The primary objectives of this study are to: * estimate vaccine response in rocatinlimab group vs placebo group, assessed using antibody anti-tetanus response at Week 24 * estimate vaccine response in rocatinlimab group vs placebo group, assessed using antibody anti-meningococcal response at Week 24
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Enrollment
221
Subcutaneous (SC) injection
SC injection
Number of Participants with a Positive Anti-tetanus Response
Time frame: Week 20 to week 24
Number of Participants with a Positive Anti-meningococcal Response
Time frame: Week 20 to week 24
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