About this data
Pipeline and clinical trial information here comes primarily from ClinicalTrials.gov. A listing on ClinicalTrials.gov means a study has been registered — not that a treatment is proven safe, effective, or FDA-approved. Investigational treatments may never be approved. Who can join a trial is decided only by that trial's own study team.
Darifenacin Hydrobromide
- Company
- Oliver Blanchard
- Mechanism
- Mechanism not yet reported
- Route
- Route not yet reported
- Recruiting trials
- 1 recruiting
Efficacy results: Not yet reported
1 recruiting study currently listed on ClinicalTrials.gov.
Data source: ClinicalTrials.gov · trial data as of Oct 10, 2026
Find a Clinical Trial Near Me
See recruiting studies for Darifenacin Hydrobromide and check eligibility with the study team.
Trial details
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Recruiting NCT NCT06249867
A Study to Assess the Safety, Tolerability, and Pharmacology of Darifenacin in Patients With ALS
Not yet reported Oliver Blanchard 60 participants Est. completion 2027-11 2 sites Stand-aloneOther conditions: Amyotrophic Lateral SclerosisView official trial listing → -
Completed NCT NCT00127270
Using Behavioral Therapy in Combination With Darifenacin for Symptoms of Overactive Bladder
Not yet reported Novartis 395 participants Est. completion 2006-02 67 sites Stand-aloneOther conditions: Urinary IncontinenceView official trial listing → -
Completed NCT NCT00170755
A Long-Term Safety, Tolerability and Efficacy Study of Darifenacin in Adult Patients With Overactive Bladder
Not yet reported Novartis 718 participants Est. completion 2005-01 1 site Stand-aloneOther conditions: Overactive Bladder SyndromeView official trial listing → -
Completed NCT NCT00170768
Cognitive Effects of Darifenacin and Oxybutynin Extended Release in Volunteers Aged 60 and Over
Not yet reported Novartis 150 participants Est. completion 2005-05 1 site Stand-aloneOther conditions: Healthy VolunteersView official trial listing → -
Completed NCT NCT00171145
A 12-Week Study to Evaluate the Efficacy of Darifenacin to Increase the Warning Time in Patients With Overactive Bladder.
Not yet reported Novartis 445 participants Est. completion 2004-12 1 site Stand-aloneOther conditions: Overactive Bladder SyndromeView official trial listing → -
Completed NCT NCT00171184
Efficacy, Safety, and Tolerability of Darifenacin in Patients Aged > 65 Years With Overactive Bladder
Not yet reported Novartis 400 participants Est. completion 2006-06 1 site Stand-aloneOther conditions: Overactive BladderView official trial listing → -
Completed NCT NCT00366002
Patient's Perception of Treatment Outcome With Darifenacin by Patients With Overactive Bladder
Not yet reported Novartis 500 participants Est. completion 2007-09 82 sites Stand-aloneOther conditions: Overactive Bladder (OAB)View official trial listing → -
Completed NCT NCT00413426
Study to Compare How the Body Changes the Blood Level of Darifenacin Tablet Form vs. the Modified Release Liquid Form in Healthy Subjects
Not yet reported Novartis 28 participants Est. completion 2007-09 1 siteOther conditions: HealthyView official trial listing → -
Completed NCT NCT00413790
Pharmacologic Effects of Darifenacin and Tolterodine on Cardiovascular Parameters in Healthy Subjects
Not yet reported Novartis 162 participants Est. completion 2007-09 12 sites Stand-aloneOther conditions: HealthyView official trial listing → -
Completed NCT NCT00547378
InSite for Over Active Bladder
Not yet reported MedtronicNeuro 571 participants Est. completion 2016-08Other conditions: Urinary Incontinence, Urgency-frequency, Overactive BladderView official trial listing → -
Completed NCT NCT00703703
Pharmacologic Effects of Darifenacin and Tolterodine on Cardiovascular Parameters in Healthy Subjects
Not yet reported Novartis 117 participants Est. completion 2008-10 21 sites Stand-aloneOther conditions: HealthyView official trial listing → -
Terminated NCT NCT00712322
A Two-week Open-label Pharmacodynamic and Pharmacokinetic Study of Multiple Doses of a Darifenacin Liquid Oral Suspension in Children (2 - 15 Years) With Neurogenic Detrusor Overactivity
Not yet reported Warner Chilcott 35 participants Est. completion 2013-05-23 12 sites Stand-aloneOther conditions: Neurogenic Detrusor OveractivityView official trial listing → -
Completed NCT NCT00786448
Post Marketing Surveillance Study on Emselex After Launch in Germany
Bayer 5821 participants Est. completion 2006-02 1 siteOther conditions: Overactive BladderView official trial listing → -
Completed NCT NCT00800462
Comparative Study of the Efficacy and Safety of Muscarinic M3 Receptors Antagonists in the Treatment of Neurogenic Detrusor Overactivity
Not yet reported Toronto Rehabilitation Institute 23 participants Est. completion 2012-12 2 sitesOther conditions: Spinal Cord Injury, Neurogenic Detrusor OveractivityView official trial listing → -
Terminated NCT NCT00845338
Study of Darifenacin in Patients Suffering From Multiple Sclerosis and Neurogenic Detrusor Overactivity
Not yet reported Bayer 7 participants Est. completion 2007-10 15 sites Stand-aloneOther conditions: Multiple Sclerosis, Overactive DetrusorView official trial listing → -
Completed NCT NCT00892450
Anticholinergic Therapy for Overactive Bladder in Parkinson's Disease
Not yet reported US Department of Veterans Affairs 12 participants Est. completion 2014-09 1 site Stand-aloneOther conditions: Parkinson's Disease, Overactive BladderView official trial listing → -
Completed NCT NCT00921245
FREEDOM - First Real-Life Evaluation of Enablex Done in ZA Overactive Bladder Patients During a 3 Months Period
Bayer 9 participants Est. completion 2009-02 1 siteOther conditions: Overactive BladderView official trial listing → -
Withdrawn NCT NCT01018225
Exploratory Study Evaluating the Effects of Darifenacin on Nocturia, Sleep and Daytime Wakefulness
Not yet reported Cognitive Research Corporation Est. completion 2010-07 Stand-aloneOther conditions: NocturiaView official trial listing → -
Terminated NCT NCT01189071
Preoperative Use of Darifenacin (Enablex) to Alleviate Postoperative Ureteral Stent Pain
Not yet reported University of Missouri-Columbia 3 participants Est. completion 2011-07 1 siteOther conditions: Overactive Bladder, Renal Colic, Pain, PostoperativeView official trial listing → -
Status unknown NCT NCT01227811
Single Dose Two-periods Crossover Bioequivalence Study of Darifenacin Tablets in Healthy Volunteers.
Not yet reported Center for Clinical Pharmacology Research Bdbeq S.A. 24 participants Est. completion 2011-03 1 site Stand-aloneOther conditions: BioequivalencyView official trial listing → -
Status unknown NCT NCT01229280
Single Dose Bioequivalence Study of Darifenacin Tablets 7.5 mg in Fed Healthy Volunteers.
Not yet reported Center for Clinical Pharmacology Research Bdbeq S.A. 24 participants Est. completion 2011-02 1 site Stand-aloneOther conditions: BioequivalencyView official trial listing → -
Completed NCT NCT02143570
Efficacy of Darifenacin and Physiotherapy for the Treatment of Overactive Bladder in Women
Not yet reported Universidad de Valparaiso 80 participants Est. completion 2016-04 1 site Stand-aloneOther conditions: Overactive BladderView official trial listing → -
Completed NCT NCT02386072
A Prospective, Observational, Multicenter Study of Patients Following Initiation of a New Course of Treatment for Overactive Bladder (OAB)
Astellas Scientific & Medical Affairs, Inc. 1524 participants Est. completion 2017-08-04 92 sitesOther conditions: Urinary Bladder Overactive, Overactive Bladder, Urinary Bladder Diseases, Urologic DiseasesView official trial listing → -
Completed NCT NCT03543566
Bladder Antimuscarinic Medication and Accidental Bowel Leakage
University of Alabama at Birmingham 32 participants Est. completion 2019-01-18 1 siteOther conditions: Urinary Incontinence, Urge, Fecal IncontinenceView official trial listing → -
Completed NCT NCT03572231
A Registry Study of Patients Initiating a Course of Drug Therapy for Overactive Bladder in Taiwan, Korea and China
Astellas Pharma Singapore Pte. Ltd. 805 participants Est. completion 2020-03-30 15 sitesOther conditions: Overactive Bladder (OAB)View official trial listing → -
Completed NCT NCT03602508
Treatment Persistence Among Patients With Overactive Bladder: A Retrospective Secondary Data Analysis in Asia Oceania
Astellas Pharma Singapore Pte. Ltd. 5589 participants Est. completion 2019-09-13 2 sitesOther conditions: Overactive Bladder (OAB)View official trial listing → -
Completed NCT NCT03662893
Behavioural Therapy With Checklist for Overactive Bladder
Not yet reported Ankara Training and Research Hospital 120 participants Est. completion 2018-04-15 1 siteOther conditions: Overactive BladderView official trial listing → -
Completed NCT NCT06616675
Darifenacin x Parasacral Transcutaneous Electric Nerve Stimulation for OAB in Patients Infected With Human T-Lymphotropic Virus 1
Not yet reported Hospital Universitário Professor Edgard Santos 42 participants Est. completion 2023-12-20 1 siteOther conditions: HTLV-1, Overactive Bladder SyndromeView official trial listing → -
Completed NCT NCT07016451
Efficacy of Low-Intensity Shockwave Therapy in Treating Radiation Cystitis
Not yet reported Thanakrit Visuthikosol 25 participants Est. completion 2026-03-31 1 site Stand-aloneOther conditions: Radiation CystitisView official trial listing → -
Completed NCT NCT07206706
Efficacy and Tolerability of Tadalafil Versus Darifenacin in Management of Ureteric Stent-Related LUTS
Not yet reported, Not yet reported Ain Shams University 150 participants Est. completion 2022-12-28 1 site Stand-aloneOther conditions: Management of Ureteric Stent Related LUTS and PainView official trial listing →
Efficacy history
Not yet reported.
Safety
Not yet reported.
Sources
Also known as: Darifenacin Hydrobromide, Darifenacin, Darifenacin 7.5 MG Extended Release Oral Tablet
Related On The Pen coverage
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This drug may be investigational and not yet approved for any use. Whether someone can join a clinical trial is determined only by that trial's own study team — On The Pen does not determine eligibility. Information here can change; always confirm current details on the official ClinicalTrials.gov listing or with the sponsor.
