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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02319005
Study type Interventional
Source Alnylam Pharmaceuticals
Contact
Status Completed
Phase Phase 3
Start date December 2014
Completion date March 30, 2017

See also
  Status Clinical Trial Phase
Not yet recruiting NCT05974644 - Southeastern ATTR Amyloidosis Consortium: SEATTRAC Family Registry
Recruiting NCT05879874 - Prospective Evaluation of NfL as a Biomarker in ATTRv
Recruiting NCT05489549 - Subclinical Transthyretin Cardiac Amyloidosis in V122I TTR Carriers
Completed NCT01960348 - APOLLO: The Study of an Investigational Drug, Patisiran (ALN-TTR02), for the Treatment of Transthyretin (TTR)-Mediated Amyloidosis Phase 3
Active, not recruiting NCT03759379 - HELIOS-A: A Study of Vutrisiran (ALN-TTRSC02) in Patients With Hereditary Transthyretin Amyloidosis (hATTR Amyloidosis) Phase 3
Recruiting NCT05873868 - Myocardial Effects in Patients With ATTRv With Polyneuropathy Treated With Patisiran or Vutrisiran
Approved for marketing NCT02939820 - Expanded Access Protocol of Patisiran for Patients With Hereditary ATTR Amyloidosis (hATTR)
Approved for marketing NCT03400098 - ATTR Expanded Access Program (EAP) by Ionis