Efficacy and Safety of a Single Dose of Emodepside Compared to a Single Dose of Albendazole in Adolescents and Adults Infected With Trichuris Incognita

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age12+
SponsorJennifer Keiser

About this trial

The purpose of this clinical trial is to compare the efficacy and safety of emodepside with the standard treatment, albendazole, in adolescents (12 years and older) and adults infected with Trichuris incognita.

Eligibility criteria

Qualifiers

Aged 12 years and above.

Written informed consent signed by participant and, in the case of minors, parents/caregivers.

Agree to comply with study procedures, including provision of two stool samples at the beginning (screening) and at follow-up assessment 14-21 days after treatment.

Having at least two slides of the quadruple Kato-Katz thick smears positive for Trichuris incognita and infection intensities of at least 48 eggs per gram (EPG).

Disqualifiers

Presence or signs of major systemic illnesses, e.g. body temperature ≥ 38 °C, severe anemia (Hb below 80g/l) upon initial clinical assessment etc.

History of severe acute or unmanaged severe chronic disease (i.e., condition is not as therapeutically controlled as necessary).

Positive malaria rapid diagnostic test (RDT) and temperature ≥ 38 °C.

Abnormal liver and renal function assessed by biochemical blood-based analyses.

Trial design

Treatments tested in this trial

  • Emodepside
  • Albendazole 400 mg

Treatment groups

100 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

Jennifer Keiser

Lead sponsor

Swiss Tropical & Public Health Institute

Sponsor institution

Centre Suisse de Recherches Scientifiques en Cote d'Ivoire

Collaborator

Université Félix Houphouët-Boigny

Collaborator

Bayer

Collaborator