An adaptive phase II/III safety and efficacy randomized controlled trial of single day or three-day fixed-dose albendazole-ivermectin co-formulation versus albendazole for the treatment of and other STH infections. ALIVE trial protocol.

Journal: Gates open research

Volume: 6

Issue: 

Year of Publication: 

Affiliated Institutions:  Barcelona Institute for Global Health (ISGlobal), Hospital Clínic-Universitat de Barcelona, Barcelona, Spain. College of Medicine and Health Science, Bahir Dar University, Bahir Dar, Ethiopia. Department of Parasitology, Centre of Infectious Diseases, Leiden University Medical Centre (LUMC), Leiden, The Netherlands. Eastern and Southern Africa Centre of International Parasite Control, Kenya Medical Research Institute (KEMRI), Nairobi, Kenya. Centro de Investigação em Saúde de Manhiça (CISM), Maputo, Mozambique. Instituto de Ganadería de Montaña, CSIC-Universidad de León, Grulleros, León, Spain. Liconsa SA, Azuqueca de Henares, Guadalajara, Spain. Institut d'Investigació Biomèdica Sant Pau (IIB SANT PAU), Barcelona, Spain. Wellcome Sanger Institute, Hinxton, Cambridgeshire, UK.

Abstract summary 

Soil-transmitted helminths (STH) are targeted for control through mass drug-administration campaigns to prevent morbidity affecting at-risk groups in endemic regions. Although broadly successful, the use of albendazole and mebendazole achieved variable progress, with deficiencies against and a predictable low efficacy against . Novel drug combinations offer a potential solution, providing they can be delivered safely and maintain efficacy against all STH species. Here we present the protocol of a clinical trial to evaluate a fixed-dose combination (FDC) tablet containing albendazole and ivermectin that will be compared against albendazole against STH An adaptive phase II/III randomized controlled trial will be undertaken in STH endemic sites in Ethiopia, Kenya and Mozambique to evaluate an oral FDC of 400 mg albendazole and either 9- or 18 mg ivermectin. FDC will be administered as a single dose or single doses over three-consecutive days and assessed against a single dose of 400 mg albendazole. In the phase II trial, 126 -infected children weighting 15 to 45 kg will be treated in a dose-escalation manner to determine safety objectives. In the phase III trial, 1097 participants aged 5 to 18 years old infected with hookworm and will be recruited to determine safety and efficacy. The trial will be open-label with blinded outcome assessors. Cure rate measured 21-days after-treatment in duplicate Kato-Katz is the primary efficacy outcome. Secondary objectives include efficacy evaluation by quantitative polymerase chain reaction (PCR) as an outcome measurement, description of pharmacokinetic parameters, palatability and acceptability evaluations, and monitoring of anthelmintic resistance. This trial with registrational goals seeks to evaluate an innovative fixed-dose combination of albendazole and ivermectin co-formulated tablets, with the goal of providing an anthelmintic regimen with improved efficacy and spectrum of coverage against STH. NCT05124691 (18/11/2021).

Authors & Co-authors:  Krolewiecki Enbiale Gandasegui van Lieshout Kepha Messa Junior Bengtson Gelaye Escola Martinez-Valladares Cambra-Pellejà Algorta Martí-Soler Fleitas Ballester Doyle Williams Legarda Mandomando Mwandawiro Muñoz

Study Outcome 

Source Link: Visit source

Statistics
Citations :  World Health Organization: Accelerating Work to Overcome the Global Impact of Neglected Tropical Diseases: A Roadmap for Implementation.(World Health Organizaiton, Geneva, Switzerland, 2012). WHO Press,2012. Reference Source
Authors :  21
Identifiers
Doi : 62
SSN : 2572-4754
Study Population
Male,Female
Mesh Terms
Other Terms
Albendazole;Antihelmintics;Hookworm;Ivermectin;STH;Strongyloides;Trichuris trichiura
Study Design
Study Approach
Quantitative
Country of Study
Mozambique
Publication Country
United States