Halofantrine was administered as prophylaxis for malaria to mine worke
rs returning from endemic areas of Papua New Guinea. The men were rand
omly assigned to receive 500 mg of halofantrine daily for 3 days (n =
195) or 6 days (n = 150) or a total dose of 1,500 mg of chloroquine ov
er 3 days (n = 55). None of the men receiving halofantrine developed f
alciparum malaria during the subsequent 28 days, whereas three men rec
eiving chloroquine did develop this disease (P < .02). The administrat
ion of halofantrine after departure from an endemic area is one strate
gy for the prevention of falciparum malaria after short-term exposure.