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The U.S. FDA approved tafenoquine for prevention of relapse of vivax malaria on July 20, 2018. Tafenoquine is an 8-aminoquinoline, a synthetic analog of primaquine, and has a long elimination half-life (average terminal half-life, 15 days). The drug is active against all stages of Plasmodium vivax, including the dormant liver hypnozoite. It has slow clearance of blood stage parasites, so it is taken in combination with a faster-acting blood schizonticide, chloroquine.
In three double-blind, randomized, multicountry clinical trials (>1000 total participants) tafenoquine was efficacious in preventing relapses of vivax malaria (NEJM JW Infect Dis Feb 2014 and Lancet 2014; 383:1049).
Dosage and administration: A single dose of 300 mg (two 150-mg …