FDA approves Auriga’s oral Liquadd for ADHD
The company has said that Liquadd will be launched during the second quarter of 2008. Frank Greico, CEO of Auriga, said: “This new product further solidifies company’s commitment
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 trial (study 06CCL3-001) is a multi-centre, randomized, double-blind, parallel-arm study that will compare the efficacy and safety of company’s twice-daily tramadol-acetaminophen combination product. The study, which is