Skip to content

An interventional, Open-label Study to Evaluate the effect of lebrikizumab on eczema and Skin Barrier Function parameters in lesional and non-lesional skin in Adults and Adolescents with Moderate to Severe Atopic Dermatitis

Status
Not yet recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-519811-32-00
Enrollment
30
Registered
2026-02-12
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atopic dermatitis

Brief summary

The percentage of patients achieving EASI-75 (≥75% reduction from Baseline in EASI score) at Week 24, the final visit of the study.

Detailed description

Alternative clinically evaluated endpoint measures (IGA ≤1 and≥2 point improvement; DLQI≥4 point improvement; NRS ≥4 point improvement);, Registry-based (EG: SwedAD) PROMS (POEM, MADRS-S, RECAP), Skin physiological outcome measures in the form of EIS in all patients and evaporimetry, Epsilon and TiVi in a subgroup, NMF and Skin lipid sampling (tape stripping in all and biopsy for ToF-SIMS in an adult subgroup, Vitamin D status in blood and skin biopsy (adults only)

Interventions

Sponsors

Region Oestergoetland
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
0 Years to 64 Years

Design outcomes

Primary

MeasureTime frame
The percentage of patients achieving EASI-75 (≥75% reduction from Baseline in EASI score) at Week 24, the final visit of the study.

Secondary

MeasureTime frame
Alternative clinically evaluated endpoint measures (IGA ≤1 and≥2 point improvement; DLQI≥4 point improvement; NRS ≥4 point improvement);, Registry-based (EG: SwedAD) PROMS (POEM, MADRS-S, RECAP), Skin physiological outcome measures in the form of EIS in all patients and evaporimetry, Epsilon and TiVi in a subgroup, NMF and Skin lipid sampling (tape stripping in all and biopsy for ToF-SIMS in an adult subgroup, Vitamin D status in blood and skin biopsy (adults only)

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 13, 2026