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Study The Effects Of Different Doses Of UK-369,003 In Men With Overactive Bladder

Pfizer logo

Pfizer

Status and phase

Completed
Phase 2

Conditions

Urinary Bladder, Overactive

Treatments

Drug: Placebo
Drug: UK-369,003

Study type

Interventional

Funder types

Industry

Identifiers

NCT00479505
A3711047

Details and patient eligibility

About

This is a 12 week study in which different doses of UK-369,003 will be administered to patients with a diagnosis of overactive bladder. Patients will complete a series of questionnaires before treatment, during treatment and after treatment, to assess whether UK-369,003 has improved their symptoms of overactive bladder and erectile function.

Enrollment

275 estimated patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male subjects aged 18 years and above
  • documented clinical diagnosis of overactive bladder with urinary frequency >= 8 times / 24 hours and number of urgency episodes > 1 episode / 24 hours.

Exclusion criteria

  • Neurological diseases known to affect bladder function.
  • Urinary tract infection.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

275 participants in 2 patient groups, including a placebo group

Active
Experimental group
Treatment:
Drug: UK-369,003
Placebo
Placebo Comparator group
Treatment:
Drug: Placebo

Trial contacts and locations

52

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Data sourced from clinicaltrials.gov

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