drugset / Trial / NCT05493969

Efficacy and Tolerability of DTG Plus 3TC in HIV Infected Adults With Virologically Suppression and TDF Toxicity

NCT05493969

Phase 4 Unknown 100 enrolled Shanghai Public Health Clinical Center
NaSingle-groupOpen-labelTreatment

Summary

To investigate the efficacy and tolerability of the regimen of dolutegravir plus lamivudine in HIV infected adults who are virologically suppressed and with evidence of TDF toxicity.

Timeline

Start
2022-08
Primary completion
2025-08
Completion
2026-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Dolutegravir Other / unclassified 50 mg
Subject Lamivudine Other / unclassified 300 mg

Indications