Zimmer Biomet
Trial Pipeline
Zimmer Biomet-RibFix Titan
NCT07485829
Mymobility Knee ROM
NCT06863428
Z1 Hip System: Post-Market Clinical Follow Up Study
NCT07104279
MDR - Comprehensive Primary Revision Stems PMCF
NCT06788717
Persona OsseoTi Keel Compatibility Study (Total Knee Arthroplasty)
NCT05787821
Affixus Natural Nail System Humeral Nail PMCF
NCT05019664
Zimmer Biomet Shoulder Arthroplasty PMCF
NCT04984291
G7 Acetabular System With Vivacit-E or Longevity Liner PMCF Study
NCT04754087
Persona Revision Knee System Outcomes
NCT04821154
JuggerStitch Post Market Clinical Follow-up Study
NCT04228367
MDR - PMCF Study for Taperloc Complete Stems
NCT04028687
Clinical Outcomes Study of the Nexel Total Elbow
NCT02469662
Comprehensive SRS Regenerex Tissue Attachment
NCT06615739
Cemented vs Cementless Persona Keel RCT
NCT05630053
A.L.P.S. Clavicle Plating System PMCF
NCT05327959
Avenir Complete Post-Market Clinical Follow-Up Study
NCT04731077
Persona Ti-Nidium Post-Market Clinical Follow-up
NCT04817969
MDR - Biomet Cannulated Screws
NCT04002518
Post-Market Study of Comprehensive Reverse Augmented Glenoid and Mini Humeral Tray in Total Shoulder Arthroplasty
NCT03726554
Post Market Clinical Follow-up (PMCF) Study of the A.L.P.S. Proximal Humerus Plating System
NCT03626038
SCP Hip Outcomes Study
NCT03494660
Prospective G7 Dual Mobility Total Hip PMCF
NCT03308929
Persona Partial Knee Clinical Outcomes Study
NCT03034811
Persona Total Knee Arthroplasty Outcomes Study
NCT02255383
Zimmer Trabecular Metal Total Ankle PMCF
NCT02038140
Vivacit-E Post-market Follow-up Study
NCT03226808
A Prospective, Clinical Investigation of the Vanguard 360 Revision Knee
NCT01542580
Zimmer Continuum Metal on Polyethylene (MoP) PostMarket Clinical Followup (PMCF) Study
NCT01307384
Database Retrieval for the Comprehensive Shoulder
NCT03409718
Outcomes Study of the Trabecular Metal (TM) Reverse Shoulder System
NCT01480440
ROSA Robot Used in Total Knee Replacement Post Market Study
NCT03969654
A Prospective Multicenter Longitudinal Cohort Study of the Mymobility Platform
NCT03737149
NexGen TM Tibia Clinical Outcomes Study
NCT03272373
BioWick SureLock Clinical Outcomes Study
NCT03199391
Zimmer® MotionLoc® in Distal Tibia Fractures
NCT02717546
BOLD MRI as a Surrogate of Improved Muscle Oxygenation Following Endovascular Therapy for the Treatment of CLI
NCT02601430
Comprehensive Shoulder System Nano IDE
NCT01936259
An MRI Investigation of Soft Tissues in Total Hip Arthroplasty
NCT01750606
Evaluation of Subchondroplasty™ for Defects Associated With Bone Marrow Lesions
NCT01621893
MaxAn Post Market Surveillance Validation
NCT01343693
Continuum™ Metal Bearing System in Total Hip Arthroplasty
NCT03382652
Regenerex Tibial Tray Multi-Center Data Collection
NCT00859963
A Clinical Investigation of ArComXL® Polyethylene in Total Hip Replacement
NCT00698152
Spine Patient Outcomes Registry for Biomet/EBI (Electro-Biology, Inc)
NCT00726284
MIS MiLIF Versus Open
NCT00792129
Performance of the Hedrocel(R) Cervical Fusion Device
NCT00758758
Evaluation Of Spinelink® Fixation In The Treatment Of Degenerative Spondylolisthesis And Spinal Instability
NCT00726310
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 3 | 1 |
Therapeutic Areas
What the Pipeline for Zimmer Biomet Shows
According to the ClinicalTrials.gov registry, Zimmer Biomet is linked to 102 US clinical trials across every stage of research activity. Of those, 67 studies are currently recruiting — about 66% of the sponsor's indexed portfolio — and 17 are already marked complete, representing roughly 17% of the total. Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.
The phase mix for Zimmer Biomet reports 1 late-stage studies (Phase 3 and Phase 4 combined) and 0 earlier-phase studies (Phase 1 and Phase 2). A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work — safety, dosing, and early signal detection — and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.
The top therapeutic focus area indexed for Zimmer Biomet is Rheumatoid Arthritis with 13 linked trials, and 9 other condition areas appear in the top list above. That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice — verify current details directly with ClinicalTrials.gov before relying on any figure here.
Read our methodology — how this data is sourced, computed, and verified.