Skip to main content

Urinary Incontinence, Urge

2
Pipeline Programs
5
Companies
3
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
0
Early DiscoveryClinical DevelopmentMarket

Competitive Landscape

4 companies ranked by most advanced pipeline stage

Human BioSciences
Human BioSciencesWV - Martinsburg
1 program
1
InterStim® devicePhase 31 trial
Active Trials
NCT01502956Completed386Est. Jul 2016
Oregon Therapeutics
Oregon TherapeuticsFrance - Paris
1 program
1
InterStim® devicePhase 3
AbbVie
AbbVieNORTH CHICAGO, IL
1 program
Bladder Antimuscarinic Medication and Accidental Bowel LeakageN/A1 trial
Active Trials
NCT03543566Completed32Est. Jan 2019
Coloplast
ColoplastAustralia - Mulgrave
1 program
INTIBIA TherapeuticN/A1 trial
Active Trials
NCT05250908Active Not Recruiting208Est. Jun 2026

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
Human BioSciencesInterStim® device
ColoplastINTIBIA Therapeutic
AbbVieBladder Antimuscarinic Medication and Accidental Bowel Leakage

Clinical Trials (3)

Total enrollment: 626 patients across 3 trials

Refractory Overactive Bladder: Sacral NEuromodulation v. BoTulinum Toxin Assessment (ROSETTA)

Start: Feb 2012Est. completion: Jul 2016386 patients
Phase 3Completed
NCT05250908ColoplastINTIBIA Therapeutic

INTIBIA Pivotal Study

Start: Mar 2022Est. completion: Jun 2026208 patients
N/AActive Not Recruiting
NCT03543566AbbVieBladder Antimuscarinic Medication and Accidental Bowel Leakage

Bladder Antimuscarinic Medication and Accidental Bowel Leakage

Start: May 2018Est. completion: Jan 201932 patients
N/ACompleted

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
5 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.