Rare 2030 Action Campaign Pushing for European Plan for Rare Diseases
Eurordis opened a campaign, called Rare 2030 Action, that is seeking to establish a European action plan for rare diseases to ensure that none of the 30 million people in Europe living with rare diseases are left behind by the start of a new decade. As part of the...
SMA Added to North Carolina’s Newborn Screening Program
As of this May, all babies born in North Carolina are now being tested at birth for spinal muscular atrophy (SMA). Newborn screening involves genetic testing of infants immediately after birth for mutations that are known causes of diseases like SMA — the most common...
UK NICE Expands Access to Spinraza for SMA Type 3
A decision from England’s National Institute for Health and Care Excellence (NICE) will make Spinraza (nusinersen) available to people with spinal muscular atrophy (SMA) type 3 who are unable to walk. In England, Spinraza is available through a managed access...
German Study Urges Newborn SMA Screening, Citing Better Outcomes
Newborn screening can aid in the early diagnosis and prompt treatment of spinal muscular atrophy (SMA), which can lead to better clinical outcomes, according to a German study. “We strongly recommend that newborn screening for SMA ought to become universal in...HCP — SMA News Today
BioNews Services, LLC
3 W Garden St
Suite 354
Pensacola, FL 32502
Email: [email protected]
Phone: 1-800-936-1363