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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02510261
Other study ID # ALN-TTR02-006
Secondary ID 2014-003877-40
Status Completed
Phase Phase 3
First received
Last updated
Start date July 16, 2015
Est. completion date November 23, 2022

Study information

Verified date November 2023
Source Alnylam Pharmaceuticals
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


Recruitment information / eligibility

Status Completed
Enrollment 211
Est. completion date November 23, 2022
Est. primary completion date November 23, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: - Have completed a patisiran study (i.e., completed the last efficacy visit in the parent study) and, in the opinion of the investigator, tolerated study drug - Be willing and able to comply with the protocol-required visit schedule and visit requirements and provide written informed consent Exclusion Criteria: - Any new or uncontrolled condition that could make the participant unsuitable for participation

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Patisiran
Patisiran was administered IV.

Locations

Country Name City State
Argentina Clinical Trial Site Buenos Aires
Australia Clinical Trial Site Westmead
Brazil Clinical Trial Site Rio de Janeiro
Brazil Clinical Trial Site São Paulo
Bulgaria Clinical Trial Site Sofia
Canada Clinical Trial Site Vancouver British Columbia
Cyprus Clinical Trial Site Nicosia
France Clinical Trial Site Creteil
France Clinical Trial Site Fort De France Martinique
France Clinical Trial Site Le Kremlin-bicetre
France Clinical Trial Site Lille
France Clinical Trial Site Marseille Cedex
France Clinical Trial Site Saint-Pierre Reunion Island
Germany Clinical Trial Site Cologne
Germany Clinical Trial Site Heidelberg
Germany Clinical Trial Site Muenster
Italy Clinical Trial Site Pavia
Italy Clinical Trial Site Rome
Italy Clinical Trial Site Sicily
Japan Clinical Trial Site Ehime
Japan Clinical Trial Site Fukuoka
Japan Clinical Trial Site Hiroshima
Japan Clinical Trial Site Kumamoto
Japan Clinical Trial Site Nagano
Japan Clinical Trial Site Oita
Japan Clinical Trial Site Okawasuji
Japan Clinical Trial Site Ono
Korea, Republic of Clinical Trial Site Seoul
Malaysia Clinical Trial Site Kuala Lumpur
Mexico Clinical Trial Site Tlalpan
Netherlands Clinical Trial Site Groningen
Portugal Clinical Trial Site Lisbon
Portugal Clinical Trial Site Porto
Spain Clinical Trial Site Barcelona
Spain Clinical Trial Site Huelva
Spain Clinical Trial Site Madrid
Spain Clinical Trial Site Palma De Mallorca
Sweden Clinical Trial Site Umeå
Taiwan Clinical Trial Site Taipei
Taiwan Clinical Trial Site Taipei
Turkey Clinical Trial Site Istanbul
United Kingdom Clinical Trial Site London
United States Clinical Trial Site Aurora Colorado
United States Clinical Trial Site Baltimore Maryland
United States Clinical Trial Site Boston Massachusetts
United States Clinical Trial Site Chicago Illinois
United States Clinical Trial Site Columbus Ohio
United States Clinical Trial Site Cooperstown New York
United States Clinical Trial Site Detroit Michigan
United States Clinical Trial Site Jacksonville Florida
United States Clinical Trial Site Joplin Missouri
United States Clinical Trial Site La Mesa California
United States Clinical Trial Site New York New York
United States Clinical Trial Site New York New York
United States Clinical Trial Site Rochester Minnesota
United States Clinical Trial Site Saint Louis Missouri

Sponsors (1)

Lead Sponsor Collaborator
Alnylam Pharmaceuticals

Countries where clinical trial is conducted

United States,  Argentina,  Australia,  Brazil,  Bulgaria,  Canada,  Cyprus,  France,  Germany,  Italy,  Japan,  Korea, Republic of,  Malaysia,  Mexico,  Netherlands,  Portugal,  Spain,  Sweden,  Taiwan,  Turkey,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of Participants With Adverse Events (AEs) Leading to Study Discontinuation AE is any untoward medical occurrence in a participant or clinical investigational subject administered a medicinal product and which does not necessarily have a causal relationship with this treatment. First dose up to 28 days after last dose of study drug (approximately 5.6 years)
Secondary Change From Baseline in the Total Neuropathy Impairment Score (NIS) at Year 5 The NIS assessment is a 244-point composite measure of neurologic impairment which includes a physical exam of lower limbs, upper limbs, and cranial nerves to assess the components: motor strength/weakness (NIS-W), reflexes (NIS-R), and sensation (NIS-S). NIS total score is obtained by combining all the component scores, ranging from 0 to 244. Higher scores represent a greater severity of disease. A positive change from baseline indicates the worsening of neuropathy. Baseline, Year 5
Secondary Change From Baseline in the Total Modified NIS (mNIS +7) Composite Score At Year 3 The mNIS+7 is a composite measure of neurologic impairment which includes the following components: physical exam of lower limbs, upper limbs, and cranial nerves to assess motor strength/weakness (192 points), reflexes (20 points), electrophysiologic measurement of small and large nerve fiber function (10 points), sensory testing (80 points), and postural blood pressure (2 points). The total mNIS+7 composite score is obtained by combining all the component scores, ranging from 0 (no impairment) to 304 (maximum impairment). A negative change from baseline indicates an improvement in neuropathy. Baseline, Year 3
Secondary Change From Baseline in the NIS+7 Total Score at Week 52 The NIS+7 provides additional, objective measures of nerve fibre function and autonomic nerve function in participants with diabetic neuropathy. The NIS+7 includes the full NIS, sum of 5 nerve conduction studies (NCS) (Sural sensory nerve action potential [SNAP], tibial motor nerve distal latency, peroneal compound motor action potential [CMAP], motor nerve conduction velocity, motor nerve distal latency), vibration detection threshold, and pulse rate response to deep breathing. The total NIS+7 score is obtained by combining all the component scores, ranging from 0 (no impairment) to 270 points (maximum impairment). A positive change from baseline indicates worsening. Baseline, Week 52
Secondary Change From Baseline in the Norfolk Quality of Life-Diabetic Neuropathy (QoL-DN) Questionnaire Total Score at Year 5 The Norfolk QoL-DN questionnaire is a standardized 47-item patient-reported outcomes measure, sensitive to the perception of the effects of diabetic neuropathy by the participant. The scores range from -4 (best possible QOL) to 136 (worst possible QOL). A negative change from baseline represents improved QOL. Baseline, Year 5
Secondary Change From Baseline in the EuroQOL-5 Dimensions-5 Levels (EQ-5D-5L) Index Score at Year 5 The EQ-5D-5L is a patient-reported measure of QoL based on 5 dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. The overall score is rated on a scale from 0 (worst) to 1 (no impairment). Higher scores indicate a higher QoL. A negative change from baseline indicates worsening of QoL. Baseline, Year 5
Secondary Change From Baseline in the EuroQoL Visual Analogue Scale (EQ-VAS) Score at Year 5 EQ-VAS measures the participant's self-rated health on a vertical scale evaluated on a scale of 0 ("worst health you can imagine") to 100 ("best health you can imagine"). Higher scores indicate a higher QOL. A negative change from baseline indicates worsening of QoL. Baseline, Year 5
