HELIXBIOPHARMA
Annual Report 2017
Breaking Down Cancer Barriers
Message to Shareholders
Focus and accelerate. These are the defining strategic ac�ons that the management team has undertaken in 2017.
Upon the transi�on of key management members in early 2017, a review was conducted to examine the
opera�ons of the company. The review resulted in streamlining the Company’s opera�on, priori�zing key
development programs and establishing measurable near term and long-term objec�ves.
The key value driver of the company is L-DOS47. Management is priori�zing all available resources to accelerate
the clinical development of this drug candidate. Three clinical studies in non-small cell lung cancer (NSCLC) are
currently underway to establish the safety and efficacy of this compound as a standalone therapeu�c or as a
combina�on product with chemotherapy. Concurrent preclinical research shows L-DOS47 can influence the body
immune defense against cancer and therefore a combina�on of L-DOS47 with immunotherapy such as checkpoint
inhibitors may benefit pa�ents.
In addi�on to L-DOS47, the Company’s Polish subsidiary is on-track to develop V-DOS47. V-DOS47 is supported in
part by a European agency grant. Due to the design of V-DOS47, this compound may be useful in trea�ng several
different solid tumors including breast cancer. V-DOS47 will be ready for formal preclinical studies and eventual
clinical evalua�ons, pending results from ongoing experiments.
In 2018, the company expects to receive addi�onal data from ongoing L-DOS47 trials. V-DOS47 will have also
made significant preclinical progress. This will help validate the DOS47 pla�orm and drive partnership discussions.
Management is preparing for an intensive and exci�ng year.
In addi�on to DOS47 development, the Company is also leveraging its knowledge in tumor microenvironment and
know-how in single domain an�body technology to develop novel cell-based therapies. The Company has
partnered with the Moffi� Cancer Ins�tute and the Na�onal Research Council Canada to advance this program.
Through our Polish subsidiary, the Company is establishing �es with Polish hospitals and stakeholders to plan for a
cell therapy unit. Currently the Company is reviewing strategic op�ons to best posi�on Helix in this exci�ng new
field of cancer treatment.
While the company has made significant strides in our development programs, we lack sufficient funds to fully
implement our objec�ves. The Company is ac�vely seeking new funding. We are grateful for our shareholders
and partners who are helping us to meet our financial needs. We are op�mis�c and management will con�nue to
work diligently to meet our goals.
I want to personally thank all our staff, shareholders and agents for your support.
Sincerely,
Heman Chao, PhD
Chief Execu�ve and Chief Scien�fic Officer
This le�er contains certain forward-looking statements. By their nature,forward-looking statements require us to make assump�ons and are
subject to inherent risks and uncertain�es. Please refer to the cau�on regarding Forward-Looking Statements and Informa�on on page 2 of this
Annual Report for a discussion of such risks and uncertain�es and the material factors and assump�ons related to these statements.
TABLE OF CONTENTS
MESSAGE TO SHAREHOLDERS……………………………………….…………………… Inside Front Cover
MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND OPERATIONS
FORWARD LOOKING INFORMATION……...…………………………………………………………………………
OVERVIEW…………………………………………………………………………………......………….…….……….
RESEARCH AND DEVELOPMENT ACTIVITIES…….……………………….……………………….………….....
SELECTED FINANCIAL INFORMATION AND SUMMARY OF QUARTERLY RESULTS ……………….…….. 13
14
RESULTS FROM OPERATIONS ………………………………………………………………………….…….…….
15
CRITICAL ACCOUNTING ESTIMATES ………………………………………………………………….…….……..
15
SIGNIFICANT ACCOUNTING POLICIES……………………………………………………………………….….….
15
NEW ACCOUNTING STANDARDS AND PRONOUNCEMENTS NOT YET ADOPTED …………………….….
16
LIQUIDITY AND CAPITAL RESOURCES…………………………………………………………………..……...….
17
RELATED PARTY TRANSACTIONS ……………………………………………………………………………….…
17
FINANCIAL INSTRUMENTS ……………………………………………………………………………..………….…
18
INTELLECTUAL PROPERTY…...………………………………………………………………………………………
19
OFF BALANCE SHEET ARRANGEMENTS ……………………………………………………………………….…
19
TABULAR DISCLOSURE OF CONTRACTUAL OBLIGATIONS………………………………………..……….….
19
QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISKS………………………….….…
21
OUTSTANDING SHARE DATA …………………………………………………………………………….……….…
SUBSEQUENT EVENTS …………………………………………………………………………………………….…
21
DISCLOSURE CONTROLS AND PROCEDURES AND
2
4
5
INTERNAL CONTROL OVER FINANCIAL REPORTING …………………………………….…………….….
RISKS AND UNCERTAINTIES …………………………………………………………...…………….….……….…
RISK FACTORS IN OTHER PUBLIC FILINGS………………………………………...…………….….……..…….
ADDITIONAL INFORMATION ………………………………………...…………….….……..……………………….
21
22
30
31
CONSOLIDATED FINANCIAL STATEMENTS OF HELIX BIOPHARMA CORP
MANAGEMENT’S RESPONSIBILITY FOR FINANCIAL INFORMATION ……...…………………………..…..… 33
INDEPENDENT AUDITOR’S REPORT ……...………………………………………………………….…….…...… 34
CONSOLIDATED STATEMENT OF FINANCIAL POSITION ……...……………………………….…………....… 35
CONSOLIDATED STATEMENT OF NET LOSS AND COMPREHENSIVE LOSS ……...……………….…....… 36
CONSOLIDATED STATEMENT OF CHANGES IN SHAREHOLDERS’ EQUITY ……...…………………..…… 37
CONSOLIDATED STATEMENT OF CASH FLOWS ……...…………………………………………………...….… 38
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS ……...…………………………………..……....….… 39
CORPORATE INFORMATION……………………………………………………………...… Inside Back Cover
Page | 1
MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION
AND RESULTS OF OPERATIONS
This Management’s Discussion and Analysis of Financial Condition and Results of Operations (“MD&A”) should be read in
conjunction with the consolidated financial statements of Helix BioPharma Corp. (the “Company” or “Helix”) for the years ended
July 31, 2017 and 2016 and the accompanying notes thereto. This MD&A is based on financial statements which have been
prepared in accordance with International Financial Reporting Standards (“IFRS”). All amounts are depicted in Canadian currency
unless otherwise noted.
Additional information relating to the Company can be found in the Company’s Annual Information Form, which is available on
SEDAR at www.sedar.com.
FORWARD-LOOKING INFORMATION
This MD&A contains forward-looking information (collectively, “forward-looking information”) within the meaning of applicable
Canadian securities laws. Forward-looking information means disclosure regarding possible events, conditions or financial
performance that is based on assumptions about future economic conditions and courses of action and includes financial
projections and estimates; statements regarding plans, goals, objectives, intentions and expectations with respect to the
Company’s future business, operations, research and development, including the focus of the Company on L-DOS47 which is the
Company’s primary drug candidate, Topical Interferon Alpha-2b and other information relating to future periods. Forward-looking
information includes, without limitation, statements concerning (i) the Company’s ability to continue to operate on a going concern
basis being dependent mainly on obtaining additional financing; (ii) the Company’s growth and future prospects being dependent
mainly on the success of L-DOS47; (iii) the Company’s priority continuing to be L-DOS47; (iv) the Company’s development
programs, including but not limited to, extension of the current drug candidate(s) to other indications and the identification and
development of further tumour-targeting antibodies for DOS47; (v) the anticipated timeline for completion of enrolment and other
matters relating to the Company’s European Phase I/II clinical study for L-DOS47 in Poland, including the number of cohorts
required to reach Maximum Tolerable Dose (“MTD”) and the Company’s U.S. Phase I clinical study for L-DOS47, (vi) seeking
strategic partner support and therapeutic market opportunities; (vii) the nature, design and timing of future clinical trials (including
the Company’s anticipated reassessment of the re-design of the LDOS003 study to focus on advanced stage lung cancer patients
by combining L-DOS47 with Vinorelbine/Cisplatin (“VIN/CIS”) and commercialization plans; (viii) the Company’s advancement in
the area of cell based therapy via its subsidiary Helix Immuno-Oncology S.A. (formerly Helix Immuno-Oncology Sp. z.o.o. and
Helix Polska Sp. z o.o.) (“HIO”) (ix) future expenditures, insufficiency of the Company’s current cash resources and the need for
financing and the Company’s possible response for such matters; (x) future financing requirements, the seeking of additional
funding (including the possible receipt of grants) and anticipated future operating losses; (xi) changes in the application of
accounting standards and interpretations; and (xii) industry performance, competition (including potential developments relating
to immunotherapies and the Company’s possible response to such developments), prospects, and general prevailing business
and economic conditions. Forward-looking information can further be identified by the use of forward-looking terminology such
as “expects”, “plans”, “designed to”, “potential”, “believe”, “intended”, “continues”, “opportunities”, “anticipated”, “2017”, “2020”,
“next”, “ongoing”, “seek”, “objective”, “estimate”, “future”, or the negative thereof or any other variations thereon or comparable
terminology referring to future events or results, or that events or conditions “will”, “may”, “could”, “would”, or “should” occur or be
achieved, or comparable terminology referring to future events or results.
Forward-looking information includes statements about the future and are inherently uncertain, and are necessarily based upon a
number of estimates and assumptions that are also uncertain. Although the Company believes that the expectations reflected in
such forward-looking information are reasonable, such statements involve risks and uncertainties, and undue reliance should not
be placed on such statements. Forward-looking information, including financial outlooks, are intended to provide information about
management’s current plans and expectations regarding future operations, including without limitation, future financing
requirements, and may not be appropriate for other purposes. The Company’s actual results could differ materially from those
anticipated in the forward-looking information contained in this MD&A as a result of numerous known and unknown risks and
uncertainties, including, but not limited to:
the Company’s need for additional capital which may not be available in a timely manner or at all (whether from additional
issuances of the Company’s securities, grant applications or otherwise) and which, if not obtained, will have a material
adverse impact on the Company and its ability to continue as a going concern;
the risk that the Company may have to suspend or terminate one or more of its clinical trials for lack of funding, as the
Company does not have sufficient funds to complete them and will need to raise additional funding, which is not assured;
uncertainty as to whether the Company’s drug product candidate(s), especially L-DOS47, will be successfully developed
and marketed;
developments in immunotherapies may result in significant changes in the treatment of cancer and may result in a
reduction, which may be significant, in the potential patient population and/or treatment protocols available to
chemotherapies and other treatments currently in development, such as the Company’s primary drug product L-DOS47;
the possibility of dilution to current shareholders from future equity financings;
Page | 2
the impact of the ongoing volatility in the economic environment which has negatively affected the availability and terms
of debt and equity financings and may have a negative effect on the Company’s ability to raise further financing and its
research and development initiatives;
risk relating to the difficulty in enrolling patients in clinical trials which may result in delays or cancellation of clinical trials;
intellectual property risks, including the possibility that patent applications may not result in issued patents, that issued
patents may be circumvented or challenged and ultimately struck down, that any expiry of an issued patent, may
negatively impact the further development or commercialization of the underlying technology, and that the Company may
not be able to protect its trade secrets or other confidential proprietary information;
research and development risks, including without limitation, the fact that the Company’s drug product candidate(s) are
complex compounds and the Company faces difficult challenges in connection with the manufacture of clinical batches,
and the risk of obtaining negative findings or factors that may become apparent during the course of research or
development, any of which may result in the delay or discontinuation of the research or development projects;
partnership/strategic alliance risks and the need to secure new strategic relationships, which are both not assured;
the Company’s dependence on third parties, including without limitation, contract research organizations, contract
manufacturing organizations, clinical trial consultants, collaborative research consultants, regulatory affairs advisors, and
others, whose performance and interdependence can critically affect the Company’s performance and the achievement
of its milestones;
the Company’s dependence on assurances from third parties regarding licensing of proprietary technology owned by
others, including the Company’s dependence on its license of the L-DOS47 antibody;
the need for future clinical trials, the occurrence and success of which cannot be assured, and the fact that results seen
in earlier clinical trials may not be repeated in later trials;
manufacturing risks, the need to manufacture to regulatory standards, uncertainty whether the manufacturing process
for the Company’s drug candidates can be further scaled-up successfully or at all and the risk that clinical batches of the
Company’s drug candidate may not be able to be produced in a timely manner or at all, which would have a negative
effect on the timing and/or occurrence of planned clinical trials and the potential commercialization of the drug candidates;
uncertainty as to the size and existence of a market opportunity for, and market acceptance of the Company’s drug
product candidate(s) including as a result of possible changes in the market for the Company’s drug candidates resulting
from development in immunotherapies or other future cancer treatments;
uncertainty as to the availability of raw materials that the Company utilizes to manufacture its products, and in particular,
Good Manufacturing Practice (“GMP”) grade materials, on acceptable terms or at all, and that the Company may not be
able to timely obtain alternative suppliers upon commercially viable terms or at all, which could have a material adverse
effect on the further development and commercialization of any or all of the Company’s drug product candidate(s);
product liability and insurance risks;
uncertainty as the Company’s ability to maintain product liability insurance required by third parties and the risk of
the risk of lawsuits and other legal proceedings against the Company;
the effect of competition, especially from the new immunotherapy treatments for non-small cell lung cancer (“NSCLC”);
the risk of unknown side effects arising from the development, manufacture or use of the Company’s products;
corresponding agreement being terminated;
the risk of misconduct on the part of employees and consultants, including non-compliance with regulatory standards
and requirements;
the need to attract and retain key personnel and reliance on key personnel;
that the Company has no sales, marketing and distribution experience;
government regulation, including drug price regulation, and the need for regulatory approvals for both the development
and profitable commercialization of products, which are not assured;
risks associated with the fact that the U.S. Food and Drug Administration (the “FDA”) and any other regulatory agency
that the Company has consulted are not bound by their scientific advice, nor are any approvals given by one regulatory
body binding on another;
rapid technological change and competition from pharmaceutical companies, biotechnology companies and universities,
which may make the Company’s technology or products obsolete or uncompetitive;
risks associated with claims, or potential claims, of infringement of third party intellectual property and other proprietary
rights;
the risk of unanticipated expenses;
the impact on the Company’s finances resulting from shifts in foreign exchange rates, credit risk and interest rate risk,
risks relating to changes in the Company’s tax rates;
risk relating to a failure to maintain an effective system of internal controls;
risks relating to the requirements of being a public company;
Page | 3
and other risk factors that are discussed above and elsewhere in this MD&A or identified in the Company’s other public filings
under the Company’s profile on SEDAR at www.sedar.com (together the “Helix Risk Factors”), any of which could cause actual
results to vary materially from current results or the Company’s anticipated future results. Certain material factors, estimates or
assumptions have been applied in making forward-looking information in this MD&A, including, but not limited to, the safety and
efficacy of the Company’s drug product candidate(s); the Company’s cost and timing in connection with the Phase I U.S. clinical
trial for L-DOS47; the cost and timing for achieving MTD in the Company’s European Phase I/II clinical trial for L-DOS47 in Poland;
that additional and sufficient financing will be obtained in a timely manner or at all to allow the Company to continue operations;
the timely provision of services and supplies or other performance of contracts by third parties; future costs; the absence of any
material changes in business strategy or plans, the timely receipt of required regulatory approvals, strategic partner support; and
that the Helix Risk Factors will not cause the Company’s actual results or events to differ materially from the forward-looking
information.
For all of the reasons set forth above, which do not represent an exhaustive list of factors that may affect the forward-looking
information, investors should not place undue reliance on forward looking information. The forward-looking information is based
on the beliefs, assumptions, opinions and expectations of the Company’s management at the time they are made, and the
Company does not assume any obligation to update any forward-looking information should those beliefs, assumptions, opinions
or expectations, or other circumstances change, except as required by law.
Data relevant to estimated market sizes in connection with Company’s lead products under development are presented in this
MD&A. These data have been obtained from a variety of published resources, including published scientific literature, websites
and information generally available through publicized means. The Company attempts to source reference data from multiple
sources whenever possible for confirmatory purposes. Although the Company believes the data is reliable, the Company has not
independently verified the accuracy and completeness of this data.
OVERVIEW
Helix is an immuno-oncology company primarily focused in cancer drug development. The Company is developing products for
the treatment and prevention of cancer based on its proprietary technologies. The Company’s product development initiatives are
focused primarily on technologies that modulate the tumour microenvironment.
To date, the Company’s proprietary technology platform, DOS47 has yielded two new drug product candidates, L-DOS47 and V-
DOS47. L-DOS47 is currently under clinical study for the treatment of NSCLC. L-DOS47 has completed extensive preclinical
testing and manufacturing development, following which, regulatory approvals to conduct a Phase I/II clinical trial In Poland and a
Phase I study in the U.S. were obtained. V-DOS47 has been licensed to the Company’s wholly owned Polish subsidiary for
preclinical and clinical development. The V-DOS47 drug candidate uses the Company’s proprietary DOS47 technology
conjugated to anti-VEGFR2 antibody targeting a wide range of cancers.
The Company continues to actively pursue additional new antibody based technologies for cell-based therapies. In September
2016 the Company announced that it was developing a novel Chimeric Antigen Receptor T-Cell (CAR-T) therapeutic. The
Company believes CEACAM6 specific CAR immune cells may have broad applications in a number of cancer types and is
working on two camelid single domain antibodies that target CEACAM6.
The Company currently believes that its growth and future prospects are mainly dependent on the success of its DOS47 drug
product candidates, and the successful development of cell-based therapies.
On December 23, 2016, the Company announced, it signed an exclusive out-license agreement with Xisle Pharma Ventures Trust
(“Xisle”) for the Company's late-stage, Biphasix™ technology platform, including the lead product candidate, interferon alpha.
Xisle is responsible for the continued clinical development and subsequent commercialization of the product for the treatment of
HPV-induced, low-grade, cervical intraepithelial lesions. As part of its asset development strategy, Xisle has initiated collaboration
with senior pharmaceutical executives at Altum Pharmaceuticals Inc., who possess regulatory, clinical, and product development
expertise. Under the terms of the agreement, Xisle paid an up-front fee of USD125,000 and agreed to pay subsequent milestone
payments as they advance the technology to registration and market approvals and royalties. As part of the agreement, Helix
retains marketing rights for Belarus, Bulgaria, Czech Republic, former Eastern Germany, Hungary, Moldova, Poland, Romania,
Russia, Slovakia and Ukraine. In addition, the Company also retains non-exclusive rights for co-promotion in Canada.
The Company subsequently assigned the foregoing marketing rights which it retained to HIO, its wholly-owned subsidiary in
Poland pursuant to an agreement between the Company and HIO with the agreement being subject to the restrictions and
limitations associated with the out-license agreement signed between the Company and Xisle. In addition, HIO will be responsible
for commercialization with milestone and royalty payments to be paid back to the Company upon successful product development
through to commercialization.
The Company finances its research and development programs primarily from the issuance of its securities. In addition, the
Company is also looking at alternative sources of additional financing. On July 21, 2016, the Company announced that it’s wholly-
owned subsidiary in Poland had been awarded a funding grant from the Polish National Centre for Research and Development
Page | 4
(“PNCRD”) to develop V-DOS47. There can be no assurance that the Company will be successful in qualifying and/or receiving
any additional grant money or that it will obtain additional financing or that the V-DOS47 program will be successful.
The Company expects to incur additional losses for the foreseeable future and will require additional financial resources to fund
the Company’s ongoing research and development activities and overhead costs.
The Company continues to not have sufficient cash reserves to meet anticipated cash needs for working capital and capital
expenditures through the next twelve months. The Company’s cash reserves as at July 31, 2017 of $897,000 are not sufficient
to see the current research and development initiatives through to completion or properly allocate scarce cash resources efficiently
and as such, the Company will require additional financing in the very near term. Securing additional sufficient financing continues
to be of critical importance to the Company.
Given the possibility of not being able to secure sufficient additional financing, whether on a timely basis or not at all, the Company
may be required to reduce, delay or cancel one or more of its planned research and development initiatives, including clinical trials
along with further reductions in overhead, any of which could impair the current and future value of the Company.
RESEARCH AND DEVELOPMENT ACTIVITIES
Background
The immune system utilizes two strategies in attacking different types of pathogens. The humoral immune system uses antibodies
their
as its main weapon. Antibodies are proteins that bind to extracellular foreign invaders, such as bacteria, and lead to
destruction. The cellular immune system utilizes specialized immune cells, called T-cells to identify and bind to abnormal
cells and subsequently destroy them.
Cancer cells have adopted and developed several strategies for evading the immune system. In some cases, proteins are
expressed on the surface of tumour cells that “turn off” attacking T-cells. By using antibodies to block these interactions
(such as anti-PD1), T-cells are reactivated to kill the tumours. Although anti-PD1 and anti-PDL1 therapies (checkpoint inhibitors)
have improved outcomes for patients, there are many that do not respond to these treatments. One possible explanation suggests
that the unique metabolism of cancer cells creates an acidic tumour microenvironment and this acidity has the effect of
interfering with T-cell function. The Company believes it has developed a novel system to raise pH at the tumour site, thus breaking
the physiologic barrier that acts to defend against tumour-killing T-cells.
Alkalization using Urease
Urease is an enzyme that catalyzes the hydrolysis of urea into carbon dioxide and ammonia ((NH2)2CO + H2O → CO2 + 2NH3).
The Company has conjugated urease to an antibody that specifically targets lung cancer cells, thus delivering the urease directly
to the site of the tumour. L-DOS47, the Company’s first drug product candidate, is currently in a phase I/II monotherapy trial in
Poland and a Phase I combination trial with carboplatin and pemetrexed in the United States. By delivering urease to the tumour
site, the company expects the pH of the tumour microenvironment to increase and activity of tumour-killing T-cells to be enhanced.
The Company believes the urease system can be used with any tumour specific antibody as a general method for modifying
the tumour microenvironment, and as such, could be combined with any of the current checkpoint inhibitor products to improve
patient outcomes.
CAR-T Cells
To date, success in Adoptive Cell Transfer (“ACT”) with engineered T-cells such as Chimeric Antigen Receptor T- cells (“CAR-
T”) has occurred mainly in the area of hematological malignancies. As of the end of 2016, 220 CAR T cell trials were documented
of which approximately 188 are ongoing including nine long
up studies. Of the current trials, 133 target hematological
term follow
malignancies and 78 solid tumors (Hartman et. al, EMBO Mol Med (2017) 9: 1183–1197). Most clinical trials have used autologous,
‐
2 for stimulation resulting in a CAR-T cell
unselected peripheral blood mononuclear cells (“PBMC”) as the starting material and IL
product consisting of CD4 and CD8 T cells with an activated effector T
cell phenotype. In five trials, more than 85% of treated
patients reached complete response (“CR”) as best clinical outcome (Hartman et. al, EMBO Mol Med (2017) 9: 1183–1197).
‐
‐
‐
While CAR-T cell therapy has shown impressive clinical benefit, it is sometimes associated with a variety of toxicities that can be
threatening. Several death cases have been reported, especially in the last year. These were due to neurotoxicity caused by
life
CAR trials sponsored by Juno Therapeutics. Whether neurological toxicities are solely restricted to
cerebral edemas in the CD19
‐
CD19
specific CAR-T cells or generally associated with CAR-T cell therapy remains to be elucidated (Hartman et. al, EMBO Mol
Med (2017) 9: 1183–1197).
‐
‐
A direct connection to another frequent side effect, the cytokine
been the most frequently observed adverse drug reaction. On
many targeted tumor antigens are also expressed on normal tissue (Hartman et. al, EMBO Mol Med (2017) 9: 1183–1197).
‐
release syndrome (“CRS”), also appears likely. CRS has so far
tumor recognition has become a relevant concern, since
target, off
‐
‐
Page | 5
On August 30, 2017, the FDA approved Novartis’ Kymriah (tisagenlecleucel) for certain pediatric and young adult patients with a
form of acute lymphoblastic leukemia (“ALL”). Kymriah is a genetically-modified autologous T-cell immunotherapy. Each dose of
Kymriah is a customized treatment created using an individual patient’s own T-cells.
Solid tumours have created challenges and as such, it is hypothesized that the failure of CAR-T therapies to date may be the result
of the acidic tumour microenvironment surrounding the cancer cell that inhibits CAR T-cell activity. The Company believes it is well
positioned to use its proprietary urease-antibody technology to alkalinize the tumour microenvironment and improve the ability of
CAR-T cells to destroy solid tumours.
Check Point Inhibitors
Dr. Robert J. Gillies of the Moffitt Cancer Center in Tampa Florida demonstrated some interesting results when treating acidic
tumours in animal models. Dr. Gillies demonstrated that in alkalized tumour cells, the activity of antibodies that target PD-L1, is
enhanced. This would indicate that tumour acidosis may protect tumours from immune check-point inhibitors. Since tumour
acidosis is experimentally shown to occur in cancers such as breast, colon, lung and pancreas, the Company believes
methodologies that can alkalize the tumour microenvironment, such as the Company’s proprietary DOS47 platform technology,
may work beneficially with check-point inhibitors.
DOS47 – A broad anti-cancer therapeutic platform
DOS47 is based upon a naturally occurring enzyme isolated from the jack-bean plant called urease that breaks down a natural
substance found in the body, urea, into metabolites that include ammonia and hydroxyl ions. By doing so at the site of cancerous
tissues in the body, the Company believes DOS47 can modify the micro environmental conditions of cancerous cells in a manner that
leads to apoptosis.
DOS47 stimulates an increase in the pH of the microenvironment surrounding the cancerous cells, effectively reversing the acidic
extra-cellular conditions that are believed to act to defend the tumour. This acidic environment can also reduce or negate the
effectiveness of some commonly used anti-neoplastic agents. The local production of ammonia at the site of cancerous tissues
is thought to readily diffuse into the cancer cells to exert a potent cytotoxic effect by interfering with their critical metabolic functions.
Enzymatic action of urease at the site of cancerous cells is potentially repetitive and sustainable due to the plentiful supply of urea.
The Company is pursuing the development of DOS47 both as a monotherapy and as an adjunct therapy in combination with certain
chemotherapeutics and/or radiation regimens, with a view to maximizing the DOS47 commercial potential.
DOS47 candidates are produced by conjugating urease with a targeting antibody or antibody fragment that can specifically direct
the urease to the surface of a cancer cell. Once docked to the cell, the urease produces ammonia enzymatically through the
conversion of urea found throughout the body. These conjugates of antibodies to urease are called DOS47 candidates. By
selecting antibodies that are selective to different tumour cell surface receptors, the Company believes that DOS47 candidates
can be used in several types of solid tumours.
In fiscal 2015, the Company entered into a collaborative research agreement with Affilogic to assess proprietary anti-tumour
targeting agents in combination with DOS47. The agreement calls for a feasibility study using a targeting agent in conjugation
with DOS47. Continuing development of these new conjugates is subject to a successful feasibility study, execution of a formal
development and licensing agreement, and the availability sufficient financial resources.
The Company continues to reach out to third parties in order to identify and test additional tumour-targeting antibodies for
conjugation with DOS47. In the event that antibody candidates worthy of further development are identified, the Company will
need to discuss development and licensing arrangements, which may not be available on terms acceptable to the Company or at
all.
L-DOS47
The Company believes that its DOS47 candidates may have potential anti-cancer activity by stimulating an increase in the pH of
the microenvironment surrounding the cancerous cells. The local production of ammonia at the site of cancerous tissues is thought
to readily diffuse into the cancer cells and may exert a potent cytotoxic effect by interfering with their critical metabolic functions.
In addition, the Company believes that the use of DOS47 candidates may also have a synergistic effect on the efficacy of other
marketed chemotherapeutics, such as vinka alkyloid analogues, where low pH can inhibit the cellular uptake of these agents. The
Company believes the enzymatic action of urease to increase the pH at the site of cancerous cells is repetitive and sustainable
due to the plentiful supply of urea that is furnished by the body.
L-DOS47 is the Company’s first targeted therapeutic immune-conjugate under development based on the DOS47 technology.
L-DOS47 is an antibody protein conjugate where the urease component enzymatically converts naturally occurring urea to
ammonia. The L-DOS47 drug molecule includes a highly specialized camelid-derived single domain antibody, designed to identify
a unique CEACAM6 antigenic site associated with NSCLC cells. By delivering the conjugate in a targeted manner, the Company
Page | 6
believes L-DOS47 stimulates an increase in the pH of the microenvironment surrounding the NSCLC cells, reversing the acidic
extra-cellular conditions that are shown to be favourable for cancer cell survival.
L-DOS47 is intended to offer an innovative approach to the first-line treatment of inoperable, locally advanced, recurrent or
metastatic NSCLC. However, other emerging therapies, including immunotherapy, may alter the treatment paradigm in
NSCLC. Therefore, the eventual approval for L-DOS47 as a first-line treatment for NSCLC will depend on both successful clinical
trials and on the treatment landscape shaped by these new therapies. The Company continues to monitor developments in this
area and to consider their effect on its L-DOS47 program, including its focus on L-DOS47 as a first-line treatment for NSCLC.
In 2005, the Company entered into a worldwide exclusive license with the National Research Council of Canada (“NRC”), through
which it obtained the rights to combine this highly specialized camelid-derived single domain antibody with Helix’s DOS47
technology. As a result, the Company has certain royalty and milestone payment obligations pursuant to the license agreement.
The license agreement with the NRC has been filed under the Company’s profile on SEDAR at www.sedar.com. The NRC filed
patent applications in respect of the antibody in Canada, the United States and other countries. On March 2, 2011, the NRC was
issued a U.S. patent in respect of the antibody.
In addition to being a key for cancer progression by promoting invasiveness and metastatic behaviors of cancer cells, the acidic
tumour microenvironment protects cancer cells from immunotherapy by suppressing the proliferation and cytotoxic activities of
local immune cells. The interactions of programmed cell death protein 1 (PD-1) on Jurkat cells with its ligand PD-L1 were studied.
The human cancer cell lines MDA-MB231 and BxPC-3 were stimulated with Interferon gamma (IFNγ) to express PD-L1 on the
cell surface. The IFNγ-stimulated cell lines were found to inhibit IL-2 production in co-incubated Jurkat cells by as much as 40%
when compared to non-stimulated cells. The addition of L-DOS47/urea to the culture medium partially restored cytokine
production in Jurkat cells, suggesting a potential role of L-DOS47 in the process of PD-1/PD-L1 interactions.
On July 11 and 18, 2017, the Company announced that it had entered into a collaboration agreement with Moffitt Cancer Center
to perform basic research studies to further investigate the pharmacodynamics of L-DOS47 and determine the potential benefits
of combining L-DOS47 with immune checkpoint inhibitors. Under the research plan Moffitt Cancer Center will perform in vitro and
in vivo research studies to study the pharmacodynamics of L-DOS47 and its effect when combined with check-point blockage
agents using their unique tumor models.
V-DOS47
V-DOS47 is an antibody DOS47 conjugate that targets the vascular endothelial growth factor 2 receptor (VEGFR2). V-DOS47 is
the second immuno-oncology drug candidate derived from the Company’s DOS47 technology platform.
In January 2016, the Company granted a world-wide exclusive license for V-DOS47 to its wholly-owned subsidiary, HIO in Poland.
The Company expects that day-to-day development activities in respect of V-DOS47 will be coordinated by HIO with coordination
and oversight from some of the Company’s scientists in Canada.
In order to advance the V-DOS47 initiative in Poland the Company is establishing a wet lab facility with the majority of the funding
coming from the grant application with the PNCRD.
The Company had previously developed four V-DOS47 research candidates and conducted in vitro feasibility studies to establish
the potential clinical applications for these molecules. HIO is expected to leverage this know-how to develop a V-DOS47 clinical
drug product candidate. The Company will assist HIO by sharing its extensive knowledge in GMP manufacturing, preclinical
research and clinical experiences. HIO will collaborate with several Polish institutes through the grant to complete the development
of the first v-DOS47 clinical drug product candidate. The development of the clinical drug product candidate for Phase I testing is
expected to take two to three years. The actual duration of the development process will depend on successful completion of
preclinical research favorable for clinical testing and establishment of cGMP manufacturing processes. The Company expects
to enter clinical trials in 2019 provided success is achieved during the preclinical and there are sufficient funds.
The Company is also leveraging its know-how in manipulating the tumour microenvironment, and its expertise in developing unique
single domain antibody therapeutics to develop CAR-T novel cell based treatments. Helix intends to develop CARs for ACT for
solid and hematological malignancies. The Company has selected CEACAM6 and VEGFR2 specific CARs for solid tumour. For
hematological malignancies the Company has selected CD19 and CD22.
As announced by the Company in August of 2017, a peer-review of V-DOS47 was published in the "Frontiers in Immunology”
journal. V-DOS47 is Helix’s second DOS47 development candidate following L-DOS47, which is currently in clinical testing for the
treatment of triple negative breast cancer. The article, entitled "Development and Characterization of a Camelid Single Domain
Antibody–Urease Conjugate That Targets Vascular Endothelial Growth Factor Receptor 2", describes the design and construction
of V-DOS47 for breast cancer and other potential indications.
Page | 7
CAR-T solid tumours
CEACAM6 specific CARs
Expression of CEACAM6 protein has been reported in a variety of normal human tissues including granulocytes. However, its
expression is elevated in many types of solid tumours such as breast, pancreatic, ovarian, lung and colon. CEACAM6 is envisaged
as a biomarker and potential therapy target for pancreatic ductal adenocarcinoma and pancreatic intraepithelial neoplasia
(Duxbury et al., 2004a, 2004c, 2004d). Recently CEACAM6 is suggested to be check point molecule in multiple myeloma.
The Company believes CEACAM6 specific CAR immune cells may have broad applications in a number of cancer types. The
Company is working on two camelid single domain antibodies that target CEACAM6.
2A3 is a camelid single domain antibody isolated from a whole cancer cell immunized llama library. The antibody binds specifically
to the CEACAM6 antigen with high affinity and inhibits the proliferation of CEACAM6-expressing cancer cells in vitro. The efficacy
of CEACAM6-CAR-T cells in xenograft model was examined in vivo. The results strongly support that CEACAM6-CAR-T cells
can be used as an effective immunotherapy agent against CEACAM6-expressing cancers, and that camelid single domain
antibodies can be easily adopted for CAR-T type therapies.
Vascular epithelial growth factor receptor 2 (VEGFR2) CARs
Most solid tumours and some hematologic malignancies are characterized by an angiogenic phenotype that is an absolute
requirement for tumour survival, progression, and metastasis. Therapeutic approaches targeting molecules involved in tumour
angiogenesis can inhibit tumour growth. Proliferating endothelial cells in the vessels within solid tumours aberrantly express high
levels of angiogenic growth factors, receptors, and adhesion molecules that are absent or barely detectable in established blood
vessels, which are normally quiescent. Among these, VEGF and its receptors appear to be the dominant regulators of
angiogenesis responsible for the vascularization of normal and neoplastic tissues. Overexpression of VEGF and its receptors is
associated with tumour angiogenesis, survival, invasion, metastasis, recurrence, and prognosis in human cancers. VEGF
stimulates angiogenesis mainly through VEGFR-2 (also known as Flk1 in mice and KDR in humans), a tyrosine kinase receptor
that is overexpressed in tumour endothelial cells and on some tumour cells. Pharmacologic approaches to inhibit VEGF, using
monoclonal antibodies or small molecules, are of value in cancer treatment, though the cytostatic rather than cytotoxic nature of
these interventions and the redundancy of angiogenic pathways have limited the curative potential of these treatments). The
Company believes VEGFR2 specific CAR immune cells may have broad applications in a number of cancer types. Helix is working
on two camelid single domain antibodies that target VEGFR2.
The Company is also leveraging its know-how in manipulating the tumour microenvironment, and its expertise in developing unique
single domain antibody therapeutics to develop CAR-T novel cell based treatments. Helix intends to develop CARs for ACT for
solid and hematological malignancies. The Company has selected CEACAM6 and VEGFR2 specific CARs for solid tumour. For
hematological malignancies the Company has selected CD19 and CD22.
The Company is also exploring opportunities for collaboration on complementary technologies to advance Company development
in cell based immune-oncology therapies.
The Company has also approached five Polish hospitals with plans to establish centers of excellence (European Center for Cancer
Immunotherapy (“ECCI”) that will participate in the development of their proprietary immune therapies. The Company will be seeking
investment in the establishment of the ECCI in Poland once a business/strategic plan has been finalized and approved by the
Company’s Board of Directors.
Clinical study initiatives
Regulatory approvals were granted to conduct a Phase I/II monotherapy (LDOS002) and a Phase I combination study (LDOS001)
of L-DOS47 in Poland and the U.S. respectively, for the treatment of NSCLC. In addition, the Company plans to initiate study
LDOS003, a clinical trial of L-DOS47 in combination with VIN/CIS in NSCLC patients with metastatic solid tumours.
U.S. Phase I clinical study (“LDOS001”)
On February 7, 2011, the Company announced it received approval by the FDA to conduct a U.S. Phase I clinical study with L-
DOS47. The Company originally planned to commence the L-DOS47 U.S. Phase I study during fiscal 2012 but, given the
Company’s limited cash resources, the Company had prioritized the LDOS002 European Phase I/II clinical study with L-DOS47
in Poland while deferring the previously planned commencement of the U.S. Phase I clinical study with L-DOS47.
On April 22, 2014, the Company announced an IND approval by the FDA to commence a study for an L-DOS47 Phase I, open
label, dose escalation study in combination with standard doublet therapy of pemetrexed/carboplatin in patients with Stage IV
recurrent or metastatic non-squamous NSCLC. The Company has initiated three U.S. sites: Dr. Sarina Piha-Paul at the MD
Anderson Cancer Center, Dr. Chandra Belani at Penn State University and the Milton S. Hershey Medical Center, and Dr. Afshin
Dowlati at University Hospitals Case Medical Center.
Page | 8
Nine patients were successfully dosed at the first two L-DOS47 dose levels 0.59 and 0.78 µg/kg respectively.
On November 30, 2016 the Company announced that after reviewing safety data from the Phase I/II study of L-DOS47 in non-
squamous non-small cell lung cancer (LDOS002), the FDA had accepted an accelerated escalation scheme for L-DOS47 dosing
in the U.S. Phase I study (LDOS001) up to 12µg/kg in combination with pemetrexed/carboplatin.
The Company provided an update to the LDOS001 study at the Biotech Showcase meeting on January 10, 2017 in San Francisco.
Highlights of the presentation included the following:
No dose limiting toxicities reported at doses up to 0.78µg/kg;
Partial responses were reported in three (3) of the first six (6) patients dosed;
Best tumour response reported was a 44% reduction in the sum of target lesions measured; and
Three (3) patients continued L-DOS47 monotherapy following induction therapy of L-DOS47 in combination with
pemetrexed/carboplatin.
On May 26, 2017, the Penn State Cancer Institute (PSCI) the closure of the site due to limited enrollment activity. The site has
subsequently been closed and no longer actively recruiting patients.
On June 29, 2017, the MD Anderson Electronic Protocol Accrual Auditing Committee (ePAAC) met to review the LDOS001
protocol due to slow patient recruitment. The committee decided to keep the protocol open for for an additional six months at
which time, another review will be conducted.
On July 25, 2017 the Company announced the opening of patient screening in the third dosing cohort. After a review of safety
data, the Safety Review Committee (“SRC”) recommended that Helix begin enrollment of patients into the third dosing cohort of
study LDOS001. Patients enrolled in the third dosing cohort will receive 1.50 micrograms of L-DOS47 per kilogram of patient body
weight in combination with pemetrexed/carboplatin.
On September 27, 2017 the Company announced that the FDA had approved an amendment to their U.S. Phase I study, protocol
LDOS001, accelerating the dose escalation phase of the study. In order to maximize the number of patients receiving a potentially
active dose of L-DOS47, the study will implement an accelerated dose design up to 6µg/kg followed by a standard 3+3 design for
the final two dosing cohorts, 9 and 12 µg/kg respectively.
To date, of the nine (9) patients in the LDOS001 study dosed to date, four (4) patients have had a confirmed partial response (as
defined by RECIST v1.1) following treatment of L-DOS47 in combination with pemetrexed/carboplatin. Four (4) patients continued
weekly L-DOS47 weekly maintenance therapy, of which two (2) were progression free for greater the one year after the initiation
of treatment.
To address patient enrollment issues, the Company request a protocol amendment, which was approved by the FDA, to reduce
the number of patients required to complete the study. Furthermore, in the next fiscal year, the Company plans to open additional
sites.
The Company continues to have insufficient cash resources to see the entire LDOS001 U.S. Phase I clinical study through to
completion. Given the Company’s limited current cash resources and the possibility of not being able to obtain additional financing
on a timely basis, the Company may be required to reduce, delay or cancel one or more of its planned research and development
programs, including clinical trials along with further reductions in overhead, any of which could impair the current and future value
of the business.
European Phase I/II clinical study in Poland (“LDOS002”)
On July 25, 2011, Helix announced that the Company had received approval from the Central Register of Clinical Trials at the
Polish Ministry of Health to perform a European Phase I/II clinical study with L-DOS47 and, on May 14, 2012, announced that
clinical site initiation and patient recruitment activities had commenced for its European Phase I/II clinical study of L-DOS47. On
October 23, 2012, the Company announced that its first patient had been enrolled and the first dose had been administered in
this study.
The study is being conducted at five Polish centers under the direction of Dr. Dariusz Kowalski at The Maria Sklodowska-Curie
Memorial Cancer Centre & Institute of Oncology as the overall coordinating investigator, together with four other principal
investigators: Prof. Cezary Szczylik, MD, PhD at the Military Medical Institute, Prof. Elzbieta Wiatr, MD, PhD at the National
Tuberculosis and Lung Diseases Research Institute, Dr. Aleksandra Szczensa, MD, PhD at the Mazovian Center of Pulmonary
Diseases and Tuberculosis in Otwock and Prof. Rodryg Ramlau, MD, PhD at Med. Polonia Hospital Poznan.
The study is being conducted in patients with inoperable, locally advanced, recurrent or metastatic, non-squamous stage IIIb/IV
NSCLC. The study, which is now well underway, recruits patients eligible for inclusion into escalating doses of L-DOS47 given
Page | 9
as a monotherapy. The study utilizes an open-label design, allowing for periodic status updates through its course. The study is
intended to demonstrate valuable safety and proof-of-concept efficacy data for L-DOS47.
Patients in the study receive weekly doses of L-DOS47, administered as an intravenous infusion over 14 days, followed by seven
days' rest (one treatment cycle is three weeks). Once the MTD of L-DOS47 has been determined in Phase I, an estimated 20
patients will be enrolled to evaluate the preliminary efficacy of L-DOS47 in the Phase II portion of the study.
Enrolment in the Phase I component of the study is now complete. A total of 55 male and female patients, at least 18 years of
age, with histologically confirmed non-squamous NSCLC were dosed at 16 L-DOS47 dose levels. Patients have an Eastern
Cooperative Oncology Group performance status of 0 – 2 at the screening visit for this study, and have at least one site of
measurable disease per RECIST v1.1.
The Phase II component enrols the same patient population as the Phase I at an L-DOS47 dose of 13.55µg/kg. Patients in the
study are dosed twice weekly over 14 days (Days 1, 4, 8, 11) followed by a 7-day rest. To date, a total of 21 patients have been
dosed in the first stage of the Phase II component of the study.
To date, the Company has completed four interim data reviews in connection with the LDOS002 study.
On October 15, 2013, the Company announced the completion of an interim data review of the first four cohorts for this study.
The release stated that L-DOS47 was well tolerated for all patients treated within all cohorts. None of the treatment related
adverse events reported to date has met the definition of a dose-limiting toxicity. Adverse events reported as of that date are
those normally expected for the population under study.
A review of available pharmacokinetic (“PK”) and immunogenicity data showed that these data so far, are consistent with trends
seen within pre-clinical animal studies of L-DOS47. Results from these reviews, together with safety data will provide guidance
on the treatment schedule and dosing for the Phase II portion of the study.
Based on Radiologic Evaluations, patients assigned a status of “Progressive Disease” following any such assessment were
withdrawn from the study. At least one patient in each of the four cohorts dosed had a radiological assessment of “Stable
Response”. Duration of treatment increased with each dose escalation up to Cohort 4. One patient in Cohort 3 was dosed for 6
cycles without disease progression. None of the patients treated to date have had a partial or complete response as defined by
RECIST v1.1 definition.
On September 30, 2014, the Company announced the completion of a further interim data review for the first eight cohorts for the
LDOS002 study. The review included all available data, including patient demographics, safety assessments, PK data,
immunogenicity and radiological tumour assessments. The following observations were made:
adverse events reported are those expected for investigational product and population under study;
no Dose Limiting Toxicities (“DLTs”) have been reported;
stable disease observed in radiological assessments of 12 of 24 (50%) of patients treated; and
two patients completed six cycles of treatment each.
On September 8, 2015, the Company announced the presentation and update of the ongoing clinical study LDOS002 for the
Company’s drug candidate L-DOS47 during the 16th World Conference on Lung Cancer held in Denver Colorado. The
presentation included the following data:
40 patients were enrolled in the first twelve dosing cohorts;
L-DOS47 was well tolerated at the dose levels up to 4.33 µg/kg;
No DLTs were reported for Cohorts 1-12;
One (1) DLT was reported for Cohort 13;
adverse events reported to date were expected for the population under study;
21 of the 40 patients had an overall response of stable disease based on radiological assessment after completing two
cycles of L-DOS47;
11 of these 21 patients continued with a response of stable disease based on radiological assessment after completing
four cycles of L-DOS47;
one (1) patient in cohort 9 was dosed for 10 cycles (approximately seven (7) months) without disease progression;
the study is currently enrolling patients in the thirteen-dosing cohort (5.76 µg/kg).
