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Artivion

🇺🇸United States
Ownership
-
Employees
1.5K
Market Cap
-
Website
Introduction

Artivion, Inc. engages in the research and development of solutions which address cardiac and vascular surgeons' clinical challenges in treating patients with aortic diseases. Its products include aortic stents and stent grafts, prosthetic heart valves, cryopreserved cardiac and vascular allografts, and surgical sealants. It operates through the Medical Devices and Preservation Services segments. The Medical Devices segment includes aortic stents and stent grafts, surgical sealants, and On-X products. The Preservation Services segment offers cardiac and vascular tissue preservation services. The company was founded on January 19, 1984, and is headquartered in Kennesaw, GA.

Clinical Trials

5

Active:1
Completed:2

Trial Phases

2 Phases

Phase 3:1
Not Applicable:3

Drug Approvals

0

Drug Approvals

No drug approvals found

This company may not have drug approvals in our database

Clinical Trials

Distribution across different clinical trial phases (4 trials with phase data)• Click on a phase to view related trials

Not Applicable
3 (75.0%)
Phase 3
1 (25.0%)

Retrospective Evaluation of Photo-oxidized Decellularized Bovine Pericardium in Cardiac Repair or Reconstruction Surgery

Terminated
Conditions
Congenital Heart Disease
Cardiac Anomaly
First Posted Date
2022-04-06
Last Posted Date
2023-01-13
Lead Sponsor
Artivion Inc.
Target Recruit Count
10
Registration Number
NCT05314868
Locations
🇺🇸

Children's Hospital of Boston, Boston, Massachusetts, United States

PERSEVERE- a Trial to Evaluate AMDS in Acute DeBakey Type I Dissection

Not Applicable
Active, not recruiting
Conditions
Acute Aortic Dissection
First Posted Date
2022-01-03
Last Posted Date
2025-01-15
Lead Sponsor
Artivion Inc.
Target Recruit Count
115
Registration Number
NCT05174767
Locations
🇺🇸

University of Alabama at Birmingham, Birmingham, Alabama, United States

🇺🇸

University of Southern California, Los Angeles, California, United States

🇺🇸

Stanford University, Palo Alto, California, United States

and more 22 locations

PROACT Xa - A Trial to Determine if Participants With an On-X Aortic Valve Can be Maintained Safely on Apixaban

Phase 3
Terminated
Conditions
Aortic Valve Disease
Aortic Valve Stenosis
Aortic Valve Failure
Interventions
Device: On-X Aortic Mechanical Valve
First Posted Date
2019-10-29
Last Posted Date
2024-03-20
Lead Sponsor
Artivion Inc.
Target Recruit Count
863
Registration Number
NCT04142658
Locations
🇺🇸

Tucson Heart Center, Tucson, Arizona, United States

🇺🇸

CHI St. Vincent Heart Institute, Little Rock, Arkansas, United States

🇺🇸

Loma Linda University Medical Center, Loma Linda, California, United States

and more 59 locations

Post-market, Prospective Evaluation of PHOTO-oxidized Bovine Pericardium in Vascular Surgery

Not Applicable
Completed
Conditions
Peripheral Arterial Disease
Carotid Artery Diseases
Abdominal Aortic Aneurism
Vascular Diseases
Hemodialysis Access Failure (Disorder)
First Posted Date
2018-09-13
Last Posted Date
2024-10-07
Lead Sponsor
Artivion Inc.
Target Recruit Count
94
Registration Number
NCT03669042
Locations
🇺🇸

University of Arizona, Tucson, Arizona, United States

🇺🇸

Iowa Heart Center, Des Moines, Iowa, United States

🇺🇸

Brigham and Women's Hospital, Boston, Massachusetts, United States

and more 6 locations

Prospective, Multicenter, Multidisciplinary, Controlled Clinical Investigation Evaluating the Safety and Efficacy of PerClot® Polysaccharide Hemostatic System

Not Applicable
Completed
Conditions
Blood Loss, Surgical
First Posted Date
2015-02-10
Last Posted Date
2022-03-17
Lead Sponsor
Artivion Inc.
Target Recruit Count
324
Registration Number
NCT02359994
Locations
🇺🇸

Indiana University d/b/a/ Methodist Research Institute, Indianapolis, Indiana, United States

News

Artivion's AMDS Hybrid Prosthesis Receives FDA Humanitarian Device Exemption for Acute Aortic Dissections

Artivion's AMDS Hybrid Prosthesis has received FDA Humanitarian Device Exemption for treating acute DeBakey Type I aortic dissections with malperfusion.

Endospan Completes Enrollment in TRIOMPHE Trial for NEXUS Aortic Arch Stent Graft

Endospan has concluded enrollment in the primary arm of the TRIOMPHE study, evaluating the NEXUS stent graft for aortic arch disease treatment.

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