Secondary Change From Baseline in the Composite Autonomic Symptom Score (COMPASS 31) Total Score at Week 52 COMPASS 31 questionnaire measures autonomic symptoms in participants with neuropathy. The questionnaire consists of 31 clinically selected questions evaluating 6 autonomic domains (orthostatic intolerance, secretomotor, gastrointestinal, bladder, and pupillomotor). COMPASS 31 is measured on a scale from 0 to 100, with 100 representing maximum impairment. Baseline, Week 52
Secondary Change From Baseline in the Modified Body Mass Index (mBMI) at Year 5 Nutritional status of participants was evaluated using the mBMI, calculated as BMI (kilograms per square meter [kg/m^2]) multiplied by the concentration of serum albumin (grams per liter [g/L]). A positive change from baseline indicates improvement in nutritional status. Baseline, Year 5
Secondary Change From Baseline in the Rasch-built Overall Disability Scale (R-ODS) at Year 5 The R-ODS is a 24-item patient-reported questionnaire that specifically captures activity and social participation limitations. It measures the level of disability on a scale of 0 (worst) to 48 (best, no limitations), higher score indicates a better outcome. A negative change from baseline indicates worsening of disability. Baseline, Year 5
Secondary Change From Baseline in the NIS+7 Component: NIS-Weakness (NIS-W) Score at Year 5 The NIS+7 provides additional, objective measures of nerve fiber function and autonomic nerve function in participants with diabetic neuropathy. The NIS+7 includes the full NIS (NIS-W, NIS-R, NIS-S), sum of 5 nerve conduction studies (NCS) (Sural SNAP, tibial motor nerve distal latency, peroneal CMAP, motor nerve conduction velocity, motor nerve distal latency), vibration detection threshold, and pulse rate response to deep breathing. NIS-W is a measure of motor strength, comprised of cranial nerve and both upper and lower limb motor assessments. The score ranges from 0 to 192. A higher score indicates greater severity of disease. Baseline, Year 5
Secondary Change From Baseline in the 10-meter Walk Test (10-MWT) Speed at Year 5 10-MWT is a measure of ambulatory ability and walk speed. It measures the speed (in meters per second [m/s]) of a participant to walk 10 meters. A negative change from baseline represents decreased ambulatory ability. Baseline, Year 5
Secondary Change From Baseline in the Hand Grip Strength at Week 52 Hand grip strength was measured by dynamometer. Grip strength in the dominant arm is a measure of motor function, with a higher grip strength indicating better motor function. The mean change from baseline in the hand grip strength was reported. Baseline, Week 52
Secondary Number of Participants With Change From Baseline in the Polyneuropathy Disability (PND) Stage PND measures changes in the ambulatory ability including the need of walking aids on the following stages: 0 (no symptoms), I (sensory disturbances but preserved walking capability), II (impaired walking capability but ability to walk without a stick or crutches), IIIA (walking with help of 1 stick/crutch), IIIB (with help of 2 sticks/crutches), and IV (confined to wheelchair or bedridden). Lower scores indicate greater ambulatory function. The number of participants with change in the stage from baseline was reported as: Improved or worsened. Baseline, Year 5
Secondary Number of Participants With Change From Baseline in the Familial Amyloidotic Polyneuropathy (FAP) Stage FAP measures changes in the ambulatory ability including the need of walking aids on the following stages: 0 (no symptoms), I (unimpaired ambulation; mostly mild sensory, motor, and autonomic neuropathy in the lower limbs), II (assistance with ambulation required; moderate impairment of the lower limbs, upper limbs, and trunk), and III (wheelchair-bound or bedridden; severe sensory, motor, and autonomic involvement of all limbs). Lower scores indicate greater ambulatory function. The number of participants with change in the stage from baseline was reported as: Improved or worsened. Baseline, Year 5
