42
Participants
Start Date
October 13, 2022
Primary Completion Date
January 5, 2023
Study Completion Date
January 5, 2023
Treatment A
Participants will receive single Dose A dose of ALXN2050 tablet (3 × Dose B) orally under fasted conditions.
Treatment B
Participant will receive single Dose A of ALXN2050 tablet (1 × Dose A) orally under fasted conditions.
Treatment C
Participants will receive single Dose A of ALXN2050 tablet (1 × Dose A) orally with a high-fat meal.
Research Site, Baltimore
Lead Sponsor
Collaborators (1)
Parexel
INDUSTRY
Alexion Pharmaceuticals, Inc.
INDUSTRY