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Clinical Trial Summary

Primary Objective:

- To demonstrate the non-inferiority of corrected adequate clinical and parasitological response at Day 28 of Artesunate Amodiaquine (ASAQ) versus chloroquine

Secondary Objectives:

- To assess the non inferiority on the same way as the main criteria:

- at Day 28 before corrected cure rate

- at Day 14 and Day 42 before and after corrected cure rate

- To compare the two groups of treatment in terms of:

- Efficacy:

- Proportion of aparasitaemic patients at 24, 48 an 72 hours

- Proportion of afebrile patients at 24, 48 and 72 hours

- Percentage of gametocyte carriers during follow-up

- Evolution of the mean of gametocytes during the 42 days of follow-up

- Evolution of haemoglobin value between Day 0 and Day 7, Day 0 and Day 28

- Clinical and biological tolerability:

- Proportion of any adverse event

- Biological safety: haematology (Red blood cells, Haemoglobin, White Blood Cells, neutrophils, platelets), biochemistry (creatinine, transaminases (alanine amino transferase/ALT), bilirubins)

- ECG (electro encephalogram) (Day 0, Day 3,Day 28) only for patients 10 years old and above


Clinical Trial Description

Each patient will be followed for a period of 42 days ;


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01378286
Study type Interventional
Source Sanofi
Contact
Status Completed
Phase Phase 3
Start date January 2012
Completion date June 2013

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