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Completed Phase 1 Interventional

Monotherapy Versus Placebo Over 7 Days-Non-Nucleoside Reverse Transcriptase Inhibitor-Experienced HIV1 Infected Adults

ClinicalTrials.gov ID: NCT00090077

Public ClinicalTrials.gov record NCT00090077. 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 May 11, 2026, 10:28 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

A Phase I, Multicenter, Randomized, Parallel, Double-Blinded Dose Ranging, Placebo-Controlled Study to Compare Antiviral Effect, Safety, Tolerability and Pharmacokinetics of Four Oral Dosage Regimens of GW695634G Monotherapy Versus Placebo Over 10 Days in ART-Naive HIV-1 Infected Adults.

Study identification

NCT ID
NCT00090077
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
50 participants

Conditions and interventions

Conditions

Interventions

  • GW695634 Drug

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
Mar 31, 2004
Primary completion
Not listed
Completion
Not listed
Last update posted
Feb 26, 2006

Started 2004

United States locations

U.S. sites
18
U.S. states
12
U.S. cities
18
Facility City State ZIP Site status
GSK Clinical Trials Call Center Phoenix Arizona 85006
GSK Clinical Trials Call Center Fountain Valley California 92708
GSK Clinical Trials Call Center San Francisco California 94115
GSK Clinical Trials Call Center West Hollywood California 90069
GSK Clinical Trials Call Center Washington D.C. District of Columbia 20007
GSK Clinical Trials Call Center Fort Lauderdale Florida 33308
GSK Clinical Trials Call Center Miami Florida 33136
GSK Clinical Trials Call Center Miami Beach Florida 33140
GSK Clinical Trials Call Center Orlando Florida 32804
GSK Clinical Trials Call Center Vero Beach Florida 32960
GSK Clinical Trials Call Center Atlanta Georgia 30308
GSK Clinical Trials Call Center Boston Massachusetts 02215
GSK Clinical Trials Call Center Las Vegas Nevada 89102
GSK Clinical Trials Call Center New York New York 10008
GSK Clinical Trials Call Center Charlotte North Carolina 28209
GSK Clinical Trials Call Center Oklahoma City Oklahoma 73104
GSK Clinical Trials Call Center Fort Worth Texas 76104
GSK Clinical Trials Call Center 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 NCT00090077, 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 Feb 26, 2006 · Synced May 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00090077 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →