This double-blind, placebo-controlled trial (n=45) will assess the safety and efficacy of two doses of intravenous (2R,6R)-Hydroxynorketamine (RR-HNK) in adults with obsessive-compulsive disorder (OCD). Participants will receive either 17.5mg/70kg or 35mg/70kg of RR-HNK, or a placebo, via a single infusion.
Led by Dr Carolyn Rodriguez at Stanford University, this study aims to understand how RR-HNK affects the brain and whether it can reduce OCD symptoms.
Participants, aged 18–65, must have a confirmed OCD diagnosis and have either failed at least one prior standard OCD treatment (such as serotonin reuptake inhibitors or cognitive-behavioural therapy) or declined these treatments. EEG and behavioural tests will be conducted before and after the infusion to assess changes in OCD severity, measured using the Yale-Brown Obsessive Compulsive Scale (YBOCS). The trial is funded by the National Institutes of Health (NIH) and is expected to run from December 2024 to November 2029.
Trial Details
The purpose of this study is to understand how RR-HNK works in the brain to bring about a reduction in OCD symptoms. This protocol examines the safety and efficacy of 2 dosage levels of intravenous RR-HNK administration in individuals with OCD.Trial Number NCT06575075
Sponsors & Collaborators
Stanford UniversityResearchers at Stanford are exploring the potential of ketamine, MDMA and psilocybin by connecting neuroscience, psychiatry and anesthesiology.
National Institutes of Health
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