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

NCT00002323 · ClinicalTrials.gov registry record · NA

A Multi-Center, Placebo-Controlled, Double-Blind, Randomized Trial Comparing the Virologic and Immunologic Activities of 400 Mg Nevirapine in Combination With Zidovudine Versus Zidovudine Alone in Asymptomatic HIV-1 Infected Patients With 4-12 Months of Prior Zidovudine Therapy and 200-500 CD4+ Cell

A NA study, sponsored by Boehringer Ingelheim.

Completed
Registry status
NA
Development phase
60
Enrollment target

NCT00002323 is a NA study that has completed, run by Boehringer Ingelheim. The registered enrollment target is 60 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00002323, a NA study, has completed, sponsored by Boehringer Ingelheim.

COMPLETED
Registry status
NA
Development phase
60 participants
Enrollment target

Study Summary

PRIMARY: To compare the virologic activity (quantitative RNA PCR, quantitative PBMC) of the combination of nevirapine and zidovudine (AZT) versus AZT alone after 3 and 6 months of treatment. To compare the effects of these two regimens on CD4 T-cell count and percentage. SECONDARY: To compare and evaluate other markers of immunologic and virologic activity in patients receiving nevirapine/AZT versus AZT alone. To compare the effects of the two regimens on clinical signs and symptoms. To evaluate the safety and tolerance of the two regimens.

Interventions

  • DRUG Zidovudine
  • DRUG Nevirapine

Trial Details

FieldValue
Enrollment Target 60 participants
Phase NA

Sponsor

Boehringer Ingelheim

515 total trials

What the Registry Record Tells You About NCT00002323

The ClinicalTrials.gov registry entry for NCT00002323 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Boehringer Ingelheim, which has 515 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Zidovudine is the first listed.

NCT00002323 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00002323 about?

NCT00002323 is a clinical study titled "A Multi-Center, Placebo-Controlled, Double-Blind, Randomized Trial Comparing the Virologic and Immunologic Activities of 400 Mg Nevirapine in Combination With Zidovudine Versus Zidovudine Alone in Asymptomatic HIV-1 Infected Patients With 4-12 Months of Prior Zidovudine Therapy and 200-500 CD4+ Cell". PRIMARY: To compare the virologic activity (quantitative RNA PCR, quantitative PBMC) of the combination of nevirapine and zidovudine (AZT) versus AZT alone after 3 and 6 months of treatment. To compare the effects of these two regimens on CD4 T-cell count and percentage. SECONDARY: To compare and e...

What is the current status of trial NCT00002323?

This trial is currently completed. It is a NA study. The enrollment target is 60 participants.

What interventions are being tested in trial NCT00002323?

The interventions under investigation include: Zidovudine (DRUG), Nevirapine (DRUG).

Who is sponsoring clinical trial NCT00002323?

This trial is sponsored by Boehringer Ingelheim, which has 515 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.