Anteris Technologies Enrolls First Patients in U.S. Heart Valve Trial
Written by Emily J. Thompson, Senior Investment Analyst
Updated: May 05 2026
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Should l Buy AVR?
Anteris Technologies announced that the first patients in the United States have been enrolled and successfully treated in the DurAVR Transcatheter Heart Valve global pivotal trial for patients with severe calcific aortic stenosis. The procedures were performed by Azeem Latib, M.D. at Montefiore Medical Center, New York, United States.
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Analyst Views on AVR
Wall Street analysts forecast AVR stock price to rise
3 Analyst Rating
3 Buy
0 Hold
0 Sell
Strong Buy
Current: 6.580
Low
15.00
Averages
17.33
High
22.00
Current: 6.580
Low
15.00
Averages
17.33
High
22.00
About AVR
Anteris Technologies Global Corp. is a structural heart company, which is engaged in providing cardiac care by science-driven and measurable advancements to restore heart valve patients to healthy function. Its lead asset, the DurAVR Transcatheter Heart Valve System (THV) consists of a single-piece, biomimetic valve made with its ADAPT tissue-enhancing technology and deployed with its ComASUR balloon-expandable delivery system. DurAVR THV is a novel transcatheter aortic valve for the treatment of aortic stenosis that is shaped to mimic the performance of a healthy human aortic valve. DurAVR THV’s single-piece design mimics the native anatomy of a human aortic valve, as compared to traditional three-piece aortic valves. The Company's ADAPT is its proprietary anti-calcification tissue shaping technology that is designed to reengineer xenograft tissue into a pure, single-piece collagen bioscaffold. Its ComASUR delivery system is a physician-developed balloon expandable delivery system.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
Anteris Secures US Medicare Coverage for PARADIGM Trial
- Coverage Milestone: Anteris Technologies has secured US Medicare reimbursement eligibility for its global pivotal PARADIGM Trial, expected to provide treatment for approximately 1,000 patients with the DurAVR® heart valve, significantly enhancing the company's market competitiveness in cardiac care.
- Trial Design and Objectives: This prospective randomized controlled trial will compare the safety and efficacy of DurAVR® against existing TAVR devices, primarily assessing one-year all-cause mortality, stroke, and cardiovascular hospitalization rates to ensure the non-inferiority of DurAVR®.
- Accelerating Operational Momentum: By obtaining Medicare coverage, Anteris anticipates accelerating the activation of US study sites, driving operational momentum across participating centers, and further solidifying its leadership position in the structural heart disease sector.
- Technological Advantages and Market Potential: The DurAVR® heart valve utilizes Anteris' patented ADAPT® tissue technology, clinically used in over 55,000 patients worldwide, demonstrating strong clinical outcomes and poised to capture a larger share in the rapidly growing heart valve market.
See More
Anteris Treats First US Patients in DurAVR Pivotal Trial
- Trial Milestone: Anteris has successfully enrolled and treated the first US patients in the global pivotal trial of its DurAVR® Transcatheter Heart Valve, marking a significant advancement that is expected to enhance the company's market share in cardiac treatment.
- Medical Collaboration: Following CMS approval, the Anteris team worked closely with physicians to achieve rapid patient enrollment, demonstrating the company's efficient execution in clinical trials and strengthening partnerships with medical institutions.
- Trial Design: The PARADIGM trial is designed to evaluate the safety and effectiveness of the DurAVR THV, aiming to enroll approximately 1,000 patients with a 1:1 random assignment, intending to provide comparative data to support future patient care decisions.
- Medicare Coverage: Anteris has secured US Medicare reimbursement eligibility for procedures under the PARADIGM trial, utilizing a Coverage with Evidence Development model that ensures financial support for patients while generating clinical data during the trial.
See More
Anteris Technologies Begins U.S. Trials for DurAVR Heart Valve
- Trial Launch: Anteris Technologies announced that the first U.S. patients have been treated in the pivotal PARADIGM trial evaluating DurAVR, a next-generation transcatheter heart valve aimed at restoring natural valve function in patients with severe symptomatic aortic stenosis.
- Study Design: The PARADIGM study is a multicenter, prospective, single-arm pivotal trial intended to enroll patients eligible for transcatheter aortic valve replacement (TAVR), assessing safety and performance outcomes, including valve function and clinical improvement.
- Technological Innovation: DurAVR features a unique single-piece, 3D-shaped leaflet design that mimics the natural motion of a healthy aortic valve, with early clinical data indicating promising hemodynamic performance that may enhance long-term durability.
- Market Outlook: The treatment of the first U.S. patients marks a significant milestone in the global development of DurAVR, with additional enrollment expected across the U.S., Europe, and Australia through 2026, reflecting increasing clinical adoption of this technology across multiple regions.
See More
ANTERIS TECHNOLOGIES REPORTS TREATMENT OF FIRST U.S. PATIENTS IN GLOBAL PIVOTAL PARADIGM TRIAL
Announcement of First Patients: Anteris Technologies has announced the treatment of its first patients in the U.S. as part of the Global Pivotal Paradigm Trial.
Significance of the Trial: This trial is crucial for evaluating the effectiveness and safety of Anteris' innovative medical technology in a global context.
See More
ANTERIS TECHNOLOGIES GLOBAL CORP - ENDING OF A SIGNIFICANT DEFINITIVE AGREEMENT
Global Corporate Termination: Antaris Technologies has announced the global termination of a material definitive agreement.
Impact on Operations: This decision may affect the company's operational strategies and partnerships moving forward.
See More
Anteris Secures U.S. Medicare Reimbursement Eligibility
- Reimbursement Milestone: Anteris Technologies announced that its global pivotal PARADIGM Trial has secured U.S. Medicare reimbursement eligibility under CMS's national coverage policy, which is expected to accelerate U.S. site activation and enhance operational momentum.
