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12-Week, Randomized, Double-Blind, Double-Dummy, Placebo-Controlled, Parallel-Group, Multicenter Trial To Evaluate The Efficacy And Safety Of Fesoterodine In Comparison To Tolterodine ER In Patients With Overactive Bladder.

Trial Profile

12-Week, Randomized, Double-Blind, Double-Dummy, Placebo-Controlled, Parallel-Group, Multicenter Trial To Evaluate The Efficacy And Safety Of Fesoterodine In Comparison To Tolterodine ER In Patients With Overactive Bladder.

Completed
Phase of Trial: Phase III

Latest Information Update: 31 Aug 2018

At a glance

  • Drugs Fesoterodine (Primary) ; Tolterodine
  • Indications Overactive bladder
  • Focus Therapeutic Use
  • Acronyms FACT2
  • Sponsors Pfizer
  • Most Recent Events

    • 31 Aug 2018 Results (n=6689) of pooled analysis from 6 studies (A0221008, A0221012, A0221013, A0221046, A0221094, A0221095) characterising patient symptom response resented at the 48th Annual Meeting of the International Continence Society
    • 31 Aug 2018 Results (n=6689) of pooled analysis from 6 studies (A0221008, A0221012, A0221013, A0221046, A0221094, A0221095) examining efficacy and safety presented at the 48th Annual Meeting of the International Continence Society
    • 31 Aug 2018 Results (n=6689) of pooled analysis from 6 studies (A0221008, A0221012, A0221013, A0221046, A0221094, A0221095) examing the relationship between disease variable resolution end of 4, 8 or 12 weeks treatment with fesoterodine and the proportion of patients achieving a significant improvement in Patient Reported Outcome Measures (PROM) resented at the 48th Annual Meeting of the International Continence Society
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