AMDL announces corporate restructuring
The new divisions include an in vitro diagnostics (IVD) division specifically focused on accelerating AMDL’s market launch for the AMDL-ELISA DR-70 (FDP) cancer test; a cancer therapeutics division
The US Food and Drug Administration (FDA) has expanded the approved indication for Bristol Myers Squibb’s (BMS) Camzyos (mavacamten) to treat symptomatic obstructive hypertrophic cardiomyopathy (oHCM) in adults and paediatric patients weighing at least 30kg (66lb).
According to the company, preclinical studies demonstrated that INS-20 and the FDA-approved Neulasta are comparable in both their pharmacological and toxicological profile. Detailed analytical characterization also demonstrated that