BLAINJECTIONINJECTABLE
Approved
Sep 2024
Lifecycle
Growth
Competitive Pressure
30/100
Clinical Trials
3
Data completeness
4/8 — Partial
EBGLYSS (lebrikizumab-lbkz) by Eli Lilly and Company is interleukin-13 antagonists [moa]. Approved for interleukin-13 antagonist [epc]. First approved in 2024.
Drug data last refreshed 21h ago · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
EBGLYSS (lebrikizumab-lbkz) is a monoclonal antibody that blocks interleukin-13, a key inflammatory cytokine driving atopic dermatitis pathology. Administered as a subcutaneous injection, it represents a targeted biologic approach to moderate-to-severe AD in patients inadequately controlled by topical therapies. The drug entered a competitive landscape dominated by JAK inhibitors but offers a distinct IL-13-specific mechanism.
Growth
Early-stage growth product with significant runway; commercial teams will expand as market adoption accelerates and real-world evidence accumulates.
Mechanism of Action
Interleukin-13 Antagonists
Pharmacologic Class:
Interleukin-13 Antagonist
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (3)
A Study of (LY3650150) Lebrikizumab to Assess the Safety and Efficacy of Adult and Adolescent Participants With Moderate-to-Severe Atopic Dermatitis and Skin of Color
Started Jan 2023
90 enrolled
Atopic Dermatitis
Long-term Safety and Efficacy Study of Lebrikizumab (LY3650150) in Participants With Moderate-to-Severe Atopic Dermatitis (ADjoin)
Started Jun 2020
1,153 enrolled
Atopic Dermatitis
Study to Assess the Safety and Efficacy of Lebrikizumab (LY3650150) in Adolescent Participants With Moderate-to-Severe Atopic Dermatitis
Started Feb 2020
206 enrolled
Atopic Dermatitis
Career Relevance
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.