Key Highlights

Risk & Performance

Pipeline Risk Assessment

Based on historical performance

High Risk

Score: 90/100

Failure Rate

38.5%

10 terminated/withdrawn out of 26 trials

Success Rate

58.3%

-28.2% vs industry average

Late-Stage Pipeline

15%

4 trials in Phase 3/4

Results Transparency

43%

6 of 14 completed trials have results

Key Signals

6 with results7 terminated

Enrollment Performance

Analytics

N/A

5(55.6%)

Phase 4

3(33.3%)

Phase 3

1(11.1%)

9Total

N/A(5)

Phase 4(3)

Phase 3(1)

Activity Timeline

Global Presence

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Clinical Trials (26)

Showing 20 of 26 trials

NCT04122157Completed

Prospective Single-center Long-term Observation of the SL-PLUS® MIA Stem

Role: lead

NCT03247023Terminated

Long Term Follow-up of Integra® Cadence™ Total Ankle System in Primary Ankle Joint Replacement

Role: collaborator

NCT04399928Completed

EU Safety and Efficacy Study Regarding the R3 Acetabular Hip System

Role: lead

NCT05815953Not ApplicableActive Not Recruiting

Polarstem Versus Corail; a Comparison of Micromotion and Periprosthetic Bone Remodelling of Two Femoral Stems

Role: collaborator

NCT03691298Completed

Safety and Performance of the SUTUREFIX ULTRA and SUTUREFIX CURVED Suture Anchors in Shoulder and Hip Arthroscopic Repair

Role: lead

NCT03877484Completed

Evaluation of the Safety and Effectiveness of ALLEVYN Gentle Border

Role: lead

NCT03566082Completed

Post-Approval Study of the R3 Biolox Delta Ceramic Acetabular System - Europe

Role: lead

NCT02211794Active Not Recruiting

Journey II BCS EU Observational Trial

Role: lead

NCT04036279Terminated

NANOS Neck Preserving Hip Stem

Role: lead

NCT04036071Terminated

Clinical Observation Study of the Hydroxylapatite-coated SLPLUS™MIA Hip Shaft

Role: lead

NCT04121585Terminated

Clinical Observation Study of the Hydroxylapatite-coated SL-PLUS™ Hip Shaft

Role: lead

NCT04425603Completed

Anthology Hip Replacement System - Orthopaedic Data Evolution Panel (ODEP) Surveillance Study

Role: lead

NCT04989998Not ApplicableWithdrawn

Patient Outcomes Using HIP7 Software as Compared to Conventional THA

Role: lead

NCT04976972Not ApplicableWithdrawn

A Comparison of Patients Receiving a Total Knee Replacement With Robotic Assistance or With Conventional Instrumentation

Role: lead

NCT04992078Not ApplicableWithdrawn

A Comparison of Patients Receiving a Unicompartmental Knee Replacement With Robotic Assistance or With Conventional Instrumentation

Role: lead

NCT00925496Completed

Patient Benefit From the New Modular Shoulder Prosthesis PROMOS

Role: lead

NCT04172129Completed

Assessment of Implant Fixation and SF-36 for Short Hip-Stems - A Prospective Clinical Study

Role: lead

NCT02664272Completed

Intraoperative Case Series Study: Trial Rasp Position Versus SL-PLUS™ MIA Ti/HA Femoral Hip Stem Position

Role: lead

NCT03065101Not ApplicableTerminated

Trigen InterTAN vs Sliding Hip Screw RCT

Role: lead

NCT02338661Completed

Clinical Observation Study With the SBG Stem

Role: lead