drugset / Trial / NCT03457532
A Phase I Study of SCC244 in Patients with Advanced MET Alterations Solid Tumors
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |