Global study tracks Real-World impact of new heart drug
NCT ID NCT07358078
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study will follow about 2000 adults with a heart condition called ATTR-CM, where abnormal proteins build up and weaken the heart. Researchers want to see how patients do on a drug called vutrisiran in everyday medical care, not just in a controlled trial. They will measure symptoms, quality of life, and how often patients need hospital care over time.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for TRANSTHYRETIN AMYLOIDOSIS WITH CARDIOMYOPATHY are added.
By submitting, you agree to our Terms of use
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
By submitting, you agree to our Terms of use
Study contacts
-
Contact
Phone: •••-•••-•••• Email: •••••@•••••
-
Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
-
Clinical Trial Site
RECRUITINGNaples, Florida, 34102, United States
-
Clinical Trial Site
RECRUITINGBoston, Massachusetts, 02215, United States
-
Clinical Trial Site
RECRUITINGNew Brunswick, New Jersey, 08901, United States
-
Clinical Trial Site
RECRUITINGMemphis, Tennessee, 38120, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- New study tracks safety of eplontersen in patients with liver transplants
- Gene-Editing breakthrough: could a single dose stop a deadly heart condition?
- New drug patisiran aims to help hearts stiffened by rare protein disease
- Hope for rare heart disease: new drug aims to slow deadly protein clumps
- Vutrisiran shows promise for Long-Term control of rare heart condition
- New drug aims to cut deaths and heart crises in rare amyloidosis