drugset / Trial / NCT01985555

Phase I Study of the Volitinib (HMPL-504) in Patients With Advanced Solid Tumors

NCT01985555

Phase 1 Completed 85 enrolled Hutchison Medipharma Limited
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety and tolerability of single and multiple doses of volitinib administered to patients with locally advanced or metastatic solid tumors and determine MTD (Maximum Tolerated Dose) or RPTD(recommended Phase 2 dose).

Timeline

Start
2013-05
Primary completion
2019-04
Completion
2019-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Savolitinib Small molecule 400 mg
Subject Savolitinib Small molecule 500 mg
Subject Savolitinib Small molecule 600 mg
Subject Savolitinib Small molecule 800 mg

Indications