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Completed Phase 2 Interventional

TMC114-C202: A Study of Safety, Efficacy, and Tolerability of TMC114 and Low Dose Ritonavir in HIV-1 Infected Patients

ClinicalTrials.gov ID: NCT00071097

Public ClinicalTrials.gov record NCT00071097. 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 Jul 21, 2026, 4:22 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 II Randomized, Controlled, Partially Blinded Trial to Investigate Dose Response of TMC114/RTV in 3-class-experienced HIV-1 Infected Patients, Followed by an Open-label Period on the Recommended Dose of TMC114/RTV.

Study identification

NCT ID
NCT00071097
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Tibotec Pharmaceuticals, Ireland
Industry
Enrollment
330 participants

Conditions and interventions

Conditions

Interventions

  • TMC114/rtv Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 99 Years
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
Sep 30, 2003
Primary completion
Jan 31, 2005
Completion
Oct 31, 2007
Last update posted
Sep 19, 2016

2003 – 2007

United States locations

U.S. sites
38
U.S. states
20
U.S. cities
38
Facility City State ZIP Site status
Not listed Birmingham Alabama
Not listed Phoenix Arizona
Not listed Beverly Hills California
Not listed Long Beach California
Not listed Los Angeles California
Not listed Oakland California
Not listed San Diego California
Not listed San Francisco California
Not listed West Hollywood California
Not listed Denver Colorado
Not listed Washington D.C. District of Columbia
Not listed Altamonte Springs Florida
Not listed Fort Lauderdale Florida
Not listed Miami Florida
Not listed Miami Beach Florida
Not listed Tampa Florida
Not listed Vero Beach Florida
Not listed Atlanta Georgia
Not listed Macon Georgia
Not listed Chicago Illinois
Not listed Baltimore Maryland
Not listed Boston Massachusetts
Not listed Springfield Massachusetts
Not listed Camden New Jersey
Not listed Albany New York
Not listed New York New York
Not listed Huntersville North Carolina
Not listed Cincinnati Ohio
Not listed Cleveland Ohio
Not listed Hershey Pennsylvania
Not listed Philadelphia Pennsylvania
Not listed Columbia South Carolina
Not listed Dallas Texas
Not listed Galveston Texas
Not listed Houston Texas
Not listed Hampton Virginia
Not listed Seattle Washington
Not listed Milwaukee Wisconsin

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00071097, 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 Sep 19, 2016 · Synced Jul 21, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00071097 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →