Non-Interventional Study Of Celsentri® In Treatment Experienced Patients With CCR5-Tropic HIV-Infection

NCT00850395 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 79

Last updated 2012-11-07

Study results available
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Summary

Aim of the study is to gain more knowledge about efficacy of CELSENTRI® in daily clinical practice and obtain information about the quality of life of patients using CELSENTRI®.

Conditions

Interventions

DRUG

maraviroc

No intervention; any procedure at the discretion of the treating physician, in line with the SmPC

Sponsors & Collaborators

  • Pfizer

    collaborator INDUSTRY
  • ViiV Healthcare

    lead INDUSTRY

Principal Investigators

  • Pfizer CT.gov Call Center · Pfizer

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-07-31
Primary Completion
2011-10-31
Completion
2011-10-31

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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 NCT00850395 on ClinicalTrials.gov