drugset / Trial / NCT04904406

Changes in Weight, Body Composition and Cardiac Risk After Discontinuing Abacavir Treatment in HIV-infected Individuals

NCT04904406

Phase 4 Completed 81 enrolled Thomas Benfield
RandomizedParallel-groupOpen-labelTreatment

Summary

Randomized controlled parallel open-label study in people living with HIV and at least 6 month of treatment with dolutegravir/abacavir/lamivudine prior to inclusion. Participants (n=95) are randomized to continue 3 drug-regimen dolutegravir/abacavir/lamivudine (control) or switch to two-drug regimen with dolutegravir/lamivudine (intervention). Follow-up is 48 weeks. Data is collected at baseline and week 48. Primary outcome is changes in weight from baseline of more than 2 kg. Secondary outcomes are changes in cardiac risk, composition and calcification of the heart tissue, and changes in body composition and metabolism, inflammation and coagulation. A MRI substudy is applied to focus on the cardiac adverse effects of abacavir.

Timeline

Start
2020-10-22
Primary completion
2023-12-01
Completion
2023-12-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Background Dolutegravir Other / unclassified 50 mg Oral
Background Lamivudine Other / unclassified 300 mg Oral