Following swiftly on its US regulatory approval last week, biotech major Amgen (Nasdaq: AMGN) yesterday announced that its Evenity (romosozumab-aqqg) is now available for shipment to wholesalers in the USA.
Evenity’s US approval is for the treatment of osteoporosis in postmenopausal women at high risk for fracture and is a successor to s a successor to the company’s $2 billion a year osteoporosis blockbuster Prolia (denosumab), which is approaching patent expiry.
"Osteoporosis is a silent disease that can lead to devastating consequences. Unfortunately, only 20 percent of women who have experienced a fracture receive any type of osteoporosis treatment post-fracture," said Murdo Gordon, executive vice president of global commercial operations at Amgen. "This is unacceptable for the millions of women who have suffered from an osteoporosis-related fracture. We need to urgently make postmenopausal osteoporosis a women's health priority," he added.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze