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HMPL-A83

Phase 1

Advanced Tumors | Small molecule | Oncology |HUTCHMED (China) Limited|Last Updated: Jun 17, 2025

Success Probability

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Market & Valuation

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Trial Design

UNCONTROLLED
Total Trials1
Total Enrollment40

FDA Designations

No designations recorded

Clinical trial landscape

HMPL-A83 · 1 trial · 1 indication

Phase 1 1
NCT05429008A Phase I Clinical Study of HMPL-A83 in Patients With Advanced Malignant NeoplasmAdvanced Tumors
COMPLETED40 Analytics
PHASE1COMPLETED
A Phase I Clinical Study of HMPL-A83 in Patients With Advanced Malignant Neoplasm
Advanced TumorsUnlock trial analytics

Study Design & Arms

Interventions

NameTypeDescription
HMPL-A83 injectionDRUGDay 1,8,15,22 dose; 28 day treatment cycles.
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Frequently asked questions about HMPL-A83

What is HMPL-A83 used for?

HMPL-A83 is an investigational small molecule being studied for the treatment of advanced tumors. It is currently in Phase 1 clinical development for this oncology indication. The drug is not yet approved and remains under investigation.

Who makes HMPL-A83?

HMPL-A83 is being developed by HUTCHMED (China) Limited, a biopharmaceutical company listed on the stock exchange under the ticker HCM. The company is conducting clinical trials to evaluate the drug's safety and efficacy in patients with advanced tumors.

What phase is HMPL-A83 in?

HMPL-A83 is in Phase 1 clinical development. A Phase 1 study has been completed, involving 40 patients with advanced tumors. The drug is investigational and has not yet received regulatory approval.

What clinical trials is HMPL-A83 in?

HMPL-A83 has one completed clinical trial, registered under NCT05429008. This Phase 1 study, titled 'A Phase I Clinical Study of HMPL-A83 in Patients With Advanced Malignant Neoplasm,' enrolled 40 patients with advanced tumors. The trial was uncontrolled and not randomized or double-blinded.

Is HMPL-A83 the same as any other drug?

No alternative names for HMPL-A83 have been reported. The drug is identified solely by its code name HMPL-A83 in clinical trial registries and development documentation.