Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

High Risk

Score: 90/100

Failure Rate

55.6%

15 terminated/withdrawn out of 27 trials

Success Rate

34.8%

-51.7% vs industry average

Late-Stage Pipeline

0%

0 trials in Phase 3/4

Results Transparency

63%

5 of 8 completed trials have results

Key Signals

5 with results15 terminated

Enrollment Performance

Analytics

N/A
2(100.0%)
2Total
N/A(2)

Activity Timeline

Global Presence

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Clinical Trials (27)

Showing 20 of 27 trials
NCT07563803Not Yet Recruiting

The restor3d Outcomes Registry

Role: lead

NCT06311331Enrolling By Invitation

Prospective Evaluation of Clinical and Radiographic Outcomes Following Total Talus Replacement (PROCLAIM)

Role: lead

NCT02494544Not ApplicableTerminated

A Multicenter Study to Evaluate Functional Outcome After Knee Replacement

Role: lead

NCT03289754Not ApplicableTerminated

A Prospective Study to Evaluate the iTotal Knee and iPoly XE Tibial Inserts

Role: lead

NCT05114356Terminated

Cervical Interbody Fusion Device Patient Registry

Role: lead

NCT05231304Completed

Retrospective Evaluation of Clinical and Radiographic Outcomes Following Total Talus Replacement

Role: lead

NCT03738462Terminated

A Study to Evaluate the Conformis Hip System

Role: lead

NCT04180423Terminated

TKA Operating Room Efficiency for TKA Using Customized Implant Techniques

Role: lead

NCT01861028Terminated

Study Comparing Fit of the iTotal Versus Standard Total Knee Implants

Role: lead

NCT03289000Completed

A Retrospective Study to Evaluate the ConforMIS iTotal® Posterior Stabilized (PS) Knee Replacement System

Role: lead

NCT01564654Completed

A Retrospective Study of the iTotal CR Knee Replacement System

Role: lead

NCT02251522Completed

A Single Time-Point Study to Evaluate the ConforMIS iTotal® (CR) Knee Versus Off-the-Shelf

Role: lead

NCT01899417Completed

Costs and Benefits of ConforMIS iTotal® Knee Replacement System Versus Standard Total Knee

Role: lead

NCT03152357Completed

A Retrospective Study to Evaluate the ConforMIS iUni, iDuo & iTotal® KRS

Role: lead

NCT01117571Terminated

Multi-Center Study to Evaluate the ConforMIS iUni Knee Implant

Role: lead

NCT01717001Completed

Comparison of Knee Kinematics for Subjects Implanted With Either a ConforMIS or Traditional Knee Implant

Role: lead

NCT01820676Terminated

iUni G2+ Prospective Study

Role: lead

NCT01564641Terminated

Study of the ConforMIS iDuo(R) G2

Role: lead

NCT04667559Terminated

A Study to Evaluate the Conformis iTotal Identity Knee Replacement System

Role: lead

NCT03146819Terminated

A Single Time-Point Study to Evaluate the ConforMIS iTotal (PS) Knee Replacement System Versus Off-the-Shelf

Role: lead