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United Kingdom's MHRA Approves YORVIPATH® (palopegteriparatide) in Great Britain for the Treatment of Adults with Chronic Hypoparathyroidism

COPENHAGEN, Denmark, April 24, 2024 (GLOBE NEWSWIRE) Ascendis Pharma A/S (Nasdaq: ASND) today announced that the United Kingdom’s Medicines & Healthcare products Regulatory Agency (MHRA) has granted marketing authorization for YORVIPATH® (palopegteriparatide; developed as TransCon™ PTH) in Great Britain as a parathyroid hormone (PTH) replacement therapy indicated for the treatment of adults with chronic hypoparathyroidism, and has also granted YORVIPATH orphan drug status. YORVIPATH is a prod ....

United States , United Kingdom , Great Britain , Ascendis Pharma , Endocrine Society Guidelines , European Commission , European Society Of Endocrinology Consensus Statement , International Consensus Statement , European Medicines Agency , Exchange Commission , Regulatory Agency , Camilla Harder Harvig , Executive Vice President , Chief Commercial Officer , Marketing Authorisation Application , European Union , Society Guidelines , European Society , Endocrinology Consensus , Ascendi Annual Report , Great Britain , European Medicines Agency , Parathyroid Hormone , Forward Looking Statements ,

Medications Help Cut Risk Of Premature Death In ADHD Patients: Study

The latest study included 148,000 individuals in Sweden who were diagnosed with ADHD. The researchers noted that starting ADHD medications reduced their overall mortality risk, particularly from ....

Lin Li , Zheng Chang , International Consensus Statement , World Federation , Jama Network , Consensus Statement , Healthy Living , Premature Death , Early Death , Unnatural Causes ,

ADHD push warrants more attention

ADHD push warrants more attention
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