Genocea Reports Third Quarter 2017 Financial Results
- SITC presentation to highlight ATLAS™ ability in neoantigen selection -
- IND filing for neoantigen cancer vaccine, GEN-009, expected in Q1 2018 -
- Conference call today at
"We believe our proprietary ATLASTM technology sets us apart among developers of neoantigen cancer vaccines, as it offers a potential solution to one of the most significant challenges in the field - namely, identifying true neoantigens
for those vaccines from up to thousands of potential candidates," said
GEN-009 is a personalized vaccine consisting of adjuvanted synthetic long peptides of true neoantigens identified by ATLAS.
- The company expects to file an Investigational New Drug (IND) application in early 2018.
- Genocea plans to initiate a Phase 1 clinical trial in patients with a range of tumor types in the first half of 2018, and expects to report initial immunogenicity data in the first half of 2019.
Upcoming Scientific Presentations
Genocea announced today that it will present three posters at the upcoming
- Poster #430 entitled "Neoantigen identification using ATLAS™ across multiple tumor
types highlights limitations of prediction algorithms," will be presented during the session on Personalized Vaccines and Technologies/Personalized Medicine on
Saturday, November 11, 2017,
- Poster #8 entitled "T cell response profiling in colorectal carcinoma patients reveals an enrichment in responses to specific tumor-associated antigens," and
- Poster #28 entitled "Profiling of T cell responses to tumor-associated antigens in lung cancer patients treated with checkpoint inhibitors," will both be presented during the session on Biomarkers and Immune Monitoring on
Saturday, November 11, 2017.
Following its announced restructuring at the end of the third quarter, Genocea continues to explore, alongside its advisors, strategic alternatives for GEN-003, the company's Phase 3-ready investigational immunotherapy to treat the large patient population infected with genital herpes, many of whom are dissatisfied with their current treatment options.
Genocea expects that its existing cash and cash equivalents are sufficient to support its operating expenses and capital expenditure requirements into the middle of 2018.
Third-Quarter 2017 Financial Results
- Cash Position: Cash and cash equivalents as of
September 30, 2017were $22.0 millioncompared to $35.2 millionas of June 30, 2017.
- Restructuring: A corporate restructuring was implemented following the Company's strategic shift to immuno-oncology, resulting in a
charge of approximately
$1.1 millionfor employee severance, benefits, and related costs. These amounts will be paid in the fourth quarter of 2017. In addition, Genocea incurred approximately $0.5 millionof expense due to contract termination clauses that the Company anticipates will result in future cash payments and approximately $1.0 millionin non-cash asset impairment charges.
- Research and Development (R&D) Expenses: R&D expenses for the quarter ended
September 30, 2017increased $1.3 million, to $10.2 millionfrom the same period in 2016. The increase was primarily driven by higher external manufacturing-related expenses and increases in compensation to support both the clinical drug supply and clinical trial planning activities in support of the previously planned GEN-003 Phase 3 program, partially offset by reduced clinical costs, due to timing of activities in support of clinical trials. Spending increases on Genocea's immuno-oncology and cancer vaccine programs were driven primarily by increased manufacturing and compensation, consulting and professional services in anticipation of Genocea's expected filing of an IND application for GEN-009 in the first quarter of 2018. Increased spending on these programs was offset by lower costs on infectious disease programs previously discontinued in 2016.
- General and Administrative (G&A) Expenses: G&A expenses for the third quarter of 2017 were
$3.8 million, compared to $3.6 millionfor the same period in 2016, reflecting marginal increases in consulting and professional services offset by reductions in depreciation expense, with all other expenditures across various activities remaining consistent with the same quarter in the prior year.
- Net Loss: Net loss was
$16.9 millionfor the quarter ended September 30, 2017, compared to a net loss of $12.8 millionfor the same period in 2016.
