Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06511180

Introduction of Dispersible 3HP Formulations for TB Preventive Treatment in Children: a Multi-country Evaluation

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
1,200 (estimated)
Sponsor
The Aurum Institute NPC · Academic / Other
Sex
All
Age
Healthy volunteers
Accepted

Summary

The WHO has recommended TB preventive therapy (TPT) for children living with HIV (CLHIV) and household contacts of people living with TB, however, the scale-up and implementation of TPT has been sub-optimal globally particularly in children. A safe and effective short-course TPT regimen, 3HP (rifapentine and isoniazid given once weekly for three months), is available but there is a lack of child-friendly formulations resulting in increased pill burden and there is a need to improve acceptability and adherence among children. The introduction of a dispersible rifapentine formulation has potential to improve uptake, treatment adherence and completion. Overall goal is to generate critical knowledge to improve delivery of TPT and, more specifically, of dispersible 3HP, in children in routine programs. This evaluation will create an important understanding of TPT uptake and completion among children and assess the impact of the introduction of a dispersible 3HP formulation. These results will provide actionable information for improving service delivery and the scale-up of TPT in the respective countries.

Conditions

Timeline

Start date
2024-08-01
Primary completion
2025-06-01
Completion
2025-06-01
First posted
2024-07-19
Last updated
2024-07-19

Source: ClinicalTrials.gov record NCT06511180. Inclusion in this directory is not an endorsement.