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A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study of YM672 in the Treatment of Painful Bladder Syndrome/Interstitial Cystitis

Update Il y a 5 ans
Reference: EUCTR2005-003367-23

Woman and Man

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Extract

To evaluate the efficacy and safety of YM672 administered orally in the treatment of painful bladder syndrome (PBS)/interstitial cystitis (IC). The primary efficacy endpoint is success, defined as ‘Moderately Improved’ or ‘Markedly Improved’ PBS/IC on the subject-rated 7-point Global Response Assessment (GRA) at the Week 12 and/or End of Treatment (ET) visit.

Inclusion criteria

  • Interstitial Cystitis / Painful Bladder Syndrome

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