Roche's Genentech Receives FDA Priority Review For Enspryng As First At-Home Subcutaneous Treatment For Thyroid Eye Disease

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ROCHE HOLDINGS AG

ROCHE HOLDINGS AG

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  • The filing application is based on improvements seen across key efficacy endpoints from the global Phase III SatraGO-1 and SatraGO-2 studies, including proptosis (bulging eyes) and diplopia (double vision) in active TED
  • Enspryng (satralizumab) has the potential to become the first at-home subcutaneous disease-modifying standard of care for TED
  • TED is an autoimmune disease affecting approximately 155 out of every 100,000 people that can lead to facial disfigurement and vision-threatening complications if left untreated