Condition: HIV Infections · Sponsor: ViiV Healthcare
The purpose of this study is long-term evaluation of long-acting injectable cabotegravir (CAB LA) for HIV pre-exposure prophylaxis (PrEP) in eligible participants who have completed DAIDS (Division of AIDS) sponsored studies HPTN 083 and HPTN 084 and associated sub-studies. Participants will continue receiving CAB LA and be followed for new HIV diagnosis, SAEs (serious adverse events), Grade 3 and Grade 4 ISRs (injection site reactions), and AEs (adverse events) leading to withdrawal.
This description comes directly from the study's public registry record.
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| GSK Investigational Site | Almagro, Argentina | Recruiting |
| GSK Investigational Site | Buenos Aires, Argentina | Recruiting |
| GSK Investigational Site | Francistown, Botswana | Recruiting |
| GSK Investigational Site | Porto Alegre, Brazil | Recruiting |
| GSK Investigational Site | Rio de Janeiro, Brazil | Recruiting |
| GSK Investigational Site | São Paulo, Brazil | Recruiting |
| GSK Investigational Site | São Paulo, Brazil | Recruiting |
| GSK Investigational Site | Mbabane, Eswatini | Recruiting |
| GSK Investigational Site | Kisumu, Kenya | Recruiting |
| GSK Investigational Site | Blantyre, Malawi | Recruiting |
| GSK Investigational Site | Lilongwe, Malawi | Recruiting |
| GSK Investigational Site | Lima, Peru | Recruiting |
+ 22 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT06134362