This study focuses on Sickle Cell Disease, a condition where red blood cells become crescent-shaped and can block blood vessels, causing pain and other complications. The study will use crizanlizumab, which is given through an intravenous infusion (delivered directly into a vein). This medication is designed to help prevent blood cells from sticking together and forming blockages in blood vessels.
The purpose of this research is to continue providing crizanlizumab treatment to patients with Sickle Cell Disease who have previously participated in other studies of this medication. The treatment will be administered through an intravenous line every few weeks, with each dose calculated based on the patient’s weight. The maximum dose will be 7.5 milligrams per kilogram of body weight.
During the study, which may last up to 120 months, patients will receive regular infusions of crizanlizumab. The medical team will monitor the patients’ health and track any side effects that may occur during the treatment. This monitoring will help ensure patient safety throughout the study period.



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