Condition: Primary Sclerosing Cholangitis · Sponsor: Aparna Goel
Primary objective: To evaluate the efficacy of hymecromone plus standard of care compared with standard of care alone in the treatment of adolescents and adults with primary sclerosing cholangitis (PSC). Secondary objectives: To evaluate the change in Alkaline Phosphatase (ALP) from baseline to 6 months post-treatment following treatment with hymecromone plus standard of care compared with standard of care. To evaluate changes in biomarkers of PSC disease during hymecromone treatment, namely: (a) fibrotic effect (FibroScan); (b) inflammatory biomarkers (serum Hyaluronan (HA)); and, (c) T-cell count.
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| Stanford Clinic | Redwood City, California, United States | Recruiting |
| Stanford Clinic | Stanford, California, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05295680