Ferroquine and artesunate in African adults and children with Plasmodium falciparum malaria: a phase 2, multicentre, randomised, double-blind, dose-ranging, non-inferiority study.
Abstract | BACKGROUND: METHODS: We did a phase 2, multicentre, parallel-group, double-blind, randomised, dose-ranging non-inferiority trial at eight African hospitals (two in Gabon, three in Burkina Faso, one in Benin, and two in Kenya). We recruited patients presenting with acute P falciparum monoinfection (1000-200,000 parasites per μL), and a central body temperature of at least 37·5°C or history of fever in the past 24 h. We assessed patients in two sequential cohorts: cohort 1 contained adults (bodyweight >50 kg) and adolescents (aged ≥14 years, >30 kg), and cohort 2 contained children (aged 2-13 years, 15-30 kg). We randomly assigned patients (1:1:1:1) to receive artesunate 4 mg/kg per day plus ferroquine 2 mg/kg, 4 mg/kg, or 6 mg/kg, given double-blind once per day for 3 days, or ferroquine monotherapy 4 mg/kg per day given single-blind (ie, allocation was only masked from the patient) once per day for 3 days. We did 14 patient visits (screening, 3 treatment days and 48 h post-treatment surveillance, a visit on day 7, then one follow-up visit per week until day 63). The primary endpoint was non-inferiority of treatment in terms of PCR-corrected cure rate against a reference value of 90%, with a 10% non-inferiority margin, assessed in patients treated without major protocol deviations for parasitologically confirmed malaria. We assessed safety in all treated patients. This study is registered with ClinicalTrials.gov, number NCT00988507, and is closed. FINDINGS: Between Oct 16, 2009, and Sept 22, 2010, we randomly assigned 326 eligible patients to treatment groups, with last follow-up visit on Dec 1, 2010. 284 patients (87%) were available for per-protocol analyses. At day 28, PCR-confirmed cure was noted in 68 (97%, 95% CI 90-100) of 70 patients treated with ferroquine 2 mg/kg plus artesunate, 73 (99%, 93-100) of 74 with ferroquine 4 mg/kg plus artesunate, 71 (99%, 93-100) of 72 with ferroquine 6 mg/kg plus artesunate, and 54 (79%, 68-88) of 68 with ferroquine 4 mg/kg monotherapy. The three dose groups of ferroquine plus artesunate met the non-inferiority hypothesis. The most common adverse events were headache in cohort 1 (30 [19%] of 162 patients) and worsening malaria in cohort 2 (23 [14%] of 164 patients); occurrences were similar between treatment groups. INTERPRETATION: FUNDING: Sanofi.
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Authors | Jana Held, Christian Supan, Carmen L O Salazar, Halidou Tinto, Léa N Bonkian, Alain Nahum, Bancole Moulero, Ali Sié, Boubacar Coulibaly, Sodiomon B Sirima, Mohamadou Siribie, Nekoye Otsyula, Lucas Otieno, Ahmed M Abdallah, Robert Kimutai, Marielle Bouyou-Akotet, Maryvonne Kombila, Kimiko Koiwai, Cathy Cantalloube, Chantal Din-Bell, Elhadj Djeriou, John Waitumbi, Benjamin Mordmüller, Daniel Ter-Minassian, Bertrand Lell, Peter G Kremsner |
Journal | The Lancet. Infectious diseases
(Lancet Infect Dis)
Vol. 15
Issue 12
Pg. 1409-19
(Dec 2015)
ISSN: 1474-4457 [Electronic] United States |
PMID | 26342427
(Publication Type: Clinical Trial, Phase II, Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2015 Elsevier Ltd. All rights reserved. |
Chemical References |
- Aminoquinolines
- Antimalarials
- Artemisinins
- Ferrous Compounds
- Metallocenes
- Artesunate
- ferroquine
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Topics |
- Adolescent
- Adult
- Aged
- Aminoquinolines
(therapeutic use)
- Antimalarials
(therapeutic use)
- Artemisinins
(therapeutic use)
- Artesunate
- Child
- Child, Preschool
- Double-Blind Method
- Drug Administration Schedule
- Drug Therapy, Combination
- Female
- Ferrous Compounds
(therapeutic use)
- Humans
- Malaria, Falciparum
(drug therapy, parasitology, pathology)
- Male
- Metallocenes
- Middle Aged
- Plasmodium falciparum
(drug effects, physiology)
- Treatment Outcome
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