Gritstone Oncology Reports Third Quarter 2019 Financial Results and Recent Highlights
EMERYVILLE, Calif., Nov. 12, 2019 (GLOBE NEWSWIRE) — Gritstone Oncology, Inc. (Nasdaq: GRTS), a clinical-stage biotechnology company developing the next generation of cancer immunotherapies to fight multiple cancer types, today reported recent business highlights and financial results for the third quarter ended September 30, 2019.
“We are making good progress in advancing our ongoing Phase 1 dose escalation studies of GRANITE and SLATE, with preliminary immunogenicity data to be shown at the ESMO-IO meeting in December,” said Andrew Allen, M.D., Ph.D., co-founder, president and chief executive officer of Gritstone Oncology. “We view a key outcome of this first-in-human data is to show that our immunotherapies can, uniquely, prime robust tumor-specific CD8+ T cell responses to neoantigens consistently across patients. If accomplished, this would be an important and de-risking step towards our goal of destroying tumors with neoantigen-specific T cells and, ultimately, offering transformative treatments for patients with cancer.”Recent Gritstone Oncology HighlightsContinued dosing patients in a Phase 1 clinical study evaluating GRANITE, our personalized immunotherapy product candidate, for the treatment of patients with advanced solid tumors, including gastroesophageal cancer, microsatellite-stable colorectal cancer, metastatic non-small cell lung cancer, and bladder cancerBegan dosing patients in a Phase 1 clinical study of SLATE, our off-the-shelf immunotherapy product candidate, for certain patients with advanced solid tumors, including metastatic non-small cell lung cancer, pancreatic ductal adenocarcinoma and microsatellite-stable colorectal cancer, as well as in patients with other solid tumor types who have relevant mutation/human leukocyte antigen (HLA) combinationsAppointed a new board member, Elaine V. Jones, Ph.D., who has two decades of life science investing experience, has served on over 20 life science company boards, and has direct experience within biopharma research and business developmentImproved the performance of the EDGE artificial intelligence platform from a positive predictive value for HLA class I peptide presentation of approximately 55% initially to over 70% now, which is an estimated 10-fold improvement over leading public toolsPresented a poster at the Society for Immunotherapy of Cancer’s 34th Annual Meeting (SITC 2019) reviewing novel shared tumor-specific neoantigens (TSNA) derived from driver mutations (such as KRAS G12C) that were identified by Gritstone in an efficient process combining the EDGE platform with tumor HLA peptide sequencing. These neoantigens are contained within the first SLATE product candidate. Anticipated Near-term MilestonesPresent early immunogenicity and safety data from the Gritstone Phase 1 program at the European Society for Medical Oncology’s Immuno-Oncology Congress (ESMO-IO) in Geneva, Switzerland on December 12, 2019Nominate a lead bispecific antibody development candidate directed towards a novel solid tumor-specific HLA-peptide complex in the fourth quarter of 2019Report clinical data from the Phase 1 clinical trials of GRANITE and SLATE at a scientific congress in mid-2020Third Quarter 2019 Financial ResultsFor the three months ended September 30, 2019, Gritstone reported a net loss of $27.5 million, compared to a net loss of $18.6 million for the three months ended September 30, 2018.Collaboration revenue was $984 thousand for the three months ended September 30, 2019, compared to $96 thousand for the three months ended September 30, 2018. The increase was due to revenue recognized under the Research Collaboration and License Agreement with bluebird bio, Inc., which was entered into in August 2018.Total research and development expenses were $24.9 million for the three months ended September 30, 2019, compared to $15.6 million for the three months ended September 30, 2018. The increase was primarily attributable to an increase in personnel-related expenses driven by increased headcount, as well as an increase in outside services and consultants, in-house laboratory supplies and consumables, and facilities-related expenses to accommodate our manufacturing expansion.General and administrative expenses were $4.6 million for the three months ended September 30, 2019, compared to $3.1 million for the three months ended September 30, 2018. The increase was primarily attributable to an increase in personnel-related expenses driven by an increase in headcount and an increase in legal and other outside professional services required to support the company’s ongoing operations as a public company.Cash, cash equivalents, and marketable securities were $151.5 million as of September 30, 2019, compared to $153.1 million as of December 31, 2018.About Gritstone OncologyGritstone Oncology (Nasdaq: GRTS), a clinical-stage biotechnology company, is developing the next generation of cancer immunotherapies to fight multiple cancer types. Gritstone develops its products by leveraging two key pillars—first, a proprietary machine learning-based platform, Gritstone EDGE™, which is designed to predict, from a routine tumor biopsy, the tumor-specific neoantigens (TSNA) that are presented on a patient’s tumor cells; and second, the ability to develop and manufacture potent immunotherapies utilizing patients’ TSNA to potentially drive the patient’s immune system to specifically attack and destroy tumors. The company’s lead product candidate, GRANITE, is a personalized neoantigen-based immunotherapy in Phase 1 clinical testing. Gritstone’s second product candidate, SLATE, is a shared neoantigen, “off-the-shelf” immunotherapy which is also being evaluated in a Phase 1 clinical study. Novel tumor-specific antigens can also provide targets for bispecific antibody (BiSAb) therapeutics for solid tumors, and Gritstone’s BiSAb program is currently in lead optimization. For more information, please visit gritstoneoncology.com.Gritstone Forward-Looking Statements
This press release contains forward-looking statements, including, but not limited to, statements related to the expected timing of data from the Phase 1 GRANITE and SLATE studies. Such forward-looking statements involve substantial risks and uncertainties that could cause Gritstone’s research and clinical development programs, future results, performance or achievements to differ significantly from those expressed or implied by the forward-looking statements. Such risks and uncertainties include, among others, the uncertainties inherent in the drug development process, including Gritstone’s programs’ early stage of development, the process of designing and conducting preclinical and clinical trials, the regulatory approval processes, the timing of regulatory filings, the challenges associated with manufacturing drug products, Gritstone’s ability to successfully establish, protect and defend its intellectual property and other matters that could affect the sufficiency of existing cash to fund operations. Gritstone undertakes no obligation to update or revise any forward-looking statements. For a further description of the risks and uncertainties that could cause actual results to differ from those expressed in these forward-looking statements, as well as risks relating to the business of the company in general, see Gritstone’s most recent Quarterly Report on Form 10-Q filed on November 12, 2019 and any current and periodic reports filed with the Securities and Exchange Commission.ContactsMedia:
Wheelhouse Life Science Advisors