Alexza completes enrollment for second Phase III acute agitation trial
The second AZ-004 Phase III clinical trial was initiated in July 2008 with a target enrollment of 300 patients, 314 patients were enrolled and Alexza expects to announce
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).