Novartis's Farydak Enters EU As First-In-Class Myeloma Therapy
This article was originally published in Scrip
Executive Summary
Novartis AG's histone deacetylase (HDAC) inhibitor Farydak (panobinostat; also known as Faridak) has secured approval in Europe for the treatment of multiple myeloma – making it the first drug of this class to reach the European market.
You may also be interested in...
Deal Watch: Celgene Joins Line Of Partners Tapping Exscientia’s AI-Driven Discovery Engine
While the proposed Bristol/Celgene merger nears an April vote, Celgene continues a recent spate of deal-making, paying $25m up front to Exscientia to discover small molecule candidates for cancer and autoimmune disease.
Accessing Venture Debt From The EIB
Tips from Gergely Krajcsi, senior investment officer at the European Investment Bank, on how biotechs can access loans for faster growth.
In Vivo's 2024 Rising Leaders At A Glance
Top 30 leaders: see the list of industry influencers highlighted in the fifth edition of In Vivo's Rising Leaders series.