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

Study Identifier
201025-002
CT.gov Identifier
NCT02411110
EudraCT Identifier
Not available
EUCTIS ID
Not available
For general inquiries, please contact

844-663-3742 or [email protected]

Study Complete

Study Details

Medical Condition
  • Bladder Disorder - Interstitial Cystitis
  • Bladder Disorder - Bladder Pain Syndrome
    • Study Drug
    N/A
    Phase
    Phase 2
    Sex
    Female
    Age
    18+ years
    Inclusion and Exclusion Criteria
    Inclusion Criteria:
    * Diagnosis of interstitial cystitis or bladder pain syndrome
    Exclusion Criteria:
    * Diagnosis of interstitial cystitis with Hunner's lesions/ulcers * Previous treatment with LiRIS®

    Protocol Summary

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

    Study Locations

    Location
    Status
    Location
    Coastal Clinical Research, Inc.
    Mobile, Alabama, United States, 36608
    Status
    Not applicable
    Location
    IC Study LLC
    Escondido, California, United States, 92025
    Status
    Not applicable
    Location
    Tower Urology
    Los Angeles, California, United States, 90048
    Status
    Not applicable
    Location
    Tri Valley Urology Medical Group
    Murrieta, California, United States, 92562
    Status
    Not applicable
    Location
    Genesis Research LLC
    San Diego, California, United States, 92123
    Status
    Not applicable
    Location
    Sutter Health
    Vacaville, California, United States, 95688
    Status
    Not applicable
    Showing {first} - {last} of {total} Results