 156,900 Acquisition of Agera — — — — — — — — — — — 2,182,505 2,182,505 Compensation expense onoptions and warrantsissued to non-employees—4 qtr — — — — — — 34,772 — — — — — 34,772 Compensation expense onoption awards issuedto employees anddirectors—4 qtr — — — — — — 390,547 — — — — — 390,547 Compensation expense onrestricted stock toemployees—4 qtr — — — — — — 88 — — — — — 88 Cancellation of unvestedrestricted stockaward—4 qtr — — — — (15,002) (15) 15 — — — — — — Comprehensive loss: Net loss — — — — — — — — — — (35,821,406) (78,132) (35,899,538) Other comprehensivegain, foreign currencytranslationadjustment — — — — — — — — — 657,182 — — 657,182 Comprehensive loss — — — — — — — — — — — — (35,242,356) Balance 12/31/06(Predecessor) — $— — $— 34,362,731 $34,363 $111,516,561 4,000,000 $(25,974,000) $(127,462) $(127,073,044) $2,104,373 $(39,519,209) The accompanying notes are an integral part of these consolidated financial statements. F12stststndndndndndrdrdrdrdththththTable of Contents Series APreferred Stock Series BPreferred Stock Common Stock AdditionalPaid-InCapital Treasury Stock AccumulatedOtherComprehensiveIncome (Loss) AccumulatedDeficitDuringDevelopmentStage TotalShareholders’Equity(Deficit) Number ofShares Amount Number ofShares Amount Number ofShares Amount Number ofShares Amount NoncontrollingInterest Compensation expense onoptions and warrantsissued to non-employees—1 qtr — $— — $— — $— $39,742 — $— $— $— $— $39,742 Compensation expense onoption awards issuedto employees anddirectors—1 qtr — — — — — — 448,067 — — — — — 448,067 Compensation expense onrestricted stock issuedto employees—1 qtr — — — — — — 88 — — — — — 88 Issuance of commonstock for cash inconnection withexercise of stockoptions—1 qtr — — — — 15,000 15 23,085 — — — — — 23,100 Expense in connectionwith modification ofemployee stockoptions —1 qtr — — — — — — 1,178,483 — — — — — 1,178,483 Compensation expense onoptions and warrantsissued to non-employees—2 qtr — — — — — — 39,981 — — — — — 39,981 Compensation expense onoption awards issuedto employees anddirectors—2 qtr — — — — — — 462,363 — — — — — 462,363 Compensation expense onrestricted stock issuedto employees—2qtr — — — — — — 88 — — — — — 88 Compensation expense onoption awards issuedto employees anddirectors—3 qtr — — — — — — 478,795 — — — — — 478,795 Compensation expense onrestricted stock issuedto employees—3 qtr — — — — — — 88 — — — — — 88 Issuance of commonstock upon exercise ofwarrants—3 qtr — — — — 492,613 493 893,811 — — — — — 894,304 Issuance of commonstock for cash, net ofoffering costs—3qtr — — — — 6,767,647 6,767 13,745,400 — — — — — 13,752,167 Issuance of commonstock for cash inconnection withexercise of stockoptions—3 qtr — — — — 1,666 2 3,164 — — — — — 3,166 Compensation expense onoption awards issuedto employees anddirectors—4qtr — — — — — — 378,827 — — — — — 378,827 Compensation expense onrestricted stock issuedto employees—4qtr — — — — — — 88 — — — — — 88 Comprehensive loss: Net loss — — — — — — — — — — (35,573,114) (246,347) (35,819,461) Other comprehensive gain,foreign currencytranslationadjustment — — — — — — — — — 846,388 — — 846,388 Comprehensive loss — — — — — — — — — — — — (34,973,073) Balance 12/31/07(Predecessor) — $— — $— 41,639,657 $41,640 $129,208,631 4,000,000 $(25,974,000) $718,926 $(162,646,158) $1,858,026 $(56,792,935) The accompanying notes are an integral part of these consolidated financial statements. F13stststststndndndrdrdrdrd rdththTable of Contents Series APreferred Stock Series BPreferred Stock Common Stock AdditionalPaid-InCapital Treasury Stock AccumulatedOtherComprehensiveIncome (Loss) AccumulatedDeficitDuringDevelopmentStage TotalShareholders’Equity(Deficit) Number ofShares Amount Number ofShares Amount Number ofShares Amount Number ofShares Amount NoncontrollingInterest Compensation expense onvested options relatedto non-employees—1 qtr — $— — $— — $— $44,849 — $— $— $— $— $44,849 Compensation expense onoption awards issuedto employees anddirectors —1 qtr — — — — — — 151,305 — — — — — 151,305 Expense in connectionwith modification ofemployee stockoptions —1 qtr — — — — — — 1,262,815 — — — — — 1,262,815 Retirement of restrictedstock — — — — (165) (1) — — — — — — (1) Compensation expense onvested options relatedto non-employees—2 qtr — — — — — — 62,697 — — — — — 62,697 Compensation expense onoption awardsissued to employees anddirectors—2 qtr — — — — — — 193,754 — — — — — 193,754 Compensation expense onvested options relatedto non-employees—3 qtr — — — — — — 166,687 — — — — — 166,687 Compensation expense onoption awardsissued to employees anddirectors—3rd qtr — — — — — — 171,012 — — — — — 171,012 Compensation expense onvested options relatedto non-employees—4th qtr — — — — — — (86,719) — — — — — (86,719) Compensation expense onoption awards issuedto employees anddirectors—4th qtr — — — — — — 166,196 — — — — — 166,196 Comprehensive loss: Net loss — — — — — — — — — — (31,411,179) (1,680,676) (33,091,855) Reclassification of foreignexchange gain onsubstantialliquidation of foreignentities — — — — — — — — — (2,152,569) — — (2,152,569) Other comprehensivegain, foreign currencytranslationadjustment — — — — — — — — — 1,433,643 — — 1,433,643 Comprehensive loss — — — — — — — — — — — — (33,810,781) Balance 12/31/08(Predecessor) — $— — $— 41,639,492 $41,639 $131,341,227 4,000,000 $(25,974,000) $— $(194,057,337) $177,350 $(88,471,121) The accompanying notes are an integral part of these consolidated financial statements. F14stststndndrdTable of Contents Series APreferred Stock Series BPreferred Stock Common Stock AdditionalPaid-InCapital Treasury Stock AccumulatedOtherComprehensiveIncome (Loss) AccumulatedDeficitDuringDevelopmentStage TotalEquity(Deficit) Number ofShares Amount Number ofShares Amount Number ofShares Amount Number ofShares Amount NoncontrollingInterest Compensationexpense on vestedoptions related tonon-employees—1 qtr — $— — $— — $— $1,746 — $— $— $— $— $1,746 Compensationexpense on optionawards issued toemployees anddirectors—1 qtr — — — — — — 138,798 — — — — — 138,798 Conversion of debtinto commonstock—1st qtr2009 — — — — 37,564 38 343,962 — — — — — 344,000 Compensationexpense on optionawards issued toemployees anddirectors—2ndqtr — — — — — — 112,616 — — — — — 112,616 Conversion of debtinto commonstock – 2nd qtr2009 — — — — 1,143,324 1,143 10,468,857 — — — — — 10,470,000 Compensationexpense on optionawards issued toemployees anddirectors—2months ended8/31/09 — — — — — — 35,382 — — — — — 35,382 Balance of expensedue tocancellation ofoptions issued toemployees anddirectors inbankruptcy—2months ended8/31/09 — — — — — — 294,912 — — — — — 294,912 Comprehensiveincome: Net income — — — — — — — — — — 65,721,531 205,632 65,927,163 Comprehensiveincome — — — — — — — — — — — — 65,927,163 Balance 8/31/09(Predecessor) — — — — 42,820,380 $42,820 $142,737,500 4,000,000 $(25,974,000) $— $(128,335,806) $382,982 $(11,146,504) Cancellation ofPredecessorcommon stockand fresh startadjustments — — — — (42,820,380) (42,820) (150,426,331) (4,000,000) 25,974,000 — — — (124,495,151) Elimination ofPredecessoraccumulateddeficit andaccumulatedothercomprehensiveloss — — — — — — — — — — 128,335,806 — 128,335,806 Balance 9/1/09(Predecessor) — — — — — — (7,688,831) — — — — 382,982 (7,305,849) Issuance of11.4 millionshares ofcommon stockin connection withemergence fromChapter 11 — — — — 11,400,000 11,400 5,460,600 — — — — — 5,472,000 Balance 9/1/09(Successor) — — — — 11,400,000 11,400 (2,228,231) — — — — 382,982 (1,833,849) Issuance of2.7 millionshares ofcommon stockin connection withthe exit financing — — — — 2,666,666 2,667 1,797,333 — — — — — 1,800,000 Issuance of commonstock on Oct. 28,2009 — — — — 25,501 25 58,627 — — — — — 58,652 Compensationexpense on sharesststissued tomanagement — — — — 600,000 600 167,400 — — — — — 168,000 Compensationexpense on optionawards issued todirectors — — — — — — 326,838 — — — — — 326,838 Compensationexpense on optionawards issued tonon-employees — — — — — — 386,380 — — — — — 386,380 Comprehensive loss: Net loss — — — — — — — — — — (5,049,999) 15,493 (5,034,506) Comprehensive loss — — — — — — — — — — — — (5,034,506) Balance 12/31/09(Successor) — $— — $— 14,692,167 $14,692 $508,347 — $— $— $(5,049,999) $398,475 $(4,128,485) The accompanying notes are an integral part of these consolidated financial statements. F15Table of Contents Series APreferred Stock Series BPreferred Stock Common Stock AdditionalPaid-InCapital Treasury Stock AccumulatedOtherComprehensiveIncome (Loss) AccumulatedDeficitDuringDevelopmentStage NoncontrollingInterest TotalEquity(Deficit) Number ofShares Amount Number ofShares Amount Number ofShares Amount Number ofShares Amount Issuance of 5.1 millionshares of common stockin March 2010, net ofissuance costs of$338,100 — $— — $— 5,076,664 $5,077 $3,464,323 — $— $— $— $— $3,469,400 Warrant fair value associatedwith common sharesissued in March 2010 — — — — — — (2,890,711) — — — — — (2,890,711) Compensation expense onshares issued tomanagement—1Q10 — — — — — — 18,000 — — — — — 18,000 Compensation expense onoption awards issued todirectors/employees-1Q10 — — — — — — 324,377 — — — — — 324,377 Compensation expense onoption awards issued tonon-employees-1Q10 — — — — — — 18,391 — — — — — 18,391 Compensation expense onshares issued tomanagement—2Q10 — — — — — — 18,000 — — — — — 18,000 Compensation expense onoption awards issued todirectors/employees-2Q10 — — — — — — 222,011 — — — — — 222,011 Compensation expense onoption awards issued tonon-employees-2Q10 — — — — — — 33,206 — — — — — 33,206 Compensation expense onshares issued tomanagement—3Q10 — — — — — — 18,000 — — — — — 18,000 Compensation expense onoption awards issued todirectors/employees-3Q10 — — — — — — 183,231 — — — — — 183,231 Compensation expense onoption awards issued tonon-employees-3Q10 — — — — — — 7,724 — — — — — 7,724 Compensation expense onshares issued tomanagement—4Q10 — — — — — — 18,000 — — — — — 18,000 Compensation expense onoption awards issued todirectors/employees-4Q10 — — — — — — 104,094 — — — — — 104,094 Compensation expense onoption awards issued tonon-employees-4Q10 — — — — — — 27,507 — — — — — 27,507 Preferred Stock Series Aconversion — — — — 606,667 607 363,393 — — — — — 364,000 Comprehensive loss: Net loss — — — — — — — — — — (12,931,531) 51,898 (12,879,633) Comprehensive loss — — — — — — — — — — — — (12,879,633) Balance 12/31/10 (Successor) — $— — $— 20,375,498 $20,376 $2,437,893 — $— $— $(17,981,530) $450,373 $(15,072,888) The accompanying notes are an integral part of these consolidated financial statements. F16Table of Contents Series APreferred Stock Series BPreferred Stock Common Stock AdditionalPaid-In Capital Treasury Stock AccumulatedOtherComprehensiveIncome (Loss) AccumulatedDeficitDuringDevelopmentStage NoncontrollingInterest TotalEquity(Deficit) Number ofShares Amount Number ofShares Amount Number ofShares Amount SubscriptionReceivable Number ofShares Amount Compensation expense on sharesissued to management—1Q11 — $— — $— — $— $— $18,000 — $— $— $— $— $18,000 Compensation expense on optionawards issued todirectors/employees-1Q11 — — — — — — — 995,551 — — — — — 995,551 Compensation expense on optionawards issued to non-employees-1Q11 — — — — — — — 38,203 — — — — — 38,203 Preferred Stock warrants exercised—1Q11 — — — — 289,599 289 — 241,542 — — — — — 241,831 Preferred Stock Series A and Bconverted— 1Q11 — — — — 3,894,000 3,894 — 323,919 — — — — — 327,813 Compensation expense on sharesissued to management—2Q11 — — — — — — — 18,000 — — — — — 18,000 Compensation expense on optionawards issued todirectors/employees-2Q11 — — — — — — — 1,082,503 — — — — — 1,082,503 Compensation expense on optionawards issued to non-employees-2Q11 — — — — — — — 250,473 — — — — — 250,473 Preferred Stock warrants exercised—2Q11 — — — — 7,230,103 7,230 — 6,065,727 — — — — — 6,072,957 Preferred Stock Series A, B and Dconverted—2Q11 — — — — 11,554,000 11,554 — 4,546,768 — — — — — 4,558,322 Issuance of 1.9 million shares ofcommon stock and 0.2 warrantsin June 2011, net of issuance costsof $0.1 million — — — — 1,908,889 1,909 — 1,578,651 — — — — — 1,580,560 Stock option exercised — — — — 246,141 246 — (246) — — — — — — Compensation expense on sharesissued to management—3Q11 — — — — — — — 12,000 — — — — — 12,000 Compensation expense on optionawards issued todirectors/employees/consultants-3Q11 — — — — — — — 225,235 — — — — — 225,235 Preferred Stock warrants exercised—3Q11 — — — — 890,564 891 — 944,485 — — — — — 945,376 Preferred Stock Series A, B and Dconverted—3Q11 — — — — 7,480,000 7,480 — 3,546,584 — — — — — 3,554,064 Issuance of 41.4 million shares ofcommon stock and 15.7warrants in August 2011, net ofissuance costs of $1.6 million — — — — 41,409,461 41,409 (550,020) 21,096,029 — — — — — 20,587,418 Compensation expense on optionawards issued todirectors/employees/consultants-4Q11 — — — — — — — 259,985 — — — — — 259,985 Preferred Stock Series D converted—4Q11 — — — — 400,000 400 — 53,037 — — — — — 53,437 Comprehensive loss: Net loss — — — — — — — — — — — (31,367,550) 18,209 (31,349,341) Comprehensive loss — — — — — — — — — — — — — (31,349,341) Balance 12/31/11 (Successor) — $— — $— 95,678,255 $95,678 $(550,020) $43,734,339 — $— $— $(49,349,080) $468,582 $(5,600,501) The accompanying notes are an integral part of these consolidated financial statements. F17Table of ContentsFibrocell Science, Inc.