On December 6, 2016, the Company presented the following LDOS002 Phase I data for the Company’s drug candidate L-
DOS47 during the 17th World Conference on Lung Cancer held in Vienna, Austria:
90 patients were consented and screened for participation in the study;
55 patients were administered at least one dose of L-DOS47 at dose levels ranging from 0.12 to 13.55µg/kg;
21 patients completed four treatment cycles and 16 patients were administered additional L-DOS47 cycles;
Page | 10
comparatively, patients in cohorts 13 to 16 (5.76 to 13.55µg/kg) were exposed to more L-DOS47 for a longer duration
without a significant change to the safety profile of L-DOS47 compared to the other dosing cohorts;
44, or 80% of the patients in the safety population had at least one treatment emergent adverse events;
L-DOS47 did not elicit a dose-dependent release of cytokines at doses up to 13.55µg/kg
the MTD of L-DOS47 was not reached in the Phase I component of study LDOS002 at doses administered up to
13.55µg/kg;
L-DOS47 was well tolerated at all dose levels up to 13.55µg/kg.
a dose response trend was observed when comparing the percentage of patients who were progression free at 16 weeks
across dose ranges;
a similar trend was observed when comparing the percentage of patient who had an overall tumour response of Stable
Disease (as defined in RECIST v1.1) and had a reduction in the sum of target lesions;
11 of 14 or 79% of patients in the highest dosing cohorts (5.76 to 13.55µg/kg) had an overall tumour response of Stable
Disease following the administration of two cycles of L-DOS47;
seven (7) of 14 or 50% of patients in the same dosing cohorts had an overall tumour response of Stable Disease and a
reduction in the sum of target lesions and 57% of patients were progression free for greater than 16 weeks.
On March 8, 2016, the Company announced the following approved changes by the central ethics committee overseeing the
Phase I/II study in Poland as it relates to the Phase II component of the study, which the Company intends to initiate:
There will be no further escalations of L-DOS47 past cohort 16. If there are no further dose limiting toxicities, the cohort
16 dose, 13.55 µg/kg, will be the dose administered to patients in the Phase II dose.
The safety profile supports a more frequent administration of L-DOS47. After reviewing safety, pharmacokinetic and
immunogenicity data, L-DOS47 will be dosed twice weekly over 14 days (Days 1, 4, 8, 11) followed by a 7-day rest in the
Phase II study.
The number of patients in the Phase II study will be increased to 45 patients. Based on Simon’s optimal two-stage design,
17 evaluable patients will be enrolled in the first stage of the Phase II component of the study. If there is/are
≥ 1 response(s) out of these initial 17 evaluable patients, 22 additional evaluable patients will need to be enrolled. To
obtain 39 patients evaluable for response, enrolment of approximately 45 patients are needed.
On April 21, 2016, the Company announced the approval by the Trial Steering Committee to initiate the Phase II component of
the LDOS002 study. On April 28, 2016, the Company announced the enrolment of the first patient in the Phase II component of
the LDOS002 study. The first Phase II patient was dosed on May 10, 2016 and has now completed their first L-DOS47 cycle.
Although the Phase II L-DOS47 regimen has been well tolerated by patients enrolled in the first stage of the study, an improvement
in potential benefit to patients compared to the Phase I regimen (L-DOS47 dosed once weekly over 14 days (Days 1, 8) followed
by a 7-day rest) has not been observed. The potential complications associated with frequent intravenous administrations in
LDOS002 does not support the potential benefit to patients, past cycle four. As a result, the LDOS002 protocol was amended to
limit the number of dosing cycles to a maximum of 6 cycles. Patients are currently being followed for efficacy evaluation to
determine if the second stage of the study will be open to enrolment. Following a review of the Phase II dataset, the Company will
determine if they will pursue a clinical strategy of L-DOS47 as a monotherapy in NSCLC.
Following the review of clinical data collected to date, L-DOS47 continues to be well tolerated. The data also suggests that L-
DOS47 may provide a clinical benefit for certain patients. Enrolment in the first stage of the Phase II component of study LDOS002
(n=21) has been completed. A Trial Steering Committee Meeting will be organized before the end of the year to review safety and
efficacy data to determine next steps.
The Company continues to have insufficient cash resources to see the entire LDOS002 European Phase I/II clinical study in
Poland through to completion. Given the Company’s limited current cash resources and the possibility of not being able to obtain
additional financing on a timely basis, the Company may be required to reduce, delay or cancel one or more of its planned research
and development programs, including clinical trials along with further reductions in overhead, any of which could impair the current
and future value of the business.
Phase II clinical study (“LDOS003”)
A potential secondary yet unproven aspect of L-DOS47 action is the observation that an acidic pH microenvironment (< pH 6.8)
may limit the effectiveness of weakly basic cytotoxic drugs employed in treatment of lung and other solid tumours. An acidic
microenvironment is associated with protonation of these agents and decreased uptake and alkalinisation can result in enhanced
agent uptake and cytotoxicity. Furthermore, extracellular acidity may also inhibit the active transport of some drugs. This raises
the possible application of L-DOS47 to combination cancer therapies with agents which have little or no overlapping toxicities.
This study is designed to determine the possible chemo-enhancing properties of L-DOS47. The possibility of combining L-DOS47
with a weakly basic agent like vinorelbine may improve therapeutic outcomes for cancer patients. The vinorelbine/cisplatin
combination is used as a first-line treatment for lung adenocarcinoma.
Page | 11
The Company has initiated a Phase IIb, open-label, randomized study in male and female patients aged ≥ 18 years old with
metastatic lung adenocarcinoma. The staging will be conducted according to Tumour Node Metastases (TNM), 8th Edition. In
Part 1 of the study (Dose Escalation), patients will receive eight (8) doses of L-DOS47 over four (4) cycles. On Day 1 and Day 8
of each cycle, L-DOS47 (administered as an intravenous (“IV”) infusion) will be administered 24 hours before vinorelbine/cisplatin.
Once the maximum tolerated dose of L-DOS47 as an adjunct to vinorelbine/cisplatin is determined, patients in Part 2 of the study
(Randomized Treatment) will be randomly assigned to receive L-DOS47 in combination with vinorelbine/cisplatin or
vinorelbine/cisplatin alone.
The Company has insufficient supply of L-DOS47 to complete the LDOS003 study. As a result, the Company plans to manufacture
another batch of drug product in the next fiscal year to support the completion of the study and other planned studies. Completion
of the study will depend on the successful release and availability of new drug product.
Given the Company’s limited current cash resources and the possibility of not being able to obtain additional financing on a timely
basis, the Company may be required to reduce, delay or cancel one or more of its planned research and development programs,
including clinical trials along with further reductions in overhead, any of which could impair the current and future value of the
business.
Commercialization
The Company’s DOS47 commercialization objective is to eventually enter into a strategic partnering alliance with a large
pharmaceutical company, on an individual or multiple drug candidate basis, such as L-DOS47 or any potential new DOS47 drug
product candidate. In the meantime, the Company will continue to gather as much value-adding clinical data/findings, which
demonstrate the safety and efficacy of L-DOS47 in patients or any other new potential DOS47 drug candidate so as to maximize
value for shareholders when entering into a strategic partnering alliance.
Market and Competition
Based on information published in “Key Statistics for Lung Cancer” by the American Cancer Society (www.cancer.org), lung cancer
accounts for about one out of four of all cancer deaths and is by far the leading cause of cancer death among men and women in
the U.S. It is estimated that in 2017 there will be over 222,500 new lung cancer cases.
If detected early, surgical removal of the cancerous tissue is currently a patient’s best option. However, in the vast majority of
cases, the cancer is not typically identified until it has advanced to a level at which surgical intervention is no longer an option. In
the cases of inoperable, locally advanced, recurrent or metastatic NSCLC and with no known targetable mutations, treatment
strategies consist of one or more of today’s leading chemotherapeutic drug regimens for lung cancer (e.g. platinum therapy
together with certain leading chemotherapeutic drugs). Typically, these regimens relieve symptoms and, at best, delay
progression of the disease.
Disease progression, even with targeted therapies, is highly likely to occur, and there are no clear guidelines and/or indications
once such therapies fail. Maintenance therapy following the induction of first-line therapy is also a treatment strategy gaining
support.
Immunotherapies such as immune checkpoint inhibitors that target Programmed Death 1 (“PD-1”) or its ligands, Programmed
Death Ligand 1 or 2 (“PD-L1” and “PD-L2”, respectively) are showing significant clinical successes in NSCLC. On March 4, 2015
the FDA approved Nivolumab, the generic name for the trade drug named Opdivo®, which targets PD-1 for the treatment of
metastatic squamous NSCLC with progression on or after platinum-based chemotherapy. On October 2, 2015, the FDA granted
accelerated approval for Pembrolizumab, the generic name for the trade drug named Keytruda®, which targets PD-1 to treat
patients with advanced metastatic NSCLC whose disease has progressed after other treatments and with tumours that express
PD-L1. Anti-PD-L1 drugs such as MPDL3280A from Roche are also advancing rapidly through late stage clinical trials.
In 2015, three randomized Phase III trials found the immune checkpoint inhibitors nivolumab and pembrolizumab to have superior
efficacy and less toxicity compared with second-line docetaxel chemotherapy in patients with NSCLC. For the first time, agents
blocking a single pathway have shown significant benefit across multiple tumour types, with US Food and Drug Administration
(FDA) approval in NSCLC, melanoma, and bladder and renal cell carcinoma. Now more than 1,000 immune checkpoint clinical
trials are underway. Many possible treatment avenues are being explored with immune checkpoint inhibitors, including
combinations with radiation, chemotherapy, targeted therapy, and other checkpoint inhibitors. Some studies are also investigating
checkpoint inhibitors as front-line therapy.
As of March 2017, the FDA had approved five checkpoint inhibitor drugs: ipilimumab (Yervoy®), pembrolizumab (Keytruda®),
nivolumab (Opdivo®), atezolizumab (Tecentriq®) and avelumab (Bavencio®).
On May 10, 2017, the FDA granted accelerated approval to pembrolizumab (KEYTRUDA®, Merck and Co., Inc.) in combination
with pemetrexed and carboplatin for the treatment of patients with previously untreated metastatic non-squamous non-small cell
lung cancer (NSCLC). Approval was based on a cohort (G1) of patients enrolled in an open-label, multicenter, multi-cohort study
(KEYNOTE-021). As a result of these developments in the treatment of NSCLC, the Company is currently reassessing its L-
Page | 12
DOS47 clinical program given that: (a) its target therapeutic indication, being inoperable, locally-advanced, recurrent or metastatic
NSCLC, may be a good candidate to combine with the emerging best-in-class immunotherapies; and (b) leading therapeutics for
such oncology applications have commonly been high revenue generators for the pharmaceutical sector.
Technological competition from pharmaceutical companies, biotechnology companies and university researchers is intense and
is expected to continue to be very intense. Many competitors and potential competitors have substantially greater product
development capabilities and financial, scientific, marketing and human resources than the Company, providing them with a
competitive advantage over the Company.
The BiphasixTM Topical Formulation System
The Biphasix™ Topical Formulation System is a platform technology which the Company acquired and further developed for
microencapsulating therapeutic compounds in multilayered, lipid-based microvesicles. These microvesicles have complex
structures that include a variety of compartments into which drug molecules can be integrated. The principal application of the
technology is in the preparation of topical dosage forms for the dermal (into the skin) or mucosal (into the mucosal tissues) delivery
of large molecular weight drug compounds.
Topical Interferon Alpha-2b
The Company received investigational new drug (“IND”) approval by the FDA to conduct a U.S. Phase II/III clinical trial of Topical
Interferon Alpha-2b in low-grade cervical dysplasia patients, as well as Clinical Trial Application (“CTA”) approval by the
Bundesinstitut fur Arzneimittel und Medizinprodukte and conditional CTA approval by the Medicines and Healthcare Regulatory
Authority to conduct an identical European Phase III confirmatory trial in Germany and/or the United Kingdom, respectively.
Due to a lack of funding, a decision was made by the Company in fiscal 2012 to downsize and eventually close the Saskatoon
laboratory which supported the Topical Interferon Alpha-2b drug development program, and focus any ongoing activities to
sourcing and qualifying alternative interferon alpha-2b raw material samples, and finding suitable strategic partner(s) who would
be willing to license or acquire the product and support the remaining development costs through to commercial launch. In 2016,
the Company ceased all activities related to Topical Interferon Alpha-2b, other than maintaining existing intellectual property
associated with Topical Interferon Alpha-2b.
On December 23, 2016, the Company announced, it signed an exclusive out-license agreement with Xisle for the Company's late-
stage, Biphasix™ technology platform, including the lead product candidate, interferon alpha. Xisle is responsible for the continued
clinical development and subsequent commercialization of the product for the treatment of HPV-induced, low-grade, cervical
intraepithelial lesions. As part of its asset development strategy, Xisle has initiated collaboration with senior pharmaceutical
executives at Altum Pharmaceuticals Inc., who possess regulatory, clinical, and product development expertise. Under the terms
of the agreement, Xisle paid an up-front fee of USD125,000 and agreed to pay subsequent milestone payments as they advance
the technology to registration and market approvals and royalties. As part of the agreement, Helix retains marketing rights for
Belarus, Bulgaria, Czech Republic, former Eastern Germany, Hungary, Moldova, Poland, Romania, Russia, Slovakia and Ukraine.
In addition, the Company also retains non-exclusive rights for co-promotion in Canada.
The Company subsequently assigned the marketing rights which it retained to HIO, its wholly-owned subsidiary in Poland pursuant
to an agreement between the Company and HIO with the agreement being subject to the restrictions and limitations associated
with the out-license agreement signed between the Company and Xisle. In addition, HIO will be responsible for commercialization
with milestone and royalty payments to be paid back to the Company upon successful product development through to
commercialization.
SELECTED FINANCIAL INFORMATION AND SUMMARY OF QUARTERLY RESULTS
Net loss and total comprehensive loss, over the last eight quarters, has ranged from a high of $3,287,000 in fiscal Q1 2017 to a
low of $1,240,000 in fiscal Q4 of 2017 with fluctuations mainly dependant on the level of research and development activities and
operating, general and administration expenses. The lower Q4 fiscal 2017 net loss and comprehensive loss reflects the
Company’s initiatives to cut costs and reduce expenditures in order to preserve cash.
The higher operating, general and administration expenditures in Q1 2017 reflects higher CEO related expenses, legal, investor
and media relations and other consulting arrangements associated mainly with ongoing efforts by the Company to raise financing.
The higher operating, general and administration expenditures in Q1 of fiscal 2016 were mainly the result of stock-based
compensation expense for options granted to directors of the Company.
The Company closed several private placements during the last fiscal year (in Q4 2017 for gross proceeds of approximately
$3,029,000; in Q3 2017 for gross proceeds of $1,930,000; in Q2 2017 for gross proceeds of $1,824,000 and in Q1 2017 for gross
proceeds of $993,000). In Q4 2016, the Company closed a private placement for gross proceeds of $1,825,000 and, in fiscal Q3
2016, the Company closed a private placement for gross proceeds of $4,658,000.
Page | 13
The following table depicts selected quarterly data from continuing operations for the fiscal year ended July 31, 2017:
Research and development
Operating, general and administration
Net loss and total comprehensive loss
Basic and diluted loss per common share
Weighted average number of common shares
Cash
Working Capital / (deficiency)
Q4
917,000
382,000
$
$
$ (1,241,000)
(0.01)
$
91,797,627
$
$
897,000
(504,000)
Q3
$ 1,932,000
944,000
$
$ (2,913,000)
(0.03)
$
92,062,331
$ 1,323,000
$ (1,994,000)
Q2
$ 1,911,000
873,000
$
$ (2,618,000)
(0.03)
$
90,621,018
$ 1,423,000
(612,000)
$
Q1
$ 2,295,000
$ 1,008,000
$ (3,287,000)
(0.04)
$
88,649,140
$ 2,397,000
595,000
$
The following table depicts selected quarterly data from continuing operations for the fiscal year ended July 31, 2016:
Research and development
Operating, general and administration
Net loss and total comprehensive loss
Basic and diluted loss per common share
Weighted average number of common shares
Cash
Working Capital / (deficiency)
Q4
$ 1,729,000
872,000
$
$ (2,604,000)
(0.03)
$
87,988,842
$ 3,654,000
$ 2,929,000
Q3
$ 1,507,000
748,000
$
$ (2,243,000)
(0.02)
$
84,861,587
$ 4,929,000
$ 3,885,000
Q2
$ 1,246,000
957,000
$
$ (2,226,000)
(0.03)
$
84,683,201
$ 2,523,000
$ 1,980,000
Q1
$ 1,339,000
$ 1,259,000
$ (2,592,000)
(0.03)
$
84,654,815
$ 5,008,000
$ 4,003,000
The following table depicts selected annual data from continuing operations for the fiscal years ended July 31:
Research and development expense
Operating, general and administration expense
Net loss and total comprehensive loss
Deficit, end of year
Basic and diluted loss per common share
Weighted average number of common shares
Cash
Working capital / (deficiency)
Total assets
RESULTS FROM OPERATIONS
2017
7,055,000
3,207,000
$
$
2016
5,821,000
3,836,000
2015
4,885,000
3,892,000
$
$
$
$
(10,059,000)
$
$ 155,380,000
(9,665,000)
$
$ 145,321,000
(8,780,000)
$
$ 135,656,000
$
$
$
$
0.11
91,797,627
897,000
(504,000)
2,187,000
$
$
$
$
0.11
85,550,926
3,654,000
2,929,000
4,468,000
$
$
$
$
0.11
78,592,444
6,792,000
6,498,000
7,796,000
Net loss and total comprehensive loss from continuing operations
The Company recorded a net loss and total comprehensive loss of $10,059,000 ($0.11 loss per common share) and $9,665,000
($0.11 loss per common share) for the fiscal years ended 2017 and 2016, respectively.
Research & development
Research and development costs for fiscal 2017 and 2016 totalled $7,055,000 and $5,821,000, respectively.
The following table outlines research and development costs expensed and investment tax credits for the Company’s significant
research and development projects for the fiscal years ended July 31:
L-DOS47
V-DOS47
CAR-T
Corporate research and development expenses
Trademark and patent related expenses
Stock-based compensation expense
Depreciation expense
Research and development investment tax credit
Polish government grant subsidy (V-DOS47)
2017
$ 5,496,000
894,000
259,000
474,000
361,000
24,000
112,000
(230,000)
(335,000)
2016
$ 5,017,000
159,000
–
431,000
244,000
27,000
118,000
(175,000)
–
$ 7,055,000
$ 5,821,000
Page | 14
L-DOS47 research and development expenses for fiscal 2017 and 2016 totalled $5,496,000 and $5,017,000, respectively. L-
DOS47 research and development expenditures relate primarily to the Company’s LDOS002 European Phase I/II clinical study in
Poland and the LDOS001 U.S. Phase I clinical study in the U.S.
V-DOS47 research and development expenses for fiscal 2017 and 2016 totalled $894,000 and $159,000, respectively. In fiscal
2016 the Company established a wholly owned subsidiary in Poland and entered into a grant funding agreement with the PNCRD
for research and development expenditures associated with V-DOS47. The Company’s subsidiary received $335,000 and $nil in
fiscal 2017 and 2016, respectively, from the PNCRD.
CAR-T research and development expenses for fiscal 2017 and 2016 totalled $259,000 and $nil, respectively. During the current
fiscal year, the Company commenced development of novel CAR-T therapeutics and new antibody based technologies for cell-
based therapies.
Corporate research and development expenses were relatively flat for fiscal 2017 and 2016 and totalled $474,000 and $431,000,
respectively.
Trademark and patent related expenses for fiscal 2017 and 2016 totalled $361,000 and $244,000, respectively. The Company
continues to ensure it works to adequately protect its intellectual property.
Operating, general and administration
Operating, general and administration expenses for the fiscal 2017 and 2016 totalled $3,207,000 and $3,836,000, respectively.
The decrease in operating, general and administration expenses reflects various cost cutting initiatives and is due primarily to
lower travel related expenses, director fees, and various terminated consulting service agreements.
CRITICAL ACCOUNTING ESTIMATES
The preparation of financial statements in conformity with IFRS requires management to make judgments, estimates and
assumptions that affect the application of accounting policies and the reported amounts of assets and liabilities, revenue and
expenses and the related disclosures of contingent assets and liabilities and the determination of the Company’s ability to continue
as a going concern. Actual results could differ materially from these estimates and assumptions. The Company reviews its
estimates and underlying assumptions on an ongoing basis. Revisions are recognized in the period in which the estimates are
revised and may impact future periods.
The areas involving a higher degree of judgment or complexity, or areas where assumptions and estimates are significant to the
Company’s financial statements have been set out in Note 1 of the Company’s audited consolidated financial statements for the
fiscal year ended July 31, 2017.
SIGNIFICANT ACCOUNTING POLICIES
The significant accounting policies used in preparing the Company’s consolidated financial statements are described in Note 2 of
the Company’s audited consolidated financial statement for the fiscal year ended July 31, 2017, except for those related accounting
policies and methods of computation related to any new accounting standards and pronouncements.
NEW ACCOUNTING STANDARDS AND PRONOUNCEMENTS NOT YET ADOPTED
New accounting standards and pronouncements issued but not yet effective up to the date of issuance of the Company's
consolidated financial statements are listed below. This listing includes standards and interpretations issued, which the Company
reasonably expects to be applicable at a future date. The Company intends to adopt those standards when they become effective.
Certain pronouncements have been issued by the IASB or International Financial Reporting Interpretations Committee. Many of
these updates are not applicable or are inconsequential to the Company and have been excluded from the discussion below:
IFRS 9, Financial Instruments
The IASB has issued a new standard, IFRS 9, Financial Instruments (“IFRS 9”), which will ultimately replace IAS 39, Financial
Instruments: Recognition and Measurement (“IAS 39”). The project had three main phases: classification and measurement,
impairment and general hedging. The standard becomes effective for annual periods beginning on or after January 1, 2018 and
is to be applied retrospectively. Early adoption is permitted. The Company is evaluating the impact of the new standard on its
results of operations, financial position and disclosures.
IFRS 15, Revenue from Contracts with Customers
The IASB has issued a new standard, IFRS 15, Revenue from Contracts with Customers (“IFRS 15”). IFRS 15 contains a single
Page | 15
model that applies to contracts with customers and two approaches to recognizing revenue: at a point in time or over time. The
model features a contract-based five-step analysis of transactions to determine whether, how much and when revenue is
recognized. New estimates and judgmental thresholds have been introduced, which may affect the amount and/or timing of
revenue recognized. The standard becomes effective for annual periods beginning on or after January 1, 2018. The Company
is evaluating the impact of the new standard on its results of operations, financial position and disclosures.
IFRS 16, Leases
In January 2016, the IASB has issued IFRS 16 Leases (“IFRS 16”), its new leases standard that requires lessees to
recognize assets and liabilities for most leases on their balance sheets. Lessees applying IFRS 16 will have a single
accounting model for all leases, with certain exemptions. Lessor accounting is substantially unchanged. The new standard will
be effective from January 1, 2019 with limited early application permitted. The Company is evaluating the impact of the new
standard on its results of operations, financial position and disclosures.
LIQUIDITY AND CAPITAL RESOURCES
Since inception, the Company has mainly relied on financing its operations from public and private sales of equity. The Company
does not have any credit facilities and is therefore not subject to any externally imposed capital requirements or covenants. The
Company manages its liquidity risk by continuously monitoring forecasts and actual cash flow from operations and anticipated
investing and financing activities.
The Company reported a consolidated net loss and total comprehensive loss of $10,059,000 for the fiscal year ended July 31,
2017 (July 31, 2016 - $9,665,000). As at July 31, 2017 the Company had a working capital deficiency of $504,000, shareholders’
deficiency of $17,000 and a deficit of $155,380,000.
