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NCT02395042 · ClinicalTrials.gov registry record · Phase 2

A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis With Hunner's Lesions

A Phase 2 study, sponsored by Allergan.

Completed
Registry status
Phase 2
Development phase
59
Enrollment target

NCT02395042: Completed Phase 2 study, sponsored by Allergan.

NCT02395042 is a Phase 2 study that has completed, run by Allergan. The registered enrollment target is 59 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (56% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02395042, a Phase 2 study, has completed, sponsored by Allergan.

COMPLETED
Registry status
Phase 2
Development phase
59 participants
Enrollment target

Study Summary

This is a safety and efficacy study of LiRIS® in females with interstitial cystitis with Hunner's lesions.

Primary Outcome

The participant recorded their daily bladder pain score over the previous 24-hour period on a 7-day pain assessment tool as measured by an NRS on an 11-point scale where 0=no pain to 10=worst pain imaginable. The daily pain scores over the 7-day period were averaged. A negative change from Baseline indicates improvement. An analysis of covariance (ANCOVA) model with Baseline value as a covariate and treatment group and stratification (baseline bladder pain NRS: ≤ 5 or \> 5) as factors was used f

Interventions

  • DRUG LiRIS®
  • DRUG LiRIS Placebo

Trial Details

FieldValue
Enrollment Target 59 participants
Start Date 2015-04-15
Est. Completion 2017-11-20
Phase Phase 2
Allergan

314 total trials

What the finished NCT02395042 record still lists

NCT02395042 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 59 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (56% lower).

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

NCT02395042 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02395042 about?

NCT02395042 is a clinical study titled "A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis With Hunner's Lesions". This is a safety and efficacy study of LiRIS® in females with interstitial cystitis with Hunner's lesions.

What is the current status of trial NCT02395042?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 59 participants. The study started on 2015-04-15. Estimated completion is 2017-11-20.

What interventions are being tested in trial NCT02395042?

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

Who is sponsoring clinical trial NCT02395042?

This trial is sponsored by Allergan, which has 314 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02395042's enrollment target sits among peer trials

59 1133rd of 2000 higher than 866 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT02395042, the US trial registry maintained by the National Library of Medicine. NCT02395042 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.