(A Development Stage Company)Consolidated Statements of Cash Flows Successor Successor Successor Predecessor Year endedDecember 31,2011 Year endedDecember 31,2010 Cumulativeperiod fromSeptember 1,2009 (date ofinception) toDecember 31,2011 Cumulativeperiod fromDecember 31,1995 (date ofinception) toAugust 31,2009 Cash flows from operating activities: Net loss $(31,349,341) $(12,879,633) $(49,263,480) $(117,121,644) Adjustments to reconcile net loss to net cash used in operatingactivities: Reorganization items, net — — 72,477 (74,648,976) Expense related to stock-based compensation 2,899,950 992,541 4,773,709 10,608,999 Warrant expense 4,762,694 465,232 5,547,010 — Derivative revaluation expense 5,451,518 — 5,451,518 — Uncompensated contribution of services — — — 755,556 Depreciation and amortization 157,756 8,085 165,841 9,091,990 Provision for doubtful accounts 17,701 (7,818) (36,736) 337,810 Provision for excessive and/or obsolete inventory (45,505) (60,366) (94,207) 259,427 Amortization of debt issue costs — — — 4,107,067 Amortization of debt discounts on investments — — — (508,983) Loss on disposal or impairment of property and equipment — — — 17,668,477 Foreign exchange gain on substantial liquidation of foreignentity (2,222) (5,072) (9,908) (2,256,408) Change in operating assets and liabilities, excluding effects ofacquisition: Decrease (increase) in accounts receivable (3,524) 47,686 67,706 (91,496) Decrease (increase) in other receivables (947) (4,033) (240) 218,978 Decrease (increase) in inventory 38,096 27,459 96,478 (455,282) Decrease (increase) in prepaid expenses (437,367) 42,799 (639,473) 34,341 Decrease (increase) in other assets — — 4,120 71,000 Increase (decrease) in accounts payable 802,920 851,102 1,761,644 57,648 Increase (decrease) in accrued expenses, liabilities subjectto compromise and other liabilities 816,083 1,256,140 1,646,429 3,311,552 Increase (decrease) in deferred revenue 55,400 — 55,400 (50,096) Net cash used in operating activities (16,836,788) (9,265,878) (30,401,712) (148,610,040) Cash flows from investing activities: Acquisition of Agera, net of cash acquired — — — (2,016,520) Purchase of property and equipment (1,570,105) (29,674) (1,599,779) (25,515,170) Proceeds from the sale of property and equipment, net of selling costs — — — 6,542,434 Purchase of investments — — — (152,998,313) Proceeds from sales and maturities of investments — — — 153,507,000 Net cash used in investing activities (1,570,105) (29,674) (1,599,779) (20,480,569) Cash flows from financing activities: Proceeds from convertible debt — — — 91,450,000 Offering costs associated with the issuance of convertible debt — — — (3,746,193) Offering costs associated with the issuance of debt (100,000) — (100,000) — Proceeds from notes payable to shareholders, net — — — 135,667 Proceeds from the issuance of redeemable preferred stock series A, net — — 2,870,000 12,931,800 Proceeds from the issuance of redeemable preferred stock series B, net 193,200 4,019,570 4,212,770 — Proceeds from the issuance of redeemable preferred stock series D, net 5,642,780 1,509,400 7,152,180 — Proceeds from the exercise of warrants 2,418,646 — 2,418,646 — Proceeds from the issuance of common stock, net 22,167,978 3,469,400 27,437,378 93,753,857 Costs associated with secured loan and debtor-in-possession loan — — — (360,872) Proceeds from secured loan — — — 500,471 Proceeds from debtor-in-possession loan — — — 2,750,000 Payments on insurance loan (80,578) (63,683) (166,152) (79,319) Principal payments on 12.5% note payable (1,283,321) — (1,283,321) — Cash dividends paid on preferred stock (623,096) (139,750) (762,846) (1,087,200) Cash paid for fractional shares of preferred stock — — — (38,108) Merger and acquisition expenses — — — (48,547) Repurchase of common stock — — — (26,024,280) Repurchase of common stock — — — (26,024,280) Net cash provided by financing activities 28,335,609 8,794,937 41,778,655 170,137,276 Effect of exchange rate changes on cash balances 2,541 5,865 11,555 (36,391) Net increase (decrease) in cash and cash equivalents 9,931,257 (494,750) 9,788,719 1,010,276 Cash and cash equivalents, beginning of period 867,738 1,362,488 1,010,276 — Cash and cash equivalents, end of period $10,798,995 $867,738 $10,798,995 $1,010,276 Supplemental disclosures of cash flow information: Cash paid for interest $435,096 $— $435,096 $12,715,283 Non-cash investing and financing activities: Predecessor deemed dividend associated with beneficial conversion ofpreferred stock $— $— $— $11,423,824 Predecessor preferred stock dividend — — — 1,589,861 Successor accrued preferred stock dividend 487,421 191,417 487,421 — Predecessor uncompensated contribution of services — — — 755,556 Predecessor common stock issued for intangible assets — — — 540,000 Predecessor common stock issued in connection with conversion ofdebt — — — 10,814,000 Predecessor equipment acquired through capital lease — — — 167,154 Successor/Predecessor financing of insurance premiums 150,251 97,065 328,833 87,623 Successor issuance of notes payable — — — 6,000,060 Successor common stock issued in connection with reorganization — — — 5,472,000 Successor intangible assets — — — 6,340,656 Successor deferred tax liability in connection with fresh-start — — — 2,500,000 Elimination of Predecessor common stock and fresh start adjustment — — — 14,780,320 Successor subscription receivable 550,020 210,000 550,020 — Successor accrued warrant liability 4,994,307 7,071,010 12,381,509 — Successor conversion of preferred stock Series A balance intocommon stock 1,202,989 — 1,202,989 — Successor conversion of preferred stock derivative balance intocommon stock 7,290,647 — 7,654,647 — Successor cashless exercise of warrants recorded previously as aliability 4,841,519 — 4,841,519 — Successor accrued derivative liability 252,318 2,120,360 2,372,678 — The accompanying notes are an integral part of these consolidated financial statements. F18Table of ContentsFibrocell Science, Inc.(A Development Stage Company)Notes to Consolidated Financial StatementsNote 1—Business and OrganizationFibrocell Science, Inc. (“Fibrocell” or the “Company” or the “Successor”) is the parent company of Fibrocell Technologies (“Fibrocell Tech”) and AgeraLaboratories, Inc., a Delaware corporation (“Agera”). Fibrocell Tech is the parent company of Isolagen Europe Limited, a company organized under the laws ofthe United Kingdom (“Isolagen Europe”), Isolagen Australia Pty Limited, a company organized under the laws of Australia (“Isolagen Australia”), andIsolagen International, S.A., a company organized under the laws of Switzerland (“Isolagen Switzerland”). Operations in the foreign subsidiaries have beensubstantially liquidated.The Company is an aesthetic and therapeutic development stage biotechnology company focused on developing novel skin and tissue rejuvenationproducts. The Company’s clinical development product candidates are designed to improve the appearance of skin injured by the effects of aging, sunexposure, acne and burns with a patient’s own, or autologous, fibroblast cells produced in the Company’s proprietary Fibrocell Process. The Company’s leadproduct, LAVIV™ (LAVIV), is the first and only personalized aesthetic cell therapy approved by the FDA for the improvement of the appearance of moderateto severe nasolabial fold wrinkles in adults. The Company also markets an advanced skin care line with broad application in core target markets through itsconsolidated subsidiary, Agera. The Company owns 57% of the outstanding shares of Agera.Note 2—Basis of PresentationAs of September 1, 2009, the Company adopted fresh-start accounting in accordance with Accounting Standards Codification (“ASC”) 852-10,Reorganizations. The Company selected September 1, 2009, as the date to effectively apply fresh-start accounting based on the absence of any materialcontingencies at the August 27, 2009 confirmation hearing and the immaterial impact of transactions between August 27, 2009 and September 1, 2009. Theadoption of fresh-start accounting resulted in the Company becoming a new entity for financial reporting purposes.Accordingly, the financial statements prior to September 1, 2009 are not comparable with the financial statements for periods on or after September 1,2009. References to “Successor” or “Successor Company” refer to the Company on or after September 1, 2009, after giving effect to the cancellation ofIsolagen, Inc. common stock issued prior to the Effective Date, the issuance of new Fibrocell Science, Inc. common stock in accordance with the Plan, and theapplication of fresh-start accounting. References to “Predecessor” or “Predecessor Company” refer to the Company prior to September 1, 2009.Note 3— Development-Stage Risks and Going ConcernThe Company emerged from Bankruptcy in September 2009 and continues to operate as a going concern. At December 31, 2011, the Company hadcash and cash equivalents of approximately $10.8 million and working capital of $2.9 million.The Company will need to access the capital markets in the near future in order to fund future operations. There is no guarantee that any such requiredfinancing will be available on terms satisfactory to the Company or available at all. These matters create uncertainty relating to its ability to continue as a goingconcern. The accompanying consolidated financial statements do not reflect any adjustments relating to the recoverability and classification of assets orliabilities that might result from the outcome of these uncertainties.Further, if the Company raises additional cash resources in the near future, it may be raised in contemplation of or in connection with bankruptcy. Inthe event of a bankruptcy, it is likely that its common stock and common stock equivalents will become worthless and our creditors will receive significantlyless than what is owed to them. F19Table of ContentsThrough December 31, 2011, the Company has been primarily engaged in developing its initial product technology. In the course of its developmentactivities, the Company has sustained losses and expects such losses to continue through at least 2012. During the year ended December 31, 2011, theCompany financed its operations primarily through its existing cash received from external financings, but as discussed above it now requires additionalfinancing. There is substantial doubt about the Company’s ability to continue as a going concern.The Company’s ability to complete additional offerings is dependent on the state of the debt and/or equity markets at the time of any proposed offering,and such market’s reception of the Company and the offering terms. The Company’s ability to complete an offering is also dependent on the status of its FDAregulatory milestones and its clinical trials. There is no assurance that capital in any form would be available to the Company, and if available, on terms andconditions that are acceptable.As a result of the conditions discussed above, and in accordance with Generally Accepted Accounting Principles (“GAAP”), there exists substantialdoubt about the Company’s ability to continue as a going concern, and its ability to continue as a going concern is contingent, among other things, upon itsability to secure additional adequate financing or capital in the near future. If the Company does not obtain additional funding, or does not anticipate additionalfunding, in the near future, it will likely enter into bankruptcy and/or cease operations. Further, if it does raise additional cash resources in the near future, itmay be raised in contemplation of or in connection with bankruptcy. If the Company enters into bankruptcy, it is likely that its common stock and commonstock equivalents will become worthless and its creditors, including preferred stock, will receive significantly less than what is owed to them.Note 4—Summary of Significant Accounting PoliciesUse of EstimatesThe preparation of financial statements in conformity with GAAP requires management to make estimates and