drugset / Trial / NCT03457532

A Phase I Study of SCC244 in Patients with Advanced MET Alterations Solid Tumors

NCT03457532

Phase 1 Completed 177 enrolled Haihe Biopharma Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

This is a Phase 1a/1b multi-center and open label study to evaluate the safety, tolorability, pharmacokinetics and priliminary efficacy of SCC244 in advanced solid tumors patients with c-MET alteration

Timeline

Start
2017-12-16
Primary completion
2023-09-22
Completion
2023-09-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Gumarontinib Small molecule 25 mg Oral
Subject Gumarontinib Small molecule 50 mg Oral
Subject Gumarontinib Small molecule 100 mg Oral
Subject Gumarontinib Small molecule 200 mg Oral
Subject Gumarontinib Small molecule 400 mg Oral
Subject Gumarontinib Small molecule 600 mg Oral

Indications