Malaria Clinical Trial
Official title:
Phase 1b Clinical Trial Using Argemone Mexicana in Healthy Adults Infected or Not Infected With Plasmodium Falciparum in Mali: Pharmacokinetics and Observational Study
The main objective is to study the pharmacokinetics, pharmacodynamics and tolerability of the decoction of the aerial parts of Argemone mexicana (AM), administered in healthy volunteers.
This is an open non comparative safety and pharmacokinetic (PK) study clinical trial.
Healthy volunteers aged from 18 to 50 years old will be recruited and followed 42 days after
treatment initiation as in the current World Health Organization malaria drug protocol
efficacy assessment protocol.
Each volunteer will be take oral Argemone mexicana in decoction formulation. For the PK
assessment purposes, 3 groups have been constituted: (i) a group will receive a unique dose
of with blood withdrawal scheduled at 0 hour, 30 minutes, 1 hour, 2 hours, 4 hours, 6 hour ,
8 hours and 12 hours. (ii) a group will receive two doses (morning and evening) of Argemone
mexicana for 14 days with blood withdrawal scheduled at 0 hours, 30 minutes, 1 hour, 2
hours, 4 hours, 6 hours, 8 hours, 12 hours, 24 hours, 3 days, 7 days and 14 days. (iii) a
group will receive two doses (morning and evening) of Argemone mexicana for 14 days with
blood withdrawal scheduled at 0 hour, 12 hours, 14 hours, 16 hours, 18 hours, 20 hours, 22
hours, 24 hours, 3 days, 7 days, 14 days and 21 days Safety will be assessed clinically
(Clinical exam and Electrocardiography) and biologically (hematology and biochemistry
parameters will be measured) throughout the 42 days of thefollow-up.
;
Endpoint Classification: Pharmacokinetics/Dynamics Study, Intervention Model: Single Group Assignment, Masking: Open Label
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