Cannabis Withdrawal Study | Paid Clinical Research in the United States
Now Enrolling Across the United States

Researchers are studying ways to help adults manage cannabis withdrawal symptoms — and they need your help.

Adults ages 18–55 who have been diagnosed with cannabis use disorder may be eligible to take part in a paid clinical research study in the United States.

Ages 18 - 55 Years
Duration ~10 Weeks
Inpatient Stay ~7 Days
Location United States
About the Study

What is this study?

This is a Phase 3 clinical research study looking at whether an investigational medicine may help reduce cannabis withdrawal symptoms in adults with cannabis use disorder (CUD).

The study is randomized and double-blind, meaning neither you nor the study team will know which study treatment you are assigned to receive.

The study is sponsored by a pharmaceutical company and is conducted in accordance with Good Clinical Practice (GCP) guidelines and the Declaration of Helsinki.

Researchers are seeking adults ages 18–55 across the United States who meet the study's eligibility criteria.

Study at a Glance

Study Phase
Phase 3
Condition
Cannabis Use
Disorder (CUD)
Study Design
Randomized,
Double-Blind
Inpatient Stay
~7 Days
Total Duration
~10 Weeks
Standards
GCP &
Declaration of Helsinki
Reviewed by an independent IRB
Eligibility

Who Can Participate?

You may be eligible for this study if you meet the following criteria:

Adults ages 18 to 55 years old

Have received a diagnosis of cannabis use disorder (CUD) based on DSM-5 criteria, confirmed by a qualified study clinician

Currently use cannabis regularly and are willing to stop cannabis use after the study randomization date

Must have used cannabis during the Screening period, including on the day before randomization

Urine drug screen must be positive for THC at Screening and on the day of randomization

Urine drug screen must be negative for all other excluded or illicit substances at Screening and on the day of randomization, and negative for alcohol on the day of randomization

Think you might be a good fit?

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Important to Know

Who Should Not Participate?

This study may not be suitable for you if any of the following apply:

Individuals younger than 18 or older than 55 years of age

Individuals with a lifetime history of a DSM-5 diagnosis of schizophrenia, schizoaffective disorder, or bipolar disorder

Individuals who meet DSM-5 criteria for any current or past substance use disorder other than cannabis use disorder or nicotine use disorder

Individuals currently pregnant or breastfeeding, or who are unwilling to use acceptable contraception during the study

Individuals who have tested positive for illicit or excluded substances (other than cannabis/THC) at Screening or on the day of randomization

Individuals with a positive urine alcohol test on the day of randomization

Participation

What's Involved?

The study lasts approximately 10 weeks in total, including a screening period, a mandatory inpatient stay, outpatient visits, and a follow-up call.

PHASE 1

Week 1 (Days 1–7)

Inpatient Stay

You will stay at an inpatient research unit for approximately 7 days (overnight stays on Days 1 through 6), where the study team will monitor your health and administer the study medicine.

PHASE 2

Weeks 2–7 (Days 8–49)

Outpatient Visits

After discharge, you will attend outpatient clinic visits and complete daily evening video check-in calls with the study team through approximately Day 35, plus additional clinic visits through Day 49.

PHASE 3

Day 64 (approximately)

Follow-Up Call

A telephone follow-up call will take place approximately 30 days after your last dose to check on your health.

Compensation

Compensation

Compensation may be provided for time and travel.

Common Questions

Frequently Asked Questions

What is the purpose of this study?
Researchers are studying whether an investigational medicine may help reduce the symptoms people experience when stopping cannabis use. This is a research study — it is not a treatment program and does not guarantee any benefit.
Will I receive the investigational medicine?
This is a double-blind study with multiple treatment groups, including a placebo group. You will be randomly assigned to one group, and neither you nor the study team will know which treatment you receive during the study.
Who is sponsoring this study?
This study is sponsored by a pharmaceutical company. Full sponsor details will be provided to you by the study team during the informed consent process.
Is this study approved?
Yes. This study is approved and overseen by an Institutional Review Board (IRB), which is an independent committee that protects the rights and safety of research participants. The study follows Good Clinical Practice (GCP) guidelines and the principles of the Declaration of Helsinki.
Is participation voluntary?
Yes. Participation is completely voluntary. You may withdraw at any time without penalty and without affecting any care you currently receive.
What happens during the inpatient stay?
You will stay at a research facility for approximately 7 days. During this time, the study team will give you the study medicine, monitor your health, and collect safety information. You will be discharged once the study team confirms it is safe to do so.

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