drugset / Trial / NCT00383292

A Study of Tasisulam in Treating Participants With Malignant Melanoma

NCT00383292

Phase 2 Completed 130 enrolled Eli Lilly and Company
NaSingle-groupOpen-labelTreatment

Summary

The primary purpose of this study is to determine the objective response rate (complete and partial response) for participants who receive tasisulam after one prior systemic treatment for unresectable or metastatic melanoma.

Timeline

Start
2006-11
Primary completion
2011-09
Completion
2015-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Tasisulam Small molecule Intravenous

Indications