The purpose of this trial is to determine which doses of Lu AG09222 are recommended to help prevent migraines. People who join this trial have already tried 1 to 4 other available medications to prevent their migraines, but these medications have not helped them.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Enrollment
874
Lu AG09222 will be administered per the arm description.
Placebo matching to Lu AG09222 will be administered per the arm description
Change From Baseline in the Number of Monthly Migraine Days (MMDs)
Time frame: Baseline up to Week 12 (Weeks 1-12)
Change From Baseline in MMDs
Time frame: Baseline up to Week 12 (Weeks 1-12)
Percentage of Participants With ≥50% Reduction From Baseline in MMDs
Time frame: Baseline up to Week 12 (Weeks 1-12)
Percentage of Participants With ≥75% Reduction From Baseline in MMDs
Time frame: Baseline up to Week 12 (Weeks 1-12)
Change from Baseline in the Number of Monthly Headache Days
Time frame: Baseline up to Week 12 (Weeks 1-12)
Number of Participants with Treatment-emergent Adverse Events (TEAEs)
Time frame: Up to Week 20
Number of Participants with Anti-drug Antibodies (ADA)
Time frame: Up to Week 20
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