Lebrikizumab in Moderate-to-severe Atopic Dermatitis

PHASE4RecruitingINTERVENTIONAL
Enrollment

48

Participants

Timeline

Start Date

July 2, 2025

Primary Completion Date

July 31, 2027

Study Completion Date

July 31, 2027

Conditions
Atopic Dermatitis
Interventions
DRUG

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"

Trial Locations (4)

48109

NOT_YET_RECRUITING

University of Michigan, Ann Arbor

79104

NOT_YET_RECRUITING

University of Freiburg, Freiburg im Breisgau

95630

RECRUITING

Physioseq USA - CA, Folsom

CH-1011

NOT_YET_RECRUITING

Lausanne University Hospital, Lausanne

Sponsors
All Listed Sponsors
collaborator

Dermira, Inc.

INDUSTRY

collaborator

Almirall, S.A.

INDUSTRY

lead

Johann E Gudjonsson MD PhD

OTHER

NCT06906497 - Lebrikizumab in Moderate-to-severe Atopic Dermatitis | Biotech Hunter | Biotech Hunter