“…Indeed, although D1 and D2 receptors were coidentified, the D1 receptor remained very much a “Cinderella” site until the identification of the first selective D1 antagonists and initial evidence that D1 receptors were not only behaviorally relevant but also participated in important functional interactions with D2 receptors . Initial clinical studies with the selective D1 antagonist ecopipam (SCH 39166) indicated it and another selective D1 antagonist (NNC 01‐0687) to be without material antipsychotic activity or major adverse effects . Subsequent clinical studies with ecopipam have focused variably on cocaine abuse, obesity, gambling disorder and, most recently, Tourette syndrome.…”