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HUTCHMED launches global early-stage trial for novel ATTC cancer therapy HMPL-A580

Story Highlights
  • HUTCHMED has initiated a global Phase I/IIa trial of HMPL-A580, a first-in-class ATTC for advanced solid tumors in China and the US.
  • The study advances HUTCHMED’s next-generation ATTC platform, aiming for more targeted, less toxic oncology therapies and future partnership-led expansion.
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HUTCHMED launches global early-stage trial for novel ATTC cancer therapy HMPL-A580

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HUTCHMED (China) ( (HK:0013) ) just unveiled an announcement.

HUTCHMED has begun a Phase I/IIa global clinical trial of HMPL-A580, its second novel Antibody-Targeted Therapy Conjugate, in patients with unresectable, advanced or metastatic solid tumors in China and the US. The first-in-class candidate couples a selective PI3K/PIKK inhibitor payload to an anti-EGFR antibody, aiming to exploit synergy between PAM pathway inhibition and EGFR blockade.

The multicenter, open-label study will assess safety, tolerability, pharmacokinetics, immunogenicity and preliminary efficacy, first through dose escalation and then through expansion in selected solid tumors to define dosing for later-stage trials. The launch underscores HUTCHMED’s push to build a differentiated ATTC platform that seeks to improve tumor targeting, reduce off-tumor toxicity and position the company for future partnerships and earlier-line oncology treatment combinations.

More about HUTCHMED (China)

HUTCHMED is an innovative, commercial-stage biopharmaceutical company focused on discovering, developing and commercializing targeted therapies and immunotherapies for cancer and immunological diseases. It advances drug candidates from in-house discovery to global markets, with three medicines already marketed in China and one also approved in the US, Europe and Japan.

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