Last updated on August 2019

Long-term Safety of Tafamidis in Subjects With Transthyretin Cardiomyopathy


Brief description of study

Open label study to evaluate tafamidis for the treatment of transthyretin cardiomyopathy

Detailed Study Description

Global Phase 3, open label long term extension safety study designed to obtain additional safety data for tafamidis meglumine 20 mg and 80 mg (or tafamidis 61 mg where available), and to continue to provide enrolled subjects with tafamidis for up to 60 months, or until subject has access to tafamidis for ATTR CM via prescription, whichever occurs first.

Clinical Study Identifier: NCT02791230

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