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A SINGLE ARM, MULTICENTER, OPEN-LABEL STUDY TO EVALUATE THE EFFICACY, SAFETY, TOLERABILITY, AND PHARMACODYNAMICS OF ORALLY ADMINISTERED TAFAMIDIS MEGLUMINE IN TRANSTHYRETIN AMYLOID POLYNEUROPATHY PARTICIPANTS IN CHINA

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A SINGLE ARM, MULTICENTER, OPEN-LABEL STUDY TO EVALUATE THE EFFICACY, SAFETY, TOLERABILITY, AND PHARMACODYNAMICS OF ORALLY ADMINISTERED TAFAMIDIS MEGLUMINE IN TRANSTHYRETIN AMYLOID POLYNEUROPATHY PARTICIPANTS IN CHINA

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 15 Mar 2024

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At a glance

  • Drugs Tafamidis meglumine (Primary)
  • Indications Transthyretin-related hereditary amyloidosis
  • Focus Therapeutic Use
  • Sponsors Pfizer

    • Most Recent Events

    • 14 Mar 2023 Status changed from active, no longer recruiting to completed.
    • 19 Nov 2021 Duration of treatment has been increased from 48 weeks to 72 weeks (18 months).
    • 19 Nov 2021 Status changed from recruiting to active, no longer recruiting.

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