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Clinical Trial Summary

The purpose of this study is to evaluate the safety and efficacy of patisiran (ALN-TTR02) in patients with transthyretin (TTR) mediated amyloidosis. An open-label, single-arm, long-term follow-up extension study NCT02510261 (ALN-TTR02-006) was initiated to provide participants who completed this study with continued patisiran-LNP (lipid nanoparticle) treatment.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01960348
Study type Interventional
Source Alnylam Pharmaceuticals
Contact
Status Completed
Phase Phase 3
Start date November 2013
Completion date August 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
Active, not recruiting NCT03759379 - HELIOS-A: A Study of Vutrisiran (ALN-TTRSC02) in Patients With Hereditary Transthyretin Amyloidosis (hATTR Amyloidosis) Phase 3
Completed NCT02319005 - ENDEAVOUR: Phase 3 Multicenter Study of Revusiran (ALN-TTRSC) in Patients With Transthyretin (TTR) Mediated Familial Amyloidotic Cardiomyopathy (FAC) 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