assumptions that affect the reportedamounts in the consolidated financial statements and notes. In addition, management’s assessment of the Company’s ability to continue as a going concerninvolves the estimation of the amount and timing of future cash inflows and outflows. Actual results may differ materially from those estimates.Cash and Cash EquivalentsThe Company considers highly liquid investments with an original maturity of three months or less when purchased to be cash equivalents.Concentration of Credit RiskAs of December 31, 2011, the Company maintains the majority of its cash primarily with one major U.S. domestic bank. All of our non-interestbearing cash balances were fully insured at December 31, 2011 due to a temporary federal program in effect from December 31, 2010 through December 31,2012. Under the program, there is no limit to the amount of insurance for eligible accounts. Beginning 2013, insurance coverage will revert to $250,000 perdepositor at each financial institution, and our non-interest bearing cash balances may again exceed federally insured limits. The terms of these deposits are ondemand to minimize risk. The Company has not incurred losses related to these deposits. Cash and cash equivalents of less than $0.1 million, related toAgera and the Company’s Swiss subsidiary is maintained in two separate financial institutions. The Company invests these funds primarily in demanddeposit accounts.Allowance for Doubtful AccountsThe Company maintains an allowance for doubtful accounts related to its accounts receivable that have been deemed to have a high risk of collectability.Management reviews its accounts receivable on a monthly basis to determine if any receivables will potentially be uncollectible. One foreign customerrepresents 85% and 88% of accounts receivable, net, at December 31, 2011 and 2010, respectively. Management analyzes historical collection trends andchanges in its customer payment patterns, customer F20Table of Contentsconcentration, and creditworthiness when evaluating the adequacy of its allowance for doubtful accounts. In its overall allowance for doubtful accounts, theCompany includes any receivable balances that are determined to be uncollectible. Based on the information available, management believes the allowance fordoubtful accounts is adequate; however, actual write-offs might exceed the recorded allowance.The allowance for doubtful accounts was $46,981 and $29,280 at December 31, 2011 and 2010, respectively.InventoryInventories are determined at the lower of cost or market value with cost determined under specific identification and on the first-in-first-out method.Inventories consist of raw materials and finished goods. At December 31, 2011, Agera’s inventory of $0.3 million consisted of $0.1 million of raw materialsand $0.2 million of finished goods. At December 31, 2010, Agera’s inventory of $0.3 million consisted of $0.2 million of raw materials and $0.1 million offinished goods.Property and equipmentProperty and equipment is carried at cost less accumulated depreciation and amortization. Generally, depreciation and amortization for financialreporting purposes is provided by the straight-line method over the estimated useful life of three years, except for leasehold improvements which are amortizedusing the straight-line method over the remaining lease term or the life of the asset, whichever is shorter. The cost of repairs and maintenance is charged as anexpense as incurred.Intangible assetsIntangible assets are research and development assets related to the Company’s primary study that was recognized upon emergence from bankruptcy.The portion of the reorganization value which was attributed to identified intangible assets was $6,340,656. This value is related to research and developmentassets that are not subject to amortization. In accordance with ASC 805-20, Business Combinations, Identifiable Assets and Liabilities, and AnyNoncontrolling Interest, this amount is reported as intangibles in the consolidated balance sheets, and is not being amortized.Intangibles are tested for recoverability whenever events or changes in circumstances indicate the carrying amount may not be recoverable. Theimpairment test consists of a comparison of the fair value of the intangible asset to its carrying amount. There was no impairment of the intangible assets as ofDecember 31, 2011.Revenue recognitionThe Company recognizes revenue over the period the service is performed in accordance with ASC 605, Revenue Recognition (“ASC 605”). In general,ASC 605 requires that four basic criteria must be met before revenue can be recognized: (1) persuasive evidence of an arrangement exists, (2) delivery hasoccurred or services rendered, (3) the fee is fixed and determinable and (4) collectability is reasonably assured.Revenue from the sale of Agera’s products is recognized upon transfer of title, which is upon shipment of the product to the customer. The Companybelieves that the requirements of ASC 605 are met when the ordered product is shipped, as the risk of loss transfers to our customer at that time, the fee isfixed and determinable and collection is reasonably assured. Any advanced payments are deferred until shipment.Shipping and handling costsAgera charges its customers for shipping and handling costs. Such charges to customers are presented net of the costs of shipping and handling, asselling, general and administrative expense, and are not significant to the consolidated statements of operations. F21Table of ContentsAdvertising costAgera advertising costs are expensed as incurred and include the costs of public relations and certain marketing related activities. These costs areincluded in selling, general and administrative expenses in the accompanying consolidated statements of operations.Research and development expensesResearch and development costs are expensed as incurred and include salaries and benefits, costs paid to third-party contractors to perform research,conduct clinical trials, develop and manufacture drug materials and delivery devices, and a portion of facilities cost. Research and development costs alsoinclude costs to develop manufacturing, cell collection and logistical process improvements.Clinical trial costs are a significant component of research and development expenses and include costs associated with third-party contractors.Invoicing from third-party contractors for services performed can lag several months. The Company accrues the costs of services rendered in connection withthird-party contractor activities based on its estimate of management fees, site management and monitoring costs and data management costs. Actual clinicaltrial costs may differ from estimated clinical trial costs and are adjusted for in the period in which they become known.Other Income, NetIn November 2010, we received one grant totaling $0.2 million under the Qualified Therapeutic Discovery Project Grants Program. The QualifiedTherapeutic Discovery Project Grants Program was included in the healthcare reform legislation, and established a one-time pool of $1 billion for grants tosmall biotechnology companies developing novel therapeutics which show potential to: (a) result in new therapies that either treat areas of unmet medical need,or prevent, detect, or treat chronic or acute diseases and conditions; (b) reduce long-term health care costs in the United States; or (c) significantly advance thegoal of curing cancer within a the 30-year period. There are no matching funding requirements or other requirements necessary to receive the funding.Warrant LiabilityCertain warrants are measured at fair value and liability-classified under ASC 815, Derivatives and Hedging, (“ASC 815”) because the warrantscontain “down-round protection” and therefore, do not meet the scope exception for treatment as a derivative under ASC 815. Since “down-round protection” isnot an input into the calculation of the fair value of the warrants, the warrants cannot be considered indexed to the Company’s own stock which is arequirement for the scope exception as outlined under ASC 815. Effective December 31, 2011, we calculated the fair value of the warrants using the MonteCarlo simulation valuation method due to the changes in the product status with the approval of LAVIV. Prior to December 31, 2011, the Black-Scholesoption-pricing model was utilized due to the assumptions present prior to the approval of LAVIV. The fair value is affected by changes in inputs to that modelincluding our stock price, expected stock price volatility, the contractual term, and the risk-free interest rate. We will continue to classify the fair value of thewarrants as a liability until the warrants are exercised, expire or are amended in a way that would no longer require these warrants to be classified as a liability.Preferred Stock and Derivative LiabilityThe preferred stock has been classified within the mezzanine section between liabilities and equity in its consolidated balance sheets in accordance withASC 480, Distinguishing Liabilities from Equity (“ASC 480”) because any holder of Series A, B and D Preferred may require the Company to redeem all ofits Series A, B or D Preferred in the event of a triggering event which is outside of the control of the Company. F22Table of ContentsThe embedded conversion option for the Series A Preferred, Series B Preferred and Series D Preferred has been recorded as a derivative liability underASC 815 in the Company’s consolidated balance sheet and will be re-measured on the Company’s reporting dates. The fair value of the derivative liability isdetermined using the Black-Scholes option-pricing model and is affected by changes in inputs to that model including our stock price, expected stock pricevolatility, the expected term, and the risk-free interest rate. The Company will continue to classify the fair value of the embedded conversion option as aliability until the preferred stock is converted into common stock.Stock-based CompensationThe Company accounts for stock-based awards to employees using the fair value based method to determine compensation for all arrangements whereshares of stock or equity instruments are issued for compensation. In addition, the Company accounts for stock-based compensation to nonemployees inaccordance with the accounting guidance for equity instruments that are issued to other than employees. The Company uses a Black-Scholes option-pricingmodel to determine the fair value of each option grant as of the date of grant for expense incurred. The Black-Scholes model requires inputs for risk-freeinterest rate, dividend yield, volatility and expected lives of the options. Expected volatility is based on historical volatility of the Company’s competitor’sstock since the The Company ceased trading as part of the bankruptcy and emerged as a new entity. The risk-free rate for periods within the contractual life ofthe option is based on the U.S. Treasury yield curve in effect at the time of the grant. The expected lives for options granted represents the period of time thatoptions granted are expected to be outstanding and is derived from the contractual terms of the options granted. The Company estimates future forfeitures ofoptions based upon expected forfeiture rates.Income taxesAn asset and liability approach is used for financial accounting and reporting for income taxes. Deferred income taxes arise from temporary differencesbetween income tax and financial reporting and principally relate to recognition of revenue and expenses in different periods for financial and tax accountingpurposes and are measured using currently enacted tax rates and laws. In addition, a deferred tax asset can be generated by net operating loss (“NOLs”)carryover. If it is more likely than not that some portion or all of a deferred tax asset will not be realized, a valuation allowance is recognized.In the event the Company is charged interest or penalties related to income tax matters, the Company would record such interest as interest expense andwould record such penalties as other expense in the consolidated statements of operations. No such charges have been incurred by the Company. As ofDecember 31, 2011 and December 31, 2010, the Company had no accrued interest related to uncertain tax positions.At December 31, 2011 and December 31, 2010, the Company has provided a full valuation allowance for the net deferred tax assets, the large majorityof which relates to the future benefit of loss carryovers. In addition, as a result of fresh-start accounting, the Company may be limited by section 382 of theInternal Revenue Service Code. The tax years 2008 through 2011 