Cidara begins Phase I trial of lead antifungal product candidate CD101 IV
"The advancement of our first product candidate into the clinic ahead of schedule is a significant next step toward our mission to address the urgent need for effective
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).
CL-H1T, which contains fast-dissolving promethazine and sumatriptan, is being developed to treat migraine headache pain and migraine-induced nausea and vomiting (MINV). Charleston Laboratories chief scientific officer Bernard Schachtel