The primary objective of this study is to access the efficacy of ALXN2220 in the treatment of adult participants with ATTR-CM by evaluating the difference between the ALXN2220 and placebo groups as assessed by the total occurrences of all-cause mortality (ACM) and cardiovascular (CV) clinical events.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
1,181
Total Occurrence of ACM and CV clinical events during the Blinded Treatment Period
Time frame: Baseline up to the end study (up to Month 48)
Change From Baseline in Kansas City Cardiomyopathy Questionnaire-Overall Score (KCCQ-OS) at Month 24
Time frame: Baseline, Month 24
Time to CV-related Mortality
Time frame: Baseline up to the end of study (up to Month 48)
Change from Baseline in Six-minute Walk Test (6MWT) at Month 24
Time frame: Baseline, Month 24
Total Occurrences of CV Clinical Events
Time frame: Baseline up to the end of study (up to Month 48)
Time to ACM
Time frame: Baseline up to the end of study (up to Month 48)
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Research Site
Irvine, California, United States
Research Site
La Jolla, California, United States
Research Site
Palo Alto, California, United States
Research Site
San Francisco, California, United States
Research Site
Aurora, Colorado, United States
Research Site
Washington D.C., District of Columbia, United States
Research Site
Jacksonville, Florida, United States
Research Site
Weston, Florida, United States
Research Site
Atlanta, Georgia, United States
Research Site
Atlanta, Georgia, United States
...and 202 more locations