In order for the Company to advance its various planned preclinical and clinical research and development activities and pay for
its overhead costs, the Company will need to raise approximately $20,000,000 to $25,000,000 over the next two fiscal years. Of
this amount, planned capital expenditures are negligible totalling approximately $31,000.
Subsequent to the first quarter of fiscal 2017, which ended on October 31, 2017, the Company has been operating with a working
capital deficiency. As a result, the Company established a cost cutting plan and worked with vendors to manage its cash position
while ensuring vendors continued providing services while being paid, albeit over a longer period of time than previously agreed
terms. The Company continues to work with its vendor base and more specifically, one vendor in particular, that oversees the
Company’s clinical study in Poland The Company’s cash reserves of $897,000 as at July 31, 2017 are insufficient to meet
anticipated cash needs for working capital and capital expenditures through the next twelve months, nor are they sufficient to see
the current or any planned research and development initiatives through to completion. Subsequent to the Company’s fiscal year
ending July 31, 2017, the Company closed two additional private placements for gross proceeds of approximately $5,221,000.
Though the funds raised have assisted the Company in dealing with the working capital deficiency, additional funds are required
to advance the various clinical and preclinical programs and pay for the Company’s overhead costs. To the extent that the
Company does not believe it has sufficient liquidity to meet its current obligations, management considers securing additional
funds, primarily through the issuance of equity securities of the Company, to be critical for its development needs.
The Company’s long-term liquidity depends on its ability to access the capital markets, which depends substantially on the success
of its ongoing research and development programs, as well as economic conditions relating to the state of the capital markets
generally. Accessing the capital markets can be particularly challenging for companies that operate in the biotechnology industry.
The Company has predominately raised funds utilizing the services of ACM Alpha Consulting Management EST (“ACMest”) and
on September 8, 2017 entered into an agreement with ACMest and Oakbridge Capital Advisors Ltd., from London, England to
assist in raising capital for the Company.
While the Company has been able to raise equity financing in recent years, there can be no assurance that additional funding by
way of equity financing will continue to be available. Any additional equity financing, if secured, would result in dilution to the
existing shareholders and such dilution may be significant. The Company may also seek additional funding from or through other
sources, including technology licensing, co-development collaborations, mergers and acquisitions, joint ventures, and other
strategic alliances, which, if obtained, may reduce the Company’s interest in its projects or products or result in significant dilution
to existing shareholders. The Company may also seek additional funding from government grants. There can be no assurance,
however, that any alternative sources of funding will be available. The failure of the Company to obtain additional financing on a
timely basis may result in the Company reducing, delaying or cancelling one or more of its planned research, development and/or
marketing programs, including clinical trials, further reducing overhead, or monetizing non-core assets, any of which could impair
the current and future value of the business or cause the Company to consider ceasing operations and undergoing liquidation.
Given the Company’s conclusion about the insufficiency of its cash reserves, significant doubt may be cast about the Company’s
ability to continue operating as a going concern. The continuation of the Company as a going concern for the foreseeable future
depends mainly on raising sufficient capital, and in the interim, reducing, where possible, operating expenses (including making
changes to the Company’s research and development plans), including the delay of one or more of the Company’s research and
development programs, further reducing overhead and the possible disposition of assets.
Page | 16
The Company had a total number of, 95,711,579 common shares issued and outstanding as at July 31, 2017 (July 31, 2016 –
89,247,937 common shares). The Company reported a consolidated net loss and total comprehensive loss of $10,059,000 for
the fiscal year ended July 31, 2107 (July 31, 2016 - $9,665,000). As at July 31, 2017 the Company had a working capital deficiency
of $504,000, shareholders’ deficiency of $17,000 and a deficit of $155,380,000. As at July 31, 2016 the Company had working
capital of $2,929,000, shareholders’ equity of $3,164,000 and a deficit of $145,321,000.
RELATED PARTY TRANSACTIONS
The key management personnel of the Company includes the Chief Executive Officer, Chief Financial Officer, Chief Scientific
Officer and the Chief Operating Officer. The following table summarizes key management personnel compensation for the fiscal
years ended:
Compensation
Stock-based compensation
2017
2016
$ 1,081,000 $ 1,283,000
53,000
–
The following table summarizes non-management directors’ compensation for the fiscal years ended:
$ 1,081,000 $ 1,336,000
Directors’ fees
Stock-based compensation
Consulting fees
Sub-lease payments
2017
314,000 $
$
16,000
329,000
144,000
2016
352,000
150,000
187,000
–
$
803,000 $
689,000
The Company entered into a consulting agreement with the Chairman of the Board to act as Chief Executive Officer of the
Company. The agreement had a twelve-month term which expired on March 31, 2017. During the 2017 fiscal year, the Company
entered into an agreement with a company controlled by a director of the Company to sub-lease office space.
The following table summarizes the Board Observer’s compensation for the fiscal years ended:
Finder’s fee commission
Financial and investor relations consulting
Expense reimbursement
$
2017
972,000 $
532,000
31,000
2016
810,000
540,000
80,000
$ 1,535,000 $ 1,430,000
The Company entered into a non-exclusive financial and investor relations agreement with ACM Alpha Consulting Management
EST (“ACMest”), effective May 1, 2012. On March 7, 2014, Mr. Andreas Kandziora became an Observer to the Board of Directors
of the Company. Mr. Kandziora was also appointed to the Supervisory Board of the Company’s wholly-owned Polish subsidiary,
HIO. Mr. Kandziora is President and CEO of ACMest (also see TABULAR DISCLOSURE OF CONTRACTUAL OBLIGATIONS
below). During the 2017 fiscal year, the Board of Directors of the Company appointed Mrs. Veronika Kandziora, the spouse of
Mr. Kandziora, as Corporate Secretary of the Company.
Related party transactions are at arm’s length and recorded at the amount agreed to by the related parties.
FINANCIAL INSTRUMENTS
Fair value hierarchy
Financial instruments recorded at fair value on the balance sheet are classified using a fair value hierarchy that reflects the
significance of the inputs used in making the measurements. The fair value hierarchy has the following levels:
Level 1 reflects valuation based on quoted prices observed in active markets for identical assets or liabilities;
Level 2 reflects valuation techniques based on inputs that are quoted prices of similar instruments in active markets;
quoted prices for identical or similar instruments in markets that are not active; inputs other than quoted prices used in a
valuation model that are observable for that instrument; and inputs that are derived principally from or corroborated by
observable market data by correlation or other means; and
Level 3 reflects valuation techniques with significant unobservable market inputs.
A financial instrument is classified to the lowest level of the hierarchy for which a significant input has been considered in measuring
fair value. The financial instrument in the Company’s financial statements, measured at fair value, is cash.
Page | 17
Fair value
The fair value of financial instruments as at July 31, 2017 and July 31, 2016 approximates their carrying value because of the
near-term maturity of these instruments.
INTELLECTUAL PROPERTY
Patents and other proprietary rights are very valuable to the Company, even though the patent positions of biotechnology
companies may be uncertain and involve complex legal and factual issues. The Company has no assurance that any of its patent
applications will result in the issuance of any patents. Even issued patents may not provide the Company with a competitive
advantage against competitors with similar technologies, or who have designed around the Company’s patents. Furthermore, the
Company’s patents may be struck down if challenged. Intellectual property laws do not protect intellectual property to the same
extent from one country to another.
Because of the substantial length of time and expense associated with developing new products, the pharmaceutical, medical
device, and biotechnology industries place considerable importance on obtaining patent protection for new technologies, products,
and processes. The Company’s policy is to file patent applications to protect inventions, technology, and improvements that are
important to the development of our business and with respect to the application of our products and technologies to the treatment
of a number of disease indications. The Company’s policy also includes regular reviews related to the development of each
technology and product in light of its intellectual property protection, with the goal of protecting all key research and developments
by patent.
The Company seeks intellectual property protection in various jurisdictions around the world and owns patents and patent
applications relating to products and technologies in the United States, Canada, Europe and other jurisdictions. The scope and
duration of our intellectual property rights vary from country to country depending on the nature and extent of our intellectual
property filings, the applicable statutory provisions governing the intellectual property, and the nature and extent of our legal rights.
The Company will continue to seek intellectual property protection as appropriate and require our employees, consultants, outside
scientific collaborators, and sponsored researchers to enter into confidentiality agreements with us that contain assignment of
invention clauses outlining ownership of any intellectual property developed during the course of the individual’s relationship with
us.
Tumor Defense BreakerTM
On September 29, 2016 the Company filed a Canadian Trade Mark Application for “TUMOR DEFENSE BREAKER”. It is planned
to expand this trademark in all major markets and territories where will aim to market the products once they receive marketing
approval by appropriate regulatory authorities. On May 1, 2017, the Company was notified that the trade mark application had
been approved. A similar application was made in Europe which was not accepted and the Company is assessing whether it will
appeal this decision.
DOS47, L-DOS47 and V-DOS47
The Company currently owns two U.S. patents in respect of the DOS47 technology, and also has also licensed patent rights from
the NRC for the antibody component of L-DOS47. With respect to non-U.S. patents, the Company owns 52 DOS47 related
patents in other jurisdictions with a number of patent applications in countries around the world. The Company has recently filed
a joint patent application in the U.S. with Amorfix to cover the antibody-DOS47 conjugates derived from their collaboration. A new
U.S. patent application to cover new features of the DOS47 technology was filed by the Company during fiscal 2013. During
January 2015, an additional U.S. patent application covering specific L-DOS47 manufacturing and novel features was filed. During
fiscal 2017, a new U.S. patent application protecting the novel use of L-DOS47 in restoring T cell function for therapeutic
application was filed. In addition, two US patents covering anti-VEGFR2 antibodies and their use in DOS47 conjugates (V-DOS4)
were filed.
Cell Based Therapy
The company has recently filed a joint patent application with NRC to protect the use of an antibody for use in cell based therapies.
In addition, the company has also filed new patent application covering the use of anti-VEGFR2 antibodies in cell based therapy
in July 2017. The Company is currently in discussion with third parties to license additional intellectual properties to strengthen
the company’s portfolio.
BiphasixTM
The Company, until recently, owned six U.S. BiphasixTM patents.
On December 23, 2016, the Company announced, it signed an exclusive out-license agreement with Xisle for the Company's late-
stage, Biphasix™ technology platform, including the lead product candidate, interferon alpha. Xisle is responsible for the continued
clinical development and subsequent commercialization of the product for the treatment of HPV-induced, low-grade, cervical
Page | 18
intraepithelial lesions. As part of its asset development strategy, Xisle has initiated collaboration with senior pharmaceutical
executives at Altum Pharmaceuticals Inc., who possess regulatory, clinical, and product development expertise. Under the terms
of the agreement, Xisle paid an up-front fee of USD125,000 and agreed to pay subsequent milestone payments as they advance
the technology to registration and market approvals and royalties. As part of the agreement, Helix retains marketing rights for
Belarus, Bulgaria, Czech Republic, former Eastern Germany, Hungary, Moldova, Poland, Romania, Russia, Slovakia and Ukraine.
In addition, the Company also retains non-exclusive rights for co-promotion in Canada.
The Company subsequently assigned the foregoing marketing rights which it retained to HIO, its wholly -owned subsidiary in
Poland pursuant to an agreement between the Company and HIO with the agreement being subject to the restrictions and
limitations associated with the out-license agreement signed between the Company and Xisle. In addition, HIO will be responsible
for commercialization with milestone and royalty payments to be paid back to the Company upon successful product development
through to commercialization.
OFF-BALANCE SHEET ARRANGEMENTS
The Company has no material off-balance sheet arrangements.
TABULAR DISCLOSURE OF CONTRACTUAL OBLIGATIONS
The Company’s commitments are summarized as follows:
2018
V-DOS47 co-funded project (1)
Clinical research organizations (2)
2,165,000
Contract manufacturing organizations (3) 615,000
Collaborative research organizations (4) 321,000
Royalty and in-licensing (5)
20,000
Operating leases (6)
52,000
127,000
Financial and investor relations (7)
2021
$ 606,000 $ 1,452,000 $ 2,578,000 $1,805,000
–
–
–
–
–
–
20,000
20,000
–
26,000
–
–
–
–
–
20,000
2020
2019
–
–
$
2022
–
–
–
–
20,000
–
–
2023 and
beyond
$
Total
– $6,441,000
2,165,000
–
615,000
–
321,000
–
200,000
100,000
78,000
–
127,000
–
$ 3,906,000 $ 1,498,000 $ 2,598,000 $1,825,000 $ 20,000
$ 100,000 $9,947,000
(1) PNCRD V-DOS47 co-funding program. Subsidized amounts may be drawn in advance or on a reimbursement basis, with
varying criteria and timelines for justification of claims being made by the Company’s subsidiary. Of the $6,441,000 in total
future commitments towards this program, the Company is projecting that approximately $3,974,000 will be reimbursed by
the PNCRD.
(2) The Company has Clinical Research Organization supplier agreements in place for clinical research services related to the
management of the Company’s clinical stage programs.
(3) The Company has Contract Manufacturing Organization supplier agreements related to its L-DOS47 program, all of which
are inter-dependant with the manufacturing of L-DOS47.
(4) The Company has Collaborative Research Organization supplier agreements relating to its L-DOS47 program.
(5) Represents future minimum royalties.
(6) The Company is committed to pay $78,000 under four facility lease agreements with lease terms up to 24 months.
(7) The Company has financial advisory agreements, of which one includes investor relations services. The main agreement,
which is with ACMest, expired on May 1, 2013, the provisions of which continue on a month-to-month basis and termination
of which requires a ninety-day written notice (also see RELATED PARTY TRANSACTIONS section above).
QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK
The Company’s main objectives when managing capital are to ensure sufficient liquidity to finance research and development
activities, clinical trials, ongoing administrative costs, working capital and capital expenditures. The Company includes cash and
components of shareholders’ equity, in the definition of capital. The Company endeavours not to unnecessarily dilute shareholders
when managing the liquidity of its capital structure.
Currency risk
The Company operates internationally and is exposed to foreign exchange risks from various currencies, primarily the Euro and
U.S. dollar. Foreign exchange risks arise from the foreign currency translation of the Company’s integrated foreign operation in
Poland. In addition, foreign exchange risks arise from purchase transactions, as well as recognized financial assets and liabilities
denominated in foreign currencies.
Page | 19
Balances in foreign currencies at are as follows:
July 31, 2017
July 31, 2016
Cash
Accounts receivable
Accounts payable
Accruals
Net foreign currencies
Euros
32,000
–
US
Dollars
1,000
Zloty
276,000
– 178,000
(468,000)
(217,000)
(653,000)
(229,000)
(24,000)
(252,000)
(201,000)
(99,000)
154,000
Euros
30,000
–
(77,000)
(82,000)
(129,000)
US
Dollars
Zloty
48,000 77,000
–
(48,000) –
(90,000)
(13,000)
(165,000)
(165,000)
–
Closing exchange rate
1.4719
Impact of 1% change in exchange rate +/- 9,000
1.2485
0.3451
+/- 3,000 +/-1,000
1.4594
1.3056 0.3415
+/- 1,000 +/- 1,000 +/- 1,000
Any fluctuation in the exchange rates of the foreign currencies listed above could have an impact on the Company’s results from
operations; however, they would not impair or enhance the ability of the Company to pay its foreign-denominated expenses.
Credit risk
Credit risk is the risk of a financial loss to the Company if a customer or counterparty to a financial instrument fails to meet its
contractual obligation.
The table below breaks down the various categories that make up the Company’s accounts receivable balances:
Government related – HST/VAT
Research and development investment tax credits
Other
Interest rate risk
July 31, 2017
$ 177,000
430,000
23,000
$ 630,000
July 31, 2016
106,000
$
380,000
3,000
489,000
$
Interest rate risk is the risk that future cash flows of a financial instrument will fluctuate because of changes in interest rates, which
are affected by market conditions. The Company is exposed to interest rate risk arising from fluctuations in interest rates received
on its cash. The Company does not have any credit facilities and is therefore not subject to any debt related interest rate risk.
The Company manages its interest rate risk by maximizing the interest income earned on excess funds while maintaining the
liquidity necessary to conduct its operations on a day-to-day basis. Any investment of excess funds is limited to risk-free financial
instruments. Fluctuations in the market rates of interest do not have a significant impact on the Company’s results of operations
due to the relatively short-term maturity of any investments held by the Company at any given point in time and the low global
interest rate environment. The Company does not use derivative instruments to reduce its exposure to interest rate risk.
Liquidity risk
Liquidity risk is the risk that the Company will not be able to meet its obligations as they come due.
Since inception, the Company has mainly relied on financing its operations from public and private sales of equity. The Company
does not have any credit facilities and is therefore not subject to any externally imposed capital requirements or covenants.
The Company manages its liquidity risk by continuously monitoring forecasts and actual cash flow from operations and anticipated
investing and financing activities.
The Company’s cash reserves of $897,000 as at July 31, 2017 are insufficient to meet anticipated cash needs for working capital
and capital expenditures through the next twelve months, nor are they sufficient to see the current research and development
initiatives through to completion. To the extent that the Company does not believe it has sufficient liquidity to meet its current
obligations, management considers securing additional funds primarily through equity arrangements to be of utmost importance.
The Company’s long-term liquidity depends on its ability to access the capital markets, which depends substantially on the success
of the Company’s ongoing research and development programs, as well as economic conditions relating to the state of the capital
markets generally. Accessing the capital markets is particularly challenging for companies that operate in the biotechnology
industry.
Page | 20
OUTSTANDING SHARE DATA
As at July 31, 2017, the Company had outstanding 95,711,579 commons shares; warrants to purchase up to 27,980,975 common
shares; and incentive stock options to purchase up to 930,000 common shares. As at October 27, 2017, the Company had
outstanding 100,062,079 common shares; warrants to purchase up to 32,331,475 common shares; and incentive stock options to
purchase up to 930,000 common shares.
SUBSEQUENT EVENTS
On August 31, 2017, the Company completed a private placement, issuing a total of 1,092,500 units at $1.20 per unit for gross
proceeds of approximately $1,311,000. Each unit consisted of one common share and one common share purchase warrant.
Each common share purchase warrant entitles the holder to purchase one common share at a price of $1.50 and has an expiry
of five years from the date of issuance.
On October 19, 2017, the Company completed a private placement, issuing a total of 3,258,000 units at $1.20 per unit for gross
proceeds of approximately $3,910,000. Each unit consisted of one common share and one common share purchase warrant.
Each common share purchase warrant entitles the holder to purchase one common share at a price of $1.50 and has an expiry
of five years from the date of issuance.
DISCLOSURE CONTROLS AND PROCEDURES AND INTERNAL CONTROL OVER FINANCIAL REPORTING
Management has designed the Company’s disclosure controls and procedures to provide reasonable assurance that all relevant
information is gathered, recorded, processed, summarized and reported to the Chief Executive Officer (“CEO”) and the Chief
Financial Officer (“CFO”) of the Company so that appropriate decisions can be made within the time periods specified in securities
legislation regarding public disclosure by the Company in its annual filings, interim filings or other documents or reports required
to be filed or submitted by it under securities legislation.
Management has also designed internal controls over financial reporting (“ICFR”) to provide reasonable assurance regarding the
reliability of the Company’s financial reporting and the preparation of financial statements for external purposes in accordance
with IFRS. Because of its inherent limitations, ICFR can provide only reasonable assurance and may not prevent or detect
misstatements. Further, projections of any evaluation of effectiveness to future periods are subject to the risk that controls may
become inadequate because of changes in conditions, or that the degree of compliance with policies or procedures may
deteriorate.
Material weakness previously disclosed and now remediated
a) a failure to adhere to Company standards with respect to the control environment throughout the management structure of
the Company and its Polish subsidiary, including ineffective and non-timely communication and reporting with respect to
corporate developments, commitments and public announcements by the Company’s Polish subsidiary;
b)
the calling of special shareholder meeting(s) by the Polish Subsidiary Board and use of a limited power of attorney without
compliance of the Company’s internal policies and procedures; and
c) designating signing authorities resulting in bank accounts being opened by the Company’s Polish subsidiary with only one
signatory without compensating controls (Company policy requires two signatories and/or sufficient compensating controls to
ensure the safeguarding of assets).
Management had previously concluded that it needed to establish a program of continuous education regarding corporate
governance and Canadian public disclosure rules for certain employees, directors and certain consultants having direct
involvement in the ongoing affairs of the Company and its Polish subsidiary.
As a result, the Company has established a regular and formalized process of meetings and written communications between the
various parties with formalized minute taking and action plans to provide reasonable assurance that all relevant information is
gathered, recorded, processed, summarized and reported to the CEO and the CFO.
Compensating controls have also been established to deal with the Company’s Polish subsidiary only having one signatory. The
Compensating control requires the Chief Executive Officer and Corporate Secretary of the parent company to provide oversight
and approval of disbursements in advance of vendor payments.
Procedures have also been established whereby any engagements, commitments and dissemination of news being contemplated
by the Company’s Polish subsidiary include the involvement of the parent company management in order to ensure appropriate
decisions can be made within the time periods specified in securities legislation in Canada regarding public disclosure by the
Company in its annual filings, interim filings or other documents or reports required to be filed or submitted by it under securities
legislation. Any material agreements being proposed by the Company’s Polish subsidiary will require advance approval by both
the parent company CEO and the Chairman of the polish subsidiary’s. Board of Directors.
Page | 21
Material weakness previously disclosed but not yet remediated
The termination of the Company’s controller in the third fiscal quarter, whose position has not been filled, resulted in a lack of
resources and has in turn impacted segregation of duties associated with the financial close and reporting process.
As of July 31, 2017, management has evaluated the effectiveness of the Company’s disclosure controls and procedures and ICFR
and have concluded they are not effective due to the above noted area of concern.
Management has concluded and the board has agreed, that when taking into account the Company’s size and financial resources,
the Company does not have sufficient scale of resources to warrant the hiring of additional staff to address this concern at this
time and, accordingly, that there is a material weakness in the design of the Company’s ICFR that has the potential to result in
material misstatements in the Company’s financial statements and that this should also be considered a weakness in the design
and operating effectiveness of the Company’s disclosure controls and procedures. This material weakness is considered to be a
common area of deficiency for many smaller listed companies in Canada.
Although the CEO and CFO are not aware of the above deficiency having actually resulted in a material misstatement of a financial
statement amount or disclosure, they have determined that, the deficiency could result in business and accounting practices that
could put both the Company’s reputation and its financial reporting at risk and lead to uncertainty whether control procedures are
being carried out such that the Company’s ICFR may fail to prevent or detect a material misstatement of a financial statement
amount or disclosure on a timely basis or fail to disclose material information required to be disclosed under securities legislation
within the time periods specified in securities legislation. However, there are several mitigating procedures and other factors which
reduce the risk of a material misstatement in the financial statements, including substantive review of the financial statements by
the Company’s audit committee and day-to-day management involvement in operations and reporting.
RISKS AND UNCERTAINTIES
Helix is subject to risks, events and uncertainties, or “risk factors”, associated with being both a publicly traded company operating
in the biopharmaceutical industry, and as an enterprise with several projects in the research and development stage. As a result
of these risk factors, reported information and forward-looking information may not necessarily be indicative of future operating
results or of future financial position, and actual results may vary from the forward-looking information or reported information.
