EMA validates Amicus’ MAA for Galafold to treat Fabry patients
Galafold is the first investigational Fabry drug to be granted accelerated assessment in the European Union (EU). In the US, the company plans to carry out a pre-NDA
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).
The company presented the results of a clinical trial comparing Flublok Quadrivalent to a traditional egg-based quadrivalent inactivated vaccine. The data demonstrate superior performance of Flublok based on
PBM will have two representatives on Xalud’s Board of Directors and will also provide operational support to the Company. Xalud Therapeutics is an IND-stage platform gene therapy company