Alexion's Soliris wins US priority review in hemolytic uremic syndrome
This article was originally published in Scrip
The US FDA granted a six-month priority review to Alexion Pharmaceuticals' supplemental biologics license application (sBLA) for Soliris (eculizumab), a first-in-class terminal complement inhibitor, as a treatment for patients with atypical hemolytic uremic syndrome (aHUS), a chronic, ultra-rare disease characterized by the formation of blood clots in small blood vessels throughout the body.
You may also be interested in...
With new funding in hand, Moderna and its infectious disease venture Valera are going full-speed ahead with a Zika vaccine, taking an mRNA approach, which they said could be a more rapid strategy to try to stop the disease.
Allergan CEO Brent Saunders vows not to engage in price gouging and says his firm will limit cost increases to single-digit percentages, occurring only once per year. But it's unclear whether Saunders will stand as a lone wolf in the industry or if others will make similar pledges.
Hillary Clinton's plan to rein in high prices of older medicines, which includes creating a federal panel that has authority to impose fines, may grab headlines, but some analysts think it's unlikely to get very far in a divided Washington.