HMPL-A830 for Cancer
What You Need to Know Before You Apply
What is the purpose of this trial?
This is a first-in-human (FIH), multicenter, open-label, phase I/Ⅱa clinical study of HMPL-A830 in participants with histologically or cytologically confirmed, unresectable, advanced, or metastatic solid tumors\*, who are refractory or progressed on/after available standard treatment. The study will be conducted in 2 parts:
Dose Escalation (Part A, Phase I), approximately 57 participants will be enrolled.
Dose Optimization (Part B, Phase IIa), approximately 90 participants will be enrolled.
Are You a Good Fit for This Trial?
This trial is for adults (18+) with advanced or metastatic solid tumors that can't be removed by surgery and have not responded to standard treatments. Participants must be in good physical condition, able to care for themselves, have a life expectancy of at least 12 weeks, and at least one tumor that can be measured.Inclusion Criteria
Exclusion Criteria
What Are the Treatments Tested in This Trial?
Interventions
- HMPL-A830
Trial Overview
The study is testing a new drug called HMPL-A830 in people with advanced solid tumors. It will first find the safest dose (Phase I), then test how well it works (Phase IIa). All participants receive HMPL-A830; there is no placebo group.
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
Find a Clinic Near You
Who Is Running the Clinical Trial?
Hutchmed
Lead Sponsor
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