drugset / Trial / NCT05886374

A Study of HMPL-415S1 in Patients With Advanced Malignant Solid Tumors

NCT05886374 ↗

Phase 1 Unknown 81 enrolled Hutchmed
NaSingle-groupOpen-labelTreatment

Summary

The objective of this study is to evaluate the safety, tolerability and PK profile of HMPL-415S1 and determine MTD and/or RP2D in patients with advanced malignant solid tumor.

Timeline

Start
2023-07-06
Primary completion
2025-05-31
Completion
2026-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject HMPL-415S1 Unknown 0.5 mg Oral
Subject HMPL-415S1 Unknown 5 mg Oral
Subject HMPL-415S1 Unknown 25 mg Oral

Indications