drugset / Trial / NCT03160833

A Study of HMPL-453 in Patients With Advanced Solid Malignancies

NCT03160833

Phase 1/2 Unknown 33 enrolled Hutchison Medipharma Limited
NaSingle-groupOpen-labelTreatment

Summary

This is a dose escalation study consisting of two stages: Dose-escalation stage (stage 1): Patients will take a single dose of HMPL-453 on Day 1 and will be followed for one week for safety observations. After one week of observation, if no safety issues occur, patients can continue multiple dosing of HMPL-453 QD (quaque die) and start on the DLT (Dose Limited Toxicity) assessment cycles. Each cycle consists of 28-days. Patients are required to draw blood samples for PK and safety analysis at specific time points during the treatment; Dose-Expansion Stage (Stage 2): This stage is to further evaluate the safety, tolerability, PD (pharmacodynamics) profile, and preliminary anti-tumor activity of HMPL-453 at the RP2D (recommended phase 2 dose) in approximately 10 patients with advanced solid tumor.

Timeline

Start
2017-05-23
Primary completion
2019-12-31
Completion
2020-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject HMPL-453 Unknown 50 mg Oral
Subject HMPL-453 Unknown 100 mg Oral
Subject HMPL-453 Unknown 200 mg Oral
Subject HMPL-453 Unknown 300 mg Oral
Subject HMPL-453 Unknown 400 mg Oral
Subject HMPL-453 Unknown 500 mg Oral

Indications