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RecruitingNCT06726200

Injectable and under-the-tongue buprenorphine for people who use fentanyl

About this title

A Clinical Trial Comparing Buprenorphine Formulations for High Potency Synthetic Opioid Use

Read the official source — NCT06726200
Medication studyAges 18–65United StatesAddiction
The study in practice

Understand this study

Who could participate?

Listed age limits: 18 years to 65 years.

Listed locations
New YorkSee all locations and recruitment
Study phase
Early phase 1An early first-in-human or very early safety study, usually focused on how a treatment behaves in the body.

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: February 25, 2026
Recruitment status
Recruiting
Enrollment listed in the registry
60
Sponsor
Rachel R. Luba
Sponsor type
Individual investigator
Study type
Drug
Intervention type
Medication / drug
Study phase
EARLY Phase 1An early first-in-human or very early safety study, usually focused on how a treatment behaves in the body.
Locations
United States
Age range
From 18 Years to 65 Years
Official registry ID
NCT06726200
Official title
Show the full official title

A Randomized Controlled Trial Examining Extended-Release Injectable Buprenorphine in Those Who Use High Potency Synthetic Opioids

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Recruitment & locations

Recruiting

New York

A listed location does not confirm current availability.

FAQ

Questions about this study

Who is behind this study?

The study sponsor is Rachel R. Luba.

Does this study involve medication?

Yes. The study involves medication, including Buprenorphine + naloxone (Suboxone) and Buprenorphine Injection.

Who can participate?

Listed age limits: 18 years to 65 years.

Is this study still recruiting?

The registry lists this study as recruiting.

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