Overview

Pharmacokinetic Study of Primaquine and Chloroquine in Healthy Subjects

Status:
Completed
Trial end date:
2012-03-01
Target enrollment:
Participant gender:
Summary
This is a standard pharmacokinetic interaction study. Subjects will be randomized to be either group A or B. Group A. Subjects will have 3 hospitalizations to complete. Each hospitalization will be about 12-24 hours depends on each regimen. Subjects in A group who receive regimen 1 of primaquine (PQ) on the first admission (visit 2) will receive regimen 2 of primaquine and chloroquine combination (PQ and CQ) on second admission (visit 3) after 1 week wash out period and will finish with regimen 3 of Chloroquine (CQ) on the third admission (visit 4) after 8 weeks wash out period. Subjects in B group who receive regimen 1 of primaquine (PQ) will receive regimen 2 of chloroquine (CQ) on second admission (visit 3) after 1 week wash out period and regimen 3 of primaquine and chloroquine combination (PQ and CQ)on third admission(visit 4) with 8 week wash out period in between.
Phase:
Phase 1
Details
Lead Sponsor:
University of Oxford
Collaborator:
Mahidol University
Treatments:
Chloroquine
Chloroquine diphosphate
Primaquine