Merck terminates development of obesity drug
John Amatruda, senior vice president and research head of diabetes and obesity at Merck Research Laboratories, said: “Available Phase III data showed that both efficacy and adverse events
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).