The U.S. Food and Drug Administration (FDA) has granted orphan drug designation for Intellia Therapeutics’ (NASDAQ: NTLA) lead asset NTLA-2002, for the treatment of hereditary angioedema (HAE).
NTLA-2002 is currently being evaluated in a Phase 1/2 study in adults with Type I or Type II HAE.
Stryker Corporation (NYSE:SYK) has launched the Gamma4 System to provide surgeons with the next generation of Stryker’s intramedullary nailing system. The…
Werewolf Therapeutics (NASDAQ: HOWL) has initiated patient dosing in a Phase 1/1b clinical trial evaluating WTX-124, its lead INDUKINET molecule targeting IL-2 for the treatment of solid tumors.
Arcturus Therapeutics Holdings Inc (NASDAQ:ARCT) received an award for up to $63.2 million from the Biomedical Advanced Research and Development Authority…