Methylene blue for malaria in Africa: results from a dose-finding study in combination with chloroquine

Peter Meißner(Heidelberg University), Germain Mandi(Centre de Recherche en Santé de Nouna), Boubacar Coulibaly(Centre de Recherche en Santé de Nouna), Steffen Witte(Heidelberg University), Théophile Tapsoba(Centre de Recherche en Santé de Nouna), Ulrich Mansmann(Heidelberg University), Jens Rengelshausen(Heidelberg University), W. Schiek(DSM (Austria)), Albrecht Jahn(Heidelberg University), I. Walter‐Sack(Heidelberg University), Gerd Mikus(Heidelberg University), Jürgen Burhenne(Heidelberg University), Klaus‐Dieter Riedel(Heidelberg University), R. Heiner Schirmer(Heidelberg University), Bocar Kouyaté(Centre de Recherche en Santé de Nouna), Olaf Müller(Heidelberg University)
Malaria Journal
October 8, 2006
Cited by 122Open Access
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Abstract

The development of safe, effective and affordable drug combinations against malaria in Africa is a public health priority. Methylene blue (MB) has a similar mode of action as chloroquine (CQ) and has moreover been shown to selectively inhibit the Plasmodium falciparum glutathione reductase. In 2004, an uncontrolled dose-finding study on the combination MB-CQ was performed in 435 young children with uncomplicated falciparum malaria in Burkina Faso (CQ monotherapy had a > 50% clinical failure rate in this area in 2003). Three serious adverse events (SAE) occurred of which one was probably attributable to the study medication. In the per protocol safety analysis, there were no dose specific effects. The overall clinical and parasitological failure rates by day 14 were 10% [95% CI (7.5%, 14.0%)] and 24% [95% CI (19.4%, 28.3%)], respectively. MB appears to have efficacy against malaria, but the combination of CQ-MB is clearly not effective in the treatment of malaria in Africa.


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