Infinity Pharmaceuticals Announces Two Upcoming Presentations on PI3K-γ and Eganelisib by Dr. Judith Varner at the 2023 Annual Meeting of the American Association of Cancer Research
Infinity Pharmaceuticals (NASDAQ: INFI) has announced upcoming presentations on eganelisib, an innovative immuno-oncology therapy, at the 2023 American Association of Cancer Research (AACR) Annual Meeting from April 14-19 in Orlando, Florida. Highlights include preclinical data indicating that PI3K-γ inhibition can convert tumor-associated macrophages in head and neck squamous cell carcinoma and non-small cell lung cancer into activated immune-stimulating cells. Presentation details include sessions by Professor Judith A. Varner of UCSD Moores Cancer Center, focusing on the clinical implications of targeting myeloid cells in cancer. The ongoing MARIO-275 and MARIO-3 trials show promising results in systemic immune activation and tumor microenvironment reprogramming with eganelisib combined with other therapies, reinforcing its potential as a next-generation immunotherapeutic.
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Highlights of the presentations include preclinical and translational data further reinforcing the mechanism of action of PI3K-γ inhibition:
- Single cell transcriptomics data showing PI3K-γ knockout switches tumor associated macrophages in head and neck squamous cell carcinoma (HNSCC) and non small cell lung cancer (NSCLC) tumor models to activated, antigen-presenting, T cell-stimulating macrophages.
- Preclinical data supporting tumor growth delay of HNSCC tumor models in PI3K-γ knockout mice is mediated by intra-tumoral interleukin-12, interferon gamma and CD8+ T cells, key drivers of immune response to cancer.
- Translational data from the MARIO-275 clinical trial showing increased systemic immune activation in patients treated with nivolumab in combination with eganelisib over nivolumab alone, with enrichment of genes from interferon signaling, antigen presentation, and T cell receptor pathways.
- Translational data from the MARIO-3 clinical trial, showing immune activation within the tumor microenvironment in patients treated with eganelisib, nab-paclitaxel and atezolizumab, with up-regulation of interferon signaling, antigen presentation, and T cell receptor pathways.
- Following translational data from MARIO-1 indicating increased expression of the TGF-β activating integrin αVβ8 in HNSCC patients treated with combination of eganelisib and nivolumab, initial preclinical studies showing anti-αVβ8 monoclonal antibody treatment prevents growth of HNSCC tumor model in PI3K-γ knock-out mice.
“Our presentations describe exciting aspects of the role of PI3K-γ as a fundamental molecular switch controlling immune response by myeloid cells in the tumor microenvironment,” said
Details of the presentations are as follows:
Presentation time:
Title: Macrophages rule in cancer
Session: ED034 - Antigen Presentation: The Macrophage-Dendritic Cell Debate
Presenter:
Presentation time:
Title: Basic and clinical impacts of targeting myeloid cells in tumors
Session: Session SY14 - Next Generation of Myeloid Checkpoints in Cancer
Presenter:
About Infinity and Eganelisib
Cautionary Note Regarding Forward-Looking Statements
This press release contains forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995. Such forward-looking statements include the therapeutic potential of eganelisib including its potential as a first-in-class, oral, immuno-oncology macrophage reprogramming therapeutic. Such statements are subject to numerous important factors, risks and uncertainties that may cause actual events or results to differ materially from the Company's current expectations. For example, there can be no guarantee that eganelisib will successfully complete necessary preclinical and clinical development phases. Further, there can be no guarantee that any positive developments in Infinity's product portfolio will result in stock price appreciation. Management's expectations and, therefore, any forward-looking statements in this press release could also be affected by risks and uncertainties relating to a number of other factors, including the following: the cost, timing and results of clinical trials and other development activities that may be delayed or disrupted by the COVID-19 pandemic or otherwise; the content and timing of decisions made by the
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