Actym Therapeutics announced today that an abstract highlighting detailed in vivo and in vitro preclinical data of its lead candidate, ACTM-838, was accepted for presentation at the Society for Immunotherapy of Cancer (SITC) 37th Annual Meeting, to be held virtually and at the Boston Convention & Exhibition Center from November 8 to 12, 2022.
| Company to present data showing comprehensive reprogramming of the immunosuppressive tumor microenvironment across several cancer models at Society for Immunotherapy of Cancer (SITC) Annual Meeting BERKELEY, Calif., Nov. 7, 2022 /PRNewswire/ -- Actym Therapeutics, a Berkeley-based biotechnology company focused on the discovery and development of transformational immunotherapies to treat cancer, announced today that an abstract highlighting detailed in vivo and in vitro preclinical data of its lead candidate, ACTM-838, was accepted for presentation at the Society for Immunotherapy of Cancer (SITC) 37th Annual Meeting, to be held virtually and at the Boston Convention & Exhibition Center from November 8 to 12, 2022. ACTM-838 is Actym’s lead candidate from its proprietary STACT platform and encodes an engineered IL-15 payload (IL-15plex) and engineered STING payload (eSTING). The data showed ACTM-838 to offer powerful efficacy as a single agent, including when used in checkpoint refractory tumors, and to work synergistically when used in combination with anti-PD1 therapies.
“The data we are presenting at SITC highlights the power of ACTM-838 to overcome the highly immunosuppressive tumor microenvironment and generate durable anti-tumor immunity in preclinical models,” said Christopher Thanos, Ph.D., Actym’s President, CEO, and Cofounder. “ACTM-838 is systemically delivered, with potent, tumor-specific effects. These preclinical data give us confidence in our approach to comprehensively and broadly re-program the tumor microenvironment as we prepare to enter the clinic in 2023.” Research highlights include:
“Our preclinical work has shown ACTM-838’s efficacy in transforming the tumor microenvironment both as a potent single agent and in synergy with anti-PD1 therapies,” said Chan Whiting, Ph.D., Actym’s Chief Development Officer and Head of Research and Development. “We look forward to entering the clinic next year with this new and potentially powerful therapeutic approach, and bringing hope to cancer patients with limited treatment options.” SITC Presentation Details: About Actym Therapeutics After IV dosing, STACT naturally and selectively expands in the extracellular milieu of the TME, an environment well-known to be hospitable for bacterial growth. Once there, it is naturally internalized by phagocytic, tumor-resident immune cells, facilitating combinatorial payload delivery to these cells. This approach enables the tumor-specific delivery of payloads (and combos) too toxic to be dosed systemically via conventional modalities, in a single therapeutic composition. Actym’s lead candidate, ACTM-838 leverages these capabilities and is being tested as a single agent and in combination with anti-PD1 therapy across multiple solid tumor types. In April of 2020, Actym raised $34 million in a Series A financing, co-led by Boehringer-Ingelheim Venture Fund and Panacea Venture Healthcare, with participation from Illumina Ventures, Korea Investment Partners, and JLO Ventures. Media Contact: Corporate Contact:
SOURCE Actym Therapeutics Inc. |
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