Investigating (2R,6R)-HNK for Acute Pain

This study is looking into a new experimental drug called (2R,6R)-hydroxynorketamine (HNK) to see if it can help reduce short-term pain in healthy adults. Opioid pain medications can be addictive, and researchers are searching for new options. HNK is related to ketamine and may offer pain relief with fewer side effects. You might be able to join if you are a healthy adult between 18 and 60 years old. The main goal is to see if a single dose of HNK can reduce pain during special tests. This study aims to understand if HNK has pain-relieving effects and how it works in the brain, which could lead to new pain treatments.

Study design
This is a randomized, double-blind (you and your doctor won't know if you're getting the drug or placebo), placebo-controlled study involving 92 healthy volunteers.
What's involved
You will receive a single intravenous (IV) infusion of either HNK or a placebo over about 40 minutes. You will have inpatient and outpatient visits.
Compensation
Not stated in the trial record.
Follow-up
Pain ratings will be measured at 3-5 hours after the infusion, and secondary outcomes will be assessed immediately after infusion, after 4-5 hours, and one day later.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07504601

Investigating the Analgesic Potential of (2R,6R)-HNK in Acute Pain in Healthy Volunteers

Not Yet Recruiting
PHASE2Ages 18–60InterventionalBasic science
National Center for Complementary and Integrative Health (NCCIH)
~92 participants
Updated 2026-09-17 on ClinicalTrials.gov
What's tested:(2R,6R)-HydroxynorketaminePlacebo

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Pain ratings during quantitative sensory testing (QST)
Measured over 3-5 hours after infusion
Healthy Volunteers

NCT07504601

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • National Institutes of Health Clinical Center

    Bethesda, Marylandstudy coordinator listed

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • Lauren Y Atlas, Ph.D. · PRINCIPAL_INVESTIGATOR · National Center for Complementary and Integrative Health (NCCIH)

Opens a ready-to-send draft in your own email app — review before sending.

  • Pain ratings during quantitative sensory testing (QST)3-5 hours after infusion

    Change in pain intensity ratings in response to experimentally induced nociceptive stimuli during quantitative sensory testing (QST), comparing (2R,6R)-hydroxynorketamine (HNK) with placebo in a randomized, double blind crossover design, controlling for baseline pain sensitivity.