| Protocol No: | ECCT/25/08/03 | Date of Protocol: | 12-01-2024 |
| Study Title: |
A Phase 4, Open-Label, Rollover Study to Provide Continued Access to Cabotegravir Long-acting Injection and Rilpivirine Long-acting Injection to Participants Living with Human
Immunodeficiency Virus Type 1 (HIV-1) Infection Who Participated in Long acting Combination Therapy Studies
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| Study Objectives: |
Primary Objective
The primary objective of the study is to provide continued CAB LA + RPV LA access to participants who were enrolled and
treated with CAB LA + RPV LA in the parent studies, and who, at the time of roll-over, experience and are expected to continue
to experience clinical benefit from this treatment.
Secondary Objective
The secondary objective is to assess the long-term safety and tolerability of CAB LA + RPV LA by evaluating the incidence of
serious adverse events (SAEs), pregnancies, adverse events (AEs) leading to discontinuation of CABLA +RPV LA, and AEs
considered to be related to the study intervention
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| Laymans Summary: |
Cabotegravir (CAB) is a potent integrase strand transfer inhibitor (INSTI) with attributes allowing formulation and delivery as a long-acting (LA) parenteral product. Rilpivirine(RPV), also formulated as a LA product, is a diarylpyrimidine derivative and a potent non-nucleoside reverse transcriptase inhibitor (NNRTI) with in vitro activity against wildtype HIV-1 and select NNRTI-resistant mutants. The combination of CAB LA and RPV LA has been shown in clinical trials in virologically suppressed adults living with HIV to besafe, well-tolerated and efficacious as a complete injectable antiretroviral regimen. This study enables continued CAB LA + RPV LA access to participants who were included inthe clinical development studies for CAB LA + RPV LA (IMPAACT 2017 [MOCHA], IMPAACT 2036 [CRAYON], IMPAACT 2040 [CREATE], TMC278LAHTX3002 [CARES],TMC278LAHTX3005 [IMPALA], in the following sections referred to as the parent studies) and who continue to benefit clinically from the regimen but do not have access tolocally available CAB LA + RPV LA to continue treatment. The rollover study will be reviewed periodically to evaluate other access options.
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| Abstract of Study: |
This is a Phase 4, non-randomized, open-label, multicenter, multicountry, rollover study in participants living with HIV-1 infection who were treated in the parent studies with CAB LA + RPV LA given intramuscularly on a Q4W or Q8W dosing schedule. Final dosing information for children <12 years of age with a body weight <35 kg will be includedvia a protocol amendment once the data from the IMPAACT 2036 (CRAYON) study become available. This rollover study will be conducted primarily to enable continued accessto CAB LA + RPV LA and also to collect long-term safety and tolerability data as specified in the Schedule of Activities in participants who completed the parent studies andwho at the time of rollover, experience and are expected to continue to experience clinical benefit from the regimen, and have no other access to locally available CAB LA +RPV LA.
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