Yes, Pozelimab, marketed under the brand name Veopoz, is FDA approved. It received FDA approval for the treatment of complement hyperactivation, angiopathic thrombosis, protein-losing enteropathy (CHAPLE) syndrome in adults and children at least 1 year old.
Pozelimab is indicated for treating complement hyperactivation, angiopathic thrombosis, protein-losing enteropathy (CHAPLE) syndrome. This condition involves a rare genetic disorder that causes severe gastrointestinal problems and immune system dysfunction.
Pozelimab is a selective immunosuppressant that works by inhibiting specific components of the immune system to reduce the hyperactivation and subsequent damage caused by CHAPLE syndrome. This helps in controlling the symptoms and progression of the disease.
Common side effects include:
Serious side effects include:
Patients are advised to contact their doctor immediately if they experience any serious side effects. Side effects can also be reported to the FDA at 1-800-FDA-1088.
Pozelimab is only available through certified pharmacies and must be administered under a special program. Patients should carry a Patient Wallet Card that outlines symptoms of meningococcal or other infections to watch for and must keep this card with them at all times.
Pozelimab (Veopoz) is FDA approved for the treatment of complement hyperactivation, angiopathic thrombosis, protein-losing enteropathy (CHAPLE) syndrome in both adults and children aged 1 year and older. It is administered as an intravenous infusion followed by subcutaneous injections and requires careful monitoring due to potential serious side effects and increased risk of infections. This approval provides a significant treatment option for patients suffering from this rare and severe genetic disorder.
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