Bavarian Nordic — Marts 2021
-
The PDUFA was March 27 for the company’s marketing application for dasiglucagon for congenital hyperinsulinism.Zealand Pharma dropped sharply in December on the announcement of topline data from the first Phase 3 trial evaluating dasiglucagon as a treatment of Congenital Hyperinsulinism (“CHI”).
-
Zealand Pharma surges on news of FDA approval for dasiglucagon
-
ZEGALOGUE (dasiglucagon) injection, for subcutaneous use. Initial U.S. Approval: 2021:
https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/214231s000lbl.pdf
-
Nyhederne har vist ikke helt forstået godkendelsen. De skriver der er en godkendelse af medfødt hyperinsulism, men det er produktet CHI der retter sig mod den sygdom. Det er hypopal pennen der er blevet godkendt, og det produkt retter sig mod en lidt anden sygdom.
Hello! It looks like you're interested in this conversation, but you don't have an account yet.
Getting fed up of having to scroll through the same posts each visit? When you register for an account, you'll always come back to exactly where you were before, and choose to be notified of new replies (either via email, or push notification). You'll also be able to save bookmarks and upvote posts to show your appreciation to other community members.
With your input, this post could be even better 💗
Tilmeld Log ind
rescue pen - så er der da basis for lidt mere i løbet af ugen 
