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.