Study to Assess the Safety and Efficacy of Lebrikizumab (LY3650150) in Adolescent Participants With Moderate-to-Severe Atopic Dermatitis
Purpose
This is an open-label, single arm study of 52 weeks duration. The study will assess the safety and efficacy of lebrikizumab in adolescent participants (≥12 to <18 years weighing ≥40 kilograms) with moderate-to-severe atopic dermatitis (AD) who are candidates for systemic therapy.
Condition
- Atopic Dermatitis
Eligibility
- Eligible Ages
- Between 12 Years and 17 Years
- Eligible Genders
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Male or female adolescent (≥12 years to <18 years, and weighing ≥40 kg). 2. Chronic AD (according to American Academy of Dermatology Consensus Criteria) that has been present for ≥1 year before the screening visit. 3. Eczema Area and Severity Index (EASI) score ≥16 at the baseline visit. 4. Investigator Global Assessment (IGA) score ≥3 (scale of 0 to 4) at the baseline visit 5. ≥10% body surface area (BSA) of AD involvement at the baseline visit. 6. History of inadequate response to treatment with topical medications; or determination that topical treatments are otherwise medically inadvisable.
Exclusion Criteria
- Participation in a prior lebrikizumab clinical study. 2. Treatment with the following prior to the baseline visit: 1. An investigational drug within 8 weeks or within 5 half-lives (if known), whichever is longer. 2. Dupilumab within 8 weeks. 3. B-cell-depleting biologics, including to rituximab, within 6 months. 4. Other biologics within 5 half-lives (if known) or 16 weeks, whichever is longer. 3. Treatment with a live (attenuated) vaccine within 12 weeks of the baseline visit or planned during the study. 4. Uncontrolled chronic disease that might require bursts of oral corticosteroids. 5. Evidence of active acute or chronic hepatitis 6. History of human immunodeficiency virus (HIV) infection or positive HIV serology at screening. 7. History of malignancy, including mycosis fungoides, within 5 years before the screening visit, except completely treated in situ carcinoma of the cervix, completely treated and resolved non-metastatic squamous or basal cell carcinoma of the skin. 8. Pregnant or breastfeeding women, or women planning to become pregnant or breastfeed during the study.
Study Design
- Phase
- Phase 3
- Study Type
- Interventional
- Allocation
- N/A
- Intervention Model
- Single Group Assignment
- Primary Purpose
- Treatment
- Masking
- None (Open Label)
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental Lebrikizumab 250 mg |
Participants received two subcutaneous (SC) injections of 250 milligram(mg) Lebrikizumab at Baseline and Week 2 followed by a single injection every 2 weeks (Q2W) from Week 4 up to (but not including) Week 52. |
|
More Details
- Status
- Completed
- Sponsor
- Eli Lilly and Company