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Completed Phase 2 Interventional

Safety and Effectiveness of the Oral HIV Entry Inhibitor Vicriviroc in HIV Infected Patients

ClinicalTrials.gov ID: NCT00082498

Public ClinicalTrials.gov record NCT00082498. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 3, 2026, 2:16 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase II, Randomized, Double-Blind Study of the Safety and Efficacy of Vicriviroc (An Orally Administered HIV-1 Entry Inhibitor) in HIV-Infected, Treatment-Experienced Subjects

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

New treatment options are critical for treatment-experienced HIV infected patients with drug resistance. HIV entry inhibitors have been shown effective in patients with resistance to other anti-HIV drugs. This study will test the safety and effectiveness of three different doses of vicriviroc (formerly known as Schering D, SCH-D, or SCH 417690) in HIV infected patients.

Study identification

NCT ID
NCT00082498
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
119 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 30, 2004
Primary completion
Nov 30, 2005
Completion
Dec 31, 2010
Last update posted
Oct 31, 2021

2004 – 2011

United States locations

U.S. sites
30
U.S. states
16
U.S. cities
23
Facility City State ZIP Site status
UCLA CARE Center CRS Los Angeles California 90035
Stanford AIDS Clinical Trials Unit CRS Palo Alto California 94304-5350
UCSD Antiviral Research Center CRS San Diego California 92103
Ucsf Hiv/Aids Crs San Francisco California 94110
Santa Clara Valley Med. Ctr. San Jose California 95128
University of Colorado Hospital CRS Aurora Colorado 80045
Georgetown University CRS (GU CRS) Washington D.C. District of Columbia 20007
The Ponce de Leon Center CRS Atlanta Georgia 30308-2012
Rush University CRS Chicago Illinois 60612
Indiana Univ. School of Medicine, Infectious Disease Research Clinic Indianapolis Indiana 46202
Massachusetts General Hospital CRS (MGH CRS) Boston Massachusetts 02114
Brigham and Women's Hospital Therapeutics Clinical Research Site (BWH TCRS) CRS Boston Massachusetts 02115
Bmc Actg Crs Boston Massachusetts 02118
Washington University Therapeutics (WT) CRS St Louis Missouri 63110
Beth Israel Med. Ctr., ACTU New York New York 10003
Weill Cornell Chelsea CRS New York New York 10011
NY Univ. HIV/AIDS CRS New York New York 10016
Weill Cornell Uptown CRS New York New York 10065
Trillium Health ACTG CRS Rochester New York 14607
Univ. of Rochester ACTG CRS Rochester New York 14642
Chapel Hill CRS Chapel Hill North Carolina 27514
Case CRS Cleveland Ohio 44106
MetroHealth CRS Cleveland Ohio 44109
Ohio State University CRS Columbus Ohio 43210
Penn Therapeutics, CRS Philadelphia Pennsylvania 19104
University of Pittsburgh CRS Pittsburgh Pennsylvania 15213-2582
The Miriam Hospital Clinical Research Site (TMH CRS) CRS Providence Rhode Island 02906
Vanderbilt Therapeutics (VT) CRS Nashville Tennessee 37204
Univ. of Texas Medical Branch, ACTU Galveston Texas 77555-0435
University of Washington AIDS CRS Seattle Washington 98104

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00082498, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 31, 2021 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00082498 live on ClinicalTrials.gov.

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