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NCT00132444 · ClinicalTrials.gov registry record · Phase 1

Study of UC-781 Vaginal Microbicide

A Phase 1 study, sponsored by CONRAD.

Completed
Registry status
Phase 1
Development phase
90
Enrollment target

NCT00132444: Completed Phase 1 study, sponsored by CONRAD.

NCT00132444 is a Phase 1 study that has completed, run by CONRAD. The registered enrollment target is 90 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (50% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00132444, a Phase 1 study, has completed, sponsored by CONRAD.

COMPLETED
Registry status
Phase 1
Development phase
90 participants
Enrollment target

Study Summary

This study will help determine whether the agent UC-781, formulated as a gel, is safe when applied to the vagina twice daily for 14 days. It will also assess whether women find the gel acceptable to use.

Interventions

  • DRUG topical vaginal application of UC-781 gel

Trial Details

FieldValue
Enrollment Target 90 participants
Start Date 2005-10
Est. Completion 2008-12
Phase Phase 1
CONRAD

33 total trials

What the finished NCT00132444 record still lists

NCT00132444 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 90 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (50% higher).

The record links to 0 conditions, and to 1 intervention - of which topical vaginal application of UC-781 gel is the first listed.

NCT00132444 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00132444 about?

NCT00132444 is a clinical study titled "Study of UC-781 Vaginal Microbicide". This study will help determine whether the agent UC-781, formulated as a gel, is safe when applied to the vagina twice daily for 14 days. It will also assess whether women find the gel acceptable to use.

What is the current status of trial NCT00132444?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 90 participants. The study started on 2005-10. Estimated completion is 2008-12.

What interventions are being tested in trial NCT00132444?

The interventions under investigation include: topical vaginal application of UC-781 gel (DRUG).

Who is sponsoring clinical trial NCT00132444?

This trial is sponsored by CONRAD, which has 33 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00132444's enrollment target sits among peer trials

90 628th of 2000 higher than 1,352 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 NCT00132444, the US trial registry maintained by the National Library of Medicine. NCT00132444 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.