remain open to examination by the major taxing jurisdictions to which we are subject. Thedeferred tax liability at December 31, 2011 and December 31, 2010, relates to the intangible assets recognized upon fresh-start accounting.Income (loss) per share dataBasic income (loss) per share is calculated based on the weighted average common shares outstanding during the period. Diluted income per share(“Diluted EPS’) also gives effect to the dilutive effect of stock options, warrants, restricted stock and convertible preferred stock calculated based on thetreasury stock method. F23Table of ContentsThe following potentially dilutive securities have been excluded from the computations of diluted weighted-average shares outstanding as ofDecember 31, 2011 and 2010, as they would be anti-dilutive: For the year endedDecember 31, 2011 2010 Shares of convertible preferred stock 7,282,000 18,342,000 Shares underlying options outstanding 13,608,500 5,677,000 Shares underlying warrants outstanding 49,135,602 31,178,295 Unvested restricted stock — 150,000 Fair Value of Financial InstrumentsThe carrying values of certain of the Company’s financial instruments, including cash equivalents and accounts payable approximates fair value due totheir short maturities. The fair values of the Company’s long-term obligations are based on assumptions concerning the amount and timing of estimated futurecash flows and assumed discount rates reflecting varying degrees of risk. The carrying values of the Company’s long-term obligations approximate their fairvalues.The fair value of the reorganization value which applies in fresh-start accounting was estimated by applying the income approach and a marketapproach. This fair value measurement is based on significant inputs that are not observable in the market and, therefore, represents a Level 3 measurement asdefined in ASC 820, Fair Value Measurements.Note 5—InventoryInventories consist of the following: December 31, December 31, 2011 2010 Raw materials $102,220 $129,863 Finished goods 164,128 129,076 Total $266,348 $258,939 Note 6—Fair Value MeasurementsThe Company adopted the accounting guidance on fair value measurements for financial assets and liabilities measured on a recurring basis. Theguidance requires fair value measurements be classified and disclosed in one of the following three categories: • Level 1: Unadjusted quoted prices in active markets that are accessible at the measurement date for identical, unrestricted assets or liabilities; • Level 2: Quoted prices in markets that are not active or inputs which are observable, either directly or indirectly, for substantially the full term ofthe asset or liability. • Level 3: Prices or valuation techniques that require inputs that are both significant to the fair value measurement and unobservable (i.e., supportedby little or no market activity). F24Table of ContentsThe following fair value hierarchy table presents information about each major category of the Company’s liabilities measured at fair value on arecurring basis as of December 31, 2011 and 2010: Fair value measurement using Quoted prices inactive markets(Level 1) Significantotherobservableinputs (Level 2) Significantunobservableinputs(Level 3) Total At December 31, 2011 Liabilities Warrant liability $— $— $13,087,000 $13,087,000 Derivative liability — — 533,549 533,549 Total $— $— $13,620,549 $13,620,549 Fair value measurement using Quoted prices inactive markets(Level 1) Significantotherobservableinputs (Level 2) Significantunobservableinputs(Level 3) Total At December 31, 2010 Liabilities Warrant liability $— $— $8,171,518 $8,171,518 Derivative liability — — 2,120,360 2,120,360 Total $— $— $10,291,878 $10,291,878 The reconciliation of warrant liability measured at fair value on a recurring basis using unobservable inputs (Level 3) is as follows: WarrantLiability Balance at January 1, 2010 $635,276 Issuance of additional warrants 7,071,010 Change in fair value of warrant liability 465,232 Balance at December 31, 2010 $8,171,518 Issuance of additional warrants 4,994,307 Exercise of warrants (4,841,519) Change in fair value of warrant liability 4,762,694 Balance at December 31, 2011 $13,087,000 The fair value of the warrant liability is based on Level 3 inputs. For this liability, the Company developed its own assumptions that do not haveobservable inputs or available market data to support the fair value. See Note 13 for further discussion of the warrant liability.The reconciliation of derivative liability measured at fair value on a recurring basis using unobservable inputs (Level 3) is as follows: DerivativeLiability Balance at January 1, 2010 $— Record fair value of derivative liability 2,120,360 Balance at December 31, 2010 2,120,360 Issuance of additional preferred stock and other 252,318 Conversion of preferred stock (7,290,647) Change in fair value of derivative liability 5,451,518 Balance at December 31, 2011 $533,549 F25Table of ContentsThe fair value of the derivative liability is based on Level 3 inputs. For this liability, the Company developed its own assumptions that do not haveobservable inputs or available market data to support the fair value. See Note 12 for further discussion of the derivative liability.Note 7—Property and EquipmentAs of December 31, 2011 and 2010, property and equipment consisted of the following: December 31,2011 December 31,2010 Lab equipment $402,192 $18,685 Computer equipment and software 137,251 10,989 Leasehold improvements 298,781 — Construction-in-process 761,555 — 1,599,779 29,674 Less: Accumulated depreciation (165,841) (8,085) Property and equipment, net $1,433,938 $21,589 Depreciation expense was $157,756 and $8,085 for the year ending December 31, 2011 and 2010, respectively.Note 8—Accrued ExpensesAccrued expenses consist of the following: December 31,2011 December 31,2010 Accrued professional fees $702,106 $413,384 Accrued compensation 6,426 7,076 Dividend on preferred stock payable 55,742 191,417 Accrued other 161,867 177,605 Accrued expenses $926,141 $789,482 Note 9—DebtThe Company’s outstanding debt at December 31, 2011 and December 31, 2010 consists of $6.7 million and $7.3 million, respectively, of 12.5%Unsecured Promissory Notes (“Notes”). Unpaid interest has been accreted to the principal at a rate of 15%. The Notes have the following features: (1) 12.5%interest payable quarterly in cash or, at the Company’s option, 15% payable in kind by capitalizing such unpaid amount and adding it to the principal as ofthe date it was due; (2) maturing June 1, 2012; (3) at any time prior to the maturity date, the Company may redeem any portion of the outstanding principal ofthe Notes in cash at 125% of the stated face value of the Notes. There is a mandatory redemption feature that requires the Company to redeem all outstandingNotes if: (1) the Company successfully completes a capital campaign raising in excess of $10 million; or (2) the Company is acquired by, or sells a majoritystake to, an outside party.Since the Company consummated a single offering of at least $10 million in August 2011, certain note holders were entitled to a mandatory redemptionof the outstanding principal plus any interest payable in cash within three business days of the consummation. Approximately $1.7 million including interestwas paid in 2011 after consummation of the offering. The remaining note holders signed amendments to their notes raising the mandatory redemption for asingle offering or a series of offerings within a six-month period from $10 million to $30 million. The Note is due June 2012.Note 10—Income TaxesFibrocell and Fibrocell Tech file a consolidated U.S. Federal income tax return. Agera files a separate U.S. Federal income tax return. The Company’sforeign subsidiaries, which comprise loss from discontinued operations, file income tax returns in their respective jurisdictions. The geographic source of lossfrom continuing operations is the United States. F26Table of ContentsThe components of the income tax expense/(benefit) related to continuing operations, are as follows: Year endedDecember 31,2011 Year endedDecember 31,2010 U.S. Federal: Current $— $— Deferred — — U.S. State: Current — — Deferred — — $— $— The reconciliation between income tax benefit at the U.S. federal statutory rate and the amount recorded in the accompanying consolidated financialstatements is as follows: Year endedDecember 31,2011 Year endedDecember 31,2010 Tax benefit at U.S. federal statutory rate $(10,958,402) $(4,490,789) Increase in domestic valuation allowance 8,880,185 5,077,136 State income tax benefit before valuation allowance, net of federal benefit (1,370,399) (789,894) Derivative revaluation expense 1,908,031 — Warrant revaluation expense 1,666,943 162,831 Other (126,358) 40,716 $— $— The components of the Company’s net deferred tax liabilities at December 31, 2011 and 2010 are as follows: December 31,2011 December 31,2010 Deferred tax liabilities: Intangible assets $2,500,000 $2,500,000 Total deferred tax liabilities $2,500,000 $2,500,000 Deferred tax assets: Loss carryforwards $39,059,449 $31,162,384 Property and equipment 1,390,315 1,460,890 Accrued expenses and other 1,165,103 1,285,007 Stock compensation 2,103,702 930,103 Total deferred tax assets 43,718,569 34,838,384 Less: valuation allowance (43,718,569) (34,838,384) Total deferred tax assets $— $— Net deferred tax liabilities $2,500,000 $2,500,000 As of December 31, 2011, the Company had generated U.S. net operating loss carryforwards of approximately $96.5 million which expire in yearsthrough 2031 and net loss carryforwards in certain non-US F27Table of Contentsjurisdictions of approximately $24.4 million. The U.S. net operating loss carryforwards were reduced by approximately $74 million as a result of theCompany’s emergence from bankruptcy. The net operating loss carryforwards are available to reduce future taxable income. However, a change in ownership,as defined by federal income tax regulations, could significantly limit the Company’s ability to utilize its U.S. net operating loss carryforwards. Additionally,because federal tax laws limit the time during which the net operating loss carryforwards may be applied against future taxes, if the Company fails to generatetaxable income prior to the expiration dates it may not be able to fully utilize the net operating loss carryforwards to reduce future income taxes. As theCompany has had cumulative losses and there is no assurance of future taxable income, valuation allowances have been recorded to fully offset the deferredtax asset at December 31, 2011 and 2010. The valuation allowance increased by $8.9 million and $5.1 million during 2011 and 2010, respectively, due to theimpact from the current year net losses incurred.Note 11—CommitmentsLeasesAs stated in Note 16, in 2012, the Company renewed its lease for the office, warehouse and laboratory facilities in Exton, Pennsylvania under a non-cancelable operating lease through 2023. Future minimum lease commitments for the amended lease agreement are as follows: Year Ending December 31, 2012 $884,173 2013 1,070,438 2014 1,081,250 2015 1,211,000 2016 1,254,250 2017 and thereafter 8,704,063 Total $14,205,174 For each of the years ended December 31, 2011 and 2010, rental expense totaled $1.4 million.Note 12-EquityCommon Stock Private PlacementsOn August 3, 2011, the Company entered into agreements with certain accredited investors, pursuant to which the Company agreed to sell to thepurchasers an aggregate of 41,409,461 shares of Company common stock at a purchase price of $0.55 per share in a private placement. Each purchaser alsoreceived a warrant to purchase 0.35 shares of common stock for every share of common stock acquired in the offering with an exercise price of $0.75 pershare and a term of 5 years from issuance. The warrants are callable by the Company if the common stock trades over $1.75 for 20 consecutive trading daysat any time after the shares underlying the warrants are registered or eligible for resale pursuant to Rule 144. The aggregate purchase price paid by thepurchasers at closing for the common stock and the warrants was $22.8 million. As of December 31, 2011, there was a subscription receivable of $0.6million. The placement agents for the transaction received cash compensation of $1.6 million and warrants to purchase 1,252,761 shares of Companycommon stock at an exercise price of $0.5454 and fair value of $440,330. Cash issuance costs of $1.6 million were netted against the gross proceeds.On June 16, 2011, the Company completed a private placement, pursuant to which it sold an aggregate of 1,908,889 shares of Company commonstock to eight accredited investors