Key Highlights

Risk & Performance

Pipeline Risk Assessment

Based on historical performance

High Risk

Score: 70/100

Failure Rate

29.8%

17 terminated/withdrawn out of 57 trials

Success Rate

67.3%

-19.2% vs industry average

Late-Stage Pipeline

18%

10 trials in Phase 3/4

Results Transparency

60%

21 of 35 completed trials have results

Key Signals

2 recruiting21 with results15 terminated

Enrollment Performance

Analytics

N/A

31(70.5%)

Phase 3

6(13.6%)

Phase 4

4(9.1%)

Phase 2

3(6.8%)

44Total

N/A(31)

Phase 3(6)

Phase 4(4)

Phase 2(3)

Activity Timeline

Global Presence

Loading network data...

Clinical Trials (57)

Showing 20 of 57 trials

NCT04929678Not ApplicableTerminated

Study of the Braive Growth Modulation System for Progressive Pediatric Scoliosis

Role: lead

NCT07414745Not ApplicableNot Yet Recruiting

MDT-0123 Japan Study

Role: lead

NCT05856370Not ApplicableRecruiting

The Ailliance Post-Market Clinical Study

Role: lead

NCT04073563Not ApplicableActive Not Recruiting

Transforaminal Lumbar Interbody Fusion (TLIF)

Role: lead

NCT02617563Completed

5-Year Global Study on MAST™ Minimally Invasive Fusion Procedures to Treat Degenerative Lumbar Spine (MASTERS-D2)

Role: lead

NCT03118505Not ApplicableActive Not Recruiting

A Study of Infuse® Bone Graft With Mastergraft® Strip and Posterior Fixation for Posterolateral Fusion (PLF) Treatment of Multi-Level Degenerative Lumbosacral Spinal Conditions

Role: lead

NCT05299762Recruiting

A Post Market Surveillance on INFUSE Bone Graft

Role: lead

NCT03062657Not ApplicableTerminated

An Investigation of the Metal Concentration in Patients Implanted With the PRESTIGE LP™ Cervical Disc at Two Contiguous Levels in the Cervical Spine

Role: lead

NCT00667459Phase 3Completed

Study of Safety & Effectiveness of PRESTIGE® LP Cervical Disc vs. Anterior Cervical Fusion in Cervical DDD

Role: lead

NCT01491386Not ApplicableCompleted

Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fusion in Patients With Symptomatic Degenerative Disc Disease

Role: lead

NCT01494493Not ApplicableTerminated

Pivotal Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody Fusion in Patients With Symptomatic Degenerative Disc Disease

Role: lead

NCT01491399Not ApplicableCompleted

INFUSE™ BONE GRAFT/CORNERSTONE-SR™ Allograft Ring/ATLANTIS™ Anterior Cervical Plate- Pilot Study

Role: lead

NCT01495234Not ApplicableCompleted

Pilot Study of rhBMP-2/BCP in Patients With Spinal Degeneration With Instability Requiring Surgical Fusion

Role: lead

NCT01494454Not ApplicableCompleted

Clinical Study of rhBMP-2/BCP With the TSRH® Spinal System for Posterolateral Lumbar Fusion in Patients With Degenerative Disc Disease

Role: lead

NCT01494441Not ApplicableCompleted

Pilot Study of rhBMP/BCP With or Without the TSRH® Spinal System for Posterolateral Lumbar Fusion in Patients With Degenerative Disc Disease

Role: lead

NCT01491542Not ApplicableCompleted

INFUSE® Bone Graft and MASTERGRAFT® Granules With CD HORIZON® for Posterolateral Lumbar Fusion in Patients With Degenerative Disc Disease - Pilot Study

Role: lead

NCT01491425Not ApplicableCompleted

A Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fusion in Patients With Degenerative Disc Disease

Role: lead

NCT01491451Not ApplicableCompleted

A Pilot Study of rhBMP-2/ACS With the INTERFIX™ Device for the AnteriorLumbar Interbody Fusion in Patients With Degenerative Disc Disease

Role: lead

NCT01491464Not ApplicableTerminated

A Pivotal Study of rhBMP-2/ACS/INTER FIX™ Device for Posterior Lumbar Interbody Fusion in Patients With Degenerative Disc Disease

Role: lead

NCT01494428Not ApplicableCompleted

A Pilot Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody Fusion in Patients With Symptomatic Degenerative Disc Disease

Role: lead