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Pharmacokinetic Study of Cabotegravir Long-acting in Healthy Adult Volunteers

Status
Planned
Phase
I
Principal Investigator(s)
GSK Clinical Trials, ViiV Healthcare
Objective

Cabotegravir (CAB) long-acting (LA) is a promising candidate for human immunodeficiency virus (HIV) pre exposure prophylaxis (PrEP) due to its potent antiretroviral activity and infrequent dosing requirements. Currently, the CAB concentrations achieved in the anatomical sites associated with sexual HIV transmission following the proposed 800 milligram (mg) intramuscular PrEP dose are unknown. These data will enhance further our understanding of CAB distribution to the anatomical mucosal tissue believed to be relevant to sexual HIV-1 transmission and supplement the data available to support future PrEP clinical trial development. The primary objective is to determine the PK concentrations of CAB following LA administration in blood plasma and in vaginal tissue (VT), cervical tissue (CT), and cervicovaginal fluid (CVF) in healthy women and in rectal tissue (RT) and rectal fluid (RF) in healthy men and women following a single 800 mg IM (split injection) dose. 

Prevention Option(s)
PrEP
Study Design
Open label
Arms and Assigned Interventions
Description
Subject will receive CAB 30 mg tablet once daily oral dose for 28 days (4 weeks) followed by a washout period of 14 to 21 days. After the washout, subject will receive a single dose of CAB LA 800 mg (2 x 400mg split injection) IM to gluteal region.
Mode of Delivery
Tablet
ARMs
Experimental
Trial Sponsors
ViiV Healthcare
April 2016
June 2017
Enrollment
16
18
Years
55
Years
Population
Women
Men