Medicrea International
8
0
0
6
Key Highlights
Risk & Performance
Pipeline Risk Assessment
Pipeline Risk Assessment
Based on historical performance
High Risk
Score: 75/100
25.0%
2 terminated/withdrawn out of 8 trials
75.0%
-11.5% vs industry average
0%
0 trials in Phase 3/4
17%
1 of 6 completed trials have results
Key Signals
Enrollment Performance
Analytics
Activity Timeline
Global Presence
Clinical Trials (8)
The Degen Study: Post-market Clinical Follow-up on the PASS LP, PASS Degen and PASS Tulip Systems (PASS DEGEN)
Role: lead
Prospective Clinical Study to Evaluate the Efficacy of the Stand-alone Cervical Interbody Cage C-CURVE ( Titanium) Manufactured by MEDICREA®
Role: lead
UNiD Rods Register
Role: lead
PASS OCT® Post-market Clinical Follow-up
Role: lead
PASS MIS® Post-market Clinical Follow-up
Role: lead
UNiD 3D VBR Register
Role: lead
Sagittal Plane Correction With Pass-LP Device in Adult Deformity Patients
Role: lead
GRANVIA®-C Cervical Disc Prosthesis Multicenter European Pilot Study
Role: lead
All 8 trials loaded