drugset / Trial / NCT02133157

Phase I Study of Sulfatinib(HMPL-012) in Patients With Advanced Solid Tumors

NCT02133157

Phase 1 Completed 71 enrolled Hutchison Medipharma Limited
NaSingle-groupOpen-labelTreatment

Summary

Sulfatinib (HMPL-012) is a novel oral small molecule that selectively inhibits vascular endothelial growth factor receptors (VEGFR) 1, 2, and 3 and inhibits FGFR kinase activity has demonstrated potent inhibitory effects on multiple human tumor xenografts. This first-in-human study is conducted to assess the maximum tolerated dose (MTD) and recommended dose for phase II ,to evaluate the pharmacokinetics , safety and preliminary anti-tumor activity of HMPL-012 at single doses and multiple doses .

Timeline

Start
2010-04
Primary completion
2014-10
Completion
2014-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Surufatinib Small molecule 25 mg Oral
Subject Surufatinib Small molecule 50 mg Oral
Subject Surufatinib Small molecule 100 mg Oral

Indications