A Study of HMPL-453 in Patients With Advanced Solid Malignancies
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |