drugset / Trial / NCT04726969
Efficacy and Safety of MOX/ALB Co-administration
Phase 3
Completed
255 enrolled
Jennifer Keiser
Centre Suisse de Recherches Scientifiques en Cote d'Ivoire · collab
RandomizedParallel-groupQuadruple-blindTreatment
Summary
This study is a double-blind randomized controlled superiority trial aiming at providing evidence on the efficacy and safety of co-administered moxidectin and albendazole versus albendazole monotherapy (standard of care) against whipworm (T. trichiura) infections in adolescents and adults (12-60 years) in Côte d'Ivoire. One arm of patients will be treated with albendazole-ivermectin. As measure of efficacy of the treatment the cure rate (percentage of egg-positive subjects at baseline who become egg-negative after treatment) will be determined 14-21 days post-treatment.
Timeline
- Start
- 2021-06-15
- Primary completion
- 2021-09-09
- Completion
- 2021-09-09
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Albendazole | Small molecule | 400 mg | Oral |
| Subject | Ivermectin | Small molecule | 200 ug/kg | Oral |
| Subject | Moxidectin | Other / unclassified | 8 mg | Oral |