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Pilot Study of Budesonide for Patients With Primary Sclerosing Cholangitis

Pilot Study of Budesonide for Patients With Primary Sclerosing Cholangitis

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00004842
Enrollment
22
Registered
2000-02-25
Start date
1997-05-31
Completion date
1999-04-30
Last updated
2017-05-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cholangitis, Sclerosing, Liver Cirrhosis, Biliary

Keywords

cirrhosis, gastrointestinal disorders, primary biliary cirrhosis, primary sclerosing cholangitis, rare disease

Brief summary

OBJECTIVES: I. Assess the safety and effectiveness of budesonide in patients with primary sclerosing cholangitis or primary biliary cirrhosis experiencing a suboptimal response to ursodeoxycholic acid. II. Estimate the efficacy of this therapy in these patient groups as a means of evaluating the feasibility of a long-term randomized trial.

Detailed description

PROTOCOL OUTLINE: Patients receive budesonide by mouth 3 times daily for a minimum of 6 months. If liver biochemistries become normal, dosage is reduced to once daily. Treatment discontinues after 1 year.

Interventions

DRUGbudesonide

Oral budesonide, 9 mg daily was administered for 1 year

Sponsors

Mayo Clinic
CollaboratorOTHER
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Lead SponsorNIH

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

PROTOCOL ENTRY CRITERIA: --Disease Characteristics-- Pathologically confirmed primary sclerosing cholangitis (PSC) meeting the following criteria: * Chronic cholestatic disease for at least 6 months * Liver biopsy within the past 6 months compatible with the diagnosis of PSC Intra and/or extrahepatic biliary duct obstruction, beading, or narrowing OR Pathologically confirmed primary biliary cirrhosis (PBC) that is experiencing suboptimal response to ursodeoxycholic acid and meeting the following criteria: * Chronic cholestatic liver disease for at least 6 months * Positive antimitochondrial antibody * No biliary obstruction by ultrasound, CT, or cholangiography * Prior liver biopsy compatible with diagnosis of PBC * Received ursodeoxycholic acid for at least 6 months --Prior/Concurrent Therapy-- Biologic therapy: * At least 3 months since prior D-penicillamine * No planned transplantation for at least 1 year Chemotherapy: * At least 3 months (6 months for PBC) since prior cyclosporin, colchicine, azathioprine, or methotrexate * At least 6 months since prior chlorambucil (PBC only) Endocrine therapy: At least 3 months (6 months for PBC) since prior corticosteroids Surgery: No prior intraductal stones or operations on the biliary tree except cholecystectomy (PSC only) Other: * At least 3 months since prior pentoxifylline, ursodeoxycholic acid, or nicotine (PSC only) * At least 6 months since prior chenodeoxycholic acid (PBC only) --Patient Characteristics-- Life expectancy: At least 3 years Hematopoietic: Not specified Hepatic: * Alkaline phosphatase at least 2 times upper limits of normal * No chronic hepatitis B infection * No hepatitis C infection * No autoimmune hepatitis * Bilirubin no greater than 4 mg/dL (PBC only) Cardiovascular: No severe cardiopulmonary disease Other: * No concurrent advanced malignancy * At least 3 months since prior inflammatory bowel disease requiring specific treatment except maintenance therapy (PSC only) * No anticipated need for transplantation within 1 year * Not pregnant * No liver disease of other etiology such as: Chronic alcoholic liver disease Hemochromatosis Wilson's disease Congenital biliary disease Cholangiocarcinoma No recurrent ascending cholangitis requiring hospitalization more than 2 times per year (PSC only) At least 1 year since prior active peptic ulcer No recurrent variceal bleeds No spontaneous encephalopathy No diuretic-resistant ascites

Design outcomes

Primary

MeasureTime frame
Change in serum alkaline phosphatase1 year

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026