Fatty Acid Amide Hydrolase (FAAH) Inhibitor Treatment of Cannabis Use Disorder (CUD)

Cannabis Use Disorder Clinical Trial

— FAAH-I MULTI  

Official title:

A Phase 2B, 8-week, Randomized, Double-Blind, Placebo-Controlled, Parallel Study to Evaluate Efficacy, Safety and Tolerability of the Fatty Acid Amide Hydrolase (FAAH) Inhibitor PF-04457845 in Adults With DSM5 Current Cannabis Use Disorder (CUD)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03386487
• Other study ID #: 2000022450
• Secondary ID: 1U01DA045372-01
• Status: Completed
• Phase: Phase 2
• Start date: January 14, 2019
• Est. completion date: July 25, 2022

Study information

• Verified date: February 2024
• Source: Yale University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A Phase 2B, 8-Week, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Efficacy, Safety and Tolerability of the Fatty Acid Amide Hydrolase (FAAH) Inhibitor PF-04457845 in Adults with DSM-5 Current Cannabis Use Disorder (CUD)

Description:

The efficacy, safety and tolerability of the FAAH Inhibitor PF-0447845 in reducing cannabis use will be studied in a 4-site randomized, double-blind, placebo-controlled, parallel-group, outpatient clinical trial comparing PF-04457845 (4mg) and placebo in DSM-5 CUD individuals. Participants will be randomized in a 1:1 ratio to either PF-04457845 or placebo using random block sizes of 2 and 4, stratified by site and degree of cannabis use. Participants will receive motivational interviewing for 2 weeks before being randomized to receive study medication to make a quit attempt within the first week of treatment. Participants will receive active or placebo PF-04457845 for 8 weeks during which time they will be evaluated weekly in face to face visits. In addition, daily assessment of adherence to study medication and cannabinoid use will be conducted daily by cellphone. Measures of cannabinoid exposure (self-reported and urine toxicology), and problems related to the use of cannabis, will be assessed.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 228
• Est. completion date: July 25, 2022
• Est. primary completion date: July 25, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 60 Years

Eligibility

Inclusion Criteria:

1. Ages 18-60 years, inclusive.

2. Male or Female.

3. Individuals with DSM-V criteria for Cannabis Use Disorder .

4. Positive for urinary THC-COOH at both screening visits.

5. Must express a willingness at screening to set a date within the first week of randomization to attempt to quit using cannabis.

Exclusion Criteria:

1. Clinically significant unstable medical disorders (as determined by the site investigator).

2. Laboratory tests with clinically significant abnormalities (as determined by the site investigator)

3. Pregnancy by history and or laboratory confirmation (serum HCG).

4. Lactation.

5. Physiological dependence on another substance.

Related Conditions & MeSH terms

• Cannabis Use Disorder
• Marijuana Abuse

Intervention

Drug:
• PF 04457845
Study medication will be administered at 4mg by mouth daily for eight weeks.
• Placebo Oral Tablet
Placebo comparator will be administered by mouth daily for eight weeks.

Locations

Country	Name	City	State
United States	Johns Hopkins University	Baltimore	Maryland
United States	Medical University of South Carolina	Charleston	South Carolina
United States	Connecticut Mental Health Center	New Haven	Connecticut
United States	Columbia University Medical College / New York State Psychiatric Institute	New York	New York

Sponsors (5)

Lead Sponsor	Collaborator
Yale University	Columbia University, Johns Hopkins University, Medical University of South Carolina, National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Time Line Follow Back (TLFB) for Cannabis Use	Change in the average number of times per day of self-reported cannabis consumption measured by the Timeline Follow Back approach for Cannabis Use in which participants quantify and report their frequency of cannabis use prior to study participation and throughout the study. Differences between groups in the change from baseline use (2 weeks prior to randomization) in the average number of times per day of self-reported consumption of cannabis or a cannabis containing product in the last 4 weeks of treatment captured using the daily TLFB data collected during CAROMA calls.	Change from baseline in self reported cannabis use as measured by the TLFB approach at baseline and then weekly average daily use over 8 weeks.
Primary	Urinary Levels of THC-COOH (ng/ml)	Assay of the levels of the principal metabolite of THC (THC-COOH) in urine samples at baseline and bi-weekly over 8 weeks.	baseline, week 1, week 3, week 5, week 7, and week 9 visits