Double-blind, randomised, placebo-controlled, multi-centre phase III clinical study comparing the combination of ursodeoxycholic acid capsules plus budesonide capsules to ursodeoxycholic acid capsules plus placebo in the treatment of primary biliary cirrhosis - Ursodeoxycholic acid plus budesonide vs. ursodeoxycholic acid alone in PBC
- Conditions
- Patients with PBC and with risk of a progression of this disease.MedDRA version: 9.1Level: LLTClassification code 10036680Term: Primary biliary cirrhosis
- Registration Number
- EUCTR2007-004040-70-IT
- Lead Sponsor
- DR. FALK PHARMA GMBH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- 62
1.Signed informed consent 2.Age ≥ 18 years 3.UDCA treatment for at least 6 months prior to inclusion 4.Liver biopsy compatible with PBC 5.Liver biopsy performed within the last 6 months prior to inclusion 6.PBC patients at risk of disease progression based on one or more of the following criteria:- Serum alkaline phosphatase ≥ 3 times the upper limit of normal at any time since diagnosis of PBC and ALT ≥ 2 times upper limit of normal or- Total Bilirubin ≥ 1.0 mg/dl (≥ 17 µmol/L) or- Moderate to severe periportal or periseptal lymphocytic interface hepatitis or- Periportal and portal fibrosis with numerous septa (Ludwig stage III) without cirrhosis 7.Type 2 anti-mitochondrial antibodies > 1:40 by direct immunofluorescence 8.Women of child-bearing potential have to apply appropriate contraceptive methods, e.g., hormonal contraception, intrauterine device (IