drugset / Trial / NCT01430416

Safety and Efficacy of AEB071 in Metastatic Uveal Melanoma Patients

NCT01430416

Phase 1 Completed 153 enrolled Novartis Pharmaceuticals
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This study has two parts, dose escalation and dose expansion. For dose escalation, the primary objective is to estimate the maximum tolerated dose (MTD) of AEB071 in patients with uveal melanoma. For dose expansion, the primary objective is to characterize the safety and tolerability of the MTD of AEB071 in patients with uveal melanoma.

Timeline

Start
2011-12-20
Primary completion
2019-05-22
Completion
2019-05-22

Drugs

EvaluationDrugModalityDoseRoute
Subject sotrastaurin Small molecule Oral

Indications