Long-term Study in Patients Under Anti-retroviral Combination Therapy Switching to Viramune®

NCT02191293 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 228

Last updated 2014-07-16

No results posted yet for this study

Summary

Collecting data on maintaining anti-retroviral activity (quantitative HIV RNA determination) and immunological activity (CD4 cells) after switching from protease inhibitor or NNRTI to Nevirapine (Viramune®) and collecting of routinely observed laboratory data on lipids, and liver enzymes.

Conditions

  • HIV Infections

Interventions

DRUG

Viramune® tablets

Sponsors & Collaborators

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2002-05-31
Primary Completion
2006-09-30

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02191293 on ClinicalTrials.gov