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Clinical Trial Summary

Stage 1 proposed study will provide evidence to support the use of twice-daily dose 50mg DTG in children (20-35kgs) co-treated with RIF. Note: An amendment has been added to include children from 3kgs and a dose of 10mg dispersible DTG


Clinical Trial Description

This is a single centre, open-label, non-randomised, prospective study evaluating the steady-state pharmacokinetics of twice-daily dose DTG administered during concurrent RIF treatment and assessing safety and tolerance in HIV-TB co-infected children weighing 20 to 35 kg. DTG will be administered as a twice-daily dose 50mg tablet formulation both before starting and after completion of the standard six-month RIF-based anti-TB treatment. The NRTI background and anti-TB drugs will be prescribed following the national weight band dosing guidelines. Those initially diagnosed with TB are likely to be sicker, and the recommendation is to start anti-TB treatment first and follow with ART two weeks later. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04746547
Study type Interventional
Source University of KwaZulu
Contact Moherndran Archary, MBChB, PhD
Phone +27312604318
Email archary@ukzn.ac.za
Status Recruiting
Phase Phase 4
Start date August 19, 2021
Completion date July 31, 2025

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