The Company cannot predict all of the risk factors, nor can it assess the impact, if any, of such risk factors on the Company’s
business or the extent to which any factor, or combination of factors, may cause future results or financial position to differ
materially from either those reported or those projected in any forward-looking information. Accordingly, reported financial
information and forward-looking information should not be relied upon as a prediction of future actual results. Some of the risks
and uncertainties affecting the Company, its business, operations and results which could cause actual results to differ materially
from those reported or from forward-looking information include, either wholly or in part, those described elsewhere in this MD&A,
as well as the following:
The Company does not have any source of operating income and is dependent solely on outside sources of financing
The Company’s operations consist of research and development activities, which do not generate any revenue.
Accordingly, the Company has no source of revenue, positive operating cash flow or operating earnings to subsidize its
ongoing research and development and other operating activities and the ability of the Company to continue as a going
concern is dependent upon the Company’s ability to rely on cash on hand, and on outside sources of financing to fund
its ongoing research and development and other operating activities. Such sources of financing involve risks, including
that the Company will not be able to raise such financing on terms satisfactory to the Company or at all, and that any
additional equity financing, if secured, would result in dilution to existing shareholders, and that such dilution may be
significant. While the Company has been able to raise equity financing in recent years, there can be no assurance that
additional funding by way of equity financing will continue to be available. Any additional equity financing, if secured,
would result in dilution to the existing shareholders and such dilution may be significant. The Company may also seek
additional funding from or through other sources, including technology licensing, co-development collaborations, mergers
and acquisitions, joint ventures, and other strategic alliances, which, if obtained, may reduce the Company’s interest in
its projects or products or result in significant dilution to existing shareholders. The Company may also seek additional
funding from government grants. There can be no assurance, however, that any alternative sources of funding will be
available. The failure of the Company to obtain additional financing on a timely basis may result in the Company reducing,
delaying or cancelling one or more of its planned research, development and/or marketing programs, including clinical
trials, further reducing overhead, or monetizing non-core assets, any of which could impair the current and future value
of the business or cause the Company to consider ceasing operations and undergoing liquidation. Given the Company’s
conclusion about the insufficiency of its cash reserves, significant doubt may be cast about the Company’s ability to
continue operating as a going concern. The continuation of the Company as a going concern for the foreseeable future
depends mainly on raising sufficient capital, and in the interim, reducing, where possible, operating expenses (including
making changes to the Company’s research and development plans), including the delay of one or more of the
Company’s research and development programs, further reducing overhead and the possible disposition of assets.
Page | 22
The Company has a history of losses and expects to continue to incur additional losses for the foreseeable future
The Company’s primary focus continues to be on its research and development of pharmaceutical product candidates.
The research and development of pharmaceutical products requires the expenditure of significant amounts of cash over
a relatively long-time period. The Company expects to continue to incur losses from continuing operations, for the
foreseeable future. The Company’s cumulative deficit as at July 31, 2017 is $155,380,000. There can be no assurance
that the Company will record earnings in the future.
The Company requires additional funding
The Company’s cash reserves will not be sufficient for the Company to fully fund its existing European Phase I/II clinical
trial with L-DOS47 in Poland or its U.S. Phase I trial or any of the Company’s other ongoing research and development,
operating activities, working capital or capital expenditures for the next twelve months.
The Company has no sources of external liquidity, such as a bank loan or line of credit. The Company will therefore
continue to rely on equity financing to fund its ongoing research and development activities and other expenses for the
foreseeable future.
Equity financing has historically been the Company’s primary source of funding; however, the market for equity financings
for companies such as the Company is challenging. While the Company has been able to raise equity financing in recent
years, there can be no assurance that additional funding by way of equity financing will continue to be available. Any
additional equity financing, if secured, would result in dilution to the existing shareholders which may be significant. The
Company may also seek additional funding from or through other sources, including grants, technology licensing, co-
development collaborations, disposition of assets, mergers and acquisitions, joint ventures, and other strategic alliances,
which, if obtained, may reduce the Company’s interest in its projects or products or result in significant dilution to existing
shareholders. There can be no assurance, however, that any alternative sources of funding will be available.
The failure of the Company to obtain additional financing on a timely basis may result in the Company reducing, delaying
or cancelling one or more of its planned research and development, including any clinical trials, further reducing
overhead, or monetizing non-core assets, any of which could impair the current and future value of the business or cause
the Company to consider ceasing operations and undergoing liquidation.
The Company faces risks in connection with competition and technological change;
The biotechnology and pharmaceutical industries are subject to rapid and substantial technological change.
Technological competition from pharmaceutical companies, biotechnology companies and university researchers is
intense and is expected to continue to be intense.
The rapid advancement of immunotherapies now has the potential to significantly change the treatment of cancer and
may result in a reduction, which may be significant, in the potential patient population and/or treatment protocols available
to chemotherapies and other treatments currently in development, such as the Company’s primary drug product
candidate, L-DOS47. Furthermore, developments in immunotherapies may require the Company to reposition its L-
DOS47 drug product candidate from a front-line monotherapy to a combination therapy with immunotherapies or other
treatment protocols, and any such repositioning, would likely result in additional expenses being incurred by the Company
and in delays in the anticipated development timeline for L-DOS47, or in the Company determining that its L-DOS47 drug
product candidate is no longer viable.
The Company cell based therapies initiative may face significant hurdles. The Company’s effort is mainly at research
proof-of-concept stage. It is possible that the selected targets or choice of antibodies are not optimal. This can delay the
initiation of formal preclinical and clinical development significantly. The Company has chosen to develop cell based
therapy for solid tumour. While there are many successful examples of cell based therapy treatment in hematological
malignancies, similar success in solid tumour is less certain.
Many of the Company’s competitors have substantially greater financial, technical and human resources and significantly
greater experience in conducting preclinical testing and human clinical trials of product candidates, scaling up
manufacturing operations and obtaining regulatory approvals of products. Accordingly, the Company’s varying competitors
may succeed in obtaining regulatory approval for products more rapidly. The Company’s ability to compete successfully
will largely depend on:
the efficacy and safety profile of our product candidates relative to marketed products and other product
candidates in development;
our ability to develop and maintain a competitive position in the product categories and technologies on which
we focus;
the time it takes for our product candidates to complete clinical development and receive marketing approval;
our ability to obtain required regulatory approvals;
Page | 23
our ability to commercialize any of our product candidates that receive regulatory approval;
our ability to establish, maintain and protect intellectual property rights related to our product candidates; and
acceptance of any of our product candidates that receive regulatory approval by physicians and other healthcare
providers and payers.
Competitors have developed and may develop technologies that could be the basis for products that challenge the
differentiated nature and potential for best-in-class product development programs and discovery research capabilities of
the DOS47 platform tehcnology. Some of those products may have an entirely different approach or means of
accomplishing the desired therapeutic effect than our product candidates and may be more effective or less costly than
our product candidates. The success of our competitors and their products and technologies relative to our technological
capabilities and competitiveness could have a material adverse effect on the future preclinical studies a nd clinical trials
of our product candidates, including our ability to obtain the necessary regulatory approvals for the conduct of such clinical
trials. This may further negatively impact our ability to generate future product development programs with improved
pharmacological properties.
If we are not able to compete effectively against our current and future competitors, our business will not grow and our
financial condition and operations will substantially suffer.
The Company is conducting early stage research and development initiatives for products under development which
may not be accepted by the market and may never generate revenue and the Company has limited sales, marketing and
distribution experience
The Company is conducting early stage research and development initiatives and is currently in the process of developing
new products that require further time consuming and costly research and development. It will be a number of years, if
ever, before its products in development begin to generate revenues, if at all. There can be no assurance that any of the
drug product candidates will ever be successfully developed or commercialized.
Even with regulatory approval, the Company may not achieve market acceptance, which depends on a number of factors,
including the establishment and demonstration in the medical community of the clinical utility of the Company’s products,
and their potential advantage over alternative treatment methods. There is also the risk that the actual market size or
opportunity for the Company’s drug candidates is not certain. Failure to gain market acceptance of either of the
Company’s products currently under development or an incorrect estimate in the nature and size of their respective
markets could have a material adverse effect on the Company.
The Company has limited sales, marketing and distribution experience, and there is no assurance that the Company will
be able to establish adequate sales, marketing, and distribution capabilities or make arrangements with any collaborators,
strategic partners, licensees, or others to perform such activities, or that such efforts will be successful. The Company’s
objective for its drug candidate products is to enter into strategic alliances with appropriate pharmaceutical partners.
There can be no assurance that any such strategic alliance will be maintained or achieved, or if achieved, that it will result
in revenue to the Company.
The timing of the Company’s internal goals and projected timelines may not be met
The Company sets internal goals for and makes public statements regarding its expected timing of meeting the objectives
material to its success, including the commencement, duration and completion of clinical trials and anticipated regulatory
approvals. The actual timing of these forward-looking events can vary dramatically due to a number of factors, including,
without limitation, delays in scaling-up of drug product candidates, delays or failures in clinical trials, additional data
requirements from the regulators, the Company failing to obtain required financing, and other risks referred to herein.
Without limiting the generality of the foregoing, it is possible that required regulatory approvals may be delayed or denied,
including those related to undertaking or continuing clinical trials, manufacturing of drug products, and marketing such
products.
The Company has expressed certain estimated timelines for its European Phase I//II clinical trials for L-DOS47 in Poland,
the U.S. Phase I study. The timeline for the European Phase I/II trials and any future timelines are contingent on the
Company having adequate financing to complete the trials and the assumption that the trials will be completed according
to the current schedules. A failure to obtain necessary financing or a change in the schedule of the trials (which may
occur if certain cost-deferral measures are taken, or due to factors beyond the Company’s reasonable control, such as
scheduling conflicts, the occurrence of serious adverse events, interruption of supplies of study drugs, withdrawals of
regulatory approvals, or slow patient recruitment) could delay their commencement or completion, or result in their
suspension or early termination, which could have a material adverse effect on the Company.
Page | 24
The Company faces intellectual property risks, including the loss of patent protection, the potential termination of
licences, the inability to protect proprietary property, and possible claims of infringement against the Company or against
a third-party from whom the Company licenses intellectual property
The Company’s success depends, in part, on its ability to secure and protect its intellectual property rights and to operate
without infringing on the proprietary rights of others or having third parties circumvent the rights owned or licensed by the
Company. However, the Company cannot predict the enforceability of its patents or its ability to maintain trade secrets
that may not be protected by patents. Patent risks include the fact that patent applications may not result in issued
patents, issued patents may be circumvented, challenged, invalidated or insufficiently broad to protect the Company’s
products and technologies; blocking patents by third parties could prevent the Company from using its patented
technology; it may be difficult to enforce patent rights, particularly in countries that do not have adequate legal enforcement
mechanisms, and enforcing such rights may divert management attention and may cause the Company to incur significant
expenses; and any expiry of an issued patent may negatively impact the underlying technology.
To protect its trade secrets, the Company enters into confidentiality undertakings with parties that have access to them,
such as the Company’s current and prospective distributors, collaborators, employees and consultants, but a party may
breach the undertakings and disclose the Company’s confidential information or competitors might learn of the information
in some other way, which could have a material adverse effect on the Company.
The Company uses processes, technology, products, or information, the rights to certain of which are owned by others,
such as a license from the NRC of the lung antibody used by the Company for L-DOS47. Termination or expiry of any
licenses or rights during critical periods, and an inability to obtain them on commercially favourable terms or at all could
have a material adverse effect on the Company and its drug candidates’ development.
The Company operates in an industry that experiences substantial litigation involving the manufacture, use and sale of
new products that are the subject of conflicting proprietary rights. The Company or one or more of its licensors may be
subject to a claim of infringement of proprietary rights by a third party. It is possible that the Company’s products and
technologies do infringe the rights of third parties, and the Company or such licensor could incur significant expenses,
and diversion of management attention, in defending allegations of infringement of proprietary rights, even if there is no
infringement. Furthermore, the Company or such licensors may be required to modify its products or obtain licenses for
intellectual property rights as a result of any alleged proprietary infringement. The inability to modify products or obtain
licenses on commercially reasonable terms, in a timely manner or at all, could adversely affect the Company’s business.
The Company faces research and development risks, including the need to prove the Company’s drug candidates are
safe and effective in clinical trials
The Company’s drug candidates are complex compounds and the Company faces difficult challenges in connection with
the manufacture of clinical batches of each of them, which could further delay or otherwise negatively affect the
Company’s planned clinical trials, or required regulatory approvals.
There is also the risk that the Company could obtain negative findings or factors that may become apparent during the
course of research or development. The results from preclinical and clinical trials may not be predictive of results obtained
in any ongoing or future clinical trials. A number of companies in the biotechnology and pharmaceutical industry have
suffered significant setbacks in advanced clinical trials, even after achieving promising results in earlier trials and pre-
clinical trials.
The timing and success of the Company’s clinical trials also depend on a number of other factors, including, but not
limited to: (a) obtaining additional financing, which is not assured; (b) sufficient patient enrolment, which may be affected
by the incidence of the disease studied, the size of the patient population, the nature of the protocol, the proximity of
patients to clinical sites, the eligibility criteria for a patient to participate in the study and the rate of patient drop-out; (c)
regulatory agency policies regarding requirements for approval of a drug, including granting permission to undertake
proposed human testing; (d) the Company’s capacity to produce sufficient quantities and qualities of clinical trial materials
to meet the trial schedule; (e) performance by third parties, on whom the Company relies to carry out its clinical trials;
and (f) the approval of protocols and/or protocol amendments.
Clinical trials are complex, expensive and uncertain, and have a high risk of failure, which can occur at any stage. Data
obtained from pre-clinical and clinical trials may be interpreted in different ways, or be incorrectly reported, which could
delay or prevent further development of the drug candidate studied. Failure to complete clinical trials successfully and
to obtain successful results on a timely basis could have a material adverse effect on the Company.
Even if the Company’s drug candidates successfully complete the clinical trials and receive the regulatory approval
necessary to market the drug candidates to the public, there is also the risk of unknown side effects, which may not
appear until the drug candidates are on the market and may result in delay or denial of regulatory approval or withdrawal
of previous approvals, product recalls or other adverse events, which could materially adversely affect the Company.
Page | 25
While the Company continues to explore opportunities to expand its drug product pipeline with new DOS47-based
therapeutics pending the identification of further tumour targeting agents, there can be no assurance that any such
tumour targeting agents will be identified or that any new DOS47-based therapeutics will be developed.
Difficulty in enrolling patients in the Company’s clinical trials, could result in delays or cancellation of clinical trials
As the Company’s product candidates advance from preclinical testing to clinical testing, and then through progressively
larger and more complex clinical trials, the Company will need to enroll an increasing number of patients that meet various
eligibility criteria. There is significant competition for recruiting cancer patients in clinical trials, and the Company may not
be unable to enroll the patients it needs to complete clinical trials on a timely basis or at all. The factors that affect the
Company’s ability to enroll patients is largely uncontrollable and include, but are not limited to, the following:
size and nature of the patient population;
eligibility and exclusion criteria for the trial;
design of the study protocol;
competition with other companies for clinical sites or patients;
the perceived risks and benefits of the product candidate under study;
the patient referral practices of physicians; and
the number, availability, location and accessibility of clinical trial sites.
The Company is dependent on a number of third parties and the failure or delay in the performance of one of these third
parties’ obligations may adversely affect the Company
The Company is dependent on third parties to varying degrees in virtually all aspects of its business, including without
limitation, on contract research organizations, contract manufacturing organizations, clinical trial consultants, raw material
suppliers, collaborative research consultants, regulatory affairs advisers, medical and scientific advisors, clinical trial
investigators, business service providers and other third parties. Critical supplies may not be available from third parties
on acceptable terms, or at all, including GMP grade materials. Service providers may not perform, or continue to perform,
as needed, or be available to provide the required services on acceptable terms or at all. Any lack of or interruption in
supplies of raw materials or services, or any change in supply or service providers or any inability to secure new supply
or service providers, would have an adverse impact on the development and commercialization of the Company’s
products. For example, the Company has previously experienced delays in the manufacturing of both engineering and
clinical batches of L-DOS47, which have in turn caused delays in the progression of its development program, and there
may be further delays. The Company relies on a third party for its supply of urease and if the contract with the third-party
urease supplier is terminated early, the Company will have to find a new supplier of urease, as well as a new manufacturer
of bulk drug product for future clinical testing programs. There can be no assurance that a new supplier or manufacturer
can be contracted in a timely manner or at all, and this could negatively impact the Company’s development plans for L-
DOS47.
With respect to L-DOS47, the Company is currently dependent on, in addition to third party suppliers, manufacturers and
consultants, the NRC and its license to the Company of a lung cancer antibody in order to develop and commercialize
L-DOS47. Early termination of the license with NRC would have a material adverse effect on the further development of
L-DOS47 and may require the cessation of such development, which would have a material adverse effect on the
Company.
Given the Company`s lack of financing, expertise, infrastructure and other resources to support a new drug product from
clinical development to marketing, the Company also requires strategic partner support to develop and commercialize its
drug candidates. There can be no assurance that such strategic partner support will be obtained upon acceptable terms
or at all.
The Company relies heavily on contract manufacturers for the production of product required for its clinical trials, product
formulation work, scaling-up experiments and commercial production. The Company may not be able to obtain new, or
keep its current, contract manufacturers to provide these services. Even if the Company does, contract manufacturers
may not be reliable in meeting its requirements for cost, quality, quantity or schedule, or the requirements of any
regulatory agencies. The Company may not be able to manufacture products in quantities or qualities that would enable
the Company to meet its business objectives, and failure to do so would materially adversely affect the Company’s
business.
If the Company can successfully develop markets for its products, the Company would have to arrange for their scaled-
up manufacture. There can be no assurance that the Company will, on a timely basis, be able to make the transition
from manufacturing clinical trial quantities to commercial production quantities successfully or be able to arrange for
scaled-up commercial contract manufacturing. Any potential difficulties experienced by the Company in manufacturing
scale-up, including recalls or safety alerts, could have a material adverse effect on the Company’s business, financial
condition, and results of operations.
Page | 26
The marketability of the Company’s products may be affected by delays and the inability to obtain necessary approvals,
and following any market approval, the Company’s products will be subject to ongoing regulatory review and
requirements which may continue to affect their marketability, including but not limited to regulatory review of drug
pricing, healthcare reforms or the payment and reimbursement policies for drugs by the various insurers and other
payors in the industry
The research, development, manufacture and marketing of pharmaceutical products are subject to regulation by the
FDA, and comparable regulatory authorities in other countries. These agencies and others regulate the testing,
manufacture, safety and promotion of the Company’s products. The Company must receive applicable regulatory
approval of a product candidate before it can be commercialized in any particular jurisdiction. Approval by a regulatory
authority of one country does not ensure the approval by regulatory authorities of other countries. Changes in regulatory
approval policies or regulations during the development period may cause delays in the approval or rejection of an
application. Regulatory authorities have substantial discretion in the approval process and may refuse to accept any
application, or may decide that our data are insufficient for approval, or require additional preclinical, clinical or other trials
and place the Company’s IND submissions on hold for an indeterminate amount of time. The development and regulatory
approval process in each jurisdiction takes many years, requires the expenditure of substantial resources, is uncertain
and subject to delays, and can adversely affect the successful development and commercialization of our drug
candidates.
Even if the Company obtains marketing approval in a particular jurisdiction, there may be limits on the approval and the
Company’s products likely will be subject to ongoing regulatory review and regulatory requirements in that jurisdiction.
Pharmaceutical companies are subject to various government regulations, including without limitation, requirements
regarding occupational safety, laboratory practices, environmental protection and hazardous substance control, and may
be subject to other present and future regulations.
The availability of reimbursement by governmental and other third-party payors, such as private insurance plans, will
affect the market for any pharmaceutical product, and such payors tend to continually attempt to contain or reduce the
costs of healthcare. Significant uncertainty exists with respect to the reimbursement status of newly approved healthcare
products.
The Company operates in an industry that is more susceptible than others to legal proceedings and, in particular, liability
claims
The Company operates in an industry that is more susceptible to legal proceedings than firms in other industries, due to
the uncertainty involved in the development of pharmaceuticals. Defense and prosecution of legal claims can be
expensive and time consuming, and may adversely affect the Company regardless of the outcome due to the diversion
of financial, management and other resources away from the Company’s primary operations. Negative judgments
against the Company, even if the Company is planning to appeal such a decision, or even a settlement in a case, could
negatively affect the cash reserves of the Company, and could have a material negative effect on the development of its
drug products.
The Company may be exposed, in particular, to liability claims which are uninsured or not sufficiently insured, and any
claims may adversely affect the Company’s ability to obtain insurance in the future or result in negative publicity regarding
the efficacy of its drug products. Such liability insurance is expensive, its ability is limited and it may not be available on
terms that are acceptable to the Company, if at all.
The use of any of the Company’s unapproved products under development, the use of its products in clinical trials, and,
if regulatory approval is received, the sale of such products, may expose the Company to liability claims which could
materially adversely affect the Company’s business. The Company may not be able to maintain or obtain commercially
reasonable liability insurance for future products, and any claims under any insurance policies may adversely affect its
ability to maintain existing policies or to obtain new insurance on existing or future products. Even with adequate
insurance coverage, publicity associated with any such claim could adversely affect public opinion regarding the safety
or efficacy of the Company’s products. As a result, any product liability claim or recall, including in connection with
products previously sold by the Company through its former distribution business, could materially adversely affect the
Company’s business.
If the Company were unable to maintain product liability insurance required by our third parties, the corresponding
agreements would be subject to termination, which could have a material adverse impact on our operations.
Some of our licensing and other agreements with third parties require or might require us to maintain product liability
insurance. If the Company cannot maintain acceptable amounts of coverage on commercially reasonable terms in
accordance with the terms set forth in these agreements, the corresponding agreements would be subject to termination,
which could have a material adverse impact on the Company’s operations.
Page | 27
The Company is dependent upon key personnel; Director residency requirements
The Company’s ability to continue its development of potential products depends on its ability to attract and maintain
qualified key individuals to serve in management and on the Board. However, the Company does not currently have a
formal succession plan for members of its senior management team or for its Board and, because competition for qualified
key individuals with experience relevant to the industry in which the Company operates is intense, the Company may not
be able to attract and/or retain such personnel. Additionally, applicable corporate law requires that at least 25% of the
Company’s directors be resident Canadians, and the Company’s articles provide that the Company cannot have fewer
than five directors at any time.
Consequently, if the Company is unable to attract and/or loses and is unable to replace key personnel, its business could
be negatively affected and, in particular, if the Company loses one or more of its three current resident Canadian directors
in the future and is unable to find a sufficient number of resident Canadian directors to fill the resulting vacancy(ies), the
Board will be prevented from taking any action other than appointing additional resident Canadian directors until such
time as a sufficient number of new resident Canadian directors have been appointed such that at least 25% of the
Company’s directors are resident Canadians.
In addition, the Company does not carry key-man insurance on any individuals.
The Company’s employees and consultants may engage in misconduct or other improper activities, including non-
compliance with regulatory standards and requirements, which could have a material adverse effect on the Company’s
business.
