Clinical trial
Phase 2
Interventional
Ages 18 and up
Nemolizumab for the Treatment of Moderate to Severe Chronic Hepatic Pruritus
Run by Mayo Clinic · NCT07843420 · Data updated 2026-11-12
Not yet open. This study is not taking new participants. Its registered completion date is 2028-11.
The purpose of this research is to investigate the efficacy of nemolizumab in the treatment of adults with moderate to severe chronic hepatic pruritus.
Quick facts
| Phase | Phase 2 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 15 (estimated) |
| Sponsor | Mayo Clinic Academic / other |
| Drugs / interventions | Nemolizumab-ilto |
| Locations | 1 site (United States) |
| Trial ID | NCT07843420 on ClinicalTrials.gov |
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Cholestatic pruritus secondary primary biliary sclerosis (PBS) or primary sclerosing cholangitis (PSC) * Pruritus that is chronic in duration (greater equal to 6 months) * Pruritus severity with a peak pruritus numerical rating score of ≥ 5 (moderate severity) * Model for End-Stage Liver Disease (MELD) score \< 15. This will capture patients with chronic stable liver disease without significant comorbid conditions and/or signs of rapidly progressive or decompensated liver failure * Willingness and ability to comply with scheduled clinic visits, physical exams, laboratory tests, questionnaires, effective contraception use, and other trial procedures Exclusion Criteria: * Pruritus due to a primary inflammatory skin dermatosis or other forms of psychogenic pruritus utilizing skin biopsies to exclude as needed * Pregnant females. Urine pregnancy test required at screening * History of intrahepatic cholestasis of pregnancy * Any form of chronic hepatic pruritus associated with underlying malignancy * Liver transplant recipients * Drug-induced liver pruritus * ALT or AST greater than 3 times the upper limit of normal or total bilirubin greater than 2 times upper normal limit * Advanced liver disease indicators including, ascites requiring therapeutic paracentesis, history of spontaneous bacterial peritonitis, any grade of hepatic encephalopathy, or a documented history of variceal bleeding within the preceding six months * Severe coagulopathy with INR \> 15 * Any form of acute cholestatic liver disease * Allergy to nemolizumab or its ingredients * Inability to provide informed consent
Where it's running
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Mayo Clinic
Jacksonville, Florida, United States
Study contacts
- Principal investigator: Jason Sluzevich, MD — Mayo Clinic
- Study coordinator: Reagan E. Dukes, MHA
- Email: dukes.reagan@mayo.edu
- Phone: 904-953-3302
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
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Last reviewed 2026-11-15 by the Find a Trial editorial team.
Information on this page is for educational purposes and is not medical advice.
Always consult qualified healthcare professionals about clinical trial participation.