Clinical and Therapeutic Evaluation of the Infection by HIV/AIDS

NCT02191215 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 442

Last updated 2014-07-16

No results posted yet for this study

Summary

The aim of the Post Marketing Study (PMS) is to evaluate the efficacy and safety profile of nevirapine in the management of the HIV/AIDS in an open environment.

Conditions

  • Acquired Immunodeficiency Syndrome

Interventions

DRUG

Nevirapine (Viramune®)

Sponsors & Collaborators

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-06-30
Primary Completion
2004-05-31

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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 NCT02191215 on ClinicalTrials.gov