Assessment of Onset, Safety & Toleration of UK-369,003 in Male Erectile Dysfunction

Completed · Phase 2

Conditions studied: Impotence

In brief

To determine the onset of action, safety and toleration of different formulations and doses of UK-369,003 in patients with erectile dysfunction. Patients should have been previously treated with PDE5 inhibitors and have been responders to the drugs. Duration of treatment is 4 weeks.

Key facts

Study ID
NCT00141349
Run by
Pfizer
People needed
300
Starts
2005-02-01
Expected to finish
2005-08-01
Last updated by the study team
2006-07-25

Who can join

Age: 18 and older, up to 65. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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