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Clinical Trial Summary

The purpose of this study is to evaluate the safety and tolerability of long-term dosing with ALN-TTR02 (patisiran) in patients with transthyretin (TTR) mediated amyloidosis (ATTR).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01961921
Study type Interventional
Source Alnylam Pharmaceuticals
Contact
Status Completed
Phase Phase 2
Start date October 2013
Completion date August 2016

See also
  Status Clinical Trial Phase
Completed NCT02292186 - A Extension Study to Evaluate Revusiran (ALN-TTRSC) in Patients With Transthyretin (TTR) Cardiac Amyloidosis Phase 2
Completed NCT01960348 - APOLLO: The Study of an Investigational Drug, Patisiran (ALN-TTR02), for the Treatment of Transthyretin (TTR)-Mediated Amyloidosis Phase 3
Completed NCT01617967 - Safety and Tolerability of Patisiran (ALN-TTR02) in Transthyretin (TTR) Amyloidosis Phase 2
Completed NCT01814839 - A Phase 1, Single- and Multi-Dose, Dose Escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Subcutaneously Administered ALN-TTRSC (Revusiran) in Healthy Volunteers Phase 1
Completed NCT01559077 - Trial to Evaluate Safety, Tolerability, and Parmacokinetics of ALN-TTR02 in Healthy Volunteer Subjects Phase 1
Completed NCT01981837 - Phase 2 Study to Evaluate ALN-TTRSC (Revusiran) in Patients With Transthyretin (TTR) Cardiac Amyloidosis Phase 2
Approved for marketing NCT02939820 - Expanded Access Protocol of Patisiran for Patients With Hereditary ATTR Amyloidosis (hATTR)