Synosia SYN115 Study Shows Positive Results
The phase IIa trial was a randomised, double-blind, placebo-controlled, cross-over study in 24 parkinson’s patients using doses up to 120mg/day for one week. The effects of SYN-115 as
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).