drugset / Trial / NCT07087938
Cannabichromene Safety in Rheumatoid Arthritis
RandomizedParallel-groupSingle-blindTreatment
Summary
For this quantitative study, the investigators will collect data on human safety and side-effects of Cannabichromene (CBC) and whether CBC reduces blood inflammatory markers and Rheumatoid Arthritis (RA) disease activity. The participants will participate in an ABAB design with 2 doses of CBC across the A phases. They will attend 5 in-person clinic visits where they will have physical evaluations, complete self-report forms, and have blood drawn for the following tests: hs-CRP, ESR, IL-6, TNF, Complete Blood Count \[CBC\], and CMP.
Timeline
- Start
- 2028-07-15
- Primary completion
- 2030-05-31
- Completion
- 2030-05-31
Outcome
Outcome not reported
Stopped (Enrollment): “This study was put on clinical hold with the FDA prior to beginning enrollment due to insufficient preclinical evidence.”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Cannabichromene | Small molecule | 400 mg | — |
| Comparator | Cannabichromene | Small molecule | 600 mg | — |