This real-world study examined initiation strategies and subsequent outcomes for solriamfetol (Sunosi®), a wake-promoting agent used to treat excessive daytime sleepiness (EDS) in obstruc...
This study assessed safety and efficacy of low-sodium oxybate (LXB) in participants with narcolepsy both with and without comorbid psychiatric disorders in a phase 3 clinical study. Safet...
Zuranolone 50 mg initiated alone (WATERFALL Study) or co-initiated with a standard-of-care antidepressant (CORAL Study) was well-tolerated in adults with major depressive disorder. In WAT...
This study aimed to assess the efficacy of the Obsessive Compulsive Inventory questionnaire (OCI-4), a four-item OCD screening tool used to detect OCD, in a cohort of college students. Th...
The American Association of Psychiatric Pharmacists (AAPP) has sought to operationalize the concept of psychotropic stewardship through formalizing a consensus-based set of outcomes and m...
In the EMERGENT-3 phase 3 trial, KarXT, a combination of xanomeline (M1/M4 muscarinic receptor agonist) and trospium chloride (muscarinic receptor antagonist), demonstrated significant ef...
Antipsychotic (AP) and vesicular monoamine transporter type 2 inhibitor (VMAT2i) treatment patterns post-tardive dyskinesia (TD) diagnosis are unclear. Deutetrabenazine (DTBZ) is a VMAT2i...
START is an ongoing, noninterventional, prospective, single-arm, 2-cohort (tardive dyskinesia [TD] and Huntington disease) study evaluating the effectiveness of deutetrabenazine initiated...
The Pathway Platform supports MBC for patients with MDD by integrating a patient-facing app with EHR. This real-world Pathway Platform implementation study in primary care demonstrated si...