RecruitingPhase 2NCT06511908

Investigation of the Antidepressant Effects of (2R,6R)-HNK, an Enhancer of Synaptic Glutamate Release, in Treatment-Resistant Depression

An Investigation of the Antidepressant Effects of (2R,6R)-HNK, an Enhancer of Synaptic Glutamate Release, in Treatment-Resistant Depression


Sponsor

National Institute of Mental Health (NIMH)

Enrollment

50 participants

Start Date

Nov 6, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

Background: Major depressive disorder (MDD) is a serious mental illness that can put people at risk of self-harm and death. Many drugs are used to treat MDD, but it can take a long time for them to be effective. Researchers want to know if a faster-acting drug, (2R,6R)-hydroxynorketamine (HNK), can better treat the symptoms of MDD. Objective: To test a study drug (HNK) in people with MDD. Eligibility: People aged 18 to 70 years with MDD. They must have had a screening assessment under protocol 01-M-0254. Design: Participants will be tapered off their current MDD drugs over 2 to 5 weeks. They will stay off of the drugs for up to 2 weeks prior to starting the study medication and procedures. They will have a physical exam with blood tests. They will have tests of their heart function, mood, and thinking. They will answer questions about their symptoms. They may choose to have imaging scans and scans of their brain activity. HNK is given through a tube attached to a needle inserted into a vein. Participants will receive infusions on this schedule: They will receive 4 infusions over 2 weeks. They will stay in the clinical center overnight after each infusion or for the duration of the study. They will receive no drugs for 2 to 3 weeks. They will have 4 more infusions over 2 weeks, with overnight stays after each or for the duration of the study. One set of 4 infusions will be the HNK. The other set of 4 infusions will be a placebo. A placebo looks just like the real drug but contains no medicine. Participants will not know when they are getting the HNK or placebo. ...


Eligibility

Min Age: 18 YearsMax Age: 70 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a compound called (2R,6R)-HNK — a natural byproduct of ketamine — to see if it can relieve depression in people who have not responded to standard antidepressants. Unlike ketamine itself, this compound may work without causing dissociative or intoxicating side effects. **You may be eligible if...** - You are between 18 and 70 years old - You have been diagnosed with major depressive disorder (MDD), currently in an active depressive episode lasting at least 2 weeks - You have not responded to multiple antidepressant medications - Your depression score is sufficiently high on standard rating scales - You have previously been screened under a related NIH protocol (01-M-0254) **You may NOT be eligible if...** - You have a history of psychosis, schizophrenia, or bipolar disorder - You have a significant substance use disorder (especially alcohol or drugs in the past year) - You have serious heart, liver, or kidney conditions - You are pregnant, breastfeeding, or planning to become pregnant - You are actively suicidal Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUG(2R,6R)-hydroxynorketamine (0.25 to 2.0 mg/kg)

Arm 1 and 2 Experimental Intervention

DRUGPlacebo

Arm 1 and 2 Control Intervention


Locations(1)

National Institutes of Health Clinical Center

Bethesda, Maryland, United States

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NCT06511908


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