Yes, Crizanlizumab, marketed under the brand name Adakveo, is FDA approved. The U.S. Food and Drug Administration (FDA) approved Crizanlizumab on November 15, 2019. This approval was specifically for its use in reducing the frequency of vaso-occlusive crises (painful episodes) in patients with sickle cell disease.
Crizanlizumab is a monoclonal antibody used to treat sickle cell disease by reducing the occurrence of vaso-occlusive crises (VOCs). These crises are painful episodes that occur when the sickled red blood cells block blood flow to different parts of the body. Crizanlizumab works by binding to a protein called P-selectin on the surface of blood vessels and certain blood cells, preventing these cells from sticking to each other and the vessel walls, thus reducing the blockage and associated pain.
Crizanlizumab is indicated for the treatment of patients with sickle cell disease to reduce the frequency of vaso-occlusive crises. It is approved for use in adults and children aged 16 years and older.
Crizanlizumab is administered as an intravenous (IV) infusion. The typical dosing schedule is:
Each infusion takes about 30 minutes to complete. The dosage is calculated based on the patient’s actual body weight and can be given with or without hydroxyurea, another medication commonly used to treat sickle cell disease.
Common Side Effects
Serious Side Effects
Some side effects may occur within 24 hours of receiving Crizanlizumab, including:
Patients should inform their healthcare provider about all medications they are taking, including prescription drugs, over-the-counter medicines, vitamins, and herbal supplements, as these can affect the efficacy and safety of Crizanlizumab.
Crizanlizumab should be stored according to the healthcare provider's instructions, typically under refrigeration until it is ready to be used.
Crizanlizumab (Adakveo) is an FDA-approved treatment that offers a new option for patients with sickle cell disease to manage and reduce the frequency of vaso-occlusive crises. Approved in November 2019, it represents a significant advancement in the management of this chronic and painful condition. Patients should work closely with their healthcare providers to understand the benefits and risks associated with this treatment.
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