The combination of
halofantrine and
primaquine therapies was calculated as a regimen for achieving radical curve of falciparum or
vivax malaria in Irian Jaya, Indonesia, and compared with combined
chloroquine and
primaquine therapies. The patients who volunteered for the study [adult, male, Indonesian immigrants with no previous exposure to endemic
malaria, normal
glucose-6-phosphate dehydrogenase (G6PD) activity, uncomplicated
malaria illness, no prior use of
antimalarials, and parasitaemias of 0.001%-1.1%] were randomized to receive either
halofantrine (24 mg base/kg bodyweight, in three equal doses over 12 h) or
chloroquine (25 mg base/kg bodyweight over 48 h, in doses of 10, 10 and 5 mg base/kg at 24-h intervals). Each patient also received concurrent daily
primaquine (0.5 mg base/kg bodyweight) for 14 days followed by the same dose on alternate days to day 28. A recurrent parasitaemia during the 28 days of follow-up constituted
drug failure. Of the 40 cases of
falciparum malaria and 26 cases of
vivax malaria treated with
halofantrine-
primaquine, none had a recurrent parasitaemia (100% efficacy). In contrast, 20 of 30 patients with
falciparum malaria and three of 27 with
vivax malaria had recurrent parasitaemias after
chloroquine-
primaquine, giving efficacies of 33% and 89%, respectively.
Halofantrine-
primaquine was significantly more effective than
chloroquine-
primaquine against
falciparum malaria (P < 0.001) but was similarly efficacious against
vivax malaria (P = 0.23). On average,
fever associated with falciparum or
vivax malaria cleared 17 h faster with
halofantrine-
primaquine (P < 0.01) although there were no significant differences (P > 0.4) in parasite-clearance times between the two regimens. The
halofantrine-
primaquine regimen was also associated with a more rapid and significant decline in
malaria-related physical complaints.