Long-term Safety of Tafamidis in Subjects With Transthyretin Cardiomyopathy
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)
Category & Conditions: Cardiovasular Diseases and Conditions
Medicine: VYNDAQEL® (TAFAMIDIS MEGLUMINE) CAPSULES AND VYNDAMAX™ (TAFAMIDIS) CAPSULES
ClinicalTrials.gov Identifier (NCT): NCT02791230
Protocol ID: B3461045
Open Plain Language Summary Result:
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