Potential Response Predictors to IMV’s Lead Compound in the DeCidE Clinical Study in Patients with Advanced, Recurrent Ovarian Cancer to be Presented at SITC Annual Meeting
IMV Inc. (NASDAQ: IMV) announced that a poster detailing translational data from the DeCidE clinical study in advanced ovarian cancer will be presented at the SITC Annual Meeting from November 10-14, 2021.
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- Poster Title: Identification of potential response predictors to maveropepimut-S (DPX-Survivac), a novel T cell activating immunotherapy, in patients with advanced recurrent ovarian cancer
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Presenter:
Oliver Dorigo , M.D., Ph.D.,
Director and Associate Professor
Division Gynecologic OncologyDepartment of Obstetrics and Gynecology Stanford University , CA - Poster Number: 353
Important dates
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November 9, 2021 : Full abstracts are made public at8 a.m. EST -
November 12, 2021 : Poster presentation-
Poster
Hall Hours : 7 a.m.–8:30 p.m. -
Dr. Dorigo will be present in person at lunch time (12:40–2:10 p.m. EST) and during the poster reception (7–8:30 p.m. EST)
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Poster
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November 12, 2021 : Poster and e-poster presentation will be available under theScientific Publications & Posters section on IMV’s website.
About IMV
IMV Forward-Looking Statements
This press release contains forward-looking information under applicable securities law. All information that addresses activities or developments that we expect to occur in the future is forward-looking information. Forward-looking statements use such word as “will”, “may”, “potential”, “believe”, “expect”, “continue”, “anticipate” and other similar terminology. Forward-looking statements are based on the estimates and opinions of management on the date the statements are made. In the press release, such forward-looking statements include, but are not limited to, statements regarding the Company’s ability to advance its development strategy, as well as the prospects, for its lead immunotherapy and its other pipeline of immunotherapy candidates. However, they should not be regarded as a representation that any of the plans will be achieved. Actual results may differ materially from those set forth in this press release due to risks affecting the Company, including access to capital, the successful design and completion of clinical trials and the timely receipt of all regulatory approvals to commence, and then continue, clinical studies and trials and the receipt of all regulatory approvals to commercialize its products.
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