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Completed Phase 2 Interventional Results available

A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome

ClinicalTrials.gov ID: NCT02411110

Public ClinicalTrials.gov record NCT02411110. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 12:39 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating Safety and Efficacy of LiRIS® 400 mg in Females With Interstitial Cystitis/Bladder Pain Syndrome

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a safety and efficacy study of LiRIS® in females with interstitial cystitis/bladder pain syndrome.

Study identification

NCT ID
NCT02411110
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Allergan
Industry
Enrollment
131 participants

Conditions and interventions

Interventions

Combination Product

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 20, 2015
Primary completion
Oct 11, 2016
Completion
Jan 8, 2017
Last update posted
Jan 3, 2018

2015 – 2017

United States locations

U.S. sites
31
U.S. states
17
U.S. cities
30
Facility City State ZIP Site status
Coastal Clinical Research, Inc. Mobile Alabama 36608
IC Study LLC Escondido California 92025
Tower Urology Los Angeles California 90048
Tri Valley Urology Medical Group Murrieta California 92562
Genesis Research LLC San Diego California 92123
Sutter Health Vacaville California 95688
Women's Health Specialty Care Farmington Connecticut 06032
Yale University New Haven Connecticut 06519
Manatee Medical Research Institute Bradenton Florida 34205
Atlanta Medical Research Instititute Alpharetta Georgia 30005
Idaho Urologic Institute Meridian Idaho 83642
Associated Surgeons and Physicians LLC DBA Women's Health Advantage Fort Wayne Indiana 46825
Regional Urology, LLC Shreveport Louisiana 71106
Anne Arundel Urology, P.A. Annapolis Maryland 21401
Chesapeake Urology Research Associates Baltimore Maryland 21237
Beyer Research Kalamazoo Michigan 49009
William Beaumont Hospital Royal Oak Michigan 48073
Washington University St Louis Missouri 63110
Saint Louis University School of Medicine Department of Obstetrics, Gynecology, and Women's Health Division of Research St Louis Missouri 63117
Cooper University Hospita/ Univeristy Urogynecology Associates Voorhees Township New Jersey 08043
Western New York Urology Associates Cheektowaga New York 14225
BRANY, as agent The Arthur Smith Institute for North Shore Long Island Jewish Health System Lake Success New York 11042
Urology Institute of Long Island Plainview New York 11803
McKay Urology Charlotte North Carolina 28207
Alliance Urology Specialist, P.A. Greensboro North Carolina 27403
Eastern Urological Associates, PA Greenville North Carolina 27834
Wake Forest University Winston-Salem North Carolina 27103
MetroHealth System Cleveland Ohio 44109
Female Sexual and Pelvic Health Institute Philadelphia Pennsylvania 19107
Integrity Medical Research (Urology Northwest) Mountlake Terrace Washington 98043
University of Washington Seattle Washington 98195

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02411110, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 3, 2018 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02411110 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →