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Terminated Phase 4 Interventional

A 48 Week Study Comparing Treatment With Saquinavir + Lopinavir/Ritonavir in Combination With Enfuvirtide HAART Versus Saquinavir + Lopinavir/Ritonavir + Other Nucleoside Combinations to See the Efficacy of These Treatments in Patients Infected With HIV-1

ClinicalTrials.gov ID: NCT00100984

Public ClinicalTrials.gov record NCT00100984. 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 Oct 17, 2026, 6:00 PM EDT

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

Brief summary

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

The main objective of this study is to compare the safety and efficacy of an enfuvirtide containing regimen to a nucleoside combination regimen. Resistance information will also be collected.

Study identification

NCT ID
NCT00100984
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 4
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
8 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
Jul 21, 2004 (Actual)
Primary completion
Jul 16, 2005 (Actual)
Completion
Jul 16, 2005 (Actual)
Last update posted
Jun 20, 2017

2004 – 2005

United States locations

U.S. sites
20
U.S. states
14
U.S. cities
16
Facility City State ZIP Site status
Not listed Hobson City Alabama 36201 —
Not listed Los Angeles California 90033 —
Not listed Los Angeles California 90036 —
Not listed Washington D.C. District of Columbia 20007 —
Not listed Washington D.C. District of Columbia 20009 —
Not listed Orlando Florida 32803 —
Not listed Atlanta Georgia 30308 —
Not listed Macon Georgia 31201 —
Not listed Chicago Illinois 60612 —
Not listed Chicago Illinois 60657 —
Not listed Baltimore Maryland 21201 —
Not listed Boston Massachusetts 02215-3318 —
Not listed Jackson Mississippi 39216-4505 —
Not listed St Louis Missouri 63139 —
Not listed Newark New Jersey 07103 —
Not listed New York New York 10011 —
Not listed New York New York 10016 —
Not listed Huntersville North Carolina 28078 —
Not listed Dallas Texas 75246 —
Not listed Houston Texas 77004 —

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 NCT00100984, 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 Jun 20, 2017 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00100984 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →