Sanofi, Lead Pharma to develop new autoimmune treatments
The research collaboration and license agreement will see new small-molecule therapies directed against the nuclear hormone receptors called ROR gamma (t) to treat these disorders. As part of
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).
Lightlake is focused on developing addiction treatments based on its expertise in opioid antagonists. In December 2014, Lightlake in partnership with the National Institute on Drug Abuse (NIDA),
A total of 2,021 patients were enrolled in the both the randomized, double-blind, placebo-controlled, multi-centered trials at participating clinics and practices in the Americas, Europe, Australia, New Zealand