Exactech
Exactech sponsors 12 registered US clinical trials on ClinicalTrials.gov, 5 of them currently recruiting, and 1 completed. 1 of these trials are in Phase 3-4 (later-stage) and 0 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Knee Arthroplasty, Total, with 2 trials.
Trial Pipeline
12 total, page 1 of 1
Exactech Hip Systems Post-Market Clinical Follow-up (PMCF)
NCT05849961
Exactech Proximal Humerus Fracture Plate System Post Market Clinical Follow-up
NCT05703958
A Post-Market Domestic (US) and International Data Collection to Assess the Truliant Knee System
NCT05653102
Exactech Vantage Total Ankle System Post Market Clinical Follow-Up - US Only
NCT05619588
Exactech Shoulder Post Market Clinical Follow-up Study
NCT05603728
Optetrak Knee System Post Market Clinical Follow-Up
NCT05788757
Exactech Humeral Reconstruction Prosthesis of Shoulder Arthroplasty PMCF (HRP)
NCT05615246
Study to Assess Exactech's Guided Personalized Surgery eGPS® in Total Knee Arthroplasty
NCT02962362
Standard Total Knee Arthroplasty Using Platelet Rich Plasma (PRP)
NCT01075230
Platelet Rich Plasma (PRP) in Total Knee Replacement
NCT00826098
Post Approval Study: NOVATION Ceramic Articulation Hip System
NCT00715143
Evaluation of Radiographic and Patient Outcomes Following Lumbar Spine Fusion Using Demineralized Bone Matrix (DBM) Mixed With Autograft
NCT00254852
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 4 | 1 |
What the Pipeline for Exactech Shows
According to the ClinicalTrials.gov registry, Exactech is linked to 12 US clinical trials across every stage of research activity. Of those, 5 studies are currently recruiting, about 42% of the sponsor's indexed portfolio, and 1 are already marked complete, representing roughly 8% of the total.
The phase mix for Exactech reports 1 late-stage studies (Phase 3 and Phase 4 combined) and 0 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for Exactech is Knee Arthroplasty, Total with 2 linked trials, and 9 other condition areas appear in the top list above.
How to read these pipeline numbers
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.
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.
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.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.