drugset / Trial / NCT02083380

Phase II Efficacy Study of Artefenomel & Piperaquine in Adults & Children With P. Falciparum Malaria.

NCT02083380 ↗

Phase 2/3 Completed 448 enrolled Medicines for Malaria Venture
RandomizedParallel-groupQuadruple-blindTreatment

Summary

A randomised, double-blind single-dose study to determine the efficacy, safety, tolerability and pharmacokinetics of OZ439 (artefenomel) in combination with piperaquine (PQP) in patients \> 0.5 years and \<= 70 years of age with uncomplicated Plasmodium falciparum malaria in Africa and Asia (Vietnam). Interim analyses for futility were planned. Adults and children will be included through progressive step-down in age following safety review by an independent safety monitoring board (ISMB). If the study were to meets its efficacy objectives, this will inform dose setting for Phase III studies.

Timeline

Start
2014-07
Primary completion
2015-10
Completion
2015-11

Outcome

Missed primary endpoint

paper none of the treatment arms reached the target efficacy of > 95% PCR-adjusted ACPR at day 28. PMID 28988541 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Artefenomel Small molecule 800 mg Oral
Subject piperaquine Small molecule 640 mg Oral
Subject piperaquine Small molecule 960 mg Oral
Subject piperaquine Small molecule 1440 mg Oral