Hutchmed begins patient dosing in phase I trial of HMPL A83 in patients with advanced malignant neoplasms in China

Hutchmed begins patient dosing in phase I trial of HMPL A83 in patients with advanced malignant neoplasms in China

By, Admin 19 July 2022

Hutchmed (China) Limited announces that it has initiated a phase I trial in China of HMPL-A83, an investigational novel IgG4-type humanized anti-CD47 monoclonal antibody. The first patient received their first dose on July 15, 2022. The phase I trial is a multicenter, open-label study to evaluate the safety, tolerability, pharmacokinetics and preliminary efficacy of HMPL-A83 in patients with advanced malignant neoplasms. The primary endpoints are dose-limiting toxicity (DLT), safety, tolerability, recommended phase II dose (RP2D) and maximum tolerated dose (MTD). The secondary endpoints include pharmacokinetics, pharmacodynamics, immunogenicity and preliminary efficacy profile. The lead principal investigators are Dr Ye Guo of Shanghai East Hospital and Dr Yuping Sun of Shandong Cancer Hospital. Dr Weiguo Su, chief executive officer and chief scientific officer of Hutchmed, said:

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