FDA extends market exclusivity for BioMarin’s Kuvan powder for oral solution and tablets
The FDA action extends KUVAN’s market exclusivity to June 2015 and is based on studies submitted in response to a written request by the FDA to investigate the
Bristol Myers Squibb (BMS) is set to merge its separate research and development (R&D) departments into a single entity, effective from 1 January 2027.
These cell banks are necessary steps in the production of the cells to be encapsulated using the cell-in-a-Box technology for Nuvilex’s Phase IIb clinical trials in advanced, inoperable