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Eurartesim® in Patients With Imported Uncomplicated Plasmodium Vivax Malaria

NCT02110784 PHASE2 TERMINATED

The aim of the present study is to investigate the efficacy, safety and tolerability of a therapeutic course of Eurartesim® in travellers who contracted malaria due to infection by P. vivax in endemic countries.

Details

Lead sponsorAlfasigma S.p.A.
PhasePHASE2
StatusTERMINATED
Enrolment27
Start dateWed Jun 18 2014 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionSun Apr 30 2017 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Interventions

Countries

France, Italy, Netherlands, Israel, Germany, Switzerland, Spain