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

NCT00000896 · ClinicalTrials.gov registry record · NA

A Study to Compare the Effectiveness of a Four Drug Anti-HIV Regimen Given Alone or in Combination With GM-CSF or IL-12 to HIV-Positive Patients

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

Completed
Registry status
NA
Development phase
24
Enrollment target

NCT00000896: Completed NA study, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

NCT00000896 is a NA study that has completed, run by National Institute of Allergy and Infectious Diseases (NIAID). The registered enrollment target is 24 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00000896, a NA study, has completed, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

COMPLETED
Registry status
NA
Development phase
24 participants
Enrollment target

Study Summary

The purpose of this study is to examine how the level of HIV is reduced in the blood when anti-HIV therapy is initiated. This study will also evaluate whether adding GM-CSF or IL-12 to the anti-HIV drug regimen will increase the rate that HIV is reduced. The anti-HIV drugs used in this study will include lamivudine (3TC), zidovudine (ZDV), indinavir (IDV), nevirapine (NVP), and stavudine (d4T). All have been used successfully to treat HIV. GM-CSF has been used to treat certain blood disorders; it will be used as an experimental drug in this study. IL-12 (interleukin-12) is a protein found naturally in the body that is thought to boost the immune system. Although GM-CSF and IL-12 have no direct effect against HIV, these drugs may improve the ability of the immune system to fight the virus.

Interventions

  • DRUG Indinavir sulfate
  • DRUG Nevirapine
  • DRUG Lamivudine/Zidovudine
  • DRUG Interleukin-12
  • BIOLOGICAL Hepatitis A Vaccine (Inactivated)

Trial Details

FieldValue
Enrollment Target 24 participants
Est. Completion 2000-10
Phase NA

What the finished NCT00000896 record still lists

NCT00000896 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 5 interventions - of which Indinavir sulfate is the first listed.

NCT00000896 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00000896 about?

NCT00000896 is a clinical study titled "A Study to Compare the Effectiveness of a Four Drug Anti-HIV Regimen Given Alone or in Combination With GM-CSF or IL-12 to HIV-Positive Patients". The purpose of this study is to examine how the level of HIV is reduced in the blood when anti-HIV therapy is initiated. This study will also evaluate whether adding GM-CSF or IL-12 to the anti-HIV drug regimen will increase the rate that HIV is reduced. The anti-HIV drugs used in this study will i...

What is the current status of trial NCT00000896?

This trial is currently completed. It is a NA study. The enrollment target is 24 participants. Estimated completion is 2000-10.

What interventions are being tested in trial NCT00000896?

The interventions under investigation include: Indinavir sulfate (DRUG), Nevirapine (DRUG), Lamivudine/Zidovudine (DRUG), Interleukin-12 (DRUG), Hepatitis A Vaccine (Inactivated) (BIOLOGICAL).

Who is sponsoring clinical trial NCT00000896?

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 NCT00000896's enrollment target sits among peer trials

24 1736th of 2000 higher than 246 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

  • NCT02331979 · 24 participants · NA

    Improving Bladder Function in SCI by Neuromodulation

  • NCT03096197 · 24 participants · NA

    Exoskeleton and Spinal Cord Stimulation for SCI

  • NCT03223922 · 24 participants · NA

    Neurocognitive Functioning With Genu-Sparing Whole Brain Radiation Therapy for Brain Metastases

  • NCT03326921 · 24 participants · Phase 1

    HA-1 T TCR T Cell Immunotherapy for the Treatment of Patients With Relapsed or Refractory Acute Leukemia After Donor Stem Cell Transplant

Source: ClinicalTrials.gov NCT00000896, the US trial registry maintained by the National Library of Medicine. NCT00000896 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.