The Company is exposed to the risk of employee and consultant fraud or other misconduct. Misconduct by employees
and consultants could include, but are not limited to the following: failure to comply with regulators, failure to provide
accurate information, failure to comply with manufacturing standards the Company has established, jurisdictional
healthcare fraud and abuse of laws and regulations, failure to report financial information or data accurately or disclose
unauthorized activities. For example, sales, marketing and business arrangements in the healthcare industry are subject
to extensive laws and regulations intended to prevent fraud, kickbacks, self-dealing, and other abusive practices. These
laws and regulations may restrict or prohibit a wide range of pricing, discounting, marketing and promotion, sales
commission, customer incentive programs and other business arrangements. Employee and consultant misconduct could
also involve the improper use of information obtained in the course of clinical trials, which could result in regulatory
sanctions and serious harm to the Company’s reputation. If any such actions are instituted against the Company, and the
Company is not successful in defending itself or asserting its rights, those actions could have a substantial impact on the
Company’s business and operating results, including the imposition of substantial fines, halt in trading of the Company’s
common shares, possible delisting and/or other sanctions.
Indemnification obligations to directors and officers of the Company may adversely affect the Company’s finances
The Company has entered into agreements pursuant to which the Company has agreed to indemnify its directors and
senior management in respect of certain claims made against them while acting in their capacity as such. If the Company
is called upon to perform its indemnity obligations, its finances may be adversely affected.
The Company’s finances may fluctuate based on foreign currency exchange rates
The Company operates internationally and is exposed to foreign exchange risks from various currencies, primarily the
U.S. dollar, the Euro and the Polish Zloty.
Unanticipated changes in the Company’s tax rates could affect its future results
Since the Company operates in different countries and is subject to taxation in different jurisdictions, its future effective
tax rates could be impacted by changes in such countries’ tax laws or their interpretations. Both domestic and
international tax laws are subject to change as a result of changes in fiscal policy, changes in legislation, evolution of
regulation and court rulings. The application of these tax laws and related regulations is subject to legal and factual
interpretation, judgment and uncertainty.
Shareholders of the Company may face dilution through exercise of stock options, warrants and future equity financings
To attract and retain key personnel, the Company has granted options to its key employees, directors and consultants to
purchase common shares and share awards as non-cash incentives. In addition, the Company has a significant number
of warrants to purchase common shares outstanding. The issuance of shares pursuant to share awards and the exercise
of a significant number of such options and warrants may result in significant dilution of other shareholders of the
Company.
Page | 28
As noted above, the Company needs additional funding and has historically turned to the equity markets to raise this
funding. The future sale of equity and warrants may also result in significant dilution to the shareholders of the Company.
The Company’s share price and trading volumes are volatile and the Company may have difficulty maintaining listing
requirements
The price of the Company’s common shares, as well as market prices for securities of biopharmaceutical and drug
delivery companies generally, have historically been highly volatile, and have from time to time experienced significant
price and volume fluctuations that are unrelated to the operating performance of particular companies.
The trading price of the Company’s common shares is subject to change and could in the future fluctuate significantly.
The fluctuations could be in response to numerous factors beyond the Company’s control, including: quarterly variations
in results of operations; announcements of technological innovations or new products by the Company, its customers or
competitors; changes in securities analysts’ recommendations; announcements of acquisitions; changes in earnings
estimates made by independent analysts; general fluctuations in the stock market; or revenue and results of operations
below the expectations of public market securities analysts or investors. Any of these could result in a sharp decline in
the market price of the common shares.
The Internet offers various avenues for the dissemination of information. The Company has no control over the
information that is distributed and discussed on electronic bulletin boards and investment chat rooms. The intention of
the people or organizations that distribute such information may not be in the Company’s best interest and the best
interests of its shareholders. This, in addition to other forms of investment information including newsletters and research
publications, could result in a sharp decline in the market price of the common shares.
In addition, stock markets have occasionally experienced extreme price and volume fluctuations. The market prices for
high-technology companies have been particularly affected by these market fluctuations and such effects have often
been unrelated to the operating performance of such companies. These broad market fluctuations may cause a decline
in the market price of the common shares.
Sales of substantial numbers of the Company’s common shares could cause a decline in the market price of such
common shares. There are minimum listing requirements for an issuer to maintain its listing on the Toronto Stock
Exchange (“TSX”), and if the Company fails to maintain these listing requirements, it may be involuntarily delisted from
the TSX. De-listing the Company or the Company shares from any securities exchange could have a negative effect on
the liquidity of the Company shares and/or the ability of a shareholder to trade in shares of the Company, and could have
an adverse effect on the Company’s ability to raise future equity financings. The Company’s common shares trade in a
very low volume compared to the number of common shares outstanding. This means a shareholder could have difficulty
disposing of common shares, especially if there are other shareholders of the Company trying to sell their shares in the
Company at the same time. Volatility in share price and trading volumes could have an adverse effect on the Company’s
ability to raise future equity financings.
The requirements of being a public company may strain the Company’s resources, divert management’s attention and
affect its ability to attract and retain qualified board members
As a public company, the Company is subject to the reporting requirements of Canadian securities regulators, the listing
requirements of the Exchange and other applicable securities rules and regulations. Compliance with these rules and
regulations may increase the Company’s legal and financial compliance costs, may make some activities more difficult,
time-consuming or costly and may increase the demand on the Company’s systems and resources. Being a public
company requires that the Company file continuous disclosure documents, including, among other things, annual and
quarterly financial statements. Management’s attention may be diverted from other business concerns, which could have
a material adverse effect on the Company’s business, financial condition and results of operations. The Company may
need to hire more employees in the future, which will increase its costs and expenses.
In addition, changing laws, regulations and standards relating to corporate governance and public disclosure create
uncertainty for public companies, increasing legal and financial compliance costs and making some activities more time
consuming. This could result in continuing uncertainty regarding compliance matters and higher costs necessitated by
ongoing revisions to disclosure and governance practices. The Company may invest resources to comply with evolving
laws, regulations and standards, and this investment may result in increased general and administrative expenses and
a diversion of management’s time and attention from revenue-generating activities to compliance activities. If the
Company’s efforts to comply with new laws, regulations and standards differ from the activities intended by regulatory
authorities, legal proceedings may be initiated against the Company and its business may be harmed.
Page | 29
Trading in the Company’s common shares outside of Canada may be subject to restrictions on trading under foreign
securities laws, and purchasers of securities under private placements by the Company will be subject to certain
restrictions on trading
The Company’s common shares trade on the TSX and are freely tradeable only in Canada. As such, shareholders
trading the Company’s common shares outside of Canada may be subject to restrictions imposed by foreign securities
laws that may restrict their ability to transfer shares freely or at all. Certain securities offered by the Company pursuant
to its private placements, including the unlisted warrants issued by the Company, are subject to certain initial hold periods
and other restrictions on trading imposed by applicable securities laws and, in the case of the warrants, pursuant to the
terms of the applicable warrant certificates. These restrictions may affect the liquidity of the investment of certain
shareholders in the securities of the Company.
General economic conditions may have an adverse effect on the Company and its business
Continuing global economic volatility and uncertainty may have an adverse effect on the Company and its business,
including without limitation the ability to raise additional financing, to obtain strategic partner support or commercialization
opportunities and alliances for the Company’s new drug candidates, and to obtain continued services and supplies.
The Company’s business involves environmental risks that could result in accidental contamination, injury, and
significant capital expenditures in order to comply with environmental laws and regulations
The Company and its commercial collaborators are subject to laws and regulations governing the use, manufacture,
storage, handling and disposal of materials and certain waste products. Although the Company believes that its safety
procedures comply with the regulations, the risk of accidental contamination or injury from these materials cannot be
eliminated. In the event of such an accident, the Company could be held liable for any damages that result and any such
liability could exceed the resources of the Company. The Company is not specifically insured with respect to this liability.
The Company (or its collaborators) may be required to incur significant costs to comply with environmental laws and
regulations in the future; and the operations, business or assets of the Company may be materially adversely affected
by current or future environmental laws or regulations.
Any failure to maintain an effective system of internal controls may result in material misstatements of our consolidated
financial statements or cause us to fail to meet our reporting obligations or fail to prevent fraud; and in that case, our
shareholders could lose confidence in our financial reporting, which would harm our business, could negatively impact
the price of our common shares and prevent the Company from raising additional capital.
Effective internal controls are necessary for the Company to provide reliable financial reports and prevent fraud. If the
Company fails to maintain an effective system of internal controls, the Company may not be able to report its financial
results accurately or prevent fraud; and in that case, the Company’s shareholders could lose confidence in our financial
reporting, which would harm our business, negatively impact the price of the Company’s common shares and also prevent
the Company from raising additional capital. Even if we were to conclude that our internal control over financial reporting
provides reasonable assurance regarding the reliability of financial reporting and the preparation of consolidated financial
statements for external purposes in accordance with IFRS as issued by the IASB, because of its inherent limitations,
internal control over financial reporting may not prevent or detect fraud or misstatements. Failure to achieve and maintain
effective internal control over financial reporting could prevent the Company from complying with its reporting obligations
on a timely basis, which could result in the loss of investor confidence in the reliability of the Company’s consolidated
financial statements, harm our business, negatively impact the trading price of our common shares and prevent the
Company from raising additional capital.
RISK FACTORS IN OTHER PUBLIC FILINGS
For all of the reasons set forth above, together with those additional risk factors identified under the headings “Forward-Looking
Statements” and “Risk Factors” in the Company’s most recent Annual Information Form filed under the Company’s profile on
SEDAR at www.sedar.com, investors should not place undue reliance on forward-looking information. Other than any obligation
to disclose material information under applicable securities laws, the Company undertakes no obligation to revise or update any
forward-looking information after the date hereof.
Data relevant to estimated market sizes and penetration for the Company’s lead products under development are presented in
this MD&A. This data has been obtained from a variety of published resources including published scientific literature, websites
and information generally available through publicized means. The Company attempts to source reference data from multiple
sources whenever possible for confirmatory purposes. Although the Company believes the foregoing data is reliable, the
Company has not independently verified the accuracy and completeness of this data.
Page | 30
ADDITIONAL INFORMATION
Additional information relating to the Company’s fiscal year ended July 31, 2017, is available under the Company’s profile on
SEDAR at www.sedar.com.
October 27, 2017
Page | 31
Consolidated Financial Statements of Helix BioPharma Corp.
Years ended July 31, 2017 and 2016
MANAGEMENT’S RESPONSIBILITY FOR
FINANCIAL INFORMATION
The accompanying consolidated financial statements of Helix BioPharma Corp. and other financial information contained in this
annual report are the responsibility of management. The consolidated financial statements have been prepared in conformity with
International Financial Reporting Standards, using management’s best estimates and judgments, where appropriate. In the
opinion of management, these consolidated financial statements reflect fairly the financial position and the results of operations
and cash flows of the Company within reasonable limits of materiality. The financial information contained elsewhere in this annual
report has been reviewed to ensure consistency with that in the consolidated financial statements.
To assist management in discharging these responsibilities, the Company maintains an effective system of procedures and
internal controls which is designed to provide reasonable assurance that its assets are safeguarded against loss from unauthorized
use or disposition, that transactions are executed in accordance with management’s authorization and that the financial records
form a reliable base for the preparation of accurate and reliable financial information.
The Board of Directors ensures that management fulfills its responsibilities for the financial reporting and internal control. The
Board of Directors exercises this responsibility through its independent Audit Committee comprising a majority of unrelated and
outside directors. The Audit Committee meets periodically with management and annually with the external auditors to review
audit recommendations and any matters that the auditors believe should be brought to the attention of the Board of Directors. The
Audit Committee also reviews the consolidated financial statements and recommends to the Board of Directors that the statements
be approved for issuance to the shareholders.
The consolidated financial statements have been audited by BDO Canada LLP, Chartered Professional Accountants, Licensed
Public Accountants, which has full and unrestricted access to the Audit Committee. BDO Canada LLP’s report on the consolidated
financial statements is presented herein.
/s/ Heman Chao
Heman Chao
Chief Executive and Science Officer
October 27, 2017
/s/ Photios (Frank) Michalargias
Photios (Frank) Michalargias
Chief Financial Officer
Page | 33
BDO Canada LLP
60 Columbia Way, Suite 300
Markham, Ontario, L3R 0C9
Canada
Telephone (905) 946-1066
Fax (905) 946-9524
www.bdo.ca
Independent Auditor's Report
To the Shareholders of
Helix BioPharma Corp.
We have audited the accompanying consolidated financial statements of Helix BioPharma Corp., and its subsidiaries, which
comprise the statements of financial position as at July 31, 2017 and 2016, the consolidated statements of net loss and
comprehensive loss, changes in shareholders’ equity, and cash flows for the years then ended and a summary of significant
accounting policies and other explanatory information.
Management’s Responsibility for the Consolidated Financial Statements
Management is responsible for the preparation and fair presentation of these consolidated financial statements in accordance with
International Financial Reporting Standards, and for such internal control as management determines is necessary to enable the
preparation of consolidated financial statements that are free from material misstatement, whether due to fraud or error.
Auditors’ Responsibility
Our responsibility is to express an opinion on these consolidated financial statements based on our audits. We conducted our
audits in accordance with Canadian generally accepted auditing standards. Those standards require that we comply with ethical
requirements and plan and perform the audit to obtain reasonable assurance about whether the consolidated financial statements
are free from material misstatement.
An audit involves performing procedures to obtain audit evidence about the amounts and disclosures in the consolidated financial
statements. The procedures selected depend on the auditor’s judgment, including the assessment of the risks of material
misstatement of the consolidated financial statements, whether due to fraud or error. In making those risk assessments, the
auditor considers internal control relevant to the entity’s preparation and fair presentation of the consolidated financial statements
in order to design audit procedures that are appropriate in the circumstances, but not for the purpose of expressing an opinion on
the effectiveness of the entity’s internal control. An audit also includes evaluating the appropriateness of accounting policies used
and the reasonableness of accounting estimates made by management, as well as evaluating the overall presentation of the
consolidated financial statements.
We believe that the audit evidence we have obtained in our audits is sufficient and appropriate to provide a basis for our audit
opinion.
Opinion
In our opinion, the consolidated financial statements present fairly, in all material respects, the financial position of Helix
BioPharma Corp., as at July 31, 2017 and 2016, and its financial performance and its cash flows for the years then ended in
accordance with International Financial Reporting Standards.
Emphasis of Matter
Without modifying our opinion, we draw attention to Note 1 in the consolidated financial statements, which indicates that Helix
BioPharma Corp.’s cash of $897,000 as at July 31, 2017 is insufficient to meet anticipated cash needs for working capital and
capital expenditures through the next twelve months. This condition, along with other matters as set forth in Note 1 in the
consolidated financial statements, indicate the existence of a material uncertainty that may cast significant doubt about Helix
BioPharma Corp.’s ability to continue as a going concern.
/s/ BDO Canada LLP
Chartered Professional Accountants, Licensed Public Accountants
October 27, 2017
Markham, Ontario
Page | 34
HELIX BIOPHARMA CORP.
Consolidated Statement of Financial Position
In thousands of Canadian dollars
As at July 31, 2017 and 2016
As at:
ASSETS
Non-current assets
Property, plant and equipment (note 4)
Current assets
Prepaid expenses
Accounts receivable
Cash
Total assets
July 31, 2017
July 31, 2016
$
487
487
173
630
897
1,700
$
235
235
90
489
3,654
4,233
$
2,187
$
4,468
SHAREHOLDERS’ EQUITY (DEFICIENCY) AND LIABILITIES
Shareholders’ equity / (deficiency) (note 5)
$
(17)
$
3,164
Current liabilities
Deferred government grant (note 11)
Accrued liabilities
Accounts payable
44
722
1,438
2,204
–
589
715
1,304
Total liabilities and shareholders’ equity (deficiency)
$
2,187
$
4,468
The accompanying notes are an integral part of these consolidated financial statements.
On behalf of the Board of Directors:
/s/ Sven Rohmann
Sven Rohmann,
Chair, Board of Directors
/s/ Sylwester Cacek
Sylwester Cacek
Chair, Audit Committee
Page | 35
HELIX BIOPHARMA CORP.
Consolidated Statement of Net Loss and Comprehensive Loss
Years ended July 31, 2017 and 2016 (In thousands of Canadian dollars, except per share amounts)
Expenses
Research and development
Operating, general and administration
Gain on sale of property, plant and equipment (note 13)
Results from operating activities before finance items
Finance items
Finance income
Finance expense
Foreign exchange gain (loss)
2017
2016
7,055
3,207
(168)
(10,094)
16
(14)
33
35
5,821
3,836
–
(9,657)
26
(17)
(17)
(8)
Net loss and total comprehensive loss
$
(10,059)
$
(9,665)
Loss per common share
Basic
Diluted
$
$
(0.11)
(0.11)
$
(0.11)
$ (0.11)
Weighted average number of common shares used in the calculation of
basic and diluted loss per share
91,797,627
85,550,926
The accompanying notes are an integral part of these consolidated financial statements.
Page | 36
HELIX BIOPHARMA CORP.
Consolidated Statement of Changes in Shareholders’ Equity
Years ended July 31, 2017 and 2016 (In thousands of Canadian dollars, except per share amounts)
In thousands of Canadian dollars, except common share and warrant numbers
Common shares warrants
Share purchase
Amount
Number Amount
Contributed
Number Options surplus
Accumulated
other
comprehensive
Total
income shareholders
equity
(loss)
Deficit
Balances, July 31, 2015 $ 112,288 84,653,837 $ 8,825 19,948,584 $2,915 $18,455 $(135,656) $ –
–
Net loss for the year
–
Common stock, issued
–
Warrants, issued
–
Warrants, expired unexercised
–
Warrants, exercised
–
Stock-based compensation
–
Options, exercised
–
Options, expired unexercised
–
–
2,081 4,355,000
(2,049) (2,571,084)
(48,500)
–
–
–
–
4,355,000
–
–
48,500
–
190,600
–
–
–
–
–
–
230
(147)
(1,286)
(9,665)
–
–
–
–
–
–
–
–
3,365
–
–
93
–
400
–
–
–
–
2,049
–
–
–
1,286
(20)
–
–
–
–
–
Balances, July 31, 2016 $ 116,146 89,247,937 $ 8,837 21,684,000 $1,712 $21,790 $(145,321) $ –
–
Net loss for the year
–
Common stock, issued
–
Warrants, issued
–
Warrants, expired unexercised
–
Warrants, exercised
–
Stock-based compensation
–
Options, exercised
–
Options, expired unexercised
–
–
2,304 6,296,975
–
–
–
–
–
–
6,296,975
–
–
–
–
166,667
–
(10,059)
–
–
–
–
–
–
–
–
–
–
–
–
159
(120)
(1,078)
–
4,195
–
–
–
–
340
–
–
–
–
–
–
–
–
1,078
–
–
–
–
–
–
–
$ 6,827
(9,665)
3,365
2,081
–
73
230
253
–
$ 3,164
(10,059)
4,195
2,304
–
–
159
220
–
Balances, July 31, 2017 $ 120,681 95,711,579 $11,141 27,980,975 $ 673 $22,868 $(155,380) $ –
$
(17)
The accompanying notes are an integral part of these consolidated financial statements.
Page | 37
HELIX BIOPHARMA CORP.
Consolidated Statement of Cash Flows
Years ended July 31, 2017 and 2016 (In thousands of Canadian dollars)
Cash flows from operating activities
Net loss and total comprehensive loss
Items not involving cash:
Depreciation of property, plant and equipment
Stock-based compensation
Foreign exchange loss
Gain on sale of property, plant and equipment
Change in non-cash working capital:
Accounts receivable
Prepaid expenses
Accounts payable
Accrued liabilities
Deferred liabilities
Net cash used in operating activities
Cash flows from financing activities
Proceeds from the issuance of common shares and
share purchase warrants, net of issue costs
Proceeds from the exercise of stock options
Proceeds from the exercise of warrants
Net cash provided by financing activities
Cash flows from investing activities
Proceeds from the sale of property, plant and equipment
Purchase of property, plant and equipment
Net cash used in investing activities
Foreign exchange gain (loss) on cash
Net decrease in cash
Cash, beginning of year
Cash, end of year
2017
2016
$
(10,059)
$
(9,665)
130
159
(33)
(168)
(141)
(83)
723
133
44
(9,295)
6,499
220
–
6,719
168
(382)
(214)
33
134
230
17
–
2
94
453
(118)
–
(8,853)
5,446
253
73
5,772
–
(40)
(40)
(17)
$
(2,757)
3,654
$
897
$
(3,138)
6,792
3,654
$
The accompanying notes are an integral part of these consolidated financial statements.
Page | 38
HELIX BIOPHARMA CORP.
Notes to Consolidated Financial Statements
Years ended July 31, 2017 and 2016
(Tabular dollar amounts in thousands of Canadian dollars, except per share amounts)
Helix BioPharma Corp. (the “Company”), incorporated under the Canada Business Corporations Act, is an immune-oncology
company primarily focused in the areas of cancer prevention and treatment. The Company has funded its research and
development activities, mainly through the issuance of common shares and warrants. The Company expects to incur additional
losses and therefore will require additional financial resources, on an ongoing basis. It is not possible to predict the outcome of
future research and development activities or the financing thereof.
1. Basis of presentation and going concern
These consolidated financial statements have been prepared on a going-concern basis, which assumes that the Company will
continue in operation for the foreseeable future and, accordingly, will be able to realize its assets and discharge its liabilities in the
normal course of operations. The Company's ability to continue as a going concern is dependent mainly on obtaining additional
financing. The Company does not have sufficient cash to meet anticipated cash needs for working capital and capital expenditures
through the next twelve months.
The Company reported a consolidated net loss and total comprehensive loss of $10,059,000 for the fiscal year ended July 31,
2017 (July 31, 2016 - $9,665,000). As at July 31, 2017 the Company had a working capital deficiency of $504,000, shareholders’
deficiency of $17,000 and a deficit of $155,380,000. As at July 31, 2016 the Company had working capital of $2,929,000,
shareholders’ equity of $3,164,000 and a deficit of $145,321,000. The Company will require additional financing in the immediate
near term and in the future to see the current research and development initiates through to completion. There can be no
assurance however, that additional financing can be obtained in a timely manner, or at all.
Not raising sufficient additional financing on a timely basis may result in delays and possible termination of all or some of the
Company’s research and development initiatives, and as a result, may cast significant doubt as to the ability of the Company to
operate as a going concern and accordingly, the appropriateness of the use of the accounting principles applicable to a going
concern. These consolidated financial statements do not include any adjustments to the carrying amount and classification of
reported assets, liabilities and expenses that might be necessary should the Company not be successful in its aforementioned
initiatives. Any such adjustments could be material. The Company cannot predict whether it will be able to raise the necessary
funds it needs to continue as a going concern.
Statement of compliance
The Company’s consolidated financial statements have been prepared in accordance with International Financial Reporting
Standards (“IFRS”) as issued by the International Accounting Standards Board (“IASB”) and interpretations of the International
Financial Reporting Interpretation Committee.
The consolidated financial statements of the Company were approved and authorized for issue by the Board of Directors on
October 24, 2017.
Use of estimates and critical judgment
The preparation of the Company’s financial statements requires management to make critical judgments, estimates and assumptions
that affect the reported amounts of expenses, assets and liabilities, and the disclosure of contingent liabilities, at the reporting
date. On an ongoing basis, management evaluates its judgments, estimates and assumptions using historical experience and
various other factors it believes to be reasonable under the given circumstances. Actual outcomes may differ from these
estimates that could require a material adjustment to the reported carrying amounts in the future.
