Yes, Ozanimod is FDA approved. The U.S. Food and Drug Administration (FDA) approved Ozanimod, marketed under the brand name Zeposia, on March 25, 2020. Ozanimod belongs to the drug class of selective immunosuppressants.
Ozanimod is an oral medication used to treat relapsing forms of multiple sclerosis (MS) in adults, which includes clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease. Additionally, it is used to treat adults with moderately to severely active ulcerative colitis.
Ozanimod works by modulating the immune system. It selectively targets and binds to sphingosine 1-phosphate receptors, which are involved in the movement of immune cells. By binding to these receptors, Ozanimod prevents the immune cells from reaching the central nervous system and gastrointestinal tract, thus reducing inflammation and the autoimmune response that contributes to the symptoms of multiple sclerosis and ulcerative colitis.
Ozanimod is available in oral capsules and follows a specific dosing schedule to minimize side effects:
This titration schedule helps to reduce the risk of side effects associated with the initiation of Ozanimod therapy.
Common side effects of Ozanimod include:
Serious side effects that require immediate medical attention include slow heartbeats, chest pain, shortness of breath, severe headache, vision changes, and symptoms of infection.
Ozanimod can interact with a variety of medications, including heart rhythm medications, antidepressants, and drugs that weaken the immune system. Patients should inform their healthcare provider about all medications they are taking to avoid potential interactions.
Ozanimod (Zeposia) is an FDA-approved medication for the treatment of relapsing forms of multiple sclerosis and moderately to severely active ulcerative colitis in adults. Approved on March 25, 2020, it offers a targeted approach to managing these conditions by modulating the immune system. Patients should follow the prescribed dosing schedule and consult their healthcare provider for monitoring and management of any potential side effects or drug interactions.
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