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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/23474
Title: Azithromycin combination therapy with artesunate or quinine for the treatment of uncomplicated Plasmodium falciparum malaria in adults: A randomized, phase 2 clinical trial in Thailand
Authors: Harald Noedl
Srivicha Krudsood
Kobsiri Chalermratana
Udomsak Silachamroon
Wattana Leowattana
Noppadon Tangpukdee
Sornchai Looareesuwan
Robert Scott Miller
Mark Fukuda
Krisada Jongsakul
Sabaithip Sriwichai
Jacqueline Rowan
Helen Bhattacharyya
Colin Ohrt
Charles Knirsch
Mahidol University
Medizinische Universitat Wien
Pfizer Inc.
WRAIR
Keywords: Medicine
Issue Date: 15-Nov-2006
Citation: Clinical Infectious Diseases. Vol.43, No.10 (2006), 1264-1271
Abstract: Background. Because antimalarial drug resistance is spreading, there is an urgent need for new combination treatments for malaria, which kills >1 million people every year. Azithromycin is a macrolide antibiotic that is particularly attractive as an antimalarial because of its safety in children and the extensive experience with its use during pregnancy. Methods. We undertook a randomized, controlled, 28-day inpatient trial involving patients with acute, uncomplicated Plasmodium falciparum malaria. We compared the safety and efficacy of 2 azithromycin-artesunate combinations and 2 azithromycin-quinine regimens in adults with malaria. Treatments were as follows: cohort 1 received 3 days of azithromycin (750 mg twice daily) plus artesunate (100 mg twice daily), cohort 2 received 3 days of azithromycin (1000 mg once daily) plus artesunate (200 mg once daily), cohort 3 received 3 days of azithromycin (750 mg twice daily) plus quinine (10 mg/kg twice daily), and cohort 4 received 3 days of azithromycin (500 mg 3 times daily) plus quinine (10 mg/kg 3 times daily). The enrollment target was 25 evaluable subjects per group. Results. The 28-day cure rates were similarly high in the artesunate and the standard-dose quinine cohorts: 92.0% (95% confidence interval [CI], 74.0%-99.0%), 88.9% (95% CI, 70.8%-97.6%), and 92.0% (95% CI, 74.0%-99.0%), for cohorts 1, 2, and 4, respectively. Late R1 treatment failures were seen in each of the artesunate and the standard-dose quinine cohorts. The cure rate for cohort 3 was 73.3% (95% CI, 44.9%-92.2%). In this cohort, 3 early treatment failures led to the termination of enrollment after 16 subjects had been enrolled. With mean parasite and fever clearance times (±SD) of 34 ± 13 h and 20 ± 20 h, the artesunate combinations were found to have led to a significantly (P < .001) faster clinical and parasitological improvement than occurred in the quinine cohorts (74 ± 32 h and 43 ± 37 h, respectively). Treatment-related adverse events were significantly more common in the quinine cohorts (P < .001). No deaths or drug-related serious adverse events were observed. In vitro results suggest that the treatment failures-particularly in the low-dose quinine cohort-were associated with decreased susceptibility to quinine, as well as with mefloquine cross-resistance. Conclusions. These data suggest that azithromycin-artesunate, even when given only once daily for 3 days, and azithromycin-quinine, given 3 times daily, are safe and efficacious combination treatments for uncomplicated falciparum malaria, and they deserve additional study in special patient populations. © 2006 by the Infectious Diseases Society of America. All rights reserved.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33750682726&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/23474
ISSN: 10584838
Appears in Collections:Scopus 2006-2010

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