drugset / Trial / NCT04647838

Tepotinib in Solid Tumors Harboring MET Alterations

NCT04647838

Non-randomizedParallel-groupOpen-labelTreatment

Summary

The aim of this study is to understand efficacy of tepotinib in patients with solid cancers harbouring c-MET amplification or exon 14 mutation who progressed after standard treatment for metastatic disease.

Timeline

Start
2020-01-16
Primary completion
2023-02-28
Completion
2024-08-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Tepotinib Small molecule 500 mg Oral

Indications