Takeda outlines strategies to expand into India
Takeda’s basic plan consists of the strategies for expanding the Takeda group’s presence in India and at the same time, to pursue productivity and cost-effectiveness as a whole
The US Food and Drug Administration (FDA) has granted accelerated approval to Bristol Myers Squibb’s (BMS) Zenbexus (iberdomide), along with daratumumab and hyaluronidase-fihj and dexamethasone (ZDd), to treat adult multiple myeloma (MM) patients.
Results from the Phase III study showed that Lixisenatide once-daily in combination with basal insulin (with or without sulfonylurea) significantly improved glycemic control. Sanofi-aventis R&D executive vice president
The DispersinB topical wound spray was manufactured by Therapure Biopharma (Mississauga, ON, Canada), under current Good Manufacturing Practices (cGMP). DispersinB is an antibiofilm enzyme, which inhibits and disperses