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NCT04108091

Vyndaqel Capsules Special Investigation (ATTR-CM)

Sponsor: Pfizer

View on ClinicalTrials.gov

Summary

Secondary Data Collection : To confirm the safety and effectiveness profiles under the actual medical practice of Vyndaqel in Japan. This study is conducted in accordance with the protocol even when Vynmac is used, and information the use of Vynmac during the observation period is also collected.

Official title: Vyndaqel Capsules Special Investigation - Investigation on Patients With Transthyretin Amyloid Cardiomyopathy

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

1214

Start Date

2019-10-03

Completion Date

2025-03-27

Last Updated

2026-05-18

Healthy Volunteers

No

Interventions

DRUG

Treatment for TTR amyloidosis

The usual adult dose is 80 mg of Tafamidis Meglumine orally once daily. The dose may be reduced if not tolerated.

DRUG

Treatment for TTR amyloidosis

The usual adult dose is 61 mg of tafamidis orally once daily.

Locations (1)

Pfizer

Tokyo, Japan