Key Insights

Highlights

Success Rate

94% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Low Risk

Score: 17/100

Termination Rate

4.5%

1 terminated out of 22 trials

Success Rate

93.8%

+7.2% vs benchmark

Late-Stage Pipeline

27%

6 trials in Phase 3/4

Results Transparency

40%

6 of 15 completed with results

Key Signals

6 with results94% success

Data Visualizations

Phase Distribution

21Total
Not Applicable (4)
P 1 (8)
P 2 (3)
P 3 (5)
P 4 (1)

Trial Status

Completed15
Recruiting3
Active Not Recruiting2
Terminated1
Withdrawn1

Trial Success Rate

93.8%

Benchmark: 86.5%

Based on 15 completed trials

Clinical Trials (22)

Showing 20 of 20 trials
NCT05621616Phase 3Active Not RecruitingPrimary

A Study to Learn How Effective and Safe the Drug 'Mirabegron' is and How Long it Stays in the Body of Children Aged 6 Months to Less Than 3 Years of Age With Neurogenic Detrusor Overactivity

NCT06596291Phase 1RecruitingPrimary

Dose Escalation Study of EG110A, Administered by Intradetrusor Injections to Adults With Neurogenic Detrusor Overactivity-related Incontinence Following Spinal Cord Injury Who Regularly Perform Clean Intermittent Catheterization

NCT06059066Not ApplicableCompleted

Optimization of OnabotulinumtoxinA (BTX-A) Injection for the Treatment of Neurogenic Lower Urinary Tract Dysfunction

NCT06515223Not ApplicableRecruiting

Improving Pelvic Rehabilitation Using Epidural Stimulation After Spinal Cord Injury

NCT01565694Phase 3CompletedPrimary

A Study to Assess the Long Term Effect, Safety and Metabolism of a Solifenacin Liquid Suspension in Participants 5 to 18 Years of Age With Neurogenic Detrusor Overactivity

NCT02751931Phase 3CompletedPrimary

Open-label Phase 3 Study With Mirabegron in Children From 3 to Less Than 18 Years of Age With Neurogenic Detrusor Overactivity

NCT02526979Phase 1Completed

A Study to Evaluate the Pharmacokinetics, Safety and Tolerability of Mirabegron Oral Suspension in Pediatric Subjects From 3 to Less Than 12 Years of Age With Neurogenic Detrusor Overactivity (NDO) or Overactive Bladder (OAB)

NCT01981954Phase 3CompletedPrimary

A Clinical Study to Investigate How Solifenacin Fluid is Taken up, How Long it Stays in the Body and How Effective and Safe it is in Treating Children Aged From 6 Months to Less Than 5 Years With Symptoms of Neurogenic Detrusor Overactivity (NDO)

NCT02211846Phase 1CompletedPrimary

A Study to Evaluate the Pharmacokinetics, Safety and Tolerability of Mirabegron OCAS (Oral Controlled Absorption System) in Pediatric Subjects With Neurogenic Detrusor Overactivity or Overactive Bladder

NCT01539707Phase 1Completed

Single Dose Study to Measure Blood Levels and Safety of a Drug for Children With Overactive Bladder

NCT05491525Phase 2RecruitingPrimary

A Study of Vibegron in Pediatric Participants 2 Years to Less Than (<) 18 Years of Age With NDO and on CIC

NCT05502614Not ApplicableActive Not Recruiting

Dorsal Genital Nerve Stimulation for Bladder Management After SCI

NCT00712322Phase 2TerminatedPrimary

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

NCT04478357Phase 1CompletedPrimary

BIOEQUIVALENCE STUDY IN HEALTHY PARTICIPANTS COMPARING 4 MG AND 8 MG FESOTERODINE EXTENDED-RELEASE TABLETS (TOVIAZ™), MANUFACTURED AT ZWICKAU VERSUS FREIBURG

NCT04452838Phase 1CompletedPrimary

Study To Assess The Bioequivalence Under Fed And Fasted Conditions Of The Fesoterodine Beads-In-Capsule SR4 And SR7 Formulations And To Estimate The Bioavailability of SR7 Beads Sprinkled On Apple Sauce Relative To The Beads-In-Capsule SR7 Formulation Administer

NCT03482037Phase 1CompletedPrimary

Effects of Rec 0/0438 in Patients With Neurogenic Detrusor Overactivity Due to Spinal Cord Injury

NCT03168828Phase 1CompletedPrimary

Safety and Tolerability of TAR-302-5018 in Subjects With Neurogenic Detrusor Overactivity Resulting From Spinal Cord Injury

NCT01043848Not ApplicableWithdrawnPrimary

Treatment of Neurogenic Detrusor Overactivity: Early Versus Late Pudendal Nerve Stimulation in Spinal Cord Injury (SCI) Patients

NCT02138149Completed

Is the Nerve Growth Factor (NGF) a Useful Biomarker in Neurogenic Bladder Dysfunction After Spinal Cord Injury?

NCT00800462Phase 4Completed

Comparative Study of the Efficacy and Safety of Muscarinic M3 Receptors Antagonists in the Treatment of Neurogenic Detrusor Overactivity

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