Sweden clears Tengion for neo-kidney augment phase 1 trial
The safety and delivery of Neo-Kidney Augment product will be assessed in around five patients with advanced chronic kidney disease (CKD) in Phase 1 trial. Tengion president and
Swedish Orphan Biovitrum (Sobi) has received a complete response letter from the US Food and Drug Administration (FDA) regarding its biologics licence application for nanoencapsulated sirolimus plus pegadricase (NASP), an investigational therapy intended for adults with uncontrolled gout.
The agreement will leverage Ra Pharmaceuticals’ Extreme Diversity platform for the development of peptide-like molecules with antibody diversity and specificity called Cyclomimetics. Ra Pharmaceuticals co-founder, president and CEO