Gamida Cell Presents New Data on Nicotinamide-Enabled NK Cell Therapy at Society for Immunotherapy of Cancer';s (SITC) 36th Annual Meeting
Gamida Cell (NASDAQ: GMDA) announced promising data on GDA-201, its nicotinamide (NAM)-enabled NK cell therapy, enhancing tumor reduction and cytotoxicity. The data will be presented at the Society for Immunotherapy of Cancer (SITC) Annual Meeting from November 10-14, 2021. NAM increases NK cell effectiveness by modulating metabolic pathways and down-regulating immune checkpoints. Gamida Cell's research utilized artificial intelligence to analyze over 1,200 genes and 100 metabolites, showcasing NAM's potential to improve clinical outcomes. GDA-201 targets hematologic and solid tumors while being in ongoing clinical trials.
- Enhanced efficacy of GDA-201 demonstrated through NAM technology, increasing NK cell cytotoxicity and tumor targeting.
- AI analysis revealed significant metabolic pathway modulation, identifying 1,204 differentially expressed genes and 100 modified metabolites.
- Potential clinical benefits highlighted, as NAM improves NK cell persistence and potency against cancer.
- None.
The presentations identify network interactions between differentially expressed genes and intracellular metabolites associated with enhanced biological functional activity of GDA-201 NK. The data show that NAM increases cytotoxicity, ADCC, homing and in vivo antitumor activity of NK cells by modulating multiple metabolic pathways, down-regulating immune checkpoint inhibitors, increasing resistance to reactive oxygen species and influencing other cellular processes. An artificial intelligence–assisted analysis identified 1,204 differentially expressed genes, and 100 significantly modified metabolites, due to the effect of NAM. These data further validate the unique benefits of the NAM technology and its potential to improve clinical outcomes.
“NAM gives us a powerful tool for preserving and enhancing desirable qualities of NK cells and a broad range of other cell types. It has been shown to improve persistence and potency against cancer and may offer advantages in overcoming an immunosuppressive tumor microenvironment,” said
About GDA-201
GDA-201 is an investigational therapy, and its safety and efficacy have not been established by the FDA or any other health authority.
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Cautionary Note Regarding Forward Looking Statements
This press release contains forward-looking statements as that term is defined in the Private Securities Litigation Reform Act of 1995, including with respect to timing of initiation and progress of, and data reported from, the clinical trials of Gamida Cell’s product candidates, anticipated regulatory filings (including the submission of the BLA for omidubicel to the FDA), commercialization planning efforts, the potentially life-saving or curative therapeutic and commercial potential of omidubicel, and Gamida Cell’s expectations regarding its projected cash to be used for operating activities and cash runway. Any statement describing Gamida Cell’s goals, expectations, financial or other projections, intentions or beliefs is a forward-looking statement and should be considered an at-risk statement. Such statements are subject to a number of risks, uncertainties and assumptions, including those related to the impact that the COVID-19 pandemic could have on our business, and including the scope, progress and expansion of Gamida Cell’s clinical trials and ramifications for the cost thereof; clinical, scientific, regulatory and technical developments; and those inherent in the process of developing and commercializing product candidates that are safe and effective for use as human therapeutics, and in the endeavor of building a business around such product candidates. In light of these risks and uncertainties, and other risks and uncertainties that are described in the Risk Factors section and other sections of Gamida Cell’s Annual Report on Form 20-F, filed with the
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1 Bachanova, et al. ASH 2020. Abstract #63.
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