Cabotegravir Plus Rilpivirine Long-acting Regimen in the Swiss HIV Cohort Study:Uptake, Outcome, and Risk Factors for Treatment Failures
- Disease/Condition
- HIV Infections
- Drug/Device/Intervention
- VOCABRIA 30Mg Tablet
- Study type
- Observational
- Intervention type
- drug
- Primary sponsor
- University of Zurich
- Location
- Zurich, Switzerland
- Phase
- N/A
- Start date
- Mar 01, 2022
- End date
- Jun 30, 2026
- Enrollment
- 600 participants
Proportion of individuals with viral blips,Proportion of individuals with confirmed viral failures,Proportion of individuals switching off CAB+RPV LA to previous or another oral regimen,Time to viral failure,Proportion of participants who discontinue treatment due to drug-related reasons,Proportion of participants who discontinue treatment due to drug-unrelated reasons,Proportion of participants by characteristics,Overall adherence to Swiss label indication in CAB+RPV LA prescriptions,Overall adherence to the proposed injection schedules,Proportion of participants by treatment adherence category
This study aims to characterize Swiss HIV Cohort Study participants initiating the CAB+RPV LA
 regimen, assess adherence to Swiss label indications, and describe treatment outcomes in this
 large, multicentre, heterogeneous, high-income setting. Moreover, the study aims to assess
 virological, immunological, demographic, clinical, and behavioural factors associated with
 viral failure under CAB+RPV LA regimen.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT06405464
- Type
- Non-Device Trial
Access comprehensive clinical trial information for NCT06405464 through Pure Global AI's free database. This phase not specified trial is sponsored by University of Zurich and is currently Recruiting. The study focuses on HIV Infections. Target enrollment is 600 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.