Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 50/100

Failure Rate

5.9%

1 terminated/withdrawn out of 17 trials

Success Rate

85.7%

-0.8% vs industry average

Late-Stage Pipeline

6%

1 trials in Phase 3/4

Results Transparency

67%

4 of 6 completed trials have results

Key Signals

3 recruiting4 with results

Enrollment Performance

Analytics

N/A
13(92.9%)
Phase 4
1(7.1%)
14Total
N/A(13)
Phase 4(1)

Activity Timeline

Global Presence

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Clinical Trials (17)

Showing 17 of 17 trials
NCT07102160Recruiting

Cleaner Long-tErm Assessment Registry - Venous Insights and Efficacy With eXtended Tracking

Role: collaborator

NCT04416321Not ApplicableCompleted

A Clinical Study to Evaluate Safety and Performance of PEEK-OPTIMA™ HA Enhanced.

Role: collaborator

NCT06513208Phase 4Recruiting

Ketorolac Effects on Post-operative Pain and Lumbar Fusion

Role: collaborator

NCT07209085Not ApplicableNot Yet Recruiting

A Study to Evaluate the Safety and Effectiveness of the FastWave Artero™ Peripheral Intravascular Lithotripsy (IVL) System in Adults With Peripheral Artery Disease (PAD)

Role: collaborator

NCT05633550Active Not Recruiting

Flexion-Extension Radiograph Imaging Protocol Reliability Study

Role: collaborator

NCT06210685Not ApplicableActive Not Recruiting

The ACES Study for Aseptic Pleural Effusion

Role: collaborator

NCT03115983Not ApplicableActive Not Recruiting

LimiFlex Clinical Trial for the Treatment of Degenerative Spondylolisthesis With Spinal Stenosis

Role: collaborator

NCT03754972Not ApplicableCompleted

Sagittal Plane Shear Index for Planning Lumbar Stenosis Surgery

Role: lead

NCT06962371Not ApplicableRecruiting

Clinical Feasibility and Evaluation Study of POINT-GUARD Embolic Protection Device During TAVR (GUARDIAN)

Role: collaborator

NCT03928041Not ApplicableCompleted

A Clinical Study to Evaluate Safety and Performance of PEEK-OPTIMA™ HA Enhanced Interbody Cages in the Lumbar Spine

Role: collaborator

NCT03734536Not ApplicableTerminated

Treatment of Partial-Thickness Rotator Cuff Tears

Role: collaborator

NCT03112200Not ApplicableCompleted

Subchondroplasty® Knee RCT

Role: collaborator

NCT03864848Not ApplicableUnknown

Epicardial Mitral Repair Trial - ENRAPT-MR

Role: collaborator

NCT05101057Unknown

A Retrospective Study to Examine the Effect of CMF Stimulation on Primary ACDF Patients

Role: collaborator

NCT05144126Not ApplicableUnknown

Safety, Radiological and Patient Reported Outcomes of i-FACTOR+ Matrix Bone Graft Device - A Canadian, Multicenter, Post-Market Clinical Investigation

Role: collaborator

NCT03621202Not ApplicableCompleted

Safety and Accuracy of the Saranas EBBMS for the Detection of Endovascular Procedure Related Bleeding Events

Role: collaborator

NCT03017261Not ApplicableCompleted

TSolution One® Total Knee Arthroplasty

Role: collaborator

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