The focus at Isis turns to the near-term prospects of an approval for the cholesterol drug Kynamro and to business development.
Now that Ionis Pharmaceuticals Inc. has received a milestone payment from partner Sanofi SA for the successful submission of an NDA for the familial hypercholesterolemia (FH) drug Kynamro (mipomersen), the biotech is turning its attention to the potential commercial launch and the next revenue drivers in the pipeline.
Isis reported second quarter financials Aug. 6 driven mainly by the $25 million milestone payment it received from Sanofi for...
Advanz Pharma would have had to show that the European Commission’s decision to revoke Ocaliva’s conditional marketing approval risked causing serious and irreparable harm, according to lawyers from Van Bael & Bellis.
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A new pilot aims to take Brazil closer to ‘digital transformation.’
While treatments for scleroderma are in development, none are approved for the condition that is associated with high morbidity and mortality. The European Medicines Agency says guidance on how to design development programs for the disorder is needed.
Madrigal Pharmaceuticals’ Rezdiffra is on track to become the first medicine approved in the EU for non-cirrhotic metabolic dysfunction-associated steatohepatitis after the European Medicines Agency recommended that it be granted conditional marketing authorization.
Highlights from Day Four of the BIO International Convention include policy concerns helping constrain dealmaking, Novartis discussing its approach to partnering, and Generate looking for funding to move into Phase III.
