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Anteris Advances DurAVR Trial with FDA Submission, Hits 100 Patients Treated

2:36am on Monday 2nd of June, 2025 AEST Healthcare
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Anteris Advances DurAVR Trial with FDA Submission, Hits 100 Patients Treated

2:36am on Monday 2nd of June, 2025 AEST
Key Points
  • FDA IDE application submitted for DurAVR pivotal PARADIGM Trial
  • 100 patients successfully treated with DurAVR Transcatheter Heart Valve
  • One-year clinical data shows sustained favorable outcomes and safety
  • Manufacturing capacity tripled to support upcoming trial and demand
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