Teva touts new efficacy and safety data with ecopipam
The US unit of Teva Pharmaceutical Industries (NYSE and TASE: TEVA) today announced new data for ecopipam, a first-in-class investigational selective D1 (dopamine) receptor antagonist for the treatment of pediatric patients with Tourette syndrome.
Presented at the International Congress of Parkinson’s Disease and Movement Disorders (MDS) in Seoul, South Korea, the data include a post hoc analysis of safety and efficacy during the initial 8 weeks of treatment with ecopipam, long-term efficacy and safety from an interim analysis of an ongoing open-label extension (OLE) study, post hoc subgroup analyses and preclinical receptor selectivity findings.
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