Kamada’s Glassia gets FDA orphan drug status for GVHD treatment
According to the preliminary human and animal studies, Glassia may be able to treat and reduce the severity of GVHD, a life threatening complication of allogeneic stem cell
The US Food and Drug Administration (FDA) has approved Pfizerās Tukysa (tucatinib) along with pertuzumab and trastuzumab as a maintenance therapy for breast cancer.
In addition to significantly strengthening the company’s balance sheet, Relmada’s CEO, Sergio Traversa, says the cash will help with its ambitious development strategy, "These funds enhance our flexibility
Developed using modern recombinant technology, Flublok is the only flu vaccine that is 100% egg-free and highly purified. Flublok also contains three times more active ingredients than traditional
Specifically designed as a supplement for biological drug production, including biosimiliars, EX-CELL Glycosylation Adjust (Gal+) allows users to easily achieve desired N-linked glycosylation by increasing the galactose site