Clinical trial

A Randomized, Double-blind, Placebo-controlled Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Oral Doses of CB1 Antagonist ANEB-001 in Healthy Occasional Cannabis Users in a THC Challenge Test.

Name
AN01AC11
Description
The aim of this study is to investigate whether ANEB-001 effectively penetrates the brain and inhibits the psychotropic effects of Δ9-Tetrahydrocannabinol (THC), the main psychoactive constituent of cannabis. This randomized, placebo-controlled, double-blind study is designed as a proof-of-pharmacology and dose finding study for the antagonistic effect of ANEB-001 during a THC challenge. Results of this study will inform the future potential use of ANEB-001 as an emergency treatment for acute cannabinoid intoxication.
Trial arms
Trial start
2021-12-15
Estimated PCD
2023-08-26
Trial end
2023-08-26
Status
Completed
Phase
Early phase I
Treatment
ANEB-001
Experimental Treatment
Arms:
Part A - ANEB-001, Part B - Cohort 1 - ANEB-001, Part B - Cohort 2 - ANEB-001, Part B - Cohort 3 - ANEB-001, Part B - Cohort 4 - ANEB-001, Part B - Cohort 5 - ANEB-001, Part B - Cohort 6 - ANEB-001, Part C - Cohort 7 - ANEB-001, Part C - Cohort 8 - ANEB-001
Placebo
Placebo comparator
Arms:
Part A - Placebo, Part B - Cohort 1 - Placebo, Part B - Cohort 2 - Placebo, Part B - Cohort 3 - Placebo, Part B - Cohort 4 - Placebo, Part B - Cohort 5 - Placebo, Part B - Cohort 6 - Placebo
Size
154
Primary endpoint
Subjective Feeling High
Day 1
Postural stability
Day 1
Subjective Alertness
Day 1
Heart Rate
Day 1
Eligibility criteria
Inclusion Criteria: * Signed informed consent prior to any study-mandated procedure * BMI between 18 and 30 kg/m2 * Minimum weight 50 kg * Occasional cannabis user Exclusion Criteria: * Evidence of active or chronic condition that could interfere with, or which the treatment of might interfere with, the conduct of the study, or that would pose an unacceptable risk to the subject in the opinion of the investigator * Clinically significant abnormalities, as judged by the investigator * Positive Hepatitis B surface antigen, Hepatitis C antibody or HIV antibody at screening * Systolic blood pressure greater than 130 or less than 90 mm Hg and diastolic blood pressure greater than 95 or less than 50 mm Hg at screening Abnormal findings in the resting electrocardiogram * Use of any medications within 7 days of study drug administration, or less than 5 half-lives (whichever is longer). Exceptions are paracetamol and ibuprofen and topical medications. * Use of any vitamin, mineral, herbal and dietary supplements within 7 days of study drug administration, or less than 5 half-lives (whichever is longer) * Participation in an investigational drug or device study (last dosing of previous study was within 90 days prior to first dosing of this study) * History of abuse of addictive substances (alcohol, illegal substances) or current use of more than 21 units alcohol per week, drug abuse, or regular user of sedatives, hypnotics, tranquilizers, or any other addictive agent other than recreative use of THC * Positive test for drugs of abuse (other than THC) at screening. * Positive test for drugs of abuse pre-dose * Clinically significant suicidal ideation in the past 5 years as judged by the investigator or any life-time suicide attempts * History of cannabis-induced psychosis, schizophrenia or other clinically relevant psychiatric disorders, as judged by the investigator. * History of a clinically significant mood disorder, including but not limited to major depressive disorder, as judged by the investigator.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE2'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'SEQUENTIAL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'QUADRUPLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR']}}, 'enrollmentInfo': {'count': 154, 'type': 'ACTUAL'}}
Updated at
2023-08-29

1 organization

2 products

1 indication

Product
Placebo
Product
ANEB-001