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NCT00002204 · ClinicalTrials.gov registry record · Phase 1

A Phase I, Observer-Blind, Placebo-Controlled Study of the Chiron Vaccine HIV p24/MF59 Administered to Healthy HIV-Seronegative Adults

A Phase 1 study, sponsored by Chiron Corporation.

Completed
Registry status
Phase 1
Development phase
40
Enrollment target

NCT00002204: Completed Phase 1 study, sponsored by Chiron Corporation.

NCT00002204 is a Phase 1 study that has completed, run by Chiron Corporation. The registered enrollment target is 40 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (33% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00002204, a Phase 1 study, has completed, sponsored by Chiron Corporation.

COMPLETED
Registry status
Phase 1
Development phase
40 participants
Enrollment target

Study Summary

To evaluate the safety and tolerability of the Chiron vaccine human immunodeficiency virus (HIV) p24(25 or 50 micrograms)/MF59 in healthy HIV-1 seronegative adults. To evaluate the immunogenicity of the HIV p24(50 micrograms)/MF59 vaccine.

Interventions

  • BIOLOGICAL HIV p24/MF59 Vaccine

Trial Details

FieldValue
Enrollment Target 40 participants
Phase Phase 1
Chiron Corporation

9 total trials

What the finished NCT00002204 record still lists

NCT00002204 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (33% lower).

The record links to 0 conditions, and to 1 intervention - of which HIV p24/MF59 Vaccine is the first listed.

NCT00002204 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00002204 about?

NCT00002204 is a clinical study titled "A Phase I, Observer-Blind, Placebo-Controlled Study of the Chiron Vaccine HIV p24/MF59 Administered to Healthy HIV-Seronegative Adults". To evaluate the safety and tolerability of the Chiron vaccine human immunodeficiency virus (HIV) p24(25 or 50 micrograms)/MF59 in healthy HIV-1 seronegative adults. To evaluate the immunogenicity of the HIV p24(50 micrograms)/MF59 vaccine.

What is the current status of trial NCT00002204?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 40 participants.

What interventions are being tested in trial NCT00002204?

The interventions under investigation include: HIV p24/MF59 Vaccine (BIOLOGICAL).

Who is sponsoring clinical trial NCT00002204?

This trial is sponsored by Chiron Corporation, which has 9 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00002204's enrollment target sits among peer trials

40 1130th of 2000 higher than 810 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT00002204, the US trial registry maintained by the National Library of Medicine. NCT00002204 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.