drugset / Trial / NCT01593046

A Study to Investigate the Safety, Tolerability and Pharmacokinetics of Repeat Dose Administration of Long-Acting GSK1265744 and Long-Acting TMC278 Intramuscular and Subcutaneous Injections in Healthy Adult Subjects

NCT01593046

Phase 1 Completed 43 enrolled ViiV Healthcare GlaxoSmithKline · collab
RandomizedParallel-groupOpen-label

Summary

LAI115428 is a Phase I, randomized, repeat dose escalation study to determine the safety, tolerability, and PK profile of intramuscular and subcutaneous injections of GSK1265744 in a long acting parenteral (LAP) formulation in healthy subjects. Subjects will be randomized to 3 monthly dosing cohorts and 1 quarterly dosing cohort with either intramuscular or subcutaneous dosing. In the monthly dosing cohorts subjects will receive GSK1265744 alone for 2 months and then in combination with TMC278 long acting parenteral (LA) for 2 months. For the quarterly dosing cohort, 2 quarterly intramuscular doses of GSK1265744 LAP will be given alone. Three dose levels of GSK1265744 will be evaluated partly in combination with TMC278 LA to adequately characterize the GSK1265744 LAP and TMC278 LA safety, tolerability, and PK profile. A total enrolment of approximately 40 healthy subjects is planned for this study.

Timeline

Start
2012-05
Primary completion
2013-11
Completion
2013-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Cabotegravir Small molecule 30 mg Oral
Subject Cabotegravir Small molecule 200 mg Oral
Subject Cabotegravir Small molecule 400 mg Oral
Subject Cabotegravir Small molecule 800 mg Oral
Subject Rilpivirine Small molecule 600 mg Intramuscular
Subject Rilpivirine Small molecule 1200 mg Intramuscular