Last reviewed · How we verify

NCT06321523

A Study to Learn About the Study Medicine Called Tafamidis 61mg in People Diagnosed With Transthyretin Amyloid Cardiomyopathy (ATTR-CM)

Completed Last updated 20 November 2025
What this trial tests

trial testing Tafamidis 61 milligrams in Transthyretin Amyloid Cardiomyopathy in 13 participants. Completed in 13 October 2025.

Timeline
19 March 2024
Primary endpoint
13 October 2025
13 October 2025

Quick facts

Lead sponsorPfizer
StatusCompleted
Study typeOBSERVATIONAL
Enrollment13
Start date19 March 2024
Primary completion13 October 2025
Estimated completion13 October 2025
Sites4 locations across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

Pfizer — full company profile →

Who can join

19 and older, any sex, with Transthyretin Amyloid Cardiomyopathy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this clinical trial is to learn about the effects of the study medicine (called Tafamidis 61milligrams (mg)) for the potential treatment of Transthyretin amyloid cardiomyopathy (ATTR-CM). This study is seeking participants who were prescribed Tafamidis 61mg after being diagnosed with ATTR-CM and have taken Tafamidis 61mg at least once. We will examine the experiences of people receiving the study medicine. This will help us determine if the study medicine is safe and effective.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Transthyretin Amyloid Cardiomyopathy

Currently open trials in the same condition.

Other Pfizer trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06321523.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing