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Urge Urinary Incontinence

4
Pipeline Programs
4
Companies
4
Clinical Trials
0
Approved Products

Pipeline by Development Stage

Preclinical
Phase 1
Phase 1/2
Phase 2
Phase 2/3
Phase 3
On Market
0
0
0
0
0
2
2
Early DiscoveryClinical DevelopmentMarket

Competitive Landscape

4 companies ranked by most advanced pipeline stage

Pfizer
PfizerNEW YORK, NY
1 program
1
FesoterodinePhase 41 trial
Active Trials
NCT00862745Completed645Est. May 2011
Astellas
AstellasChina - Shenyang
1 program
1
SolifenacinPhase 41 trial
Active Trials
NCT01559389Completed138Est. Jun 2017
Human BioSciences
Human BioSciencesWV - Martinsburg
1 program
1
Botulinum toxin APhase 31 trial
Active Trials
NCT01166438Completed249Est. May 2012
Antares Therapeutics
1 program
1
oxybutyninPhase 31 trial
Active Trials
NCT00909181Completed626Est. Nov 2010

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
AstellasSolifenacin
PfizerFesoterodine
Human BioSciencesBotulinum toxin A
Antares Therapeuticsoxybutynin

Clinical Trials (4)

Total enrollment: 1,658 patients across 4 trials

Incontinence & Intimate Partners: Assessing the Contribution of Treatment

Start: Mar 2012Est. completion: Jun 2017138 patients
Phase 4Completed
NCT00862745PfizerFesoterodine

Bringing Simple Urge Incontinence Diagnosis & Treatment to Providers (BRIDGES)

Start: Jan 2009Est. completion: May 2011645 patients
Phase 4Completed

Anticholinergic vs. Botox Comparison Study

Start: Mar 2010Est. completion: May 2012249 patients
Phase 3Completed

Study of Topically Administered Oxybutynin Gel in Patients With Urge Incontinence

Start: Mar 2009Est. completion: Nov 2010626 patients
Phase 3Completed

Phase Legend

PreclinicalLab & animal studies
Phase 1Safety & dosing
Phase 2Efficacy testing
Phase 3Large-scale trials
On MarketApproved & available

Key Insights

2 late-stage (Phase 3) programs, potential near-term approvals
4 companies competing in this space

The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.