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Lebrikizumab

Alternative Names: lebrikizumab, milr1444a, tnx-650, LY3650150, LY 3650150, LY-3650150, EBGLYSS
Latest Update: 2024-12-17
Latest Update Note: Clinical Trial Update

Product Description

Lebrikizumab is a novel, high-affinity, monoclonal antibody or biological agent that selectively inhibits interleukin 13 (IL-13) for the treatment of atopic dermatitis (eczema). (Sourced from: https://dermnetnz.org/topics/lebrikizumab)

Mechanisms of Action: IL13 Inhibitor

Novel Mechanism: No

Modality: Antibody

Route of Administration: Subcutaneous

FDA Designation: None *

Approval Status: Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Eli Lilly
Company Location: INDIANAPOLIS IN 46285
Company CEO: David A. Ricks
Additonal Commercial Interests: Almirall

Clinical Description

Map of Global Clinical Trials for Lebrikizumab

Countries in Clinic: Argentina, Australia, Austria, Belgium, Brazil, Bulgaria, Canada, China, Czech Republic, Denmark, Estonia, France, Germany, Italy, Japan, Korea, Latvia, Lithuania, Mexico, Netherlands, Poland, Romania, Singapore, Spain, Sweden, Taiwan, Ukraine, United Kingdom, United States

Active Clinical Trial Count: 33

Highest Development Phases

Phase 3: Dermatitis, Atopic|Nasal Polyposis|Rhinitis, Allergic, Perennial|Sinusitis|Skin Diseases, Genetic

Phase 1: Healthy Volunteers

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

jRCT2031240234

P3

Not yet recruiting

Sinusitis|Nasal Polyposis

2027-02-28

J2T-MC-KGBU

P3

Unknown Status

Nasal Polyposis|Sinusitis

2026-10-30

J2T-MC-KGBT

P3

Unknown Status

Rhinitis, Allergic, Perennial

2026-08-03

ADorable-2

P3

Enrolling by invitation

Dermatitis, Atopic

2026-06-26

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