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FDA approves supplemental patient cohort for HeartWare's Endurance trial

  • The FDA approves and IDE supplement allowing HeartWare International (HTWR -0.6%) to enroll an additional patient cohort for the Endurance destination therapy study.
  • Data from the new cohort will be included in a PMA application seeking a destination therapy indication for the HeartWare System. (PR)
  • More on the Endurance trial: Northland sees "glaring inconsistencies."
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