Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

High Risk

Score: 80/100

Failure Rate

26.6%

47 terminated/withdrawn out of 177 trials

Success Rate

67.1%

-19.4% vs industry average

Late-Stage Pipeline

7%

13 trials in Phase 3/4

Results Transparency

66%

63 of 96 completed trials have results

Key Signals

8 recruiting63 with results38 terminated9 withdrawn

Enrollment Performance

Analytics

N/A
88(87.1%)
Phase 4
9(8.9%)
Phase 3
4(4.0%)
101Total
N/A(88)
Phase 4(9)
Phase 3(4)

Activity Timeline

Global Presence

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Clinical Trials (177)

Showing 20 of 177 trials
NCT03720782Active Not Recruiting

Safety and Performance Study of the Legion Porous System in Total Knee Arthroplasty

Role: lead

NCT04552119Completed

Safety of Treatment of Shoulder Repair

Role: lead

NCT00611585Completed

A Safety and Efficacy Study of the Birmingham Hip Resurfacing System

Role: lead

NCT06700850Not ApplicableCompleted

Human Participant Study of Prototype Non-medicated Multilayer Foam Dressings on Intact Skin

Role: lead

NCT04849884Not ApplicableActive Not Recruiting

To Evaluate the Performance of the CORI™ KNEE TENSIONER as an Accessory to the CORI™ Surgical System.

Role: lead

NCT02353377Active Not Recruiting

OXINIUM◊ DH Total Hip Arthroplasty Pivotal Study

Role: lead

NCT04903106Completed

Safety and Performance Study of the FAST-FIX FLEX System for Meniscal Repairs and Meniscal Transplantations

Role: lead

NCT02204228Terminated

TITAN™ Reverse Shoulder System

Role: lead

NCT06564636Active Not Recruiting

A Multi-Centre Study in Patients Undergoing Total Hip Arthroplasty With the Smith+Nephew CATALYSTEM™ Primary Hip System

Role: lead

NCT04848896Not ApplicableRecruiting

Study to Evaluate the Safety and Effectiveness of the REAL INTELLIGENCE™ CORI™ in Total Knee Arthroplasty (TKA) Procedure

Role: lead

NCT03078543Active Not Recruiting

Ten Year Implant Survivorship of the ANTHEM™ PS Total Knee System

Role: lead

NCT03768128Completed

Safety and Performance of the Journey™ II UNI Unicompartmental Knee System

Role: lead

NCT06916728Enrolling By Invitation

A Post Approval Multicenter 10 Year Follow-up Observational Trial of Marketed Product - MP01 vs. Surgical Standard of Care (SSOC) Used for the Treatment of Joint Surface Lesions of the Knee

Role: lead

NCT04361487Terminated

Circumferential Compression STITCH Repairs of Complex and Horizontal Cleavage Meniscal Tears

Role: lead

NCT05197036Active Not Recruiting

A Global Clinical Study Investigating the Safety and Effectiveness of Smith and Nephew's Porous Knee System in Patients Who Need a Total Knee Replacement Due to Degenerative Arthritis, Post-traumatic Arthritis or Inflammatory Arthritis

Role: lead

NCT03687593Active Not Recruiting

Safety and Performance Using Legion™ CR Oxinium and CoCr Femoral Implants Combined With Legion™/Genesis™ II XLPE High Flex Tibial Inserts

Role: lead

NCT05204797Not ApplicableActive Not Recruiting

Efficacy of Robot-assisted Technique vs Conventional Technique in Preventing Early Micromobilisation After UKA

Role: collaborator

NCT02648152Completed

POLARSTEM Cementless Hip Stem

Role: lead

NCT05444465Not ApplicableRecruiting

Use of the REGENETEN™ Bioinductive Implant System in High Grade Partial-thickness Tears

Role: lead

NCT06510777Not ApplicableTerminated

PICO Venous Leg Ulcers (VLU) Reimbursement Study

Role: lead