Ligelizumab: Difference between revisions

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Latest revision as of 12:56, 18 March 2025

Ligelizumab is a monoclonal antibody designed for the treatment of chronic spontaneous urticaria (CSU). It is developed by Novartis, a Swiss multinational pharmaceutical company. Ligelizumab works by targeting and neutralizing immunoglobulin E (IgE), a type of antibody that plays a key role in allergic reactions.

Mechanism of Action[edit]

Ligelizumab is a monoclonal antibody that binds to IgE, preventing it from attaching to mast cells and basophils. This inhibits the release of inflammatory mediators like histamine, which are responsible for the symptoms of CSU.

Clinical Trials[edit]

Ligelizumab has undergone several clinical trials to evaluate its safety and efficacy. In a Phase IIb study, ligelizumab demonstrated superior efficacy compared to omalizumab, another IgE inhibitor, in patients with CSU who were unresponsive to antihistamines.

Approval[edit]

As of 2021, ligelizumab is not yet approved by the Food and Drug Administration (FDA) or the European Medicines Agency (EMA). However, it is under review by these regulatory bodies.

See Also[edit]

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