EMA validates Biogen and Sobi’s MAA for Alprolix to treat hemophilia B
The MAA is based on results from two global Phase III clinical trials that examined the efficacy, safety and pharmacokinetics of Alprolix for hemophilia B. The two trials
HAYA Therapeutics has secured fast track designation from the US Food and Drug Administration (FDA) for its investigational therapy, HTX-001, to treat symptomatic non-obstructive hypertrophic cardiomyopathy (nHCM).
Farydak is the first histone deacetylase (HDAC) inhibitor approved in combination with bortezomib, a type of chemotherapy, and dexamethasone, an anti-inflammatory medication, to treat these patients who received
DPX-Survivac is Immunovaccine’s new T cell activating immunotherapy, while epacadostat (INCB24360) is Incyte’s investigational oral indoleamine 2,3-dioxygenase 1 (IDO1) inhibitor. Under the deal, both the firms will co-fund