The most significant critical estimates and judgments made by management include the following:
a) Going Concern
Significant judgments related to the Company’s ability to continue as a going concern are disclosed in the first paragraph
above in Note 1.
b) Clinical study expenses
Clinical study expenses are accrued based on services received and efforts expanded pursuant to contracts with contract research
organizations (“CROs”), consultants, clinical study sites and other vendors. In the normal course of business, the Company
contracts with third parties to perform various clinical study activities. The financial terms of these agreements vary from contract
to contract and are subject to negotiations that may result in uneven payment outflows. Payments under the contracts depend on
various factors such as the achievement of certain events, the successful enrolment of patients or the completion of portions of
the clinical study and/or other similar conditions. The Company determines the accruals by reviewing contracts, vendor
agreements and purchase orders, and through discussions with internal personnel and external providers as to the progress or
stage of completion of the clinical studies or services and the agreed-upon fee to be paid for such services. However, actual costs
Page | 39
HELIX BIOPHARMA CORP.
Notes to Consolidated Financial Statements
Years ended July 31, 2017 and 2016
(Tabular dollar amounts in thousands of Canadian dollars, except per share amounts)
and timing of the Company’s clinical studies is uncertain, subject to risk and may change depending upon a number of factors,
including the Company’s clinical development plans and trial protocols.
c) Valuation of share-based compensation and warrants
Management measures the costs for share-based compensation and warrants using market-based option valuation techniques.
Assumptions are made and estimates are used in applying the valuation techniques. These include estimating the future volatility
of the share price, expected dividend yield, future employee turnover rates, a n d future exercise behaviours. Such estimates
and assumptions are inherently uncertain. Changes in these assumptions affect the fair value estimates of share-based payments
and warrants.
d)
Income taxes
the likelihood that the
Deferred tax assets, including those arising from unutilized tax losses, require management to assess
Company will generate future taxable income in future years in order to utilize any deferred tax asset which has been
recognized. Estimates of future taxable income are based on forecasted cash flows. At the current statement of financial position
date, no deferred tax assets have been recognized in these financial statements.
e)
Impairment of long-lived assets
Long-lived assets are reviewed for impairment upon the occurrence of events or changes in circumstances indicating that the
carrying value of the asset may not be recoverable. For the purpose of measuring recoverable amounts, assets are grouped
at the lowest levels for which there are separately identifiable cash flows (cash-generating units). The recoverable amount is the
higher of an asset’s fair value less costs to sell and value in use (being the present value of the expected future cash flows of the
relevant asset or cash-generating unit). An impairment loss is recognized for the amount by which the asset’s carrying amount
exceeds its recoverable amount. Management evaluates impairment losses for potential reversals when events or circumstances
warrant such consideration.
Functional and presentation currency
The functional and presentation currency of the Company is the Canadian dollar.
2. Significant accounting policies
The accounting policies set out below have been applied consistently to all periods presented in these consolidated financial
statements.
Basis of consolidation
These consolidated financial statements include the accounts of the Company and its subsidiaries listed below. Control is achieved
when the Company has the power to govern the financial and operating policies of an entity so as to obtain benefits from its
activities. Subsidiaries are fully consolidated from the date on which control is acquired by the Company. Inter-company
transactions and balances are eliminated upon consolidation. They are de-consolidated from the date that control by the Company
ceases. The consolidated financial statements include the assets and liabilities and results of operations of all subsidiaries after
elimination of intercompany transactions and balances.
As at July 31, 2017, the wholly-owned subsidiaries of the Company include: Helix BioPharma Inc., incorporated in the USA, Helix
Immuno-Oncology Sp. z.o.o., incorporated in Poland and Helix Product Development (Ireland) Limited, incorporated in Ireland.
Cash
The Company considers cash on hand, deposits in banks and bank term deposits with maturities of 90 days or less as cash.
Property, plant and equipment
Property, plant and equipment are recorded at cost less accumulated depreciation. Impairment charges are included in
accumulated depreciation.
Depreciation is provided using the following methods and estimated useful life:
Asset
Computer equipment and software
Furniture and fixtures
Research and manufacturing equipment
Leasehold improvements
Basis
Straight line
Straight line
Straight line
Straight line
Rate
3 years
5 years
4-10 years
Lease term
Page | 40
HELIX BIOPHARMA CORP.
Notes to Consolidated Financial Statements
Years ended July 31, 2017 and 2016
(Tabular dollar amounts in thousands of Canadian dollars, except per share amounts)
Research and development costs
Research costs are expensed as incurred. Development costs are expensed as incurred except for those which meet the criteria
for deferral, in which case, the costs are capitalized and amortized to operations over the estimated period of benefit. No costs
have been deferred to date.
Investment tax credits
The Company is entitled to Canadian federal and provincial investment tax credits, which are earned as a percentage of eligible
research and development expenditures incurred in each taxation year. Investment tax credits are accounted for as a reduction
of the related expenditure for items of a current nature and a reduction of the related asset cost for items of a capital nature,
provided that the Company has reasonable assurance that the tax credits will be realized.
Stock-based compensation
The Company accounts for stock-based compensation and other stock-based payments made in exchange for goods and services
provided by employees and non-employees in accordance with the fair value method. The fair value of stock options granted is
determined at the appropriate measurement date using the Black-Scholes option pricing model, and generally expensed over the
options’ vesting period for employee awards. Awards with graded vesting are considered multiple awards for fair value
measurement and stock-based compensation calculation. In determining the expense, the Company accounts for forfeitures
using an estimate based on historical trends.
Foreign currency translation
The Company’s currency of presentation is the Canadian dollar, which is also the Company’s functional currency. Foreign
currency-denominated items are translated into Canadian dollars. Monetary assets and liabilities in foreign currencies are
translated into Canadian dollars at the rates of exchange in effect at the balance sheet dates. Non-monetary items are translated
at historical exchange rates. Revenue and expenses are translated at the exchange rates prevailing at their respective transaction
dates. Exchange gains and losses arising on translation are included in income.
Income taxes
The Company follows the asset and liability method of accounting for income taxes. Under this method, deferred income tax
assets and liabilities are recognized for the future tax consequences attributable to differences between the financial statement
carrying amounts of certain existing assets and liabilities and their respective tax bases. Deferred income tax assets and liabilities
are measured using enacted or substantively enacted tax rates expected to apply to taxable income in the years in which those
temporary differences are expected to be recovered or settled. The effect on deferred tax assets and liabilities of a change in tax
rates is recognized in income in the period that includes the date of substantive enactment. Given the Company’s history of net
losses and expected future losses, the Company is of the opinion that it is probable that these tax assets will not be realized in
the foreseeable future and therefore, the deferred tax asset has not been recognized.
Financial instruments
Financial assets and financial liabilities are initially recorded at fair value and their subsequent measurements are determined in
accordance with their classification. The classification depends on the purpose for which the financial instruments were acquired
or issued and their characteristics. Cash is classified as a held-for-trading assets and is accounted for at fair value. Accounts
receivable are classified as loans and receivables, and after initial recognition are recorded at amortized cost. Accounts payable
and accrued liabilities are classified as other financial liabilities, and after initial recognition are recorded at amortized cost.
Impairment
(i) Financial assets:
A financial asset not carried at fair value through profit or loss is assessed at each reporting date to determine whether there is
objective evidence that it is impaired. A financial asset is impaired if objective evidence indicates that a loss event has occurred
after the initial recognition of the asset, and that the loss event had a negative effect on the estimated future cash flows of that
asset that can be estimated reliably.
An impairment test is performed, on an individual basis, for each material financial asset. Other individually non-material financial
assets are tested as groups of financial assets with similar risk characteristics. Impairment losses are recognized in income.
An impairment loss in respect of a financial asset measured at amortized cost is calculated as the difference between its carrying
amount and the present value of the estimated future cash flows discounted at the assets original effective interest rate. Losses
are recognized in income and reflected in an allowance account against the respective financial asset. Interest on the impaired
asset continues to be recognized through the unwinding of the discount. When a subsequent event causes the amount of
impairment loss to decrease, the decrease in impairment loss is reversed through income for all financial assets except available-
for-sale equity securities.
Page | 41
HELIX BIOPHARMA CORP.
Notes to Consolidated Financial Statements
Years ended July 31, 2017 and 2016
(Tabular dollar amounts in thousands of Canadian dollars, except per share amounts)
(ii) Non-financial assets:
The carrying amounts of the Company’s non-financial assets are reviewed at each reporting date to determine whether there is
any indication of impairment. If such an indication exists, the recoverable amount is estimated.
The recoverable amount of an asset or a cash-generating unit is the greater of its value in use and its fair value less costs to sell.
In assessing value in use, the estimated future cash flows are discounted to their present value using a pre-tax discount rate that
reflects current market assessments of the time value of money and the risks specific to the asset or cash-generating unit. For
the purpose of impairment testing, assets that cannot be tested individually are grouped together into the smallest group of assets
that generates cash inflows from continuing use that are largely independent of cash inflows of other assets or cash-generating
units. An impairment loss is recognized if the carrying amount of an asset or its related cash-generating unit exceeds its estimated
recoverable amount.
Impairment losses recognized in prior periods are assessed each reporting date for any indications that the loss has decreased
or no longer exists. An impairment loss is reversed if there has been a change in the estimates used to determine the recoverable
amount. An impairment loss is reversed only to the extent that the asset’s carrying amount does not exceed the carrying amount
that would have been determined, net of depreciation, if no impairment loss had been recognized.
Basic and diluted loss per common share
Basic loss per share is computed by dividing the net loss available to common shareholders by the weighted average number of
shares outstanding during the reporting period. Diluted loss per share is computed similarly to basic loss per share, except that
the weighted average shares outstanding are increased to include additional shares for the assumed exercise of stock options
and warrants, if dilutive. The number of additional shares is calculated by assuming that outstanding stock options and warrants
were exercised and that the proceeds from such exercises were used to acquire common shares at the average market price
during the reporting periods. The inclusion of the Company’s stock options and warrants in the computation of diluted loss per
share has an anti-dilutive effect on the loss per share and, therefore, they have been excluded from the calculation of diluted loss
per share.
Government Grants and Disclosure of Government Assistance
Government grant funds are recognised in income when there is reasonable assurance that the Company has complied with the
conditions attached to them and that the grant funds will be received. Grant funds receivable are recognized in income over the
periods in which the entity recognizes as expenses, the related costs for which the grant is intended to compensate.
3. New accounting standards and pronouncements not yet adopted
New accounting standards and pronouncements issued but not yet effective up to the date of issuance of the Company's
consolidated financial statements are listed below. This listing includes standards and interpretations issued, which the Company
reasonably expects to be applicable at a future date. The Company intends to adopt those standards when they become effective.
Certain pronouncements have been issued by the IASB or International Financial Reporting Interpretations Committee. Many of
these updates are not applicable or are inconsequential to the Company and have been excluded from the discussion below:
IFRS 9, Financial Instruments
The IASB has issued a new standard, IFRS 9, Financial Instruments (“IFRS 9”), which will ultimately replace IAS 39, Financial
Instruments: Recognition and Measurement (“IAS 39”). The project had three main phases: classification and measurement,
impairment and general hedging. The standard becomes effective for annual periods beginning on or after January 1, 2018 and
is to be applied retrospectively. Early adoption is permitted. The Company is evaluating the impact of the new standard on its
results of operations, financial position and disclosures.
IFRS 15, Revenue from Contracts with Customers
The IASB has issued a new standard, IFRS 15, Revenue from Contracts with Customers (“IFRS 15”). IFRS 15 contains a single
model that applies to contracts with customers and two approaches to recognizing revenue: at a point in time or over time. The
model features a contract-based five-step analysis of transactions to determine whether, how much and when revenue is
recognized. New estimates and judgmental thresholds have been introduced, which may affect the amount and/or timing of
revenue recognized. The standard becomes effective for annual periods beginning on or after January 1, 2018. The Company
is evaluating the impact of the new standard on its results of operations, financial position and disclosures.
IFRS 16, Leases
In January 2016, the IASB has issued IFRS 16 Leases (“IFRS 16”), its new leases standard that requires lessees to
recognize assets and liabilities for most leases on their balance sheets. Lessees applying IFRS 16 will have a single
accounting model for all leases, with certain exemptions. Lessor accounting is substantially unchanged. The new standard will
Page | 42
HELIX BIOPHARMA CORP.
Notes to Consolidated Financial Statements
Years ended July 31, 2017 and 2016
(Tabular dollar amounts in thousands of Canadian dollars, except per share amounts)
be effective from January 1, 2019 with limited early application permitted. The Company is evaluating the impact of the new
standard on its results of operations, financial position and disclosures.
4. Property, plant and equipment
Research equipment
Manufacturing equipment
Leasehold improvements
Computer equipment
Computer software
Furniture and fixtures
2017
Cost
$ 1,654
402
359
103
56
12
$ 2,586
Accumulated
depreciation
$ 1,198
402
359
72
56
12
$ 2,099
$
Net book
value
456
–
–
31
–
–
487
$
2016
Cost
$ 1,306
1,555
370
244
89
19
$ 3,583
Accumulated
depreciation
$ 1,106
1,553
370
211
89
19
$ 3,348
$
Net book
value
200
2
–
33
–
–
235
$
5. Shareholders’ equity (deficiency)
Preferred shares
Authorized 10,000,000 preferred shares.
As at July 31, 2017 and 2016 the Company had nil preferred shares issued and outstanding.
Common shares and share purchase warrants
Authorized unlimited common shares without par value.
As at July 31, 2017 the Company had 95,711,579 (2016 – 89,247,937) common shares issued and outstanding.
On April 11, 2016, the Company completed a private placement, issuing 3,105,000 units at $1.50 per unit, for gross proceeds of
$4,658,000. Each unit consisted of one common share and one common share purchase warrant. Each common share purchase
warrant entitles the holder to purchase one common share at a price of $1.98 until April 10, 2021. Of the gross proceeds amount,
$1,770,000 was allocated to the share purchase warrants based on fair value and the residual amount of $2,888,000 was allocated
to the common shares. Share issue costs totalling $700,000 were proportionately allocated to the share purchase warrants
($266,000) and the common shares ($434,000), respectively.
On July 29, 2016, the Company completed a private placement, issuing 1,250,000 units at $1.46 per unit, for gross proceeds of
$1,825,000. Each unit consisted of one common share and one common share purchase warrant. Each common share purchase
warrant entitles the holder to purchase one common share at a price of $1.82 until July 28, 2021. Of the gross proceeds amount,
$707,000 was allocated to the share purchase warrants based on fair value and the residual amount of $1,118,000 was allocated
to the common shares. Share issue costs totalling $336,000 were proportionately allocated to the share purchase warrants
($130,000) and the common shares ($206,000), respectively.
On August 18, 2016, the Company completed a private placement, issuing 644,675 units at $1.54 per unit, for gross proceeds of
$993,000. Each unit consisted of one common share and one common share purchase warrant. Each common share purchase
warrant entitles the holder to purchase one common share at a price of $1.92 until August 17, 2021. Of the gross proceeds
amount, $377,000 was allocated to the share purchase warrants based on fair value and the residual amount of $616,000 was
allocated to the common shares. Share issue costs totalling $182,000 were proportionately allocated to the share purchase
warrants ($69,000) and the common shares ($113,000), respectively.
On December 28 and 29, 2016 the Company completed two private placements, issuing a total of 1,520,000 units at $1.20 per
unit, for gross proceeds of $1,824,000. Each unit consisted of one common share and one common share purchase warrant.
Each common share purchase warrant entitles the holder to purchase one common share at a price of $1.50 until December 28
and 29, 2021. Of the gross proceeds amount, $672,000 was allocated to the share purchase warrants based on fair value and
the residual amount of $1,152,000 was allocated to the common shares. Share issue costs totalling $312,000 were proportionately
allocated to the share purchase warrants ($115,000) and the common shares ($197,000), respectively.
On March 16, 2017, the Company completed a private placement, issuing a total of 925,000 units at $1.20 per unit, for gross
proceeds of $1,110,000. Each unit consisted of one common share and one common share purchase warrant. Each common
share purchase warrant entitles the holder to purchase one common share at a price of $1.50 until March 15, 2022. Of the gross
proceeds amount, $402,000 was allocated to the share purchase warrants based on fair value and the residual amount of
Page | 43
HELIX BIOPHARMA CORP.
Notes to Consolidated Financial Statements
Years ended July 31, 2017 and 2016
(Tabular dollar amounts in thousands of Canadian dollars, except per share amounts)
$708,000 was allocated to the common shares. Share issue costs totalling $188,000 were proportionately allocated to the share
purchase warrants ($68,000) and the common shares ($120,000), respectively.
On April 28, 2017, the Company completed a private placement, issuing a total of 683,300 units at $1.20 per unit, for gross
proceeds of $820,000. Each unit consisted of one common share and one common share purchase warrant. Each common
share purchase warrant entitles the holder to purchase one common share at a price of $1.50 until April 27, 2022. Of the gross
proceeds amount, $285,000 was allocated to the share purchase warrants based on fair value and the residual amount of
$535,000 was allocated to the common shares. Share issue costs totalling $150,000 were proportionately allocated to the share
purchase warrants ($52,000) and the common shares ($98,000), respectively.
On June 7, 2017, the Company completed a private placement, issuing a total of 2,524,000 units at $1.20 per unit, for gross
proceeds of $3,029,000. Each unit consisted of one common share and one common share purchase warrant. Each common
share purchase warrant entitles the holder to purchase one common share at a price of $1.50 until June 6, 2022. Of the gross
proceeds amount, $1,022,000 was allocated to the share purchase warrants based on fair value and the residual amount of
$2,007,000 was allocated to the common shares. Share issue costs totalling $443,000 were proportionately allocated to the share
purchase warrants ($149,000) and the common shares ($294,000), respectively.
The following table provides information on share purchase warrants outstanding as at:
Exercise Price
July 31, 2017
July 31, 2016
Weighted average
remaining contractual
life (in years)
Number of share
purchase warrants
outstanding
Weighted average
remaining contractual
life (in years)
Number of share
purchase warrants
outstanding
$1.50
$1.50
$1.50
$1.50
$1.92
$1.82
$1.98
$1.54
$1.54
$2.24
$1.61
Outstanding, end of year
4.85
4.74
4.62
4.41
4.05
3.99
3.70
2.75
2.67
1.94
1.25
2,524,000
683,300
925,000
1,520,000
644,675
1,250,000
3,105,000
3,250,000
5,430,000
3,996,000
4,653,000
27,980,975
–
–
–
–
–
4.99
4.70
3.75
3.67
2.94
2.25
–
–
–
–
–
1,250,000
3,105,000
3,250,000
5,430,000
3,996,000
4,653,000
21,684,000
Stock options
The Company’s equity compensation plan reserves up to 10% of the Company’s outstanding common shares from time to time
for granting to directors, officers and employees of the Company or any person or company engaged to provide ongoing
management or consulting services. Based on the Company’s current issued and outstanding common shares as at July 31,
2017, options to purchase up to 9,571,157 common shares (2016 – 8,924,793) may be granted under the plan. As at July 31,
2017, options to purchase a total of 930,000 common shares (2016 – 1,686,484) were issued and outstanding under the equity
compensation plan.
The following table provides information on options outstanding and exercisable as at:
July 31, 2017
Exercise
Price
$2.00
$0.92
$1.50
$1.65
$1.34
$1.30
$1.68
Weighted average
remaining contractual
Number of
options
life (in years) outstanding
50,000
380,000
200,000
100,000
200,000
–
–
3.26
2.86
2.46
2.26
1.25
–
–
Number of
vested and
exercisable
options
16,667
380,000
200,000
100,000
200,000
–
–
Weighted average
remaining contractual
life (in years)
3.99
–
3.46
3.26
2.25
0.92
0.38
July 31, 2016
Number of
options
outstanding
110,000
–
300,000
150,000
234,400
200,000
692,084
Number of
vested and
exercisable
options
20,000
–
199,998
99,999
234,400
200,000
692,084
Outstanding, end of year
2.39
930,000
896,667
1.57
1,686,484
1,466,481
Page | 44
HELIX BIOPHARMA CORP.
Notes to Consolidated Financial Statements
Years ended July 31, 2017 and 2016
(Tabular dollar amounts in thousands of Canadian dollars, except per share amounts)
The following table summarized activity under the Company’s equity compensation plan for the fiscal years ended:
July 31, 2017
July 31, 2016
Outstanding, beginning of year
Granted
Exercised
Expired
Outstanding, end of year
Number
1,686,484
380,000
(166,667)
(969,817)
930,000
Vested and exercisable, end of year
896,667
Weighted average
exercise price
1.57
0.92
1.32
1.65
$
$
$
1.27
1.24
Number
2,730,084
50,000
(190,600)
(903,000)
1,686,484
1,466,481
Weighted average
exercise price
1.92
2.00
1.33
2.68
$
$
$
1.57
1.56
Weighted average market share prices for options exercised during the fiscal years 2017 and 2016 were $1.32 and $1.97
respectively.
The fair value of each option granted was estimated on the date of grant using the Black-Scholes option pricing model with the
following assumptions:
Grant
Date
June 12, 2017
November 2, 2015
January 16, 2015
November 3, 2014
November 1, 2013
Number
of options
granted
380,000
50,000
300,000
150,000
475,000
Volatility
factor
57.30 %
80.47 %
79.56 %
78.61 %
76.69 %
Risk free
interest
rate
0.88 %
0.73 %
1.02 %
1.37 %
1.62 %
Dividend
rate
Expected
life
0.00 %
0.00 %
0.00 %
0.00 %
0.00 %
5 years
5 years
5 years
5 years
5 years
Vesting
period
3 years
3 years
3 years
3 years
1 year
Fair value
of options
granted
$
$
$
$
$
136
61
333
160
379
For the year ended July 31, 2017, 530,003 options vested (2016 – 169,994) with a fair value of $301,663 (2016 – $188,353).
6. Commitments, contingent liabilities and contingent assets
The Company’s commitments are summarized as follows:
V-DOS47 co-funded project
Clinical research organizations
Contract manufacturing organizations
Collaborative research organizations
Royalty and in-licensing
Operating leases
Financial and investor relations
2018
$ 606
2,165
615
321
20
52
127
2019
$ 1,452
–
–
–
20
26
–
2020
$ 2,578
–
–
–
20
–
–
2021
$ 1,805
–
–
–
20
–
–
$
2022
–
–
–
–
20
–
–
2023 and
beyond
–
$
–
–
–
100
–
–
$ 3,906
$ 1,498
$ 2,598
$ 1,825
$ 20
$ 100
Total
$ 6,441
2,165
615
321
200
78
127
$ 9,947
Grant Funding Agreement (the “Agreement”) with the Polish National Centre for Research and Development (“PNCRD”)
Based on the Agreement, certain expenditures made commencing on March 1, 2016 are eligible for reimbursement with the final
reimbursement submission to be made no later than September 30, 2021. Total costs associated with the V-DOS47 development
program under the Agreement is PLN19,794,416 ($6,830,815). Of the total project costs of PLN19,794,416 ($6,830,815), the
PNCRD will reimburse the Company’s Polish subsidiary PLN12,506,955 ($4,316,000) for eligible expenditures, under the program.
