About this trial
The goal of this clinical trial is to learn how a investigational medicinal product (THC) affects psychological and physical responses in healthy adults with prior cannabis use experience. The main questions it aims to answer are:
\- How do different dose levels of the investigational medicinal product (THC) influence short-term subjective and physiological responses?
Researchers will compare three dose levels of the study drug to a placebo (a look-alike substance with no active ingredient) to see how responses vary across sessions.
Participants will:
* Attend four in-person study visits, each involving a single dose of either the study drug or placebo * Complete questionnaires about their moment-to-moment experiences * Have their heart rate, blood pressure, and other physical measures monitored * Undergo serial blood sampling to measure circulating biomarkers
Eligibility criteria
Qualifiers
Adults aged 18-55
No major medical or psychiatric conditions
At least one previous, well-tolerated experience with cannabis
Not currently pregnant or breastfeeding
Disqualifiers
Family history (first- or second-degree relatives) of bipolar disorder, psychosis, or schizophrenia
Significant negative reaction to cannabis in the past or known allergy to cannabis products
Currently using recreational drugs
Trial design
Treatments tested in this trial
- AVCN319301b (6mg)
- AVCN319301b (9mg)
- AVCN319301b (15mg)
- Placebo