- Trial Scale and Design: The PARADIGM Trial will enroll approximately 1,000 patients with a 1:1 randomization to compare the safety and effectiveness of the DurAVR® Transcatheter Heart Valve against commercially available TAVRs, providing critical data for market entry.
- Clinical Evaluation Standards: The trial will assess non-inferiority of the DurAVR® THV on a primary composite endpoint of all-cause mortality, all stroke, and cardiovascular hospitalization at one year, aiming to provide robust clinical evidence for the new product's market introduction.
- Technological Innovation Background: The DurAVR® THV is the first biomimetic valve utilizing Anteris's patented ADAPT® tissue technology, which has been clinically used in over 55,000 patients worldwide, further solidifying Anteris's leadership position in the structural heart disease sector.
See More
Anteris Secures US Medicare Coverage for PARADIGM Trial
- Coverage Milestone: Anteris Technologies has secured US Medicare reimbursement eligibility for its global pivotal PARADIGM Trial, expected to provide treatment for approximately 1,000 patients with the DurAVR® heart valve, significantly enhancing the company's market competitiveness in cardiac care.
- Trial Design and Objectives: This prospective randomized controlled trial will compare the safety and efficacy of DurAVR® against existing TAVR devices, primarily assessing one-year all-cause mortality, stroke, and cardiovascular hospitalization rates to ensure the non-inferiority of DurAVR®.
- Accelerating Operational Momentum: By obtaining Medicare coverage, Anteris anticipates accelerating the activation of US study sites, driving operational momentum across participating centers, and further solidifying its leadership position in the structural heart disease sector.
- Technological Advantages and Market Potential: The DurAVR® heart valve utilizes Anteris' patented ADAPT® tissue technology, clinically used in over 55,000 patients worldwide, demonstrating strong clinical outcomes and poised to capture a larger share in the rapidly growing heart valve market.
See More
Anteris Treats First US Patients in DurAVR Pivotal Trial
- Trial Milestone: Anteris has successfully enrolled and treated the first US patients in the global pivotal trial of its DurAVR® Transcatheter Heart Valve, marking a significant advancement that is expected to enhance the company's market share in cardiac treatment.
- Medical Collaboration: Following CMS approval, the Anteris team worked closely with physicians to achieve rapid patient enrollment, demonstrating the company's efficient execution in clinical trials and strengthening partnerships with medical institutions.
- Trial Design: The PARADIGM trial is designed to evaluate the safety and effectiveness of the DurAVR THV, aiming to enroll approximately 1,000 patients with a 1:1 random assignment, intending to provide comparative data to support future patient care decisions.
- Medicare Coverage: Anteris has secured US Medicare reimbursement eligibility for procedures under the PARADIGM trial, utilizing a Coverage with Evidence Development model that ensures financial support for patients while generating clinical data during the trial.
See More
Anteris Technologies Begins U.S. Trials for DurAVR Heart Valve
- Trial Launch: Anteris Technologies announced that the first U.S. patients have been treated in the pivotal PARADIGM trial evaluating DurAVR, a next-generation transcatheter heart valve aimed at restoring natural valve function in patients with severe symptomatic aortic stenosis.
- Study Design: The PARADIGM study is a multicenter, prospective, single-arm pivotal trial intended to enroll patients eligible for transcatheter aortic valve replacement (TAVR), assessing safety and performance outcomes, including valve function and clinical improvement.
- Technological Innovation: DurAVR features a unique single-piece, 3D-shaped leaflet design that mimics the natural motion of a healthy aortic valve, with early clinical data indicating promising hemodynamic performance that may enhance long-term durability.
- Market Outlook: The treatment of the first U.S. patients marks a significant milestone in the global development of DurAVR, with additional enrollment expected across the U.S., Europe, and Australia through 2026, reflecting increasing clinical adoption of this technology across multiple regions.
See More
ANTERIS TECHNOLOGIES REPORTS TREATMENT OF FIRST U.S. PATIENTS IN GLOBAL PIVOTAL PARADIGM TRIAL
Announcement of First Patients: Anteris Technologies has announced the treatment of its first patients in the U.S. as part of the Global Pivotal Paradigm Trial.
Significance of the Trial: This trial is crucial for evaluating the effectiveness and safety of Anteris' innovative medical technology in a global context.
See More
ANTERIS TECHNOLOGIES GLOBAL CORP - ENDING OF A SIGNIFICANT DEFINITIVE AGREEMENT
Global Corporate Termination: Antaris Technologies has announced the global termination of a material definitive agreement.
Impact on Operations: This decision may affect the company's operational strategies and partnerships moving forward.
See More
Anteris Secures U.S. Medicare Reimbursement Eligibility
- Reimbursement Milestone: Anteris Technologies announced that its global pivotal PARADIGM Trial has secured U.S. Medicare reimbursement eligibility under CMS's national coverage policy, which is expected to accelerate U.S. site activation and enhance operational momentum.
- Trial Scale and Design: The PARADIGM Trial will enroll approximately 1,000 patients with a 1:1 randomization to compare the safety and effectiveness of the DurAVR® Transcatheter Heart Valve against commercially available TAVRs, providing critical data for market entry.
- Clinical Evaluation Standards: The trial will assess non-inferiority of the DurAVR® THV on a primary composite endpoint of all-cause mortality, all stroke, and cardiovascular hospitalization at one year, aiming to provide robust clinical evidence for the new product's market introduction.
- Technological Innovation Background: The DurAVR® THV is the first biomimetic valve utilizing Anteris's patented ADAPT® tissue technology, which has been clinically used in over 55,000 patients worldwide, further solidifying Anteris's leadership position in the structural heart disease sector.
See More
