drugset / Trial / NCT02517736

Study Multicentre Evaluating the Effectiveness and Toxicity Sorafenib (Nexavar®) in Adult Patients With Uveal Melanoma and Metastatic Dissemination

NCT02517736 ↗

Phase 2 Completed 32 enrolled University Hospital, Caen
NaSingle-groupOpen-labelTreatment

Summary

The objective of the study is to determine the efficacy and toxicity of sorafenib in metastatic uveal melanoma. The main objective is to determine the non-tumor progression rate 24 weeks after initiation of treatment with sorafenib at a dose of 800 mg / day

Timeline

Start
2012-02
Primary completion
2015-01-13
Completion
2015-01-13

Drugs

EvaluationDrugModalityDoseRoute
Subject Sorafenib Small molecule 800 mg —

Indications