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Amphivena Therapeutics Announces First Patient Dosed in the Phase 1 Dose Expansion of AMV564

Amphivena Therapeutics Announces First Patient Dosed in the Phase 1 Dose Expansion of AMV564 News provided by Share this article SOUTH SAN FRANCISCO, Calif., Dec. 16, 2020 /PRNewswire/ Amphivena Therapeutics, a clinical-stage oncology company focused on developing a platform of bivalent T-cell engagers that restore anti-cancer immunity in patients, today announced the first patient has been dosed in the Phase 1 dose expansion study evaluating AMV564, an investigational, first-in-class agent that depletes myeloid derived suppressor cells (MDSC) and activates T cells, in adult patients with selected solid tumor indications.  The dose escalation phase of the first-in-human, multicenter, open-label study of AMV564 in solid tumors was initiated in October 2019 and established the safety, PK profile and clinical activity of AMV564 including a confirmed RECIST complete response

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