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Topical WR 279,396 for Cutaneous Leishmaniasis in Tunisia

NCT00703924Phase 2Completed

Sponsor
U.S. Army Medical Research and Development Command
Start
Mar 2003
Primary completion
Nov 2004
Modality
Small Molecules
Countries
2
01

Overview

Phase 2, randomised, double-blind trial in cutaneous leishmaniasis (CL) comparing WR 279,396 with Placebo (2 arms). Primary endpoints: Complete Clinical Response at Day 180 and Safety of WR 279,396 at 180 days. Started Mar 2003; status: completed.

02

Drugs

WR 279,396
03

Conditions

cutaneous leishmaniasis (CL)

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