Genocea will host a conference call and webcast today at
Genocea is harnessing the power of T cell immunity to develop life-changing vaccines and immunotherapies. While traditional immunotherapy discovery methods have largely used predictive methods to propose T cell targets, or antigens, Genocea has developed ATLAS™, its proprietary technology platform, to identify clinically relevant antigens of T cells based on actual human immune responses. Genocea is using ATLAS in immuno-oncology applications to develop neoantigen cancer vaccines while also exploring partnership opportunities for general cancer vaccines and a vaccine targeting cancers caused by Epstein-Barr Virus. Genocea expects to begin clinical development of its first neoantigen cancer vaccine, GEN-009, in early 2018. Genocea is exploring strategic alternatives for GEN-003, its Phase 3-ready immunotherapy candidate for the treatment of genital herpes. For more information, please visit www.genocea.com.
About Neoantigen Cancer Vaccines and GEN-009
Neoantigens are personalized tumor mutations that are seen as "foreign" by an individual's immune system. Data published in recent years have indicated that an individual's response to neoantigens drives checkpoint inhibitor efficacy and that it is possible to vaccinate an individual against their own neoantigens. Genocea's lead immuno-oncology program, GEN-009, is an adjuvanted neoantigen peptide vaccine candidate designed to direct a patient's immune system to attack their tumor. GEN-009's neoantigen peptides are identified by Genocea's proprietary ATLAS platform, which recalls a patient's pre-existing CD4+ and CD8+ T cell immune responses to their tumor. Following ATLAS neoantigen identification, Genocea will manufacture a personal vaccine for each patient.
Statements herein relating to future business performance, conditions or strategies and other financial and business matters, including expectations regarding clinical developments, are forward-looking statements within the meaning of the Private Securities Litigation Reform Act. Genocea cautions that these forward-looking statements are subject to numerous assumptions, risks, and uncertainties that change over time. Factors that may cause actual results to differ materially from the results discussed in the forward-looking statements or historical experience include risks and uncertainties, including Genocea's ability to progress any product candidates in preclinical or clinical trials; the ability of ATLAS to identify promising oncology vaccine and immunotherapy product candidates; the scope, rate and progress of its preclinical studies and clinical trials and other research and development activities; anticipated clinical trial results; anticipated timing for initiation of new clinical trials; current results may not be predictive of future results; even if the data from preclinical studies or clinical trials is positive, regulatory authorities may require additional studies for approval and the product may not prove to be safe and efficacious; Genocea's ability to enter into future collaborations with industry partners and the government and the terms, timing and success of any such collaboration; risks associated with the manufacture and supply of clinical and commercial product; the cost of filing, prosecuting, defending and enforcing any patent claims and other intellectual property rights; Genocea's ability to obtain rights to technology; competition for clinical resources and patient enrollment from drug candidates in development by other companies with greater resources and visibility; the rate of cash utilized by Genocea in its business and the period for which existing cash will be able to fund such operation; Genocea's ability to obtain adequate financing in the future to continue its clinical programs through product licensing, co-promotional arrangements, public or private equity or debt financing or otherwise; general business conditions; competition; business abilities and judgment of personnel; the availability of qualified personnel and other factors set forth under "Risk Factors" in Genocea's Annual Report on Form 10-K for the fiscal year ended
CONDENSED CONSOLIDATED BALANCE SHEETS (UNAUDITED)
|Cash, cash equivalents and investments||$||21,983||$||63,362|
|Debt, current and long-term||$||15,782||$||16,958|
|Accrued expenses and other liabilities||6,447||4,354|
|Total liabilities and stockholders' equity||$||28,044||$||69,896|
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS (UNAUDITED)
(In thousands, except per share amounts)
|Three Months Ended ||Nine Months Ended |
|Research and development||10,155||8,811||31,324||22,821|
|General and administrative||3,750||3,619||10,955||11,569|
|Refund of research and development expense||—||—||—||(1,592||)|
|Total operating expenses||16,496||12,430||44,870||32,798|
|Loss from operations||(16,4956||)||(12,430||)||(44,870||)||(32,563||)|
|Other income and expense:|
|Total other income and expense||$||(372||)||$||(335||)||$||(1,108||)||$||(976||)|
|Other comprehensive loss:|
|Unrealized gain (loss) on available-for-sale securities||$||—||$||(9||)||$||—||$||15|
|Net loss per share - basic and diluted||$||(0.59||)||$||(0.45||)||$||(1.61||)||$||(1.18||)|
|Weighted-average number of common shares used in computing net loss per share||$||28,666||$||28,276||$||28,568||$||28,214|
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