The efficacy and safety of DUPIXENT was evaluated for up to 52 weeks in two multipart, phase 3 clinical trials.

ADULTS & ADOLESCENTS AGED 12+ YEARS

Study design: Part A and Part B each consisted of a 24-week double-blind treatment period. Subjects who completed Part A or Part B were then eligible to enroll in a 28-week extended active treatment period (Part A-C or Part B-C, respectively) totaling 52 weeks of treatment.1,3,4

Overview: A total of 188 subjects aged 12+ years were enrolled in the extended active treatment period (77 in Part A-C and 111 in Part B-C). Management of the disease was evaluated through clinical, histologic, and endoscopic endpoints.1,3

CHILDREN AGED 1-11 YEARS

Study design: EoE KIDS-Part A consisted of a 16-week double-blind treatment period. Subjects who completed Part A were then eligible to enroll in a 36-week extended active treatment period (EoE KIDS-Part B) totaling 52 weeks of treatment.1

Overview: A total of 47 subjects aged 1-11 years were enrolled in the extended active treatment period. Management of the disease was evaluated through clinical, histologic, and endoscopic endpoints.1

VIEW THE study design IN
ADULTS & ADOLESCENTS
(12+ YEARS)

VIEW THE study design IN
CHILDREN (1-11 YEARS)