Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00006441 · ClinicalTrials.gov registry record · NA

Effectiveness of Adding Interleukin-2 to Anti-HIV Drugs in Patients Recently Infected With HIV

A NA study, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

Completed
Registry status
NA
Development phase
398
Enrollment target

NCT00006441: Completed NA study, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

NCT00006441 is a NA study that has completed, run by National Institute of Allergy and Infectious Diseases (NIAID). The registered enrollment target is 398 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (72% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00006441, a NA study, has completed, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

COMPLETED
Registry status
NA
Development phase
398 participants
Enrollment target

Study Summary

The purpose of this study is to see whether taking interleukin-2 (IL-2) and other anti-HIV drugs affects the course of HIV disease in patients with primary HIV infection (the time period that immediately follows infection with HIV). After primary HIV infection, the actual infection is spread through an increasing amount of HIV virus in the body. Studies have shown that, by taking a combination of anti-HIV drugs, it is possible to reduce the amount of HIV in the body to almost undetectable levels. This study will find out if starting anti-HIV drugs during primary infection will interrupt or reduce the spread of HIV in patients' bodies.

Interventions

  • DRUG Aldesleukin
  • DRUG Nelfinavir mesylate
  • DRUG Lamivudine/Zidovudine

Trial Details

FieldValue
Enrollment Target 398 participants
Start Date 2003-02
Est. Completion 2008-10
Phase NA

What the finished NCT00006441 record still lists

NCT00006441 is an interventional study that assigns participants to a tested intervention. The registered 398 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (72% lower).

The record links to 0 conditions, and to 3 interventions - of which Aldesleukin is the first listed.

NCT00006441 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00006441 about?

NCT00006441 is a clinical study titled "Effectiveness of Adding Interleukin-2 to Anti-HIV Drugs in Patients Recently Infected With HIV". The purpose of this study is to see whether taking interleukin-2 (IL-2) and other anti-HIV drugs affects the course of HIV disease in patients with primary HIV infection (the time period that immediately follows infection with HIV). After primary HIV infection, the actual infection is spread throug...

What is the current status of trial NCT00006441?

This trial is currently completed. It is a NA study. The enrollment target is 398 participants. The study started on 2003-02. Estimated completion is 2008-10.

What interventions are being tested in trial NCT00006441?

The interventions under investigation include: Aldesleukin (DRUG), Nelfinavir mesylate (DRUG), Lamivudine/Zidovudine (DRUG).

Who is sponsoring clinical trial NCT00006441?

This trial is sponsored by National Institute of Allergy and Infectious Diseases (NIAID), which has 2,006 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00006441's enrollment target sits among peer trials

398 267th of 2000 higher than 1,734 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT05365581 · 398 participants · Phase 1

    A Study of ASP2138 Given by Itself or Given With Other Cancer Treatments in Adults With Stomach Cancer, Gastroesophageal Junction Cancer, or Pancreatic Cancer

  • NCT03165734 · 399 participants · Phase 3

    A Phase 3 Study of Pacritinib in Patients With Primary Myelofibrosis, Post Polycythemia Vera Myelofibrosis, or Post-Essential Thrombocythemia Myelofibrosis

  • NCT05022862 · 399 participants · NA

    Economic Incentives and vDOT for Latent Tuberculosis Infection

  • NCT00601939 · 397 participants · NA

    Effectiveness of Empowerment Group Sessions for Treating Suicidal African American Women in Abusive Relationships

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00006441, the US trial registry maintained by the National Library of Medicine. NCT00006441 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.