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Important safety information (isi) what is hemgenix® Please see important safety information and full prescribing information on website. Gene therapy for hemophilia b aims to establish sustained factor ix activ.
In an oral presentation at the 18th annual congress of the european association for haemophilia and allied disorders (eahad), data showed that through. Hemophilia b is an ideal candidate for gene therapy Over 5 years of treatment in hemophilia b patients, gene therapy research shows sustained factor ix activity and safety.
By providing durable disease correction throughout the 24 months after gene therapy, etranacogene dezaparvovec provides a safe and effective therapeutic option for patients with severe or moderately severe haemophilia b.
48 intriguingly, the domain “dealing with hemophilia” scores. A key metric in gene therapy for genetic disease for patients, physicians, and payers is the durability of expression The phase 3 trial of etranacogene dezaparvovec is designed to follow participants for 5 years These data will thus be captured.
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