Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

High Risk

Score: 80/100

Failure Rate

35.3%

6 terminated/withdrawn out of 17 trials

Success Rate

57.1%

-29.4% vs industry average

Late-Stage Pipeline

0%

0 trials in Phase 3/4

Results Transparency

75%

6 of 8 completed trials have results

Key Signals

2 recruiting6 with results4 withdrawn

Enrollment Performance

Analytics

N/A
12(100.0%)
12Total
N/A(12)

Activity Timeline

Global Presence

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Clinical Trials (17)

Showing 17 of 17 trials
NCT04194138Recruiting

Complex Adult Deformity Surgery (CADS)

Role: collaborator

NCT06298812Not ApplicableRecruiting

REFLECT Scoliosis System Post Approval Study

Role: lead

NCT04088383Not ApplicableCompleted

Amnios™ RT Outcomes Study

Role: lead

NCT04257279Not ApplicableUnknown

Prospective Robotic Global Research Study (PROGRESS)

Role: lead

NCT03162666Withdrawn

Patient Outcomes Using an Expandable Spacer

Role: lead

NCT02184520Not ApplicableTerminated

A Prospective Randomized Postmarket Clinical Study of the TRANSITION Stabilization System

Role: lead

NCT02075554Not ApplicableCompleted

Study of an Expandable Interbody Device for the Lumbar Spine

Role: lead

NCT01861899Completed

Treatment of Sacroiliac Dysfunction With SI-LOK® Sacroiliac Joint Fixation SI-SI-LOK

Role: lead

NCT00401518Not ApplicableCompleted

A Pivotal Study of a Facet Replacement System to Treat Spinal Stenosis

Role: lead

NCT01441999Not ApplicableWithdrawn

Proximal Junctional Kyphosis Following Long Instrumented Spinal Fusion: The Effect of Implant Selection

Role: lead

NCT01198470Not ApplicableCompleted

TRIUMPH Lumbar Artificial Disc IDE: A Pilot Study

Role: lead

NCT03230279Not ApplicableWithdrawn

Sacroiliac Joint Fusion Comparison Study

Role: collaborator

NCT01156675Not ApplicableTerminated

Study Evaluating the Safety and Effectiveness of the FLEXUS(TM) Interspinous Spacer

Role: lead

NCT03371316Not ApplicableWithdrawn

Preliminary Investigation of ViaShield™ Amnion Patch as an Anti-Adhesive Barrier in Hemicraniectomies

Role: lead

NCT00882661Not ApplicableCompleted

SECURE®-C Cervical Artificial Disc Clinical Study/ SECURE-C Cervical Artificial Disc Postmarket Approval Study

Role: lead

NCT02388022Completed

A Retrospective Study Using CALIBER® TLIF Expandable Spacer in the Treatment of DDD: 2 Year Follow-up.

Role: lead

NCT02299323Completed

INDEPENDENCE Spacer for Lumbar Fusion

Role: lead

All 17 trials loaded