Secondary Number of Participants With Change From Baseline in the New York Heart Association (NYHA) Classification NYHA classification grades the severity of heart failure symptoms into the following stages: I (no symptoms; ordinary physical activity such as walking and climbing stairs does not cause fatigue or dyspnea), II (symptoms with ordinary physical activity; walking or climbing stairs rapidly, walking uphill, walking or stair climbing after meals, in cold weather, in wind or when under emotional stress causes undue fatigue or dyspnea), III (symptoms with less than ordinary physical activity; walking 1 to 2 blocks on the level and climbing more than 1 flight of stairs in normal conditions causes undue fatigue or dyspnea), IV (symptoms at rest; inability to carry on any physical activity without fatigue or dyspnea). The number of participants with change in the stage from baseline was reported as: Improved or worsened. Baseline, Year 5
Secondary Change From Baseline in the Intraepidermal Nerve Fiber Density (IENFD) at Year 5 IENFD (fibers/millimeter [mm]) is a measure for the pathologic evaluation of sensory and autonomic innervation. It is obtained by tandem 3 mm skin punch biopsies: one set of biopsies taken from the distal thigh and one set from the distal lower leg. An increase in nerve fiber density suggests improvement, while a decrease in nerve fiber density suggests worsening. Baseline, Year 5
Secondary Change From Baseline in the Sweat Gland Nerve Fiber Density (SGNFD) at Year 5 SGNFD (meter/cubic millimeter [m/mm^3]) is a measure for the pathologic evaluation of sensory and autonomic innervation. It is obtained by tandem 3 mm skin punch biopsies: one set of biopsies taken from the distal thigh and one set from the distal lower leg. An increase in nerve fiber density suggests improvement, while a decrease in nerve fiber density suggests worsening. Baseline, Year 5
Secondary Change From Baseline in the Dermal Amyloid Burden at Year 5 Dermal Amyloid Burden is a measure for the pathologic evaluation of sensory and autonomic innervation and reported as % congo red stain. It is obtained by tandem 3 mm skin punch biopsies: one set of biopsies taken from the distal thigh and one set from the distal lower leg. Baseline, Year 5
Secondary Change From Baseline in the Cardiac Biomarker: Serum Troponin I at Year 5 Manifestations of cardiac amyloid involvement were assessed through measurement of serum levels of the cardiac biomarker: troponin (micrograms per liter [µg/L]). The troponin I values <0.1 µg/L were imputed to 0.1 thus the actual changes cannot be calculated for values <0.1 µg/L. Baseline, Year 5
Secondary Change From Baseline in the Cardiac Biomarker: N-terminal Prohormone of B-type Natriuretic Peptide (NT-proBNP) at Year 5 Manifestations of cardiac amyloid involvement were assessed through measurement of serum levels of the cardiac biomarker: NT-proBNP (nanograms per liter [ng/L]). Baseline, Year 5
Secondary Change From Baseline in the Echocardiogram Parameter: Average Peak Longitudinal Strain at Year 5 The echocardiogram parameters analyzed included measures of systolic function: Average peak longitudinal strain (percentage [%]). Baseline, Year 5
Secondary Change From Baseline in the Echocardiogram Parameter: Left Ventricular (LV) Mass at Year 5 The echocardiogram parameters analyzed included measures of cardiac structure: LV mass (grams [g]). Baseline, Year 5
Secondary Change From Baseline in the Echocardiogram Parameter: LV End-diastolic Volume at Year 5 The echocardiogram parameters analyzed included measures of diastolic function: LV end-diastolic volume (milliliters [mL]). Baseline, Year 5
Secondary Change From Baseline in the Echocardiogram Parameter: LV Relative Wall Thickness at Year 5 The echocardiogram parameters analyzed included measures of cardiac structure: LV relative wall thickness (ratio). Baseline, Year 5
Secondary Change From Baseline in the Echocardiogram Parameter: Mean LV Wall Thickness at Year 5 The echocardiogram parameters analyzed included measures of cardiac structure: Mean LV wall thickness (centimeters [cm]). Baseline, Year 5
Secondary Change From Baseline in the Echocardiogram Parameter: Cardiac Output at Year 5 The echocardiogram parameters analyzed included measures of systolic function: Cardiac output (liters per minute [L/min]). Baseline, Year 5
Secondary Percent Change From Baseline in Serum TTR Levels at Year 5 Serum TTR was assessed using enzyme linked immunosorbent assay (ELISA). Baseline, Year 5
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