Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Low Risk

Score: 15/100

Failure Rate

10.3%

6 terminated/withdrawn out of 58 trials

Success Rate

87.5%

+1.0% vs industry average

Late-Stage Pipeline

16%

9 trials in Phase 3/4

Results Transparency

83%

35 of 42 completed trials have results

Key Signals

4 recruiting35 with results

Enrollment Performance

Analytics

N/A
44(80.0%)
Phase 4
8(14.5%)
Phase 2
2(3.6%)
Phase 3
1(1.8%)
55Total
N/A(44)
Phase 4(8)
Phase 2(2)
Phase 3(1)

Activity Timeline

Global Presence

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Clinical Trials (58)

Showing 20 of 58 trials
NCT06661473Not ApplicableCompleted

Interventional Study Exploring the Occurrence of Surgical Site Infections.

Role: lead

NCT07034014Not ApplicableRecruiting

An Investigation to Evaluate Wearing Properties of Three Different Investigational Devices

Role: lead

NCT04839523Not ApplicableActive Not Recruiting

Performance and Safety of Exufiber Ag+ and Exufiber on Partial Thickness Burns

Role: lead

NCT04181320Not ApplicableTerminated

A Multicentre European Study to Evaluate Granulox® Used in the Treatment Pathway of Predominantly Chronic Venous Leg Ulcers (VLUs).

Role: lead

NCT06321978Recruiting

Mepilex Border Flex Utilization Pilot Spain

Role: lead

NCT05608317Not ApplicableRecruiting

A Clinical Investigation to Follow the Progress of Exuding Chronic Venous Leg Ulcers Using a Non-Bordered Foam Dressing

Role: lead

NCT06392165Not ApplicableNot Yet Recruiting

Evaluation of Adhesion Properties in Wound Care Devices

Role: lead

NCT04753294Not ApplicableCompleted

Confirm Safety and Performance of Avance Solo and Avance Solo Adapt NPWT Systems

Role: lead

NCT04884568Not ApplicableCompleted

Confirm Performance and Safety of Exufiber When Used as Intended on Donor Sites

Role: lead

NCT03344354Not ApplicableCompleted

Durability of Double-gloving With Biogel® Surgical Gloves When Used by Clinicians/Surgeons

Role: lead

NCT05588583Not ApplicableRecruiting

A Clinical Investigation to Follow the Progress of Exuding Chronic Wounds Using Mepilex® Up as the Primary Dressing.

Role: lead

NCT05494450Not ApplicableTerminated

An Open, Non-comparative, Multicenter Investigation to Evaluate the Safety and Performance of Exufiber Ag+, a Gelling Fiber Silver Dressing, When Used in Medium to High Exuding Chronic Wounds

Role: lead

NCT04754048Not ApplicableCompleted

Confirm the Safety and Performance of Avance Solo NPWT System

Role: lead

NCT04960553Not ApplicableTerminated

A PMCF Investigation on Exuding Chronic Wounds Using Exufiber® as Primary Dressing, and Mepilex® Border Flex/Comfort

Role: lead

NCT04994145Unknown

A Post-Market Clinical Investigation on Mepilex Border Post-Op

Role: lead

NCT04942496Phase 4Unknown

A 96-hour Patch Test Study Using Healthy Human Volunteers to Assess the Skin Irritation Potential of 11 Topically Applied Formulations

Role: lead

NCT03738163Not ApplicableCompleted

A Clinical Investigation With Epaderm® Cream

Role: lead

NCT04894604Not ApplicableUnknown

A Safety and Performance PMCF Investigation of the Avance® Solo NPWT System in Surgically Closed Incisions

Role: lead

NCT04813809Not ApplicableCompleted

A Clinical Investigation With BARRIER® EasyWarm®

Role: lead

NCT03662997Not ApplicableCompleted

Clinical Study to Compare 3 Multi-Layered Foam Dressings for the Management of Chronic Wounds

Role: lead