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

NCT ID: NCT00850395

Last Updated: 2012-11-07

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

79 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-07-31

Study Completion Date

2011-10-31

Brief Summary

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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®.

Detailed Description

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Non interventional study, inclusion and exclusion criteria defined by the labelling of Celsentri (Maraviroc).

Conditions

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HIV-1

Keywords

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HIV-1 non-interventional CCR-5 tropic virus therapy experienced patients

Study Design

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Study Time Perspective

PROSPECTIVE

Study Groups

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1

Non-Interventional

maraviroc

Intervention Type DRUG

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

Interventions

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maraviroc

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

Intervention Type DRUG

Other Intervention Names

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Selzentry, Celsentri

Eligibility Criteria

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Inclusion Criteria

HIV-1 infection. CCR-5 tropic virus. Therapy experienced patient,

Exclusion Criteria

X4 or D/M tropic virus. Therapy-naive patients.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Pfizer

INDUSTRY

Sponsor Role collaborator

ViiV Healthcare

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Pfizer CT.gov Call Center

Role: STUDY_DIRECTOR

Pfizer

Related Links

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Other Identifiers

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CELTROP

Identifier Type: -

Identifier Source: secondary_id

A4001070

Identifier Type: -

Identifier Source: org_study_id