drugset / Trial / NCT05601128

A Study Evaluating the Pharmacokinetics, Efficacy, Safety and Tolerability of CABENUVA

NCT05601128

NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of CABENUVA (Long-acting Cabotegravir Plus Long-acting Rilpivirine) in patients with HIV infection and severe renal impairment. This study is considered research and is voluntary.

Timeline

Start
2023-01-01
Primary completion
2025-04-01
Completion
2025-10-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Cabotegravir Small molecule 30 mg Oral
Subject Cabotegravir Small molecule 400 mg Oral
Subject Cabotegravir Small molecule 600 mg Oral
Subject Rilpivirine Small molecule 25 mg Oral
Subject Rilpivirine Small molecule 600 mg Oral
Subject Rilpivirine Small molecule 900 mg Oral