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A PHASE 3 MULTICENTER, OPEN-LABEL STUDY TO EVALUATE THE SAFETY OF DAILY ORAL DOSING OF TAFAMIDIS MEGLUMINE (PF-06291826-83) 20 MG OR 80 MG [OR TAFAMIDIS (PF-06291826-00) 61 MG] IN SUBJECTS DIAGNOSED WITH TRANSTHYRETIN CARDIOMYOPATHY (ATTR-CM)

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A PHASE 3 MULTICENTER, OPEN-LABEL STUDY TO EVALUATE THE SAFETY OF DAILY ORAL DOSING OF TAFAMIDIS MEGLUMINE (PF-06291826-83) 20 MG OR 80 MG [OR TAFAMIDIS (PF-06291826-00) 61 MG] IN SUBJECTS DIAGNOSED WITH TRANSTHYRETIN CARDIOMYOPATHY (ATTR-CM)

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 17 Jul 2024

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At a glance

  • Drugs Tafamidis meglumine (Primary)
  • Indications Cardiomyopathies; Cardiovascular disorders; Transthyretin-related hereditary amyloidosis
  • Focus Adverse reactions
  • Acronyms ATTR-CM
  • Sponsors Pfizer

    • Most Recent Events

    • 09 Jan 2024 Status changed from active, no longer recruiting to completed.
    • 19 Dec 2023 This trial has been completed in Belgium, according to European Clinical Trials Database record (2023-10-26).
    • 17 Dec 2023 This trial has been completed in Netherlands, according to European Clinical Trials Database record (2023-10-26).

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