Transthyretin Amyloid Cardiomyopathy
Conditions
Keywords
Safety surveillance, Tafamidis
Brief summary
The purpose of this study is to learn about the safety of Tafamidis for the treatment of Transthyretin amyloid cardiomyopathy (ATTR-CM) in India. ATTR-CM is a condition that affects people's hearts. Transthyretin is a protein that is made in the liver. In some people this protein stops working and forms clumps called as amyloid. Transthyretin amyloid builds up in heart and stops the heart from pumping properly. This study is seeking for participants who are: * confirmed with ATTR-CM. * given Tafamidis capsules to be taken by mouth. The safety of Tafamidis capsules will be checked based on side effects. These side effects can happen within 6 months after taking Tafamidis. A side effect is something (expected or unexpected) that you feel was caused by a medicine or treatment you take. The study doctor will collect side effect information and put the information on patient's case form. Follow-up of the patient's will be performed via clinic re-visit or over a call. It is not a rule for the participants to visit the clinic in this study. This study will help to see if Tafamidis is safe.
Interventions
DRUGTafamidis
Patients on tafamidis will be observed
Sponsors
Pfizer
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Adult patients (age ≥18 years) with diagnosis of cardiomyopathy of wild type or hereditary transthyretin-mediated amyloidosis (ATTR-CM). * Patients to whom VyndaMx® Capsules is prescribed for the treatment of wild or hereditary ATTR-CM.
Exclusion criteria
* Patient with hypersensitivity to VyndaMx® Capsule or to any of the excipients in the product. * Patients with rare hereditary problems of fructose intolerance. * Patient who has a contraindication to VyndaMx® Capsules according to the approved local product label.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of Adverse events with Tafamidis | Baseline to 6 months | The safety of VyndaMx® Capsules is the primary objective of the study and will be assessed based on Adverse events which would occur within 6 months from first dosing. Investigator will collect the safety related data until 6 months from first dosing of Tafamidis Capsules and will record these data on the Case report Form. |
Countries
India
Outcome results
None listed