for an aggregate purchase price of $1,718,000. The placement agent for the transaction received cash compensation of$137,440 and warrants to purchase 152,711 shares of Company common stock at an exercise price of $0.90 per share. F28Table of ContentsRedeemable Preferred stockThe Redeemable Preferred stock (“Preferred Stock’) is convertible into common stock at the option of the holder on a share-for-share basis. Each of theforegoing securities are subject to the “down-round” protection and if at any time while the Preferred Stock is outstanding, the Company sells or grants anyoption to purchase or sells or grants any right to reprice, or otherwise disposes of or issues (or announces any sale, grant or any option to purchase or otherdisposition), any common stock or common stock equivalents at an effective price per share that is lower than the then conversion price of the Preferred(“Conversion Price”) or the exercise price of the warrants, then the conversion price and exercise price will be reduced to equal the lower price. The PreferredStock has been classified by the Company within the mezzanine section between liabilities and equity in its consolidated balance sheets in accordance withASC 480 because any holder of Preferred may require the Company to redeem all of its Preferred Stock in the event of a triggering event which is outside of thecontrol of the Company.In addition, the holders of the Preferred stock have no voting rights except with respect to specified matters affecting the rights of the Series A, B and DRedeemable preferred stock. The Preferred stockholders are entitled to receive cumulative dividends at the rate per share of 6% per annum.The Company records accrued dividends at a rate of 6% per annum on the Preferred Stock. As of December 31, 2011 and December 31, 2010,$55,742 and $191,417, respectively, were accrued for dividends payable. The Company paid cash of $623,096 and $139,750 for the year endedDecember 31, 2011 and December 31, 2010, respectively.On May 24, 2011, the Company sent a mandatory conversion notice to the holders of its outstanding Series A Convertible Preferred Stock and Series BConvertible Preferred Stock. Pursuant to the notice, each holder of Series A Convertible Preferred Stock and Series B Convertible Preferred Stock was notifiedthat since the volume weighted average price of the Company’s common stock had exceeded 200% of the then effective conversion price of the Preferred Stockfor twenty consecutive trading days; the Company was permitted to force the conversion of the Preferred Stock into Company common stock. The conversionwas effective on July 7, 2011; provided that holders of Preferred Stock had the right to voluntarily convert their shares of Preferred Stock prior to such date.During 2010 and 2011, 364 and 2,886 Series A preferred shares were converted into 606,667 and 5,772,000 common shares, respectively. During 2011,4,640 Series B preferred shares were converted into 9,280,000 common shares.During 2011, 4,138 Series D preferred shares were converted into 8,276,000 common shares.Preferred Stock Series BIn the third and fourth quarter of 2010, the Company entered into a Securities Purchase Agreement (the “Purchase Agreement”) with certain accreditedinvestors (the “Purchasers”), pursuant to which the Company agreed to sell to the Purchasers in the aggregate: (i) 4,640 shares of Series B Preferred, with apar value of $0.001 per share and a stated value of $1,000 per share Series B Preferred, and (ii) the Warrants to purchase 7,733,334 shares of Common Stockat an exercise price of $0.8054 per share. The aggregate purchase price for the third and fourth quarter 2010 Series B Preferred financing paid by thePurchasers for the Series B Preferred and the Warrants was $4,430,000. The Company used the proceeds for working capital purposes. As a result of theDecember 2010 Series D Preferred Stock transaction the shares and warrants were repriced to $0.50 per share. After giving effect to this anti-dilutionprovision, as of December 31, 2010, there will be 9,280,000 shares of Common Stock underlying the Series B Preferred.Preferred Stock Series DOn January 21, 2011, the Company completed a private placement of securities in which the Company sold to certain accredited investors in theaggregate: (i) 1,234 shares of Series D Convertible Preferred Stock, with a par value of $0.001 per share and a stated value of $1,000 per share, and (ii) F29Table of Contentswarrants to purchase 2,468,000 shares of Company common stock at an exercise price of $0.50 per share. The aggregate purchase price paid by thePurchasers for the Series D Preferred and the Warrants was $1,234,000 (representing $1,000 for each share of Series D Preferred together with warrants). TheCompany intends to use the proceeds for working capital purposes. The placement agents for the offering received cash compensation of $98,720 andwarrants to purchase 197,440 shares of Common Stock at an exercise price of $0.50 per share.On January 28, 2011, the Company completed a private placement of securities in which the Company sold to certain accredited investors in theaggregate: (i) 1,414 shares of Series D at a stated value of $1,000 per share, and (ii) warrants to purchase 2,828,000 shares of Common Stock at an exerciseprice of $0.50 per share. The aggregate purchase price paid by the Purchasers for the Series D Preferred and the warrants was $1,414,000 (representing $1,000for each share of Series D Preferred together with warrants). The Company intends to use the proceeds for working capital purposes. The placement agents forthe offering received cash compensation of $113,120 and warrants to purchase 226,240 shares of Common Stock at an exercise price of $0.50 per share.On February 9, 2011, the Company completed a private placement of securities in which the Company sold to certain accredited investors in theaggregate: (i) 3,436 shares of Series D at a stated value of $1,000 per share, and (ii) warrants to purchase 6,872,000 shares of Common Stock at an exerciseprice of $0.50 per share. The aggregate purchase price paid by the Purchasers for the Series D Preferred and the warrants was $3,436,000 (representing $1,000for each share of Series D Preferred together with warrants). The Company intends to use the proceeds for working capital purposes. The placement agents forthe offering received cash compensation of $274,880 and warrants to purchase 549,760 shares of Common Stock at an exercise price of $0.50 per share.On March 1, 2011, the Company completed a private placement of securities in which the Company sold to certain accredited investors in the aggregate:(i) 50 shares of Series D at a stated value of $1,000 per share, and (ii) warrants to purchase 100,000 shares of Common Stock at an exercise price of $0.50 pershare. The aggregate purchase price paid by the Purchasers for the Series D Preferred and the warrants was $50,000 (representing $1,000 for each share ofSeries D Preferred together with warrants). The Company intends to use the proceeds for working capital purposes. The placement agents for the offeringreceived cash compensation of $4,000 and warrants to purchase 8,000 shares of Common Stock at an exercise price of $0.50 per share.On December 15, 17 and 27, 2010, the Company completed a private placement of securities of Series D Preferred and warrants. The details of the2010 Series D Preferred financing are as follows:1,645 shares of Series D Preferred, with a par value of $0.001 per share and a stated value of $1,000 pershare and (ii) warrants to purchase 3,290,000 shares of Common Stock at an exercise price of $0.50 per share. The aggregate purchase price paid by thePurchasers for the Series D Preferred and the Warrants was $1,645,000 (representing $1,000 for each share of Series D Preferred together with Warrants).Conversion option of Redeemable Preferred stockThe embedded conversion option for the Preferred Stock has been recorded as a derivative liability under ASC 815 in the Company’s consolidatedbalance sheet as of December 31, 2011 and 2010 and will be re-measured on the Company’s reporting dates. The fair value of the derivative liability isdetermined using the Black-Scholes option-pricing model and is affected by changes in inputs to that model including our stock price, expected stock pricevolatility, the contractual term, and the risk-free interest rate. The Company will continue to classify the fair value of the embedded conversion option as aliability until the preferred stock is converted into common stock. F30Table of ContentsThe embedded conversion option for the Preferred Stock was valued at $533,549 and $2,120,360 at December 31, 2011 and 2010, respectively, at fairvalue using the Black-Scholes option-pricing model. The fair market value of the derivative liability was computed using the Black-Scholes option-pricingmodel with the following weighted average assumptions: December 31,2011 December 31,2010 Expected life (years) 1.1 years 1.6 years Interest rate 0.1% 1.6% Dividend yield — — Volatility 61% 63% Note 13-WarrantsWe account for stock warrants as either equity instruments or derivative liabilities depending on the specific terms of the warrant agreement. Stockwarrants are accounted for as a derivative in accordance with ASC 815 if the stock warrants contain “down-round protection” and therefore, do not meet thescope exception for treatment as a derivative. Since “down-round protection” is not an input into the calculation of the fair value of the warrants, the warrantscannot be considered indexed to the Company’s own stock which is a requirement for the scope exception as outlined under ASC 815. The fair value of theequity-classified warrants for the year ended December 31, 2011 and the fair value of the liability-classified warrants at December 31, 2010 was determinedusing the Black-Scholes option-pricing model and is affected by changes in inputs to that model including our stock price, expected stock price volatility, theexpected term, and the risk-free interest rate. The Company will continue to classify the fair value of the warrants as a liability until the warrants are exercised,expire or are amended in a way that would no longer require these warrants to be classified as a liability. Effective December 31, 2011, we calculated the fairvalue of the warrants using the Monte Carlo simulation valuation method due to the changes in the product status with the approval of LAVIV.The following table summarizes outstanding warrants to purchase Common Stock as of December 31, 2011: NumberofWarrants ExercisePrice Expiration Dates Liability-classified warrants Issued in Series A Preferred Stock offering 3,256,492 $0.50 Oct. 2014 Issued in March 2010 offering 4,917,602 0.50 Mar. 2015 Issued in Series B Preferred Stock offering 9,616,086 0.50 Jul.