Condition: Breast Cancer · Sponsor: Medical University of South Carolina
This is a randomized placebo controlled partially blinded window of opportunity trial. A maximum of 84 patients with invasive breast cancer will be enrolled. Patients will be randomized 2:2:1:1 to either CBD low dose, CBD high dose, matching low dose placebo, or matching high dose placebo using permuted block randomization with random block sizes of 6 or 12. The time window between CBD or placebo initiation and surgery will be between 5 and 56 days.
This description comes directly from the study's public registry record.
HCC Clinical Trials Office · 843-792-9321 · hcc-clinical-trials@musc.edu
Always discuss trial participation with your own doctor first.
| Medical University of South Carolina | Charleston, South Carolina, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06148038