MiMedx Group
MiMedx Group sponsors 32 registered US clinical trials on ClinicalTrials.gov, 1 of them currently recruiting, and 26 completed. 2 of these trials are in Phase 3-4 (later-stage) and 3 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Scarring, with 2 trials.
Trial Pipeline
32 total, page 1 of 1
Modified Platform Trial Evaluating PpLHACM and SOC Versus SOC Alone in the Treatment of Nonhealing DFUs
NCT06600724
Phase 2B Micronized DHACM vs. Saline in the Treatment of Knee Osteoarthritis
NCT05796765
Micronized dHACM vs. Saline in the Treatment of Osteoarthritis of the Knee
NCT03485157
Use of Human Dehydrated Amnion Chorion Allograft in Laryngectomy/Pharyngectomy
NCT03479463
Use of Human Dehydrated Amnion Chorion Allograft in Closed Hemorroidectomy
NCT03479489
Micronized dHACM Injectable for the Treatment of Achille Tendonitis
NCT03414255
Micronized dHACM Injectable for the Treatment of Plantar Fasciitis
NCT03414268
A Single Center, Prospective, Case Series of the Treatment of Pressure Ulcers and Decubitus Ulcers.
NCT03529578
Use of Human Dehydrated Amnion/Chorion (DHACM) Allograft in Partial Nephrectomy
NCT03323021
Use of Human Dehydrated Umbilical Cord Allograft in Supraspinatus Tendon Repair
NCT03084068
Protocol for the Clinical Evaluation of Lyophilized Amniotic Fluid in the Treatment of Knee Osteoarthritis
NCT03074526
Dehydrated Human Umbilical Cord Allograft in the Management of Diabetic Foot Ulcers
NCT02844660
Case Series of Weekly Applications of dHACM in Treatment of Pressure Ulcers
NCT02861560
Evaluation of Amniotic Fluid Product in Knee Osteoarthritis
NCT02768155
Dehydrated Human Amnion Chorion Membrane (dHACM) vs. Control in the Treatment of Partial Thickness Burns.
NCT02765737
DHACM in Robotic Assisted Laparoscopic Prostatectomy (RALP)
NCT02526173
dHACM Mesh In the Treatment of Diabetic Foot Ulcers
NCT02589210
Micronized dHACM Injectable for the Treatment of Plantar Fasciitis
NCT02427191
dHACM in Lumbar Decompression and Microdiscectomy Surgery
NCT02300909
Amniotic Membrane in Decompressive Craniectomy to Reduce Scarring
NCT02033824
Use of dHACM in the Treatment of Venous Leg Ulcers
NCT02011503
Amniotic Membrane in Total Knee Replacements to Reduce Scarring
NCT02088567
Dehydrated Human Amnion/Chorion Membrane Micrografts(dHACM) Injectable in the Treatment of Recalcitrant Plantar Fasciitis
NCT01996111
DHACM vs Other Commercially Available Treatments
NCT01921491
Micronized Dehydrated Human Amniotic Membrane Suspension in the Treatment of Lateral Epicondylitis
NCT01921569
Randomized Clinical Trial Using Amniotic Membrane in Robotic Assisted Laparoscopic Prostatectomy
NCT01832168
Comparative Study of Amniotic Membrane Injectable in the Treatment of Recalcitrant Plantar Fasciitis
NCT01659827
Comparative Study of Two Application Regimens of Amniotic Membrane Wound Graft In the Management of Diabetic Foot Ulcers
NCT01657474
Trial of Dehydrated Human Amnion/Chorion Membrane (dHACM) In the Management of Diabetic Foot Ulcers
NCT01693133
Comparative Study of Amniotic Membrane Wound Graft In the Management of Diabetic Foot Ulcers
NCT01552499
Human Amniotic Membrane Grafting and Standard of Care Versus Standard of Care Alone in the Treatment of Venous Leg Ulcers
NCT01552447
An Evaluation of the Effect of the AmnioFix Amniotic Membrane Allograft in Patients Undergoing Posterior Instrumentation Removal
NCT01357187
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 2 | 3 |
| Phase 3 | 2 |
Therapeutic Areas
What the Pipeline for MiMedx Group Shows
According to the ClinicalTrials.gov registry, MiMedx Group is linked to 32 US clinical trials across every stage of research activity. Of those, 1 studies are currently recruiting, about 3% of the sponsor's indexed portfolio, and 26 are already marked complete, representing roughly 81% of the total.
The phase mix for MiMedx Group reports 2 late-stage studies (Phase 3 and Phase 4 combined) and 3 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for MiMedx Group is Scarring 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.