The purpose of this study was to evaluate the safety and effectiveness of revusiran (ALN-TTRSC) in adults with transthyretin-mediated amyloidosis (ATTR), whose disease has continued to worsen after liver transplantation. Dosing has been discontinued; patients are being followed-up for safety.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
12
500mg Revusiran by subcutaneous (sc) injection
Clinical Trial SIte
Paris, France
Clinical Trial SIte
Münster, Germany
Clinical Trial SIte
Porto, Portugal
Clinical Trial SIte
Majorca, Spain
Clinical Trial Site
Umeå, Sweden
Clinical Trial SIte
London, United Kingdom
Percentage Change From Baseline in Serum TTR at Month 6
A negative percentage change from baseline at Month 6 indicates a reduction in serum TTR level.
Time frame: Month 6
Percentage Change From Baseline in Serum TTR Over 18 Months
A negative percentage change from baseline indicates a reduction in serum TTR level.
Time frame: Weeks 3, 7, 12, 18, 24, 26 (Month 6), 39 (Month 9), 52 (Month 12), 57, 78 (Month 18)
Change From Baseline in Modified Neurological Impairment Score (mNIS +7) Composite Score Over 18 Months
The mNIS+7 is a composite score that measures neurologic impairment which includes the following components: physical exam of lower limbs, upper limbs and cranial nerves to assess motor strength/weakness, electrophysiologic measurement of small and large nerve fiber function, sensory testing and postural blood pressure. The minimum and maximum values are 0 and 304, respectively. A higher score indicates a worse outcome. A negative change from baseline indicates an improvement.
Time frame: Baseline, Months 6, 12, 18
Norfolk Quality of Life-Diabetic Neuropathy (QoL-DN) Questionnaire Score
The Norfolk QoL-DN questionnaire is a standardized 35-item patient-reported outcomes measure that is sensitive to the different features of diabetic neuropathy - small fiber, large fiber, and autonomic nerve function. The minimum and maximum values are -4 and 136, respectively. A higher score indicates a worse outcome.
Time frame: Baseline, Months 6, 12, 18
Number of Participants in Each Polyneuropathy Disability (PND) Stage Based on Worst Post-Baseline Score
PND Scores: Stage 0: No symptoms, Stage 1: Sensory disturbances but preserved walking capabilities, Stage 2: Impaired walking capacity, but ability to walk without a stick or crutches, Stage 3A/B: Walking with help of 1 or 2 sticks or crutches, Stage 4: confined to wheel chair. For each stage (0-4) at baseline, the number of participants is presented at their worst post-baseline score for each stage (0-4) post-baseline. Worst post-baseline is defined the highest PND classification for a participant recorded after the first dose of study drug.
Time frame: Baseline, Months 6, 12, 18
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