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RecruitingNCT06575075

Testing two HNK doses for obsessive-compulsive symptoms

About this titleRead the official source — NCT06575075
Medication studyAges 18–65United StatesOCD
The study in practice

Understand this study

Who could participate?

This study is for people with OCD. Listed age limits: 18 years to 65 years. Other eligibility criteria apply.

What will I do during this study?

You receive one IV infusion of RR-HNK at 0.25 or 0.5 mg/kg, or a sterile-saline placebo (an inactive comparison treatment), depending on your assigned group. EEG (recording of the brain’s electrical activity) and computer-based behavioural tests are done before and after the infusion; symptom change is assessed through one week.

Listed locations
Palo AltoSee all locations and recruitment
Study phase
Phase 1 / Phase 2This study spans more than one phase, so it may combine goals such as safety, dosing, and early effectiveness.

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What to know before participating

A point to clarify

This summary does not cover all risks or eligibility requirements. What risks or changes to my care would apply to me?

Study clarity

Things to check before joining

Study start dateStarted: January 23, 2026
Recruitment status
Recruiting
Enrollment listed in the registry
45
Sponsor
Carolyn Rodriguez
Sponsor type
Unknown or unclear
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 1 / Phase 2This study spans more than one phase, so it may combine goals such as safety, dosing, and early effectiveness.
Locations
United States
Age range
From 18 Years to 65 Years
Official registry ID
NCT06575075
Official title
Show the full official title

A Double-blind, Placebo-controlled Study to Determine the Safety and Feasibility of Two Doses of Intravenous (2R, 6R)-Hydroxynorketamine (RR-HNK) in Adults With Obsessive-Compulsive Disorder

Recruitment & locations

Currently recruiting

Palo Alto

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FAQ

Questions about this study

Who is behind this study?

The study sponsor is Carolyn Rodriguez.

Does this study involve medication?

Yes. The study involves medication, including RR-HNK/Hydroxynorketamine and Placebo.

Who can participate?

This study is for people with OCD. Listed age limits: 18 years to 65 years. Other eligibility criteria apply.

Is this study still recruiting?

The registry lists this study as recruiting.

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