A Extension Study to Evaluate Revusiran (ALN-TTRSC) in Patients With Transthyretin (TTR) Cardiac Amyloidosis
Completed · Phase 2
Conditions studied: TTR-mediated Amyloidosis
In brief
The purpose of this study was to evaluate the safety and clinical activity of long-term dosing with revusiran (ALN-TTRSC). Dosing has been discontinued; patients are being followed-up for safety.
Key facts
- Study ID
- NCT02292186
- Run by
- Alnylam Pharmaceuticals
- People needed
- 25
- Starts
- 2014-10-01
- Expected to finish
- 2017-02-22
- Last updated by the study team
- 2020-07-09
Who can join
Age: 18 and older, up to 90. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Subjects who previously received and tolerated revusiran (ALN-TTRSC) in the ALN-TTRSC-002 study
- Adequate liver function
- Not Pregnant or nursing
You may not qualify if…
- Inadequate renal function
- Uncontrolled hypertension, ischemic heart disease or clinically significant cardiac arrhythmia
- Untreated hypo- or hyperthyroidism
- Prior major organ transplant
Where it is running
- Clinical Trial Site — Boston, Massachusetts, United States
- Clinical Trial Site — New York, New York, United States
- Clinical Trial Site — Cleveland, Ohio, United States
- Clinical Trial Site — Calgary, Alberta, Canada
- Clinical Trial Site — London, United Kingdom
Full record on ClinicalTrials.gov
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