Under the Agreement, the Company’s subsidiary is required to spend PLN4,437,459 ($1,531,00) towards eligible project
expenditures plus an additional PLN2,850,000 ($984,000) for manufacturing and clinical trial documentation costs that are not
eligible for subsidies from the PNCRD. Subsidized amounts may be drawn in advance or on a reimbursement basis, with varying
criteria and timelines for justification of claims being made by the Company’s subsidiary. Of the $6,441,000 in total future
commitments towards this program, the Company is projecting that approximately $3,974,000 will be reimbursed by the PNCRD.
Page | 45
HELIX BIOPHARMA CORP.
Notes to Consolidated Financial Statements
Years ended July 31, 2017 and 2016
(Tabular dollar amounts in thousands of Canadian dollars, except per share amounts)
Clinical Research Organization (“CRO”) Commitments
The Company has CRO supplier agreements in place for clinical research services related to the management of the Company’s
clinical stage programs
As at July 31, 2017, the Company accrued $1,128,000 (2016 – $446,000) for services provided by these CRO’s.
Contract Manufacturing Organization (“CMO”) commitments
The Company has CMO supplier agreements related to the Company’s L-DOS47 program, all of which are inter-dependant with
manufacturing of L-DOS47.
As at July 31, 2017, the Company accrued $38,000 (2016 – $nil) for CMO services it had received and is committed to pay $nil
for additional services.
Collaborative Research Organization Service Commitments
The Company has one collaborative research agreement relating to the Company’s L-DOS47 program. The nature of the services
includes assay development, animal studies and imaging and ongoing future clinical sample analysis.
As at July 31, 2017, the Company accrued $nil (2016 – $82,000) for collaborative research organizations services it had received.
Royalty and in-licensing commitments
Pursuant to an agreement dated April 28, 2005 with the National Research Council of Canada (the “NRC”), the Company is
required to pay a royalty to the NRC of 3% of net sales, with a minimum royalty of $10,000 per annum generated from the use of
a certain antibody to target cancerous tissues of the lung. In addition to the royalty payments, the Company is also required to
make certain milestone payments: $25,000 upon successful completion of Phase I clinical trials; $50,000 upon successful
completion of Phase IIb clinical trials; $125,000 upon successful completion of Phase III clinical trials; and $200,000 upon receipt
of market approval by regulatory authority. L-DOS47 is subject to this agreement.
Pursuant to an agreement dated September 22, 2016 with the National Research Council of Canada, the Company is required to
pay a royalty to the NRC of 3% of net sales, with a minimum royalty of $10,000 per annum generated from the use of a certain
antibody to target cancerous tissues of the lung. In addition to the royalty payments, the Company is also required to make certain
milestone payments for the first licensed product: $25,000 upon successful completion of Phase I clinical trials; $50,000 upon
successful completion of Phase IIb clinical trials; $150,000 upon successful completion of Phase III clinical trials; $200,000 upon
receipt of first regulatory approval by a regulatory authority; and $200,000 upon receipt of a second regulatory approval by a
regulatory authority. For the development of each subsequent licensed product: $200,000 upon receipt of first regulatory approval
by a regulatory authority; and $200,000 upon receipt of a second regulatory approval by a regulatory authority. As it relates to
sub-licensing arrangements, the Company is required to pay the NRC 33% of any sub-licensing revenues received. The anti-
CEACAM6 single domain antibody 2A3 is subject to this agreement.
As at July 31, 2017, the Company has $nil (2016 – $80,000) in financial obligations outstanding related to royalty and in-licensing
commitments.
Operating lease commitments
The Company is committed to pay $78,000 under four facility lease agreements with lease terms up to 24 months.
Financial and investor relations agreements
The Company entered into a non-exclusive financial and investor relations agreement with ACM Alpha Consulting Management
EST (“ACMest”), effective May 1, 2012. The agreement may now be terminated by either party at any time upon ninety days
written notice to the other party. On March 7, 2014, Mr. Andreas Kandziora was asked to act as an Observer on the Board of
Directors of the Company. Mr. Kandziora is President and CEO of ACMest. The agreement includes the following provisions:
a) a monthly fee for investor relations services of CHF33,000 and reimbursement of certain expenses;
b) a 12.5% fee on the gross proceeds on any capital raised up to six months after the termination of this agreement from
an ACMest introduced investor with residency outside Canada and the U.S.;
c) a 12.5% fee on the value of a transaction up to twelve months after the termination of the agreement from an ACMest
introduced strategic partner, including but not limited to, any cash payments to the Company as an up-front payment,
any co-development proceeds, any milestone payments and any royalties associated with the transaction; and
Page | 46
HELIX BIOPHARMA CORP.
Notes to Consolidated Financial Statements
Years ended July 31, 2017 and 2016
(Tabular dollar amounts in thousands of Canadian dollars, except per share amounts)
d) a 12.5% fee on the gross proceeds of any capital raised up to twelve months after the termination of the agreement from
an ACMest introduced strategic partner.
At July 31, 2017, the Company accrued $nil (2016 – $251,000) for services provided by ACMest. Also see Note 9 – Related
Party Transactions).
Non-disclosure agreement (“NDA”)
The Company and its wholly-owned subsidiary signed two separate non-disclosure agreements which included specific wording
as to the use of data for purposes other than those specified or in the event of disclosure to a third party of all or a part of certain
data. Under the NDA, and the event of a breach, the Company would be liable for a contractual penalty of PLN500,000 for each
case of breach under each of the NDA’s.
Legal proceedings and claims
There are two claims made against the Company in the normal course of operations that remain pending at the end of fiscal 2017.
Management believes that these claims are without merit. These actions are not sufficiently advanced for the outcome to be
presently determinable and, accordingly, no provision for these claims have been made in these financial statements.
7. Capital risk management
The Company’s main objectives when managing capital are to ensure sufficient liquidity to finance research and development
activities, clinical trials, ongoing administrative costs, working capital and capital expenditures. The Company includes cash in
the definition of capital. The Company endeavours not to unnecessarily dilute shareholders when managing the liquidity of its
capital structure.
Since inception, the Company has financed its operations from public and private sales of equity, the exercise of warrants and
stock options, and, to a lesser extent, from interest income from funds available for investment, government grants and investment
tax credits. Since the Company does not have net earnings from its operations, the Company’s long-term liquidity depends on its
ability to access capital markets, which depends substantially on the success of the Company’s ongoing research and
development programs, as well as capital market conditions and availability.
The Company does not currently have enough cash reserves to fully fund its clinical trials nor does the Company have sufficient
cash reserves to meet anticipated cash needs for working capital and capital expenditures through at least the next twelve months.
The Company does not have any credit facilities and is therefore not subject to any externally imposed capital requirements or
covenants.
8. Financial instruments and risk management
The Company has classified its financial instruments as follows:
Cash
2017
2016
Fair Value
897
$
Fair value
hierarchy
Level 1
Fair Value
$ 3,654
Fair value
hierarchy
Level 1
Fair value hierarchy
Financial instruments recorded at fair value on the balance sheet are classified using a fair value hierarchy that reflects the
significance of the inputs used in making the measurements. The fair value hierarchy has the following levels:
a. Level 1 reflects valuation based on quoted prices observed in active markets for identical assets or liabilities;
b. Level 2 reflects valuation techniques based on inputs that are quoted prices of similar instruments in active markets;
quoted prices for identical or similar instruments in markets that are not active; inputs other than quoted prices used in a
valuation model that are observable for that instrument; and inputs that are derived principally from or corroborated by
observable market data by correlation or other means; and
c. Level 3 reflects valuation techniques with significant unobservable market inputs.
A financial instrument is classified to the lowest level of the hierarchy for which a significant input has been considered in measuring
fair value.
Page | 47
HELIX BIOPHARMA CORP.
Notes to Consolidated Financial Statements
Years ended July 31, 2017 and 2016
(Tabular dollar amounts in thousands of Canadian dollars, except per share amounts)
The financial instrument in the Company’s financial statements, measured at fair value, is cash.
Fair value
The fair value of financial instruments as at July 31, 2017 and 2016 approximates their carrying value because of the near-term
maturity of these instruments.
Financial risk management
The Company is exposed to a variety of financial risks by virtue of its activities: market risk (including currency and interest rate
risk), credit risk and liquidity risk. The overall risk management program focuses on the unpredictability of financial markets and
seeks to minimize potential adverse effects on financial performance.
Risk management (the identification and evaluation of financial risk) is carried out by the finance department, in close cooperation
with management. The finance department is charged with the responsibility of establishing controls and procedures to ensure
that financial risks are mitigated in accordance with the approved policies. The Company’s Board of Directors has the overall
responsibility for the oversight of these risks and reviews the Company’s policies on an ongoing basis to ensure that these risks
are appropriately managed.
Market risk
Market risk is the risk that changes in market prices, such as interest rates and foreign exchange rates, will affect the Company’s
income or the value of its financial instruments.
Currency risk
The Company has international transactions and is exposed to foreign exchange risks from various currencies, primarily the Euro
and U.S. dollar. Foreign exchange risks arise from the foreign currency translation of the Company’s integrated foreign operation
in Poland. In addition, foreign exchange risks arise from purchase transactions, as well as recognized financial assets and
liabilities denominated in foreign currencies.
Balances in foreign currencies at July 31, 2017 and 2016 are as follows:
Cash
Accounts receivable
Accounts payable
Accruals
Net foreign currencies
EUR
32
–
(468)
(217)
(653)
2017
USD
1
–
(229)
(24)
(252)
PLN
276
178
(201)
(99)
154
EUR
30
–
(77)
(82)
(129)
2016
USD
48
–
(48)
(165)
(165)
PLN
77
–
–
(90)
(13)
Closing exchange rate
Impact of 1% change in exchange rate
1.4719
+/- 9
1.2485
+/- 3
0.3451
+/- 1
1.4594
+/- 1
1.3056
+/- 1
0.3345
+/- 1
Any fluctuation in the exchange rates of the foreign currencies listed above could have an impact on the Company’s results from
operations; however, they would not impair or enhance the ability of the Company to pay its foreign-denominated expenses.
The following summary illustrates the purchasing power of the Canadian dollar for the fiscal years 2017 and 2016 against the Euro
(EUR), the U.S. dollar (USD) and the Polish Zloty (PLN):
High
Average
Low
EUR
2017
USD
PLN
0.7232
0.8043 3.2108
0.6910 0.7556 2.9737
0.7277 2.7488
0.6569
EUR
0.7102
0.6784
0.6278
2016
USD
PLN
0.7972
3.0998
0.7531 2.9274
0.6854 2.7693
Interest rate risk
Interest rate risk is the risk that future cash flows of a financial instrument will fluctuate because of changes in interest rates, which
are affected by market conditions. The Company is exposed to interest rate risk arising from fluctuations in interest rates received
on its cash and cash equivalents. The Company does not have any credit facilities and is therefore not subject to any debt related
interest rate risk.
Page | 48
HELIX BIOPHARMA CORP.
Notes to Consolidated Financial Statements
Years ended July 31, 2017 and 2016
(Tabular dollar amounts in thousands of Canadian dollars, except per share amounts)
The Company manages its interest rate risk by maximizing the interest income earned on excess funds while maintaining the
liquidity necessary to conduct its operations on a day-to-day basis. Any investment of excess funds is limited to risk-free financial
instruments. Fluctuations in the market rates of interest do not have a significant impact on the Company’s results of operations
due to the relatively short-term maturity of any investments held by the Company at any given point in time and the low global
interest rate environment. The Company does not use derivative instruments to reduce its exposure to interest rate risk.
Credit risk
Credit risk is the risk of a financial loss to the Company if a customer or counterparty to a financial instrument fails to meet its
contractual obligation.
The table below breaks down the various categories that make up the Company’s accounts receivable balances as at July 31:
Government related – HST/VAT
Research and development investment tax credits
Other
2017
$ 177
430
23
$ 630
2016
$ 106
380
3
$ 489
Liquidity risk
Liquidity risk is the risk that the Company will not be able to meet its obligations as they come due. Since inception, the Company
has mainly relied on financing its operations from public and private sales of equity. The Company does not have any credit
facilities and is therefore not subject to any externally imposed capital requirements or covenants.
The Company manages its liquidity risk by continuously monitoring forecasts and actual cash flow from operations and anticipated
investing and financing activities.
The Company’s cash reserves of $897,000 as at July 31, 2017 are insufficient to meet anticipated cash needs for working capital
and capital expenditures through the next twelve months, nor are they sufficient to see the current research and development
initiates through to completion. To the extent that the Company does not believe it has sufficient liquidity to meet its current
obligations, management considers securing additional funds primarily through equity arrangements to be of utmost importance.
The Company’s long-term liquidity depends on its ability to access the capital markets, which depends substantially on the success
of the Company’s ongoing research and development programs, as well as economic conditions relating to the state of the capital
markets generally. Accessing the capital markets is particularly challenging for companies that operate in the biotechnology
industry.
The following are the contractual maturities of the undiscounted cash flows of financial liabilities as at July 31:
2016
2017
Accounts payable
Accrued liabilities
Carrying
amount
$ 1,438
722
Less than Greater than
one-year
one year
–
$
$ 1,438
–
722
Carrying
amount
715
589
$
Less than Greater than
one-year
one year
–
$
715
$
–
589
This table only covers liabilities and obligations relative to financial instruments and does not anticipate any income associated
with assets.
9. Related party transactions
The following table summarizes key management personnel compensation for the fiscal years ended:
Compensation
Stock-based compensation
2017
$ 1,081
–
$ 1,081
2016
$ 1,283
53
$ 1,336
Page | 49
HELIX BIOPHARMA CORP.
Notes to Consolidated Financial Statements
Years ended July 31, 2017 and 2016
(Tabular dollar amounts in thousands of Canadian dollars, except per share amounts)
The following table summarizes non-management directors’ compensation for the fiscal years ended:
Directors’ fees
Stock-based compensation
Consulting fees
Sub-lease payments
$
2017
314
16
329
144
$
2016
352
150
187
–
$
803
$
689
The Company entered into a consulting agreement with the Chairman of the Board to act as Chief Executive Officer of the
Company. The agreement had a twelve-month term which expired on March 31, 2017. During the 2017 fiscal year, the Company
entered into an agreement with a company controlled by a director of the Company to sub-lease office space.
The following table summarizes the Board Observer’s compensation for the fiscal years ended:
Finder’s fee commissions
Financial and investor relations consulting fee
Expense reimbursement
$
2017
972
532
31
$ 1,535
$
2016
810
540
80
$ 1,430
The Company entered into a non-exclusive financial and investor relations agreement with ACM Alpha Consulting Management
EST (“ACMest”), effective May 1, 2012. On March 7, 2014, Mr. Andreas Kandziora became an Observer to the Board of Directors
of the Company. Mr. Kandziora was also appointed to the Supervisory Board of the Company’s wholly-owned Polish subsidiary,
Helix Immuno-Oncology. Mr. Kandziora is President and CEO of ACMest (also see Note 6 – Commitments, contingent liabilities
and contingent assets). During the 2017 fiscal year, the Board of Directors of the Company appointed Mrs. Veronika Kandziora,
the spouse of Mr. Kandziora, as Corporate Secretary of the Company.
Related party transactions are at arm’s length and recorded at the amount agreed to by the related parties.
10. Research and development projects
As at July 31, 2017, the Company has incurred research and development expenditures primarily on the L-DOS47 research and
development program.
Included in research and development expenditures are costs directly attributable to the various research and development
functions and initiatives the Company has underway and include: salaries; bonuses; benefits; stock based compensation;
depreciation of property, plant and equipment; patent costs; consulting services; third party contract manufacturing, third party
clinical research organization services; and all overhead costs associated with the Company’s research facilities.
The following table outlines research and development costs expensed and investment tax credits for the Company’s significant
research and development projects for the fiscal years ended July 31:
L-DOS47
V-DOS47
CAR-T
Corporate research and development expenses
Trademark and patent related expenses
Stock-based compensation expense
Depreciation expense
Research and development investment tax credits
Polish government grant subsidy (V-DOS47)
11. Government grant
$
2017
5,496
894
259
474
361
24
112
(230)
(335)
$ 7,055
2016
$ 5,017
159
–
431
244
27
118
(175)
–
$ 5,821
On July 21, 2016, the Company announced that a grant funding agreement was entered into by the Company’s wholly-owned
subsidiary in Poland and the PNCRD, whereby certain expenditures made commencing on March 1, 2016 are eligible for
reimbursement with the final reimbursement submission to be made no later than September 30, 2021. Subsidized amounts may
be drawn in advance or on a reimbursement basis, with varying criteria and timelines for justification of claims being made by the
Company’s subsidiary. The Agreement may be terminated by either party upon one month’s written notice and must also state
Page | 50
HELIX BIOPHARMA CORP.
Notes to Consolidated Financial Statements
Years ended July 31, 2017 and 2016
(Tabular dollar amounts in thousands of Canadian dollars, except per share amounts)
the grounds for which the Agreement is being terminated. In certain cases of termination, the Company’s Polish subsidiary may
be obligated to return the received financial support in full within fourteen days of the day notice is served, with interest (also see
Note 6 – Commitments, contingent liabilities and contingent assets).
12. Income taxes
The Company recognizes deferred tax assets and liabilities for expected future tax consequences of temporary differences
between the carrying amounts and the tax basis of assets and liabilities and certain carry-forward balances. The Company’s
effective income tax rate in fiscal 2017 is 25.7% (2016 – 26.7%).
The tax effects of temporary differences for the Company that gives rise to the unrecorded deferred tax asset presented in the
following table:
Deferred tax assets:
Scientific Research & Experimental Development expenditure pool
Non-capital losses and other credits carried forward
Capital losses carried forward
Excess of tax basis over book basis of capital assets
Deductible share issue costs
2017
2016
$ 12,438
20,335
161
1,525
561
$ 35,040
$ 11,978
18,293
161
1,500
454
$ 32,386
Current income tax expense and non-capital tax carry-forwards
As at July 31, 2017, the Company has Canadian tax losses that can be carried forward of approximately $76,284,000 (2016 –
$68,621,000) and are available until 2037 as follows:
2025
2026
2027
2028
2029
2030
2031
2032
2033
2034
2035
2036
2037
$
862
2,113
2,904
2,438
9,188
6,552
6,793
13,242
2,437
6,727
7,256
7,883
7,889
$ 76,284
Scientific Research & Experimental Development expenditures (“SR&ED”)
Under the Income Tax Act (Canada), certain expenditures are classified as SR&ED expenditures and are grouped into a pool for
tax purposes. This expenditure pool can be carried forward indefinitely and deducted in full in any subsequent year. The SR&ED
expenditure pool at July 31, 2017 is approximately $46,883,000 (2016 – $44,911,000).
Investment tax credits
The Company has also earned investment tax credits in Canada, on eligible SR&ED expenditures at July 31, 2017 of
approximately $11,468,000 (2016 – $11,014,000), which can offset Canadian income taxes otherwise payable in future years up
to 2037. Investment tax credits are accounted for as a reduction of the related expenditure for items of a current nature and a
reduction of the related asset cost for items of a capital nature, provided that the Company has reasonable assurance that the tax
credits will be realized. During the year, the Company received cash refundable investment tax credits related to prior years in
the amount of $179,000 (2016 – $184,000). At July 31, 2017, cash refundable investment tax credits total $430,000 (2016 –
$379,000). The research and development investment tax credits recorded are based on management’s estimates of amounts
expected to be recovered and are subject to audit by the taxation authorities and, accordingly, these amounts may vary. Federal
investment tax credits are non-refundable to the Company. Refundable investment tax credits reflect eligible SR&ED expenditures
incurred in various provinces.
Page | 51
HELIX BIOPHARMA CORP.
Notes to Consolidated Financial Statements
Years ended July 31, 2017 and 2016
(Tabular dollar amounts in thousands of Canadian dollars, except per share amounts)
Tax - Poland
As at July 31, 2017, the Company has Poland tax losses that can be carried forward of approximately $777,000 (2016 – $170,000)
and are available until 2022 as follows:
2019
2020
2021
2022
$ 3
26
146
602
777
$
13. Gain on sale of property, plant and equipment
On December 23, 2016, the Company announced, it signed an exclusive out-license agreement with Xisle for the Company's late-
stage, Biphasix™ technology platform, including the lead product candidate, interferon alpha. Xisle is responsible for the continued
clinical development and subsequent commercialization of the product for the treatment of HPV-induced, low-grade, cervical
intraepithelial lesions. As part of its asset development strategy, Xisle has initiated collaboration with senior pharmaceutical
executives at Altum Pharmaceuticals Inc., who possess regulatory, clinical, and product development expertise. Under the terms
of the agreement, Xisle paid an up-front fee of USD125,000 and agreed to pay subsequent milestone payments as they advance
the technology to registration and market approvals and royalties. As part of the agreement, Helix retains marketing rights for
Belarus, Bulgaria, Czech Republic, former Eastern Germany, Hungary, Moldova, Poland, Romania, Russia, Slovakia and Ukraine.
In addition, the Company also retains non-exclusive rights for co-promotion in Canada.
The Company subsequently assigned the marketing rights which it retained over to HIO, its wholly-owned subsidiary in Poland
pursuant to an agreement between the Company and HIO with the agreement being subject to the restrictions and limitations
associated with the out-license agreement signed between the Company and Xisle. In addition, HIO will be responsible for
continuing clinical development and subsequent commercialization with milestone and royalty payments to be paid back to the
Company upon successful product development through to commercialization.
14. Subsequent Event
On August 31, 2017, the Company completed a private placement, issuing a total of 1,092,500 units at $1.20 per unit for gross
proceeds of approximately $1,311,000. Each unit consisted of one common share and one common share purchase warrant.
Each common share purchase warrant entitles the holder to purchase one common share at a price of $1.50 and has an expiry
of five years from the date of issuance.
On October 19, 2017, the Company completed a private placement, issuing a total of 3,258,000 units at $1.20 per unit for gross
proceeds of approximately $3,910,000. Each unit consisted of one common share and one common share purchase warrant.
Each common share purchase warrant entitles the holder to purchase one common share at a price of $1.50 and has an expiry
of five years from the date of issuance.
Page | 52
TRANSFER AGENT
Computershare
100 University Avenue
9th Floor, North Tower
Toronto, Ontario
Canada M5S 2Y1
Tel: 800-564-6253
EXCHANGE SYMBOLS
TSX: HBP
Frankfurt: HBP
Corporate Informa�on
DIRECTORS AND OFFICERS
Sven Rohmann, MD, PhD., MBA
Chairman
Slawomir Majewski, MD.
Director
Marek Orlowski, MD.
Director
Sylwester Cacek
Director
George Anders
Director
Theodore J. Witek, MBA, PhD
Director
Heman Chao, PhD
Chief Execu�ve and Chief Scien�fic Officer
Steve Demas, BSc.
Chief Opera�ng Officer
Pho�os (Frank) Michalargias, CPA, CA
Chief Financial Officer
HELIXBIOPHARMA
T - 905 841 2300
F - 905 841 2244
E - ir@helixbiopharma.com
9120 Leslie Street, Suite 205
Richmond Hill, Ontario L4B 3J9
Canada
helixbiopharma.com