drugset / Trial / NCT00445796

Arsucam® (Artesunate + Amiodaquine) Efficacy and TOLerance

NCT00445796 ↗

Phase 4 Completed 300 enrolled Sanofi
RandomizedParallel-groupOpen-labelTreatment

Summary

Primary Objective: To demonstrate the non-inferiority, in terms of clinical and parasitological efficacy on Day 14, of administration of Arsucam® as a single daily intake versus two daily intakes. Secondary Objective: To compare the clinical safety of the two treatment regimens.

Timeline

Start
2005-06
Primary completion
—
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject Artesunate Small molecule — —
Subject amodiaquine Other / unclassified — —

Indications