Hemostemix prepares IND application for ACP-01 to treat critical limb ischemia
The company said that the time frame for FDA review is about 30 days. CLI is caused by reduced blood flow to the legs and about half of
HAYA Therapeutics has secured fast track designation from the US Food and Drug Administration (FDA) for its investigational therapy, HTX-001, to treat symptomatic non-obstructive hypertrophic cardiomyopathy (nHCM).
The collaboration, which was facilitated by the Johnson & Johnson Innovation Center in Boston, utilizes Emulate’s Organs-on-Chips to advance the clinical goals for three Janssen R&D programs at