Status:

COMPLETED

Safety and Efficacy of MK0594 to Treat Overactive Bladder (0594-003)

Lead Sponsor:

Vyne Therapeutics Inc.

Conditions:

Urinary Incontinence

Overactive Bladder

Eligibility:

All Genders

40-74 years

Phase:

PHASE2

Brief Summary

This study is designed to investigate whether a new drug may offer safe and effective treatment for patients with overactive bladder.

Eligibility Criteria

Inclusion

  • Patients with predominantly urge incontinence overactive bladder episodes
  • Patients must meet minimum eligibility requirements (e.g., average number of micturitions/day) based on screening diary cards

Exclusion

  • History of Diabetes insipidus, uncontrolled hyperglycemia or hypercalcemia
  • Lower urinary tract symptoms associated with benign prostatic hypertrophy
  • Active or current Urinary Tract Infections (UTIs)
  • Surgery to correct prolapsed uterus or stress incontinence

Key Trial Info

Start Date :

February 21 2006

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

September 24 2007

Estimated Enrollment :

557 Patients enrolled

Trial Details

Trial ID

NCT00290563

Start Date

February 21 2006

End Date

September 24 2007

Last Update

May 19 2021

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