MedPath

Ligelizumab

Generic Name
Ligelizumab
Brand Names
-
Drug Type
Biotech
Chemical Formula
-
CAS Number
1322627-61-1
Unique Ingredient Identifier
L8LE0L691T
Background

Ligelizumab is a humanized IgG1k monoclonal antibody targeted against immunoglobulin E (IgE). Similar in mechanism to omalizumab, another IgE-directed monoclonal antibody, ligelizumab has a distinct binding epitope as compared to its peer (with a small degree of overlap) which appears to confer a greater affinity for free serum IgE and an altered sensitivity to IgE conformation.

Ligelizumab is currently under investigation for the treatment of chronic spontaneous urticaria (CSU), an autoimmune-driven inflammatory condition. While the precise pathogenesis of CSU is not entirely clear, autoantibodies against IgE receptors, and sometimes against IgE itself, are thought to exist in 30-40% of patients, and the efficacy anti-IgE antibody therapy in the treatment of CSU has been previously established with omalizumab. Initial trials of ligelizumab suggest a greater efficacy over its predecessor for the treatment of CSU.

Associated Conditions
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Associated Therapies
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Reviewing Major Dermatologic Studies of the Year: 2024

2024 dermatology studies advanced skin health understanding and patient care, highlighting treatments like ligelizumab for urticaria, ACE2 as a COVID-19 biomarker, and JNJ-77242113 for psoriasis. AI's role in dermatology and ethnic differences in vulvar dermatoses were also explored.

FDA reviews Sanofi and Regeneron's Dupixent label expansion for urticaria

FDA reviews Sanofi and Regeneron’s Dupixent for chronic spontaneous urticaria, targeting decision by April 2025. Dupixent, a monoclonal antibody, inhibits IL-4 and IL-13 pathways, showing significant itch and urticaria reduction in Study C. Already approved in Japan and UAE, Dupixent seeks EU approval and has potential revenue of $23.6bn by 2030.
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