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Clinical Trial Summary

This is a Phase I/II, multicenter, open-label, non-randomized study with four groups to characterize the pharmacokinetics and safety of Cabotegravir (CAB) and Rilpivirine (RPV) long-acting injectable (LA) during pregnancy and postpartum among people with HIV-1 viral suppression and their infants.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06336434
Study type Interventional
Source National Institute of Allergy and Infectious Diseases (NIAID)
Contact Rachel Scheckter
Phone (919) 321-3540
Email rscheckter@fhi360.org
Status Not yet recruiting
Phase Phase 1/Phase 2
Start date September 24, 2024
Completion date December 24, 2026

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