June 15, 2026

Top News
Subcutaneous Risperidone Maintains Therapeutic Levels for 56 Days in Phase 1 Trial
Substance Use
Hospital addiction consultation service may improve outcomes at low cost

A hospital-based addiction consultation service (START) for opioid use disorder improves clinical outcomes at low cost.

Diagnosis & Treatment
UNM Researchers to Study the Use of Psilocybin in Group Therapy Treatment for PTSD - UNM HSC Newsroom

A clinical trial is being conducted to evaluate the efficacy of psilocybin administered within a group therapy setting for the treatment of PTSD.

Drug Development
HMNC Brain Health raises $50M Series B to advance two depression drugs

HMNC Brain Health raised $50M in Series B funding to advance its two depression drug candidates into mid-stage clinical trials.

Drug Development
A Phase 1 Open-Label Study Assessing the Safety and Pharmacokinetics of TV-46000, an Extended-Release Injectable Suspension of Risperidone for Subcutaneous Use

A Phase 1 study confirms the safety and pharmacokinetic profile of TV-46000 (Uzedy), a subcutaneous extended-release risperidone formulation, demonstrating therapeutic plasma levels maintained for up to 56 days with no new safety signals.

Mechanism of Action
Dextromethorphan Beyond the Cough: Exploring Its Psychedelic Potential: A Systematic Review

This systematic review characterizes the dose-dependent psychedelic effects of dextromethorphan, noting hallucinatory phenomena at 300-400 mg, but concludes evidence is insufficient to define therapeutic parameters for psychiatric use.

Clinical Pearls

Bite-sized clinical takeaways from today's literature (sources from Jan 07 – Jun 15)

  • Consider pre-treatment ACKR1 genetic testing for patients prescribed clozapine to mitigate the risk of severe neutropenia.
  • Monitor closely for serious psychiatric adverse events in patients using cannabis, given high rates of hospitalization and death in pharmacovigilance data.
  • Note that Uzedy (subcutaneous extended-release risperidone) maintains therapeutic plasma levels for up to 56 days with no new safety signals in Phase 1 studies.
  • Be aware that dextromethorphan doses of 300-400 mg can induce hallucinatory phenomena, so evidence is currently insufficient to define safe psychiatric therapeutic parameters.
  • Consider prucalopride as a potential off-label repurposing option for depression-related cognitive dysfunction, based on early-phase trial data showing improvement in brain fog.
  • Evaluate the START hospital-based addiction consultation service model for improving opioid use disorder outcomes at low cost.
  • Recognize that single-dose psilocybin has shown promise in providing months of relief from chronic suicidal thoughts in preliminary studies.
  • Keep an eye on ongoing Phase 1 trials for TV-46000 to confirm long-term safety and pharmacokinetic profiles before wider clinical adoption.

Substance Use 1

Cannabis and Cannabinoid-Related Suspected Adverse Drug Reactions: Global Patterns and Cross-National Analysis Based on VigiBase® Data

A global pharmacovigilance analysis of nearly 10,000 cannabis-related adverse drug reaction reports reveals that psychiatric and nervous system disorders are the most frequent suspected side effects, with a high proportion of serious outcomes including hospitalization and death.

Diagnosis & Treatment 1

A single dose of psilocybin provides months of relief from chronic suicidal thoughts in new study - PsyPost

A single dose of psilocybin provided months of relief from chronic suicidal thoughts, highlighting a potential therapeutic application for this psychedelic compound in psychiatry.

Drug Development 1

Laxative drug could ease depression-related brain fog, early trial suggests

An early-phase trial suggests the constipation drug prucalopride, a 5-HT4 receptor agonist, may improve cognitive function in individuals with a history of depression, highlighting potential repurposing opportunities for treating depression-related brain fog.

Pharmacogenomics 1

ACKR1 genetic testing should be offered before starting clozapine treatment - Nature

This article advocates for pre-treatment ACKR1 genetic testing to mitigate the risk of severe neutropenia in patients prescribed clozapine, highlighting a pharmacogenomic approach to prescribing safety.