MedCity News August 12, 2024
Frank Vinluan

FDA approval of Ascendis Pharma’s Yorvipath is just in time for patients with hypoparathyroidism as Takeda Pharmaceutical will soon stop making the only drug therapy for the rare disorder. But competition could come from others, including an AstraZeneca peptide in late-stage development.

Patients with hypoparathyroidism have been clamoring for an alternative to a Takeda Pharmaceutical therapy set to cease production by the end of the year, leaving them with no drug treatments. FDA approval of an Ascendis Pharma drug finally gives them another one, albeit much later than expected.

Ascendis Pharma announced Monday that the FDA approved its hypoparathyroidism therapy, a peptide drug intended to bring deficient levels of thyroid hormone to within the normal range in adults. The regulatory...

Today's Sponsors

Venturous
Got healthcare questions? Just ask Transcarent

Today's Sponsor

Venturous

 
Topics: Biotechnology, FDA, Govt Agencies, Pharma, Pharma / Biotech
Amgen starts two critical late-stage trials for weight loss drug MariTide
Patient Access To Cheaper Biosimilar Drugs Varies Significantly Across Pharmacy Benefit Managers
Novo Nordisk offers Wegovy for less than half the price through new direct-to-consumer pharmacy
'Not just adding another drug to your pharmacy': CAR T, explained
Private equity firm to buy Walgreens for $10B, report says

Share This Article