PLoS neglected tropical diseases · 2026
Assessing the efficacy of high-dose rifampicin plus albendazole against onchocerciasis.
СтатьяРандомизированное исследованиеКлиническое исследование II фазыНазвание и аннотация: Перевод в очереди
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Ahiadorme Monica, Klarmann-Schulz Ute, Dubben Bettina, Nadal Jennifer, Korir Patricia Jebett, Pfarr Kenneth, Kuehlwein Janina M, Lenz-Plet Franziska, Ricchiuto Arcangelo, Kutu Emmanuel Donawobuge, Mensah Derrick Adu, Opoku Vera Serwaa, Boateng John, Opoku John, Osei-Mensah Jubin, Gyasi Charles, Obeng Prince, Kuutiero Eunice Kyaakyile, Obeng Michael Agyemang, Emikpe Benjamin, Rahamani Abu Abudu, Atisu Prince Dennis, Ayisi-Boateng Nana Kwame, Kontoh Derrick Boateng, Twumasi-Ankrah Sampson, Hoerauf Achim, Debrah Linda Batsa, Debrah Alexander Yaw
Аннотация
BACKGROUND: Onchocerciasis, also known as river blindness, remains a public health challenge in tropical regions. Despite significant gains through mass drug administration (MDA) with ivermectin, the infection remains persistent in many endemic foci. While the disease burden has reduced, elimination may require alternative strategies, including macrofilaricidal therapies. Rifampicin (RIF) has demonstrated strong anti-Wolbachia activity in vitro and in animal models, but its clinical efficacy in humans remains uncertain.
METHODS: We conducted a phase II randomised, controlled trial in Ghana to evaluate the safety and efficacy of high-dose RIF (35 mg/kg/day) combined with albendazole (ALB, 400 mg/day) as an alternative treatment for onchocerciasis. The study randomised 120 infected participants into one of four arms: RIF + ALB for 14 days (TA1), RIF + ALB for 7 days (TA2), ALB alone for 14 days (TA3), and a No Treatment control group (TA4). Treatment efficacy, including Wolbachia and microfilariae (MF) depletion, adult worm vitality and embryogenesis were assessed following treatment at 4-, 18-, and 20-months.
RESULTS: High-dose RIF + ALB was safe and well-tolerated, associated with only mild, transient adverse events. Treatment with RIF + ALB for 14 days reduced Wolbachia load in skin MF at 4 months (47.9%; p = 0.018). ALB monotherapy showed sustained reductions in skin microfilarial densities at the 18- and 20-month time points (p < 0.05). However, no macrofilaricidal effect or sustained Wolbachia depletion in adult worms was observed in any group.
CONCLUSION: High-dose RIF + ALB is safe with limited macrofilaricidal efficacy in clinical settings, contrasting with the superiority observed from preclinical trials. ALB alone shows promise as an alternative microfilaricidal treatment to ivermectin or as a complementary regimen. The lack of sustained efficacy of RIF as an anti-Wolbachia regimen may reflect suboptimal dosing, highlighting the need for further optimisation of RIF-based regimens for onchocerciasis treatment.
TRIAL REGISTRATION: PACTR202009704006025 (https://pactr.samrc.ac.za/Search.aspx). Date of trial registration: September 9, 2020.
METHODS: We conducted a phase II randomised, controlled trial in Ghana to evaluate the safety and efficacy of high-dose RIF (35 mg/kg/day) combined with albendazole (ALB, 400 mg/day) as an alternative treatment for onchocerciasis. The study randomised 120 infected participants into one of four arms: RIF + ALB for 14 days (TA1), RIF + ALB for 7 days (TA2), ALB alone for 14 days (TA3), and a No Treatment control group (TA4). Treatment efficacy, including Wolbachia and microfilariae (MF) depletion, adult worm vitality and embryogenesis were assessed following treatment at 4-, 18-, and 20-months.
RESULTS: High-dose RIF + ALB was safe and well-tolerated, associated with only mild, transient adverse events. Treatment with RIF + ALB for 14 days reduced Wolbachia load in skin MF at 4 months (47.9%; p = 0.018). ALB monotherapy showed sustained reductions in skin microfilarial densities at the 18- and 20-month time points (p < 0.05). However, no macrofilaricidal effect or sustained Wolbachia depletion in adult worms was observed in any group.
CONCLUSION: High-dose RIF + ALB is safe with limited macrofilaricidal efficacy in clinical settings, contrasting with the superiority observed from preclinical trials. ALB alone shows promise as an alternative microfilaricidal treatment to ivermectin or as a complementary regimen. The lack of sustained efficacy of RIF as an anti-Wolbachia regimen may reflect suboptimal dosing, highlighting the need for further optimisation of RIF-based regimens for onchocerciasis treatment.
TRIAL REGISTRATION: PACTR202009704006025 (https://pactr.samrc.ac.za/Search.aspx). Date of trial registration: September 9, 2020.