
Psychiatry in the News: October 2023
Key Takeaways
- Evenamide was assessed in a 6-week, randomized, rater-blinded trial in TRS patients maintained on a single non-clozapine antipsychotic, focusing on safety/tolerability at 7.5–30 mg BID.
- After 6 months of evenamide treatment, 40% of patients improved sufficiently to no longer meet TRS severity criteria, suggesting potential for meaningful symptomatic de-escalation.
Here are some updates from the world of psychiatry throughout the month of October.
Experts discussed a wide variety of psychiatric disorders, treatments, and issues at the
Study Shows 40% of Patients With TRS No Longer Meet Severity Criteria Following Treatment With NCE
A study of a new chemical entity (NCE) for treatment-resistant schizophrenia (TRS) found that 40% of patients improved to the point of no longer meeting TRS severity criteria after 6 months of treatment.
Study 014/015—a 6-week, randomized, rater-blinded study by Newron Pharmaceuticals—evaluated the safety, tolerability, and efficacy of evenamide, an investigational NCE for the management of TRS. For study 014, investigators recruited a total of 161 patients with TRS who were consistently administered a therapeutic dose of a single antipsychotic medication, excluding clozapine, with the primary aim of assessing the safety and tolerability of orally administered evenamide at 3 predefined doses: 7.5 mg, 15 mg, and 30 mg twice a day.
Study Finds Connection Between Olanzapine/Samidorphan and Reduced Health Care Utilization in Patients With Schizophrenia, Bipolar I
A study found that a combination of olanzapine and samidorphan (OLZ/SAM) can help reduce health care resource utilization in patients with schizophrenia and bipolar I disorder.
The study, which was sponsored by Alkermes Inc and shared in a poster presentation at Psych Congress® 2023, is the first to assess the efficacy of OLZ/SAM—a combination of olanzapine, an atypical antipsychotic, and samidorphan, an opioid antagonist, which is marketed as Lybalvi—in a real-world setting.
Study Finds Esketamine Nasal Spray More Likely to Induce Remission in Treatment-Resistant MDD Than Quetiapine Extended Release
A long-term clinical trial comparing esketamine CIII nasal spray with quetiapine extended release found that esketamine had greater success with inducing remission in participants with treatment-resistant major depressive disorder (MDD).
The clinical trial—a randomized, open-label, active-controlled, rater-blinded, phase 3b study called ESCAPE-TRD—aimed to evaluate the efficacy of flexibly dosed esketamine nasal spray (Johnson & Johnson’s Spravato) in comparison with the efficacy of quetiapine extended release, both when combined with a selective serotonin reuptake inhibitor (SSRI) or a serotonin-norepinephrine reuptake inhibitor (SNRI), in patients with treatment-resistant MDD.
See more recent news coverage from Psychiatric Times
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The articles and interviews featured on this page were developed by Psychiatric Times editorial staff and contributors based on presentations delivered at Psych Congress®, an annual conference produced by HMP Global, LLC. Psychiatric Times is an independent publication and is not affiliated with, endorsed by, or sponsored by HMP Global, LLC. All content on this page reflects the independent editorial judgment of Psychiatric Times and does not represent the views, positions, or communications of HMP Global, LLC.











