IMV to Showcase its DPX® Delivery Technology in Two Presentations at the AACR Annual Meeting 2022
IMV Inc. will present significant findings at the AACR Annual Meeting on its DPX technology, which enhances anti-tumor immune responses involving natural killer (NK) cells. The presentations include data from a Phase 2 basket study evaluating maveropepimut-S in combination with pembrolizumab and cyclophosphamide for advanced bladder cancer. Key insights will be shared by Dr. Olivier Rixe, highlighting the safety and efficacy of their immunotherapeutic strategies. IMV's platform aims to improve cancer treatment outcomes by activating targeted immune responses.
- IMV's DPX technology shows promising involvement of NK cells in anti-tumor responses, indicating potential for improved treatment efficacy.
- Presentation of clinical data from significant studies may increase investor confidence and attract interest in the company's immunotherapy pipeline.
- None.
- IMV’s DPX technology elicits a coordinated anti-tumor immune response involving natural killer cells in both translational and preclinical studies
- Clinical data from the Company’s basket study in advanced, metastatic bladder cancer will be presented at the “Immunotherapy Combination Strategy in Clinical Trials” mini symposium
“Data to be presented suggest that our DPX delivery platform instructs an innate immune response involving NK cells in addition to the previously recognized role for T and B cells,” said
Translational research using both clinical samples from the DeCidE ovarian cancer trial and tissues from pre-clinical models will be presented showing for the first time that natural killer (NK) cells play a distinct role in promoting anti-tumor responses to the company’s lead DPX-peptide immunotherapeutic, Maveropepimut-S.
In an oral presentation in a late-breaking session about immunotherapeutic combinations, Dr.
Presentations Details
- NK cells are involved in promoting anti-tumor responses to DPX-peptide immunotherapy
Presenter: Moamen Bydoun, Ph.D., Senior Research Scientist at IMV
Poster Number: 623
Date/Time:
- Safety, preliminary efficacy and pharmacodynamic (PD) analysis of maveropepimut-S, intermittent low-dose cyclophosphamide and pembrolizumab in patients with advanced, metastatic bladder cancer
Presenter:
Session Title: Immunotherapy Combination Strategies in Clinical Trials
Presentation Number: CT035
Session Date and Time:
About IMV
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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 and the anticipated timing of the Company’s clinical trial programs and studies. 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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