ENDEAVOUR: Phase 3 Multicenter Study of Revusiran (ALN-TTRSC) in Patients With Transthyretin (TTR) Mediated Familial Amyloidotic Cardiomyopathy (FAC)
Status: | Completed |
---|---|
Conditions: | Cardiology, Hematology |
Therapuetic Areas: | Cardiology / Vascular Diseases, Hematology |
Healthy: | No |
Age Range: | 18 - 90 |
Updated: | 7/20/2018 |
Start Date: | December 2014 |
End Date: | March 30, 2017 |
A Phase 3 Multicenter, Multinational, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of ALN TTRSC in Patients With Transthyretin (TTR) Mediated Familial Amyloidotic Cardiomyopathy (FAC)
The purpose of this study was to evaluate the safety and efficacy of revusiran (ALN-TTRSC) in
patients with transthyretin (TTR) mediated Familial Amyloidotic Cardiomyopathy. Dosing has
been discontinued; patients are being followed-up for safety.
patients with transthyretin (TTR) mediated Familial Amyloidotic Cardiomyopathy. Dosing has
been discontinued; patients are being followed-up for safety.
Inclusion Criteria:
- Documented TTR mutation
- Amyloid deposits in cardiac or non-cardiac tissue
- Medical history of heart failure
- Evidence of cardiac involvement by echocardiogram
Exclusion Criteria:
- Has known primary amyloidosis (AL), leptomeningeal amyloidosis, non-FAC hereditary
cardiomyopathy, hypertensive cardiomyopathy, or cardiomyopathy due to valvular heart
disease
- Has known peripheral vascular disease affecting ambulation
- Has a Polyneuropathy Disability score >2
- Has a New York Heart Association (NYHA) classification of IV
We found this trial at
40
sites
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