Teva reaches settlements in Nuvigil patent case
These settlements dismiss a pending appeal with the US Court of Appeals for the Federal Circuit of a trial court decision that found the ‘570 patent to be
Akeso has received approval from China’s National Medical Products Administration (NMPA) for gumokimab (AK111), an anti-Interleukin-17 (IL-17) monoclonal antibody, to treat adults with moderate-to-severe plaque psoriasis.
The Class 1 resubmission follows a complete response letter issued by the FDA that referenced previously observed deficiencies at a Boehringer Ingelheim facility where empagliflozin will be manufactured.