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  4. Efficacy of moxidectin versus ivermectin against Strongyloides stercoralis infections: a randomized controlled noninferiority trial
 
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Efficacy of moxidectin versus ivermectin against Strongyloides stercoralis infections: a randomized controlled noninferiority trial

Date Issued
2017-01-01
Author(s)
Barda, Beatrice  
Sayasone, Somphou  
Phongluxa, Khampheng  
Xayavong, Syda
Keoduangsy, Khonsavanh
Odermatt, Peter  
Puchkov, Maxim  
Huwyler, Jörg  
Hattendorf, Jan  
Keiser, Jennifer  
DOI
10.1093/cid/cix278
Abstract
Infections with Strongyloides stercoralis are of considerable public health relevance. Moxidectin, a well-established drug in veterinary medicine under consideration for regulatory submission for the treatment of onchocerciasis, might serve as an alternative to the widely used ivermectin.; We conducted an exploratory, randomized, single-blind trial to evaluate the efficacy and safety of moxidectin (8 mg) vs ivermectin (200 μg/kg) against S. stercoralis infections. Cure rate (CR) against S. stercoralis was the primary outcome. Safety and efficacy against coinfections with soil-transmitted helminths and Opisthorchis viverrini were secondary outcomes. Noninferiority required the lower limit of the 95% confidence interval (CI) of the differences in CRs not exceed 7 percentage points.; A total of 127 participants were enrolled and randomly assigned to the 2 treatments whereby 1 participant per arm was lost to follow-up. We observed a CR of 93.7% (59/63) for moxidectin compared to 95.2% (59/62) for ivermectin. Differences between CRs were estimated as -1.5% percentage points (95% CI, -9.6 to 6.5), thus the lower limit of the CI exceeds the noninferiority margin of 7 percentage points. No side effects were observed. CRs against hookworm infection were 57% (moxidectin) and 56% (ivermectin). Low efficacy for both drugs against O. viverrini was observed.; Moxidectin might be a safe and efficacious alternative to ivermectin for the treatment of S. stercoralis infection, given that only slight differences in CRs were observed. However, noninferiority could not be demonstrated. Larger clinical trials should be conducted once the drug is marketed.; Current Controlled Trials: ISRCTN11983645.
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