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Chlorproguanil/dapsone/artesunate

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This is an old revision of this page, as edited by Anypodetos (talk | contribs) at 17:46, 28 June 2016 (Anypodetos moved page Chlorproguanil hydrochloride-dapsone-artesunate to Chlorproguanil/dapsone/artesunate: Standard title for combination drugs per WP:MOSPHARM). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Chlorproguanil/dapsone/artesunate
Combination of
ChlorproguanilAntimalarial drug
DapsoneAntibiotic
ArtesunateAntimalarial drug
Legal status
Legal status
  • Development halted

Chlorproguanil/dapsone/artesunate (abbreviated CDA) was an experimental antimalarial treatment that entered Phase III clinical trials in 2006. Development was halted because it was associated with an increased risk of haemolytic anaemia in patients with glucose-6-phosphate dehydrogenase deficiency.[1]

It consists of chlorproguanil, dapsone, and artesunate. (It can also be interpreted as Lapdap+artesunate.)

Studies compared this combination against artemether/lumefantrine (Coartem) and against chlorproguanil/dapsone (Lapdap). This drug was developed in collaboration between GlaxoSmithKline, UNICEF, the World Bank, Medicines for Malaria Venture and the WHO Special Programme for Research and Training in Tropical Diseases (WHO/TDR), the Liverpool School of Tropical Medicine, and the London School of Hygiene and Tropical Medicine.[2]

References

  1. ^ Van Malderen, C; Van Geertruyden, J. P.; Machevo, S; González, R; Bassat, Q; Talisuna, A; Yeka, A; Nabasumba, C; Piola, P; Daniel, A; Turyakira, E; Forret, P; Van Overmeir, C; Van Loen, H; Robert, A; d' Alessandro, U (2012). "Glucose-6-phosphate dehydrogenase deficiency, chlorproguanil-dapsone with artesunate and post-treatment haemolysis in African children treated for uncomplicated malaria". Malaria Journal. 11: 139. doi:10.1186/1475-2875-11-139. PMC 3393623. PMID 22546009.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  2. ^ Das P (2006). "Promising anti-malarial enters phase II studies". Lancet Infect Dis. 6 (9): 551. doi:10.1016/S1473-3099(06)70571-0.