drugset / Trial / NCT03466268

Study to Evaluate the Safety and Anti-tumor Activity of SCC244

NCT03466268 ↗

Phase 1 Completed 56 enrolled Haihe Biopharma Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

This study evaluates the Safety, Tolerability, Pharmacokinetics, and Anti-tumor Activity of SCC244 in patients with advanced solid tumors with c-Met Alterations.

Timeline

Start
2017-09-14
Primary completion
2023-01-09
Completion
2023-01-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Gumarontinib Small molecule 100 mg —
Subject Gumarontinib Small molecule 200 mg —
Subject Gumarontinib Small molecule 300 mg —
Subject Gumarontinib Small molecule 400 mg —

Indications