The purpose of this study is to: * evaluate the safety and tolerability of single ascending doses of ALN-4285 in healthy volunteers * characterize the single-dose pharmacokinetics (PK) of ALN-4285
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
76
Clinical Trial Site
London, United Kingdom
Frequency of Adverse Events (AEs)
Time frame: Up to Week 24
Concentration of ALN-4285 in Plasma
Time frame: Up to Day 3
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