Transthyretin Amyloid Cardiomyopathy Clinical Trial

ENDEAVOUR: Phase 3 Multicenter Study of Revusiran (ALN-TTRSC) in Patients With Transthyretin (TTR) Mediated Familial Amyloidotic Cardiomyopathy (FAC)

Summary

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.

View Eligibility Criteria

Eligibility Criteria

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

Study is for people with:

Transthyretin Amyloid Cardiomyopathy

Phase:

Phase 3

Estimated Enrollment:

206

Study ID:

NCT02319005

Recruitment Status:

Completed

Sponsor:

Alnylam Pharmaceuticals

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There are 16 Locations for this study

See Locations Near You

Clinical Trial Site
Bakersfield California, , United States
Clinical Trial Site
Beverly Hills California, , United States
Clinical Trial Site
La Mesa California, , United States
Clinical Trial Site
Los Angeles California, , United States
Clinical Trial Site
San Francisco California, , United States
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Stanford California, , United States
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Torrance California, , United States
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Aurora Colorado, , United States
Clinical Trial Site
Washington District of Columbia, 20037, United States
Clinical Trial Site
Washington District of Columbia, 20422, United States
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Tampa Florida, , United States
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Atlanta Georgia, , United States
Clinical Trial Site
Chicago Illinois, 60611, United States
Clinical Trial Site
Chicago Illinois, 60612, United States
Clinical Trial Site
Chicago Illinois, 60637, United States
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New Orleans Louisiana, , United States
Clinical Trial Site
Baltimore Maryland, 21201, United States
Clinical Trial Site
Baltimore Maryland, 21287, United States
Clinical Trial Site
Boston Massachusetts, 02111, United States
Clinical Trial Site
Boston Massachusetts, 02118, United States
Clinical Trial Site
Boston Massachusetts, 02215, United States
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Detroit Michigan, , United States
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Rochester Minnesota, , United States
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Saint Louis Missouri, , United States
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Newark New Jersey, , United States
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Bronx New York, , United States
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New York New York, , United States
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Rosedale New York, , United States
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Durham North Carolina, , United States
Clinical Trial Site
Cleveland Ohio, 44106, United States
Clinical Trial Site
Cleveland Ohio, 44195, United States
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Columbus Ohio, , United States
Clinical Trial Site
Philadelphia Pennsylvania, 19102, United States
Clinical Trial Site
Philadelphia Pennsylvania, 19104, United States
Clinical Trial Site
Charleston South Carolina, , United States
Clinical Trial Site
Nashville Tennessee, , United States
Clinical Trial Site
Dallas Texas, , United States
Clinical Trial Site
Fort Worth Texas, , United States
Clinical Trial Site
Houston Texas, , United States
Clinical Trial Site
Richmond Virginia, , United States
Clinical Trial Site
Seattle Washington, , United States
Clinical Trial Site
Anderlecht , , Belgium
Clinical Trial Site
Hasselt , , Belgium
Clinical Trial Site
Roeselare , , Belgium
Clinical Trial Site
Toronto , , Canada
Clinical Trial Site
Bordeaux Aquitaine, , France
Clinical Trial Site
Creteil , , France
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Marseille , , France
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Paris , , France
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Heidelberg , , Germany
Clinical Trial Site
Muenster , , Germany
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Bologna , , Italy
Clinical Trial Site
Messina , , Italy
Clinical Trial Site
Pavia , , Italy
Clinical Trial Site
Barcelona , 8003, Spain
Clinical Trial Site
Barcelona , 8907, Spain
Clinical Trial Site
Madrid , , Spain
Clinical Trial Site
Umea , , Sweden
Clinical Trial Site
Croydon England, , United Kingdom
Clinical Trial Site
London England, , United Kingdom
Clinical Trial Site
Tooting , , United Kingdom

How clear is this clinincal trial information?

Study is for people with:

Transthyretin Amyloid Cardiomyopathy

Phase:

Phase 3

Estimated Enrollment:

206

Study ID:

NCT02319005

Recruitment Status:

Completed

Sponsor:


Alnylam Pharmaceuticals

How clear is this clinincal trial information?

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