FDA Grants Fast Track Status to RNS60 for Revolutionary Ischemic Stroke Treatment

FDA Grants Fast Track Status to RNS60 for Revolutionary Ischemic Stroke Treatment

Revalesio, a clinical-stage biopharmaceutical company, has been granted Fast Track designation by the U.S. Food and Drug Administration (FDA) for its lead investigational therapy, RNS60, targeting acute ischemic stroke. This designation aims to expedite the development and review of RNS60, a proprietary oxygen-enriched saline designed to protect brain tissue following ischemic injury, addressing a critical gap in stroke treatment. Acute ischemic stroke, a leading cause of long-term disability and the second leading cause of death globally, often results in permanent neurological deficits despite advances in endovascular thrombectomy, which restores blood flow but does not prevent tissue damage post-reperfusion. Currently, no FDA-approved therapies exist to mitigate brain tissue loss during or after reperfusion, underscoring the urgent need for innovative treatments.

FDA Approves SKYTROFA for Adult Growth Hormone Deficiency

FDA Approves SKYTROFA for Adult Growth Hormone Deficiency

Growth hormone deficiency (GHD) in adults, a rare disorder characterized by decreased or absent endogenous growth hormone production, leads to abnormal body composition, dyslipidemia, insulin resistance, and increased risks of metabolic syndrome, cardiovascular disease, and impaired quality of life, including cognitive and psychological issues. Sodium-glucose cotransporter-2 (SGLT2) inhibitors have shown promise in managing related comorbidities, but adherence to the standard daily somatropin injections remains a challenge. Ascendis Pharma A/S has developed SKYTROFA® (lonapegsomatropin-tcgd), a prodrug of somatropin administered weekly, previously approved by the U.S. Food & Drug Administration (FDA) in 2021 for pediatric GHD. This study evaluates its efficacy and safety for adult GHD.