Four Rivers Clinical Research | Paducah, KY
Status and phase
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About
The purpose of this study is to evaluate the safety, tolerability and efficacy of V117957 in subjects with interstitial cystitis/bladder pain syndrome, compared to placebo.
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Inclusion and exclusion criteria
Key Inclusion Criteria include:
Key Exclusion Criteria include:
Other protocol-specific inclusion and exclusion criteria may apply.
Primary purpose
Allocation
Interventional model
Masking
44 participants in 2 patient groups, including a placebo group
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Data sourced from clinicaltrials.gov
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