CompletedPhase 2NCT02411110
A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome
Studying Interstitial cystitis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Allergan
- Principal Investigator
- Till GeibAllergan
- Intervention
- LiRIS®(combination_product)
- Enrollment
- 131 target
- Eligibility
- 18 years · FEMALE
- Timeline
- 2015 – 2017
Study locations (30)
- Coastal Clinical Research, Inc., Mobile, Alabama, United States
- IC Study LLC, Escondido, California, United States
- Tower Urology, Los Angeles, California, United States
- Tri Valley Urology Medical Group, Murrieta, California, United States
- Genesis Research LLC, San Diego, California, United States
- Sutter Health, Vacaville, California, United States
- Women's Health Specialty Care, Farmington, Connecticut, United States
- Yale University, New Haven, Connecticut, United States
- Manatee Medical Research Institute, Bradenton, Florida, United States
- Atlanta Medical Research Instititute, Alpharetta, Georgia, United States
- Idaho Urologic Institute, Meridian, Idaho, United States
- Associated Surgeons and Physicians LLC DBA Women's Health Advantage, Fort Wayne, Indiana, United States
- Regional Urology, LLC, Shreveport, Louisiana, United States
- Anne Arundel Urology, P.A., Annapolis, Maryland, United States
- Chesapeake Urology Research Associates, Baltimore, Maryland, United States
- +15 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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