FDA grants priority review to bluebird bio’s BLA for SCD gene therapy
Bluebird is seeking approval for treating a rare genetic disease, SCD, in patients aged 12 years and above having a history of vaso-occlusive events. A modified form of
The US Food and Drug Administration (FDA) has approved Viatris’ Ryzumvi (phentolamine ophthalmic solution 0.75%) to treat presbyopia in adults.