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Anteris Technologies Secures CMS Reimbursement Supporting U.S. Site Activation for PARADIGM Trial

Key Takeaway: Anteris Technologies has announced that it secured U.S. Medicare reimbursement eligibility for its PARADIGM Trial, which will evaluate the DurAVR® Transcatheter Heart Valve against commercially available TAVRs. This milestone is expected to enhance U.S. site activation and operational momentum. The trial aims to enroll around 1000 patients to assess the safety and effectiveness of the DurAVR® THV.

Market Sentiment Analysis

POSITIVE FACTORS

  • Secured U.S. Medicare reimbursement eligibility for the PARADIGM Trial.
  • Expected to accelerate U.S. site activation and operational momentum.
  • The DurAVR® THV is a novel biomimetic valve designed for aortic stenosis.

Full Press Release Details

MINNEAPOLIS and BRISBANE, Australia, April 28, 2026 (GLOBE NEWSWIRE) --Anteris Technologies Global Corp.(“Anteris” or the “Company”) (NASDAQ: AVR, ASX: AVR), a global structural heart company committed to designing, developing, and commercializing cutting-edge medical devices to restore healthy heart function, today announced it has secured U.S. Medicare reimbursement eligibility for the global pivotal PARADIGM Trial under a Centers for Medicare & Medicaid Services (CMS) national coverage policy. Eligible procedures performed at participating U.S. study sites are covered under the Transcatheter Aortic Valve Replacement (TAVR) National Coverage Determination 20.32.
The CMS framework operates under a Coverage with Evidence Development (CED) model, enabling reimbursement with clinical evidence generation in the PARADIGM Trial. This milestone is expected to facilitate U.S. site activation, accelerating operational momentum across participating centers.

About the PARADIGM Trial

The PARADIGM Trial is a prospective randomized controlled trial which will evaluate the safety and effectiveness of the DurAVR®Transcatheter Heart Valve (“THV”) compared to commercially available transcatheter aortic valve replacements (TAVRs).
This head-to-head study will enroll approximately 1000 patients in the ‘All Comers Randomized Cohort’ with 1:1 randomization of patients who will receive either the DurAVR®THV or TAVR using commercially available and approved THVs. The PARADIGM Trial will assess non-inferiority on a primary composite endpoint of all-cause mortality, all stroke and cardiovascular hospitalization at one year post procedure.
For further information, please refer to ClinicalTrials.gov NCT07194265.

About Anteris

Anteris Technologies Global Corp. (NASDAQ: AVR, ASX: AVR) is a global structural heart company committed to designing, developing, and commercializing cutting-edge medical devices to restore healthy heart function. Founded in Australia, with a significant presence in Minneapolis, USA, Anteris is a science-driven company with an experienced team of multidisciplinary professionals delivering restorative solutions to structural heart disease patients.
Anteris’ lead product, the DurAVR®THV, was designed in collaboration with the world’s leading interventional cardiologists and cardiac surgeons to treat aortic stenosis – a potentially life-threatening condition resulting from the narrowing of the aortic valve. The balloon-expandable DurAVR®THV is the first biomimetic valve, which is shaped to mimic the performance of a healthy human aortic valve and aims to replicate normal aortic blood flow. DurAVR®THV is made using a single piece of molded ADAPT®tissue, Anteris’ patented anti-calcification tissue technology. ADAPT®tissue, which is FDA-cleared, has been used clinically for over 10 years and distributed for use in over 55,000 patients worldwide. The DurAVR®THV System is comprised of the DurAVR®valve, the ADAPT®tissue, and the balloon-expandable ComASUR®Delivery System.

Forward-Looking Statements

This announcement contains forward-looking statements, including statements regarding the expectation that achievement of the milestone will facilitate U.S. site activation, accelerating operational momentum across participating centers, and the PARADIGM Trial. Forward-looking statements include all statements that are not historical facts. Forward-looking statements generally are identified by the words “believe,” “project,” “expect,” “anticipate,” “estimate,” “intend,” “budget,” “target,” “aim,” “strategy,” “plan,” “guidance,” “outlook,” “may,” “should,” “could,” “will,” “would,” “will be,” “will continue,” “will likely result” and similar expressions, although not all forward-looking statements contain these identifying words. These forward-looking statements are subject to a number of risks, uncertainties, and assumptions, including those described under “Risk Factors” in Anteris’ Annual Report on Form 10-K for the fiscal period ended December 31, 2025 that was filed with the Securities and Exchange Commission and ASX. Readers are cautioned not to put undue reliance on forward-looking statements, and except as required by law, Anteris does not assume any obligation to update any of these forward-looking statements to conform these statements to actual results or revised expectations.

For more information:

Global Investor Relations Investor Relations (US)
investors@anteristech.com mchatterjee@bplifescience.com
Debbie Ormsby Malini Chatterjee, Ph.D.
Anteris Technologies Global Corp. Blueprint Life Science Group
+61 1300 550 310 | +61 7 3152 3200 +1 917 330 4269
Website www.anteristech.com
X @AnterisTech
LinkedIn https://www.linkedin.com/company/anteristech

Frequently Asked Questions

What is the PARADIGM Trial?

The PARADIGM Trial is a randomized controlled trial evaluating the DurAVR® THV's safety and effectiveness compared to existing TAVRs.

How many patients will be enrolled in the PARADIGM Trial?

Approximately 1000 patients will be enrolled in the PARADIGM Trial.

What does the CMS reimbursement cover?

The CMS reimbursement covers eligible procedures performed at U.S. study sites under the TAVR National Coverage Determination.

What is the primary endpoint of the PARADIGM Trial?

The primary endpoint is non-inferiority regarding all-cause mortality, stroke, and cardiovascular hospitalization at one year.

Last updated: Apr 28, 2026