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NCT06024642 · ClinicalTrials.gov registry record · Phase 1

Study of V117957 in Overactive Bladder Syndrome

A Phase 1 study, sponsored by Imbrium Therapeutics.

Completed
Registry status
Phase 1
Development phase
51
Enrollment target

NCT06024642: Completed Phase 1 study, sponsored by Imbrium Therapeutics.

NCT06024642 is a Phase 1 study that has completed, run by Imbrium Therapeutics. The registered enrollment target is 51 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (15% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06024642, a Phase 1 study, has completed, sponsored by Imbrium Therapeutics.

COMPLETED
Registry status
Phase 1
Development phase
51 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the safety, tolerability and efficacy of V117957 in subjects with overactive bladder syndrome, compared to placebo.

Primary Outcome

Subjects were asked to record all micturition episode components into a daily electronic diary during the 3 to 7 days prior to each scheduled clinic visit.

Interventions

  • DRUG Placebo
  • DRUG V117957

Trial Details

FieldValue
Enrollment Target 51 participants
Start Date 2022-06-30
Est. Completion 2024-05-21
Phase Phase 1
Imbrium Therapeutics

5 total trials

What the finished NCT06024642 record still lists

NCT06024642 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 51 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (15% lower).

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

NCT06024642 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06024642 about?

NCT06024642 is a clinical study titled "Study of V117957 in Overactive Bladder Syndrome". The purpose of this study is to evaluate the safety, tolerability and efficacy of V117957 in subjects with overactive bladder syndrome, compared to placebo.

What is the current status of trial NCT06024642?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 51 participants. The study started on 2022-06-30. Estimated completion is 2024-05-21.

What interventions are being tested in trial NCT06024642?

The interventions under investigation include: Placebo (DRUG), V117957 (DRUG).

Who is sponsoring clinical trial NCT06024642?

This trial is sponsored by Imbrium Therapeutics, which has 5 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06024642's enrollment target sits among peer trials

51 969th of 2000 higher than 1,028 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 NCT06024642, the US trial registry maintained by the National Library of Medicine. NCT06024642 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.