News Release

New treatment option for children with malaria

N. B. Please note that if you are outside North America the embargo date for all Lancet press material is 0001hours UK time Friday 19th April 2002

Peer-Reviewed Publication

The Lancet_DELETED

Combination of the drugs artesunate and amodiaquine could be a new treatment option for children with malaria caused by the parasite Plasmodium falciparum, conclude authors of a fast-track study in this week’s issue of THE LANCET.

Drug-resistant P. falciparum malaria is a serious problem in sub-Saharan Africa. Chloroquine resistance is a major contributor to the increase in malaria-related illness and death among African children, and resistance to sulfadoxine/pyrimethamine (an inexpensive, widely used alternative) is emerging. Bob Taylor from WHO, Geneva, Switzerland, and collaborating colleagues assessed the safety and treatment efficacy of adding artesunate to amodiaquine in three randomised trials in Kenya, Sénégal, and Gabon.

941 children (400 in Kenya, 321 in Sénégal, and 220 in Gabon) who were younger than 11 years and who had uncomplicated P. falciparum malaria took part in the study. They were randomly assigned amodiaquine (10 mg/kg per day for 3 days) plus artesunate (4 mg/kg per day for 3 days) or amodiaquine and placebo (for 3 days).

The cure rates after two weeks treatment for amodiaquine-artesunate compared with amodiaquine were: 91% versus 74% in Kenya, 93% versus 94% in Sénégal, and 98% versus 90% in Gabon. Corresponding cure rates after one month were 68% versus 41% in Kenya, 82% versus 79% in Sénégal, and 85% versus 71% in Gabon

Bob Taylor comments: “For African countries that are considering a change of their current first-line antimalarial drug, amodiaquine-artesunate is an option. Cost, access, and local efficacy data are also fundamental elements to consider before amodiaquine-artesunate or other drug combinations are implemented as policy. Longitudinal studies should now address the general question of how best to deploy artemisinin-based combinations, and the safety of amodiaquine-artesunate and its potential effect on the development of drug resistance and transmission.”

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Contact: Dr W R J Taylor, WHO/TDR, Avenue Appia 20, Geneva CH-1211, Switzerland; T) +41 22 791 3853; F) +41 22 791 4774; E) taylorw@who.ch

Contacts for the principal investigators:
(i) Gabon study: Professor P. Kremsner, Sektion Humanparasitologie, Institut fuer Tropenmedizin, Universitaet Tuebingen, Wilhelmstrasse 27, 72074 Tuebingen, Germany; T)+ 49 7071 2987179; F) +49 7071 295189; E) peter.kremsner@uni-tuebingen.de
(ii) Kenya: Dr. M. Loolpapit, African Medical and Research Foundation, PO Box 00506-27691, Nairobi, Kenya;T) +254-2-605-331; F) +254-2-609-518; E) MoresL@amrefhq.org
(iii) Senegal study: Professor P. Brasseur, Laboratoire de Parasitologie, Centre Hospitalier Universitaire, Hôpital Charles Nicolle 1, rue de Germont, 76031, Rouen, France; T) +33 2 32 88 80 15; F) + 33 2 32 88 80 17; E) philippe.brasseur@wanadoo.fr


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