-Nov. 2015 Issued in Series D Preferred Stock offering 15,446,640 0.50 Dec. 2015-Mar. 2016 33,236,820 Equity-classified warrants Issued in June 2011 equity financing 152,711 $0.90 June 2016 Issued to placement agents in August 2011 equity financing 1,252,761 0.55 August 2016 Issued in August 2011 equity financing 14,493,310 0.75 August 2016 15,898,782 Total 49,135,602 The following table summarizes the rollforward of the warrants for the two years ended December 31, 2011: Number ofwarrants Outstanding at January 1, 2010 1,168,210 Warrants issued with financing 17,359,983 Additional warrants issued due to anti-dilution provision 12,650,102 Exercised — Outstanding at December 31, 2010 31,178,295 Warrants issued with financing 29,148,222 Exercised (11,190,915) Outstanding at December 31, 2011 49,135,602 F31Table of ContentsThere were 4,837,291 warrants exercised for the year ended December 31, 2011 which resulted in receipts of $2,418,646 and the issuance of4,837,291 shares of common stock. In addition, there were 6,387,235 cashless warrants exercised for the year ended December 31, 2011 which resulted inthe issuance of 3,572,971 shares of common stock for the year ended December 31, 2011.Liability-classified WarrantsSeries D Preferred Stock Warrants and Placement Agent WarrantsIn connection with the Series D Convertible Preferred Stock transaction, the Company issued 12,268,000 warrants at an exercise price of $0.50 pershare and 981,440 placement agent warrants at an exercise price of $0.50 per share during the first quarter of 2011. The warrants are liability classified sincethey have “down-round” price protection and they are re-measured on the Company’s reporting dates. The weighted average fair market value of the warrants,at the date of issuance, granted to the accredited investors and placement agents, based on the Black-Scholes option-pricing model, is estimated to be $0.45 perwarrant.All liability-classified warrants have an exercise price of $0.50 per share as a result of the December 2010 Series D Preferred Stock financingtransaction.The fair market value of the liability-classified warrants was computed using the Black-Scholes option-pricing model for the year ended December 31,2010 with the following key weighted average assumptions as date indicated: December 31,2010 Net cashsettlementas ofDecember 31,2010(1) Calculated aggregate value $8,171,518 $11,450,000 Exercise price per share of warrant $0.50 $0.50 Closing price per share of common stock $0.51 $0.51 Volatility 63% 100% Expected term (years) 4.7 4.7 Risk-free interest rate 1.8% 1.8% Dividend yield 0% 0% Represents the net cash settlement value of the warrant as of December 31, 2010, which value was calculated utilizing the Black-Scholes option-pricingmodel specified in the warrant. Represents the volatility assumption used to calculate the net cash settlement value as of December 31, 2010.Effective December 31, 2011, the Company utilized the Monte Carlo simulation valuation method to value the liability classified warrants. Thefollowing table summarizes the calculated aggregate fair values and net cash settlement value as of the dates indicated along with the assumptions utilized ineach calculation. F32(2)(1)(2)Table of Contents December 31,2011 Net cashsettlementas of December31, 2011 Calculated aggregate value $13,087,000 $8,320,000 Exercise price per share of warrant $0.50 $0.50 Closing price per share of common stock $0.40 $0.40 Volatility 70% 100% Probability of Fundamental Transaction or Delisting 45.1% — Expected term (years) 3.7 3.7 Risk-free interest rate 0.63% 0.63% Dividend yield 0% 0% (1)Represents the net cash settlement value of the warrant as of December 31, 2011, which value was calculated utilizing the Black-Scholes option-pricingmodel specified in the warrant.(2)Represents the volatility assumption used to calculate the net cash settlement value as of December 31, 2011.Equity-classified WarrantsIn connection with the private placement transaction on August 3, 2011, the Company issued warrants to purchase 14,493,310 shares of the Companycommon stock to certain accredited investors with an exercise price of $0.75 per share and a term of 5 years from issuance. The warrants are callable by theCompany if the common stock trades over $1.75 for 20 consecutive trading days. The placement agents for the transaction received warrants to purchase1,252,761 shares of Company common stock at an exercise price of $0.5454. The Company determined the average fair value of the warrants as of the dateof the grant was $0.31 per share utilizing the Black-Scholes option-pricing model. In estimating the fair value of the warrants, the Company utilized thefollowing inputs: closing price per share of common stock of $0.63, volatility of 61.4%, expected term of 5 years, risk-free interest rate of 1.25% anddividend yield of zero.On June 16, 2011, the Company completed a private placement and issued warrants to the placement agents in the private placement to purchase152,711 shares of Company common stock at an exercise price of $0.90 per share. The Company determined the fair value of the warrants as of the date ofthe grant was $0.62 per share utilizing the Black-Scholes option-pricing model. In estimating the fair value of the warrants, the Company utilized thefollowing inputs: closing price per share of common stock of $1.08, volatility of 61.6%, expected term of 5 years, risk-free interest rate of 1.52% anddividend yield of zero.Note 14—Equity-based CompensationTotal stock-based compensation expense recognized using the straight-line attribution method in the consolidated statement of operations for the yearended December 31 is as follows: 2011 2010 Stock option compensation expense for employees and directors $2,607,210 $833,713 Restricted stock expense 48,000 72,000 Equity awards for nonemployees issued for services 244,740 86,828 Total stock-based compensation expense $2,899,950 $992,541 Our board of directors adopted the 2009 Equity Incentive Plan (the “Plan”) effective September 3, 2009. The Plan is intended to further align theinterests of the Company and its stockholders with its employees, including its officers, non-employee directors, consultants and advisors by providingincentives for such persons to exert maximum efforts for the success of the Company. The Plan originally allowed for the issuance of up to 4,000,000 shares ofthe Company’s common stock. In June 2011, the board of F33(1)(2)Table of Contentsdirectors of the Company amended the 2009 Equity Incentive Plan to increase the number of shares available for issuance under the Plan to 15,000,000 sharesof common stock. The types of awards that may be granted under the Plan include options (both nonqualified stock options and incentive stock options),stock appreciation rights, stock awards, stock units, and other stock-based awards. Notwithstanding the foregoing, to the extent the Company is unable toobtain shareholder approval of the Plan within one year of the effective date, any incentive stock options issued pursuant to the Plan shall automatically beconsidered nonqualified stock options, and to the extent a holder of an incentive stock option exercises his or her incentive stock option prior to suchshareholder approval date, such exercised option shall automatically be considered to have been a nonqualified stock option. The term of each award isdetermined by the Board at the time each award is granted, provided that the terms of options may not exceed ten years.During the years ended December 31, 2011 and 2010, the weighted average fair market value using the Black-Scholes option-pricing model of theoptions granted was $0.40 and $0.53, respectively. The fair market value of the stock options at the date of grant was estimated using the Black-Scholesoption-pricing model with the following weighted average assumptions for the year ended December 31: 2011 2010 Expected life (years) 5.4 years 5.1 years Interest rate 2.1% 2.0% Dividend yield — — Volatility 62% 64% There were 600,000 cashless stock options exercised during the year ended December 31, 2011, which resulted in the issuance of 246,141 shares ofcommon stock. Number ofshares Weighted-averageexerciseprice Weighted-averageremainingcontractualterm (in years) Aggregateintrinsicvalue Outstanding at January 1, 2010 2,807,000 $0.77 7.35 $1,082,800 Granted 2,870,000 0.95 Exercised — — Forfeited — — Outstanding at December 31, 2010 5,677,000 $0.86 7.46 $— Granted 9,628,000 $0.72 Exercised (600,000) $0.75 318,000 Forfeited (1,096,500) $0.77 Outstanding at December 31, 2011 13,608,500 $0.77 8.36 $— Exercisable at December 31, 2011 8,596,427 $0.80 8.00 $— The following table summarizes the Company’s non-vested stock options: Non-vested Options Number ofShares Weighted-Average FairValue Non-vested at January 1, 2010 677,000 $0.36 Granted 2,870,000 0.53 Vested (1,497,384) 0.49 Forfeited — — Non-vested at December 31, 2010 2,049,616 $0.50 Granted 9,628,000 0.72 Vested (5,569,043) 0.77 Forfeited (1,096,500) 0.76 Non-vested at December 31, 2011 5,012,073 $0.41 F34Table of ContentsThe total fair value of shares vested during the twelve months ended December 31, 2011 was $2.5 million. As of December 31, 2011, there was$1.4 million of total unrecognized compensation cost, related to non-vested stock options which vest over time. That cost is expected to be recognized over aweighted-average period of 1.5 years. As of December 31, 2011, there was less than $0.1 million of total unrecognized compensation expense related toperformance-based, non-vested employee stock options. That cost will be recognized when the performance criteria within the respective performance-basedoption grants become probable of achievement.Restricted stockThe following table summarizes the Company’s restricted stock activity for the year ended December 31, 2011: Non-vested Options Numberof Shares Weighted-AverageFairValue Non-vested at January 1, 2010 300,000 $0.48 Granted — — Vested (150,000) 0.48 Forfeited — — Non-vested at December 31, 2010 150,000 $0.48 Granted — — Vested (150,000) 0.48 Forfeited — — Non-vested at December 31, 2011 — $— Note 15—Segment Information and Geographical informationThe Company has two reportable segments: Fibrocell Therapy and Agera. The Fibrocell Therapy segment specializes in the development andcommercialization of autologous cellular therapies for soft tissue regeneration. The Agera segment maintains proprietary rights to a scientifically-basedadvanced line of skincare products. There is no intersegment revenue. The following table provides operating financial information for the continuingoperations of the Company’s two reportable segments: Segment Year Ended December 31, 2011 FibrocellTherapy Agera Consolidated Total operating revenue $— $812,235 $812,235 Depreciation and amortization expense 157,756 — 157,756 Segment income (loss) from continuing operations $(31,254,865) $(54,854) $(31,309,719) Segment Year Ended December 31, 2010 FibrocellTherapy Agera Consolidated Total operating revenue $— $936,369 $936,369 Depreciation and amortization expense 8,085 — 8,085 Segment income (loss) from continuing operations $(12,840,598) $9,770 $(12,830,828) F35Table of ContentsGeographical information concerning the Company’s revenue is as follows: Year Ended December 31, 2011 2010 United States $192,172 $237,286 United Kingdom 526,189 669,921 Other 93,874 29,162 $812,235 $936,369 During the year ended December 31, 2011, revenue from one foreign customer and one domestic customer represented 65% and 17% of consolidatedrevenue, respectively. During the year ended December 31, 2010, revenue from one foreign customer and one domestic customer represented 72% and 17% ofconsolidated revenue, respectively. Segment FibrocellTherapy Agera Consolidated Total assets: December 31, 2011 $19,749,479 $524,018 $20,273,497 December 31, 2010 7,681,502 596,643 8,278,145 As of December 31, 2011 and 2010, one foreign customer represented 85% and 88%, respectively, of accounts receivable, net.Note 16—Subsequent EventsOur corporate headquarters and manufacturing operations are located in one location, Exton, Pennsylvania. On February 17, 2012 the Companyrenegotiated the lease and extended it for a period of ten years until March 31, 2023. The lease is non-cancelable and the minimum annual lease payments aresummarized in Note 11. F36Exhibit 10.17AMENDMENT TO LEASETHIS AMENDMENT TO LEASE (the “Amendment”), is effective as of April 1, 2011, and is by and between THE HANKIN GROUP(“Landlord”) and FIBROCELL SCIENCE, INC., formerly known as ISOLAGEN, INC. (“Tenant”).BACKGROUNDLandlord and Tenant (then known as Isolagen, Inc.) entered into a certain lease agreement dated April 6, 2005 (the “Current Lease”) pertaining toapproximately 86,500 rentable square feet of space located at 405 Eagleview Boulevard in Eagleview Corporate Center, Route 100, Exton, UwchlanTownship, Chester County, Pennsylvania.Isolagen, Inc. filed a petition in bankruptcy under Chapter 11 of the U.S. Bankruptcy Code, following which Tenant successfully reorganized andemerged from bankruptcy under the name Fibrocell Science, Inc. Landlord and Tenant have agreed to extend the Term of the Current Lease, originallyscheduled to expire March 31, 2013, until March 31, 2023, upon the terms and conditions hereinafter set forth.NOW THEREFORE, the parties hereto, each intending to be legally bound hereby, agree that the Current Lease is hereby amended and modified asfollows:1. Extension of Term.The Term of the Lease is hereby extended for a period of ten (10) years until March 31, 2023.2. Option to Extend.(a) Provided that Landlord has not given Tenant notice of default more than two (2) times following the date of execution of this Amendment, andthere then exists no event of default by Tenant under the Lease nor any event that with the giving of notice and/or the passage of time would constitute an eventof default, Tenant shall have the right and option to extend the Term for one (1) additional period of sixty (60) months. Tenant shall exercise this right bygiving Landlord prior written notice, not sooner than fifteen (15) nor later than twelve (12) months in advance of then scheduled expiration of the Term, ofTenant’s election to extend the Term. The parties agree that time is of the essence and that this option is personal to Tenant and is non-transferable to anyassignee or sublessee (regardless of whether any such assignment or sublease was made with or without Landlord’s consent) or other party.