A Study to Evaluate the Pharmacokinetic Effects of Different Storage Conditions for a Long-Acting Nanosuspension of Rilpivirine on Pharmacokinetics
A Phase 1 Open-Label, Randomized, Parallel-Group Study in Healthy Subjects to Investigate the Effect of Different Storage Conditions of a Long-Acting Nanosuspension of Rilpivirine on the Single-Dose Plasma Pharmacokinetics of Rilpivirine After Intramuscular Injection
Sponsor: Janssen Infectious Diseases BVBA
This PHASE1 trial investigates Human Immunodeficiency Virus Type 1 and is currently completed. Janssen Infectious Diseases BVBA leads this study, which shows 7 recorded versions since 2015 — indicating limited longitudinal coverage. The change history captured here reflects the iterative nature of clinical trial conduct.
Status Flow
Change History
7 versions recorded-
Sep 2024 — Present [monthly]
Completed PHASE1
-
Jul 2024 — Sep 2024 [monthly]
Completed PHASE1
-
Jan 2021 — Jul 2024 [monthly]
Completed PHASE1
-
Sep 2020 — Jan 2021 [monthly]
Completed PHASE1
-
Dec 2018 — Sep 2020 [monthly]
Completed PHASE1
▶ Show 2 earlier versions
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Jun 2018 — Dec 2018 [monthly]
Completed PHASE1
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Jan 2017 — Jun 2018 [monthly]
Completed PHASE1
First recorded
Aug 2015
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Janssen Infectious Diseases BVBA
For direct contact, visit the study record on ClinicalTrials.gov .