Bioness Inc
9
0
0
6
Key Highlights
Risk & Performance
Pipeline Risk Assessment
Pipeline Risk Assessment
Based on historical performance
Moderate Risk
Score: 50/100
11.1%
1 terminated/withdrawn out of 9 trials
85.7%
-0.8% vs industry average
11%
1 trials in Phase 3/4
67%
4 of 6 completed trials have results
Key Signals
Enrollment Performance
Analytics
Activity Timeline
Global Presence
Clinical Trials (9)
StimRouter Registry Clinical Protocol
Role: lead
Overactive Bladder Treatment Using StimRouter Neuromodulation System: A Prospective Randomized Trial
Role: lead
StimRouter™ for Pain Management in Post-stroke Shoulder Pain
Role: lead
Acute Human Study: StimRouter for Peripheral Nerve Stimulation of Discrete Peripheral Nerves
Role: lead
Clinical Study of the L300 Versus Ankle-foot Orthosis (AFO) on Post-Stroke Subjects With Foot Drop
Role: lead
Evaluation of Usability and Human Factors in the Novus System
Role: collaborator
Bioness® StimRouter™ Neuromodulation System for Chronic Pain Therapy
Role: lead
An Implantable Microneuromodulator for the Treatment of Chronic Shoulder Pain in Chronic Post-Stroke Subjects
Role: lead
Evaluation of the Safety and Performance of the NESS L300 Plus System
Role: lead
All 9 trials loaded