Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 40/100

Failure Rate

10.5%

2 terminated/withdrawn out of 19 trials

Success Rate

80.0%

-6.5% vs industry average

Late-Stage Pipeline

11%

2 trials in Phase 3/4

Results Transparency

113%

9 of 8 completed trials have results

Key Signals

5 recruiting9 with results

Enrollment Performance

Analytics

N/A
10(83.3%)
Phase 4
2(16.7%)
12Total
N/A(10)
Phase 4(2)

Activity Timeline

Global Presence

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Clinical Trials (19)

Showing 19 of 19 trials
NCT07519954Not Yet Recruiting

Expediting Pregnancy of Unknown Location Risk Stratification Using the ROM-Plus Point of Care Test

Role: collaborator

NCT06905808Recruiting

e-Sense® Normal Values of Urodynamic Pressures Using e-Sense® Catheters

Role: lead

NCT05383274Phase 4Recruiting

Optilume PoST AppRoval Clinical Evaluation of Andrology ParaMeters

Role: collaborator

NCT07020520Not ApplicableRecruiting

EvaluatioN of Optilume Drug-Coated Balloon for the Endoscopic Treatment of UREteric Strictures

Role: collaborator

NCT06281691Completed

GreenBladder - Early Detection of Bladder Cancer in Residents in Greenland Using a Urinary Marker and a Mobile Cystoscopy Unit

Role: collaborator

NCT03499964Not ApplicableActive Not Recruiting

ROBUST III- Re-Establishing Flow Via Drug Coated Balloon For The Treatment Of Urethral Stricture Disease

Role: collaborator

NCT07206615Enrolling By Invitation

Spot Ex PMCF 01 Study

Role: lead

NCT06805240Recruiting

EvaluatIng Normal Values for traditionaL anorectaL fUnction paraMeters With aIr Charged aNd Solid State HRAM catheTErs ("ILLUMINATE" Study)

Role: lead

NCT06336304Recruiting

NXT Post-Market Clinical Follow-up

Role: lead

NCT05479422Active Not Recruiting

Optilume Registry for Treatment of Stricture of the Anterior Urethra

Role: collaborator

NCT04438499Not ApplicableCompleted

e۰Sense® Catheter Clinical Investigation

Role: lead

NCT03559946Not ApplicableTerminated

Condensed Percutaneous Tibial Nerve Stimulation (PTNS) Protocol

Role: collaborator

NCT03429270Not ApplicableCompleted

T-DOC® 5 Fr Pediatric Clinical Investigation

Role: lead

NCT03615001Not ApplicableCompleted

T-DOC® NXT Clinical Investigation

Role: lead

NCT02756182Not ApplicableCompleted

Air-charged vs Water-filled Catheters (Bonn)

Role: lead

NCT00706407Not ApplicableCompleted

Uro-NIRS Clinical Study

Role: collaborator

NCT02746406Not ApplicableCompleted

A Human Factor Study To Asses The Usability And Feasibility Of The Peritron+ During Intended Use

Role: lead

NCT00871975Phase 4Terminated

Tetra-NIRS Clinical Study

Role: lead

NCT02673944Not ApplicableCompleted

Portable Pves Study

Role: lead

All 19 trials loaded