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Clinical Trial Summary

A 2x2 randomized crossover of single dose malarone at rest and during moderate intensity exercise under controlled conditions of heat and humidity in healthy adult participants. Statistical analysis of AUC and Cmax will be performed to determine pharmacokinetic changes.


Clinical Trial Description

A clinical trial under controlled heat exposure and moderate intensity exercise, determined by VO2max testing and calibration, to determine if physiologic changes during heat exposure and exercise change the pharmacokinetics of malarone to a degree that falls outside the range of that which is considered bioequivalent or 80-125% concentration using AUC and Cmax for rate and extent of exposure. Participants will be randomized to order of rest and exercise components. Single dose malarone will be used during both arms. Single dose malarone pharmacokinetics will give insight into risk of toxicity or risk of under treatment during prophylaxis administration. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03991208
Study type Interventional
Source Walter Reed Army Institute of Research (WRAIR)
Contact
Status Withdrawn
Phase Phase 4
Start date May 24, 2019
Completion date May 23, 2021

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