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Health Matters: FDA Approves Groundbreaking Gene-Editing Tool That Could Cure Sickle Cell Disease

More Americans could have access to a life-changing treatment, but it comes at an expensive price point per patient. ....

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FDA approves world-first gene editing treatment: Sickle cell therapy gives hope to 100,000 Americans with incurable disease - but it'll cost millions of dollars per DOSE

In a ground-breaking decision, the Food and Drug Administration approved the first gene therapies to treat people with sickle cell disease ....

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Sickle Cell Disease Association of America Inc. statement about gene therapy approval

Sickle Cell Disease Association of America Inc. statement about gene therapy approval
chicagocrusader.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from chicagocrusader.com Daily Mail and Mail on Sunday newspapers.

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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

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.

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Bluebird bio Announces FDA Approval of LYFGENIA™ (lovotibeglogene autotemcel) for Patients Ages 12 and Older with Sickle Cell Disease and a History of Vaso-Occlusive Events

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. ....

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