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NCT00100984 · ClinicalTrials.gov registry record · Phase 4

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

A Phase 4 study, sponsored by Hoffmann-La Roche.

Terminated
Registry status
Phase 4
Development phase
8
Enrollment target

NCT00100984: Clinical Trial Phase 4 study, sponsored by Hoffmann-La Roche.

NCT00100984 is a Phase 4 study that was terminated before completion, run by Hoffmann-La Roche. The registered enrollment target is 8 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00100984, a Phase 4 study, was terminated before completion, sponsored by Hoffmann-La Roche.

TERMINATED
Registry status
Phase 4
Development phase
8 participants
Enrollment target

Study Summary

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.

Interventions

  • DRUG FUZEON [enfuvirtide]

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 2004-07-21
Est. Completion 2005-07-16
Phase Phase 4
Hoffmann-La Roche

909 total trials

Why NCT00100984 stopped before completion

NCT00100984 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 8 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 1 intervention - of which FUZEON [enfuvirtide] is the first listed.

NCT00100984 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00100984 about?

NCT00100984 is a clinical study titled "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". 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.

What is the current status of trial NCT00100984?

This trial is currently terminated. It is a Phase 4 study. The enrollment target is 8 participants. The study started on 2004-07-21. Estimated completion is 2005-07-16.

What interventions are being tested in trial NCT00100984?

The interventions under investigation include: FUZEON [enfuvirtide] (DRUG).

Who is sponsoring clinical trial NCT00100984?

This trial is sponsored by Hoffmann-La Roche, which has 909 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00100984's enrollment target sits among peer trials

8 1972nd of 2000 higher than 20 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00100984, the US trial registry maintained by the National Library of Medicine. NCT00100984 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.