(b) Such extension shall be under the same terms and conditions as provided in the Lease except that: (1) the Minimum Annual Rent payable byTenant shall be at the then fair market value (and in no event less than the Minimum Annual Rent payable during the immediately preceding Term) and(2) upon exercise of the option to extend, there shall be no further options to extend. 1(c) For the purposes of this Lease, the term “fair market value” shall mean Landlord’s reasonable determination of fair market value of rent foroffice/laboratory/warehouse buildings in the Eagleview Corporate Center. Landlord shall notify Tenant in writing within thirty (30) days after Tenant’s exerciseof its option to extend as to Landlord’s determination of such fair market value rent. Tenant shall execute a lease renewal agreement in form prescribed byLandlord and reasonably acceptable to Tenant utilizing such determination of fair market value within twenty (20) days after Tenant’s receipt of Landlord’snotice; if Tenant does not exercise its option to extend by the date set forth above, or having exercised its option, does not execute a lease renewal agreementwithin the time period required above, Tenant shall be deemed to have revoked its option to extend, and the Lease shall terminate, without further options toextend, at the expiration of the then current Term.(d) The provisions of this Section 2 supersede in their entirety the provisions of Section 45 of the Current Lease, which is hereby agreed to bevoid and of no further force and effect.3. Rent.(a) Paragraph 3(b) of the Current Lease is hereby deleted and amended and restated to provide as follows:(b) For each of the lease years beginning April 1, 2011 and April 1, 2012 (the “Carryover Period”), respectively, Minimum Annual Rent shallaccrue in an amount equal to the Base Rent for Adjustment Purposes, increased by one half the CPI Adjustment, but in no event shall the Minimum AnnualRent for either such year be (1) less than the Minimum Annual Rent in effect for the preceding year, nor (2) greater than $1,384,000.00 per year. For thepurposes of this Section 3(b), the Base Rent for Adjustment Purposes for the lease year beginning April 1, 2011 is $1,194,350.40, being the MinimumAnnual Rent in effect for the prior lease year beginning April 1, 2010. Notwithstanding the foregoing, during each year of the Carryover Period, Tenant shallbe permitted to pay on account of Minimum Annual Rent the sums as provided in the schedule below (without any CPI Adjustment to such amounts in theschedule), and defer payment of the difference between Minimum Annual Rent calculated in accordance with this paragraph and Minimum Annual Rent as setforth in the schedule (hereinafter “Deferred Rent Amount”) until the expiration of the Term of the Lease as extended by this Amendment, without the occurrenceof an Event of Default by Tenant, at which time Tenant’s obligation to pay the Deferred Rent Amount shall be excused. The parties agree that upon theoccurrence of an Event of Default, the Deferred Rent Amount shall be included as part of the unpaid rent due and payable to Landlord. After the CarryoverPeriod, during each remaining year of the Lease, Tenant shall be permitted to pay on account of Minimum Annual Rent the sums as provided in the schedulebelow (without any CPI Adjustment to such amounts in the schedule). 2For the purpose of this Section 3(b), the following terms shall have the meanings defined below:(i) The “CPI U” shall mean the Consumer Price Index established by the U.S. Department of Labor Bureau of Labor Statistics for allurban consumers for the Philadelphia metropolitan area (CPI-U) (1982-1984 = 100).(ii) The “Base Index” shall mean, for the lease year beginning April 1, 2011, the CPI U for March, 2010, and for each subsequent year,the CPI U for the month of March one year prior to the Comparison Index.(iii) The “Comparison Index” shall mean the CPI U for month of March immediately preceding the commencement of each lease yearbeginning April 1, 2011.(iv) The “CPI Adjustment” shall mean, for each year of the Term beginning April 1, 2011, an increase in the Base Rent for AdjustmentPurposes by the percentage increase in the Comparison Index over the Base Index, applicable to such year.The Minimum Annual Rent schedule (the amounts in which are not subject to a CPI Adjustment) is as follows: Period Rate per square foot Minimum Annual Rent Monthly Installment 4/1/11 - 3/30/13 $12.00 $1,038,000.00 $86,500.00 4/1/13 - 3/31/15 $12.50 $1,081,250.00 $90,104.17 4/1/15 - 3/31/19 $14.50 $1,254,250.00 $104,520.83 4/1/19 - 3/31/23 $17.00 $1,470,500.00 $122,541.67 (c) In addition to the Minimum Annual Rent, Tenant shall continue to pay Tenant’s Proportionate Share of Real Estate Taxes and OperatingExpenses, as well as all other items of Additional Rent on the Leased Space, determined in accordance with the terms of the Lease.4. Condition of Leased Space. Tenant acknowledges and agrees that it shall occupy the Leased Space in “as is” condition.5. Tenant Alterations. Section 8 of the Current Lease is hereby deleted in its entirety, and the following substituted in its place:8. Tenant Alterations.(a) Except as hereafter provided, Tenant shall make no alterations, additions or improvements (“Tenant Alterations”) to the Leased Spacewithout the consent of Landlord, which consent, subject to the provisions of subsection (c) below, shall not be unreasonably withheld, delayed orconditioned. 3At the time of Landlord’s consent, Landlord shall designate whether Tenant shall be required to remove the proposed Tenant Alteration upontermination of this Lease, and the absence of such designation in Landlord’s written consent shall be deemed Landlord’s agreement that Tenantshall not be obligated to remove Tenant Alterations upon the termination of this Lease. Landlord also may impose such reasonable conditions aspart of its consent as Landlord deems appropriate, taking into consideration the nature of the proposed Tenant Alteration, including, withoutlimitation, requiring Tenant to furnish Landlord with security for the payment of all costs to be incurred in connection with such work, and, ifEagleview Commercial Construction Company (“Contractor”) declines to perform such work, insurance, and copies of the plans, specificationsand permits necessary for such work. Nothing herein, however, shall be construed to obligate Tenant to construct any Tenant Alteration for whichLandlord has given its consent.(b) Subject to Tenant’s compliance with the provisions of subsection (c) below, Landlord’s consent shall not be required for Tenant Alterationswhich (i) do not adversely impact the structural integrity of the Building or the systems serving the Building or their operation, and (ii) are not visiblefrom the Building exterior.(c) All Tenant Alterations shall be done at Tenant’s expense by Contractor, on the basis of a contract between Tenant and Contractor where thecontract price is based upon the Cost of the Work plus a contractor’s fee, in which the term “Cost of the Work” shall be defined by reference to thedefinition of such term as used in the then current edition of the AIA Contract for Construction, and the fee shall be, with respect to any TenantAlterations which are for laboratory improvements, 8% of the Cost of the Work, and for any other Tenant Alterations, 12% of the Cost of the Work.The contract between Tenant and Contractor shall be on an “open book” basis, and all subcontracts for more than $25,000.00 shall be subject tocompetitive bidding. Such contract shall also require the Contractor to maintain a reasonable schedule for the performance of Tenant Alterations.Payment for Tenant Alterations by Tenant to Contractor shall be no less frequently than monthly, and shall be pursuant to invoices for completed workor materials properly stored on site. No Tenant Alterations shall be performed by any contractor other than Contractor, unless Contractor declines toperform the proposed Tenant Alterations (“Permitted Outside Contractor Alterations”), provided that Tenant shall not use a contractor to which Landlordobjects in good faith. With respect to Permitted Outside Contractor Alterations, no work shall be performed until the plans therefore have been approvedby Landlord, which approval shall not be unreasonably withheld, delayed or conditioned and shall be deemed approved unless Landlord notifiesTenant of objections to the proposed plans within ten (10) business days after delivery to Landlord of a complete set of the plans therefor, and untilTenant provides to Landlord the evidence of insurance and security for payment for such work as referenced in subsection (a) above. In connection withthe review of plans submitted by Tenant, Landlord shall be reimbursed by Tenant for Landlord’s cost in reviewing such plans at the 4rate of $125.00 per hour; subject to reasonable increase to reflect the then current hourly charge imposed for such review by Landlord for its tenants inthe Center generally, and prior to undertaking any such review, Landlord shall provide a statement of the maximum review hours to be dedicated to suchreview. With respect to Permitted Outside Contractor Alterations, Tenant shall provide Landlord with a copy of Tenant’s application for a buildingpermit therefor, if applicable (together with all attachments thereto), and no review fee shall be charged to Tenant by Landlord in connection therewithnor shall Landlord’s approval of such application be required. Tenant shall provide copies of as-built plans and specifications for all Permitted OutsideContractor Alterations to Landlord within a reasonable time of completion of the work. All Permitted Outside Contractor Alterations shall be done in afirst class, workmanlike manner and shall comply with all insurance requirements then made available to Tenant and all applicable laws, ordinances,rules and regulations of governmental authorities having jurisdiction thereover, and, where applicable, with all reasonable requirements of Landlord.Tenant shall promptly pay for all work done by contractors performing Permitted Outside Contractor Alterations, and obtain and deliver to Landlordpartial releases of lien for all work covered by invoices paid by or on behalf of Tenant for such work executed by all contractors, subcontractors andother persons entitled to file mechanic’s liens for non-payment, and final releases of mechanic’s liens upon completion of such work.(d) If, as a condition of Landlord’s consent, removal of a Tenant Alteration is required at termination of this Lease, Tenant shall promptly removesuch Tenant Alterations and repair any damage occasioned by such removal. In default thereof, Landlord may effect said removal and repairs atTenant’s expense. With respect to any Tenant Alterations which Tenant is not obligated to remove hereunder (including without limitation PermittedOutside Contractor Alterations), such Tenant Alterations, if not removed by Tenant upon the termination of this Lease, shall be deemed abandoned byTenant, and deemed a part of Landlord’s property, notwithstanding any provision of Section 16 to the contrary.(e) Landlord’s consent shall not be required for Tenant Alterations which (i) do not adversely impact the structural integrity of the Building or thesystems serving the Building or their operation, (ii) are not visible from the Building exterior and (iii) qualify under the following:(A) The Tenant Alteration is to be made to portions of the Leased Premises other than the laboratory areas and the cost thereof is $10,000 or lesswith respect to any Tenant Alteration project (or $20,000 or less in the aggregate with respect to Tenant Alteration projects undertaken over any twelve(12) consecutive month period); or(B) The Tenant Alteration is to be made to the laboratory areas of the Leased Premises and the cost thereof is $50,000 or less with respect to anyTenant Alteration project (or $100,000 or less in the aggregate with respect to Tenant Alteration projects undertaken over any twelve (12) consecutivemonth period). 5Tenant Alterations described in this subsection (e) for which Landlord’s consent is not required hereinafter are called “Permitted TenantAlterations.” Notwithstanding the foregoing, painting or carpeting of the interior of the Leased Space and like cosmetic improvements shall not bedeemed Tenant Alterations regardless of the cost thereof. Tenant shall not be obligated to remove Permitted Tenant Alterations upon the termination of thisLease unless an Event of Default has occurred which is then continuing and Landlord so requires such removal. For the purpose of this subsection (e),in calculating the “cost” of any Tenant Alteration project to determine if any proposed Tenant Alteration is a “Permitted Tenant Alteration”, “cost” shallmean the Landlord’s good faith estimate of the entire cost of the Tenant Alteration project or projects under consideration, including all permit fees,design and engineering costs, general conditions, and the cost of all work to be performed by all trade contractors to furnish and install materials neededto complete such project, and a reasonable fee to a general contractor or construction manager for overhead and profit.5. Section 23 of the Lease is hereby deleted, and the following substituted in its place:23. CONFESSION OF JUDGMENT:UPON AN EVENT OF DEFAULT, TENANT HEREBY AUTHORIZES AND EMPOWERS ANY PROTHONOTARY ORATTORNEY OF ANY COURT OF RECORD TO APPEAR FOR TENANT IN ANY AND ALL ACTIONS FOR RENT IN ARREARS ORTREATED AS IF IN ARREARS AND CHARGES, WHETHER OR NOT PAYABLE AS RENT, AND TO CONFESS JUDGMENTAGAINST TENANT FOR ALL ARREARS OR SUCH SUMS TREATED AS IF IN ARREARS AND THE SAID CHARGES, AND FORINTEREST AND COSTS, TOGETHER WITH AN ATTORNEY’S COMMISSION OF TEN PER CENT (10%) OF THE AGGREGATEOF THE FOREGOING SUMS AND CHARGES. SUCH AUTHORITY SHALL NOT BE EXHAUSTED BY ONE EXERCISE THEREOF,BUT JUDGMENT MAY BE CONFESSED FROM TIME TO TIME AS OFTEN AS ANY RENT IN ARREARS OR RENT TREATED ASIF IN ARREARS OR CHARGES FALL DUE AND ARE NOT PAID. SUCH POWERS MAY BE EXERCISED DURING AS WELL ASAFTER THE EXPIRATION OR TERMINATION OF THE TERM AND DURING, AND AT ANY TIME, AFTER ANY EXTENSION ORRENEWAL OF THE TERM.WHEN THE LEASE SHALL BE TERMINATED BY COVENANT OR CONDITION BROKEN, EITHER DURING THE ORIGINALTERM OR 6ANY RENEWALS OR EXTENSIONS THEREOF, AND ALSO WHEN AND AFTER THE TERM HEREBY CREATED OR, ANYRENEWAL OR EXTENSION THEREOF SHALL HAVE EXPIRED, IT SHALL BE LAWFUL FOR ANY ATTORNEY OF ANY COURTOF RECORD AS ATTORNEY FOR TENANT TO CONFESS JUDGMENT IN EJECTMENT AGAINST TENANT AND ALL PERSONSCLAIMING UNDER TENANT, AND A JUDGMENT FOR THE RECOVERY BY LANDLORD OF POSSESSION MAY ISSUEFORTHWITH WITHOUT ANY PRIOR WRIT OR PROCEEDINGS WHATSOEVER. IF FOR ANY REASON AFTER SUCH ACTIONSHALL HAVE BEEN COMMENCED, IT SHALL BE CANCELED OR SUSPENDED AND POSSESSION OF THE LEASED SPACEREMAINS IN OR IS RESTORED TO TENANT, LANDLORD SHALL HAVE THE RIGHT UPON ANY SUBSEQUENT DEFAULT ORTERMINATION OF THE LEASE, OR ANY RENEWAL OR EXTENSION HEREOF, TO BRING ONE OR MORE ACTIONS INCONFESSION OF JUDGMENT FOR EJECTMENT AS HEREINBEFORE SET FORTH TO RECOVER POSSESSION OF THELEASED SPACE. IF IN ANY ACTION TO CONFESS JUDGMENT IN EJECTMENT, LANDLORD SHALL CAUSE TO BE FILED INSUCH ACTION AN AFFIDAVIT SETTING FORTH THE FACTS NECESSARY TO AUTHORIZE THE ENTRY OF JUDGMENT ANDIF A TRUE COPY OF THIS INSTRUMENT (AND THE TRUTH OF THE COPY STATED IN SUCH AFFIDAVIT SHALL BESUFFICIENT PROOF) BE FILED IN SUCH ACTION, IT SHALL NOT BE NECESSARY TO FILE THE ORIGINAL AS A WARRANTOF ATTORNEY, ANY LAW, RULE OF COURT, CUSTOM OR PRACTICE TO THE CONTRARY NOTWITHSTANDING. TENANTEXPRESSLY RELEASES TO LANDLORD, AND TO ANY AND ALL ATTORNEYS WHO MAY APPEAR FOR TENANT, ALLERRORS IN THE SAID PROCEEDINGS, AND ALL LIABILITY THEREFOR. TENANT EXPRESSLY WAIVES THE BENEFIT OFALL LAWS, NOW OR HEREAFTER IN FORCE, EXEMPTING ANY GOODS WITHIN THE LEASED SPACE OR ELSEWHEREFROM DISTRAINT, LEVY OR SALE.FIBROCELL SCIENCE, INC.By: s/s Declan Daly6. Brokers.Tenant represents and warrants to Landlord that Tenant has not dealt with any broker, firm, company or person in connection with thenegotiation for or the obtaining of this Amendment, other than Newmark, Knight, Frank, Smith, Mack, whose commission shall be paid by Landlordpursuant to a separate agreement between Landlord and such broker, and each party shall indemnify, defend and hold harmless the other from and againstany claim by any other person claiming a commission or other 7form of compensation by virtue of having dealt with such party with regard to this Lease, and any attorneys fees or other expenses incurred by the other partyin connection therewith.7. Miscellaneous.(a) All capitalized terms not defined herein shall have the same meaning as the Current Lease. From and after the date hereof, except to the extentthat the context otherwise requires, the term “Lease” shall mean the Current Lease as modified by this Amendment.(b) Except as expressly modified hereby, the terms and conditions of the Current Lease remain unmodified and in full force and effect, which theparties hereby ratify and confirm. In the event of a conflict between the terms of the Current Lease and this Amendment, the latter shall control.(c) The terms and conditions of the Current Lease, as amended hereby, constitutes the whole agreement between the parties and any furtheramendments or modifications to the terms of the Current Lease must be in writing and duly executed by the parties hereto.(d) This Amendment shall be binding upon and shall inure to the benefit of the parties hereto and their respective heirs and assigns, except asspecifically provided herein or in the Current Lease, and is not intended to benefit any person or entity not a party hereto.(e) This Amendment shall be construed under the laws of the Commonwealth of Pennsylvania without regard to conflicts of laws principles.(f) This Amendment may be executed in any number of counterparts, each of which shall be deemed an original and all of which counterpartstogether shall constitute one and the same instrument. It shall not be necessary for all parties to execute the same counterpart, so long as each party shall haveexecuted at least one counterpart, but in this latter event, each party shall have delivered to it photocopies of counterparts showing signatures of all of theparties.(g) This Amendment, together with the Current Lease, constitutes the entire agreement of Landlord and Tenant with respect to the subject matterhereof, and may not be contradicted by any prior or contemporaneous representation, statement or agreement of the parties relating to the subject matter hereof,and may not be modified except by a written instrument executed by the parties hereto.THE REMAINDER OF THIS PAGE INTENTIONALLY LEFT BLANK 8IN WITNESS WHEREOF, Landlord and Tenant have executed this Amendment this 17 day of February, 2012, effective as of April 1, 2011. LANDLORD: THE HANKIN GROUP, a Pennsylvania limited partnership By: The Hankin Group, Inc., its general partner BY: /s/ Robert S. Hankin Robert S. Hankin, President TENANT: FIBROCELL SCIENCE, INC.WITNESS/ATTEST: BY: /s/ Declan Daly/s/ Sue White NAME: Declan Daly TITLE: Chief Financial Officer DATE: February 17, 2012 9thExhibit 23.1Consent of Independent Registered Public Accounting FirmWe hereby consent to the incorporation by reference in the Registration Statement on Form S-8 (File No. 333-172776) of Fibrocell Science, Inc. of our reportdated March 30, 2012, relating to the consolidated financial statements appearing in the Company’s Annual Report on Form 10-K for the year endedDecember 31, 2011. Our report contains an explanatory paragraph regarding the Company’s ability to continue as a going concern. /s/ BDO USA, LLPHouston, TexasMarch 30, 2012Exhibit 31.1OFFICER’S CERTIFICATION PURSUANT TOSECTION 302 OF THE SARBANES-OXLEY ACT OF 2002I, David Pernock, Chief Executive Officer of Fibrocell Science, Inc., certify that:1. I have reviewed this Annual Report on Form 10-K of Fibrocell Science, Inc.;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 the statementsmade, in light of the circumstances under which such statements were made not misleading with respect to the period covered by this report;3. Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the financialcondition, 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 and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in ExchangeAct 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 registrantand have:a) Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensurethat material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others within those entities,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 our supervision,to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes inaccordance 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 the effectivenessof the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; andd) Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recent fiscalquarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, theregistrant’s internal control over financial reporting; and5. The registrant’s other certifying officer 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 reasonably likelyto adversely affect the registrant’s ability to record, process, summarize and report financial information; andb) Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal control overfinancial reporting. Dated: March 30, 2012By: /s/ David PernockDavid Pernock, Chief Executive OfficerExhibit 31.2OFFICER’S CERTIFICATION PURSUANT TOSECTION 302 OF THE SARBANES-OXLEY ACT OF 2002I, Declan Daly, Chief Financial Officer of Fibrocell Science, Inc., certify that:1. I have reviewed this Annual Report on Form 10-K of Fibrocell Science, Inc.;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 the statementsmade, in light of the circumstances under which such statements were made not misleading with respect to the period covered by this report;3. Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the financialcondition, 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 and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in ExchangeAct 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 registrantand have:a) Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensurethat material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others within those entities,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 our supervision,to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes inaccordance 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 the effectivenessof the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; andd) Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recent fiscalquarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, theregistrant’s internal control over financial reporting; and5. The registrant’s other certifying officer 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 reasonably likelyto adversely affect the registrant’s ability to record, process, summarize and report financial information; andb) Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal control overfinancial reporting. Dated: March 30, 2012By: /s/ Declan DalyDeclan Daly, Chief Financial OfficerExhibit 32.1CERTIFICATION PURSUANT TO SECTION 1350 OFCHAPTER 63 OF TITLE 18 OF THE UNITED STATES CODEFor purposes of 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002, the undersigned, David Pernock, ChiefExecutive Officer of Fibrocell Science, Inc. (the “Company”), hereby certifies that: i.the Annual Report on Form 10-K of the Company for the year ended December 31, 2011, as filed with the Securities and Exchange Commissionon the date hereof (the “Report”) fully complies with the requirements of Section 13(a) or 15(d) of the Securities Exchange Commission Act of1934; and ii.the information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of the Company.Dated: March 30, 2012 By: /s/ David Pernock David Pernock Chief Executive Officer Fibrocell Science, Inc.A signed original of this written statement required by Section 906 has been provided to Fibrocell Science, Inc. and will be retained by FibrocellScience, Inc. and furnished to the Securities and Exchange Commission or its staff upon request.Exhibit 32.2CERTIFICATION PURSUANT TO SECTION 1350 OFCHAPTER 63 OF TITLE 18 OF THE UNITED STATES CODEFor purposes of 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002, the undersigned, Declan Daly, ChiefFinancial Officer of Fibrocell Science, Inc. (the “Company”), hereby certifies that: i.the Annual Report on Form 10-K of the Company for the year ended December 31, 2011, as filed with the Securities and Exchange Commissionon the date hereof (the “Report”) fully complies with the requirements of Section 13(a) or 15(d) of the Securities Exchange Commission Act of1934; and ii.the information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of the Company.Dated: March 30, 2012 By: /s/ Declan Daly Declan Daly Chief Financial Officer Fibrocell Science, Inc.A signed original of this written statement required by Section 906 has been provided to Fibrocell Science, Inc. and will be retained by FibrocellScience, Inc. and furnished to the Securities and Exchange Commission or its staff upon request.

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