48
Participants
Start Date
July 2, 2025
Primary Completion Date
July 31, 2027
Study Completion Date
July 31, 2027
lebrikizumab
"Patients will receive lebrikizumab with a 500 mg loading dose administered subcutaneously at baseline and Week 2 followed by 250 mg every 2 weeks until Week 24.~At week 24, patients with ≥ Eczema Area and Severity Index (EASI) 50 will continue in the study and begin receiving lebrikizumab 250mg every 4 weeks (Q4W), while patients with \<EASI 50 will be discontinued from the study.~At week 36, patients with EASI ≥50 to \<90 will remain on Q4W through W60 (do not enter withdrawal arm), while patients with sustained low disease activity (IGA 0/1 or EASI≥90 response for at least 3 months assessed at W24 and W36) will withdraw from lebrikizumab treatment"
NOT_YET_RECRUITING
University of Michigan, Ann Arbor
NOT_YET_RECRUITING
University of Freiburg, Freiburg im Breisgau
RECRUITING
Physioseq USA - CA, Folsom
NOT_YET_RECRUITING
Lausanne University Hospital, Lausanne
Collaborators (2)
Dermira, Inc.
INDUSTRY
Almirall, S.A.
INDUSTRY
Johann E Gudjonsson MD PhD
OTHER