bluebird bio, Inc. announced the U.S. Food and Drug Administration has approved LYFGENIA?? , also known as lovo-cel, for the treatment of sickle cell disease in patients ages 12 and older who have a.
bluebird bio Details Plans for the Commercial Launch of LYFGENIA™ Gene Therapy for Patients Ages 12 and Older with Sickle Cell Disease and a History of Vaso-Occlusive Events streetinsider.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from streetinsider.com Daily Mail and Mail on Sunday newspapers.
bluebird bio (BLUE) Announces FDA Approval of LYFGENIA for Patients Ages 12 and Older with Sickle Cell Disease and a History of Vaso-Occlusive Events streetinsider.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from streetinsider.com Daily Mail and Mail on Sunday newspapers.
Severe vaso-occlusive events were eliminated for 94% of evaluable patients and all VOEs were eliminated for 88% of evaluable patients between 6 and 18 months post-infusion
LYFGENIA is the most.
Outcomes-based contract offerings available to both commercial payers and Medicaid
LYFGENIA will be available through bluebird’s established national network of Qualified Treatment Centers.