US FDA accepts Santhera, ReveraGen’s vamorolone NDA to treat DMD
The FDA is expected to complete the NDA review in October this year and stated that it currently has no plans to hold an advisory committee meeting to
The regulatory acceptance of application for marketing authorisation of tislelizumab is to treat first-line unresectable or metastatic HCC patients. The humanised IgG4 anti-PD-1 monoclonal antibody tislelizumab has been