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Clinical trial

A Multicenter, Randomized, Double-Blind, Parallel Group, Phase II, Forced Dose Titration Study to Investigate the Efficacy and Safety of 400mg and 600mg ELB245 Given Once Daily for 12 Weeks (8 + 4 Weeks) Versus Placebo and Versus 4mg Tolterodine Given Once Daily in Patients With Incontinent Overactive Bladder (OAB)

NCT00439192 is registered in ClinicalTrials.gov with elbion AG as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Multicenter, Randomized, Double-Blind, Parallel Group, Phase II, Forced Dose Titration Study to Investigate the Efficacy and Safety of 400mg and 600mg ELB245 Given Once Daily for 12 Weeks (8 + 4 Weeks) Versus Placebo and Versus 4mg Tolterodine Given Once Daily in Patients With Incontinent Overactive Bladder (OAB)
Lead sponsor
elbion AG
Phase
Phase 2
Overall status
Terminated
Start date
February 28, 2007
Completion date
August 31, 2007
Enrollment
275 (estimated)
Sites
31

Conditions

As the registry lists them; a condition with its own page is linked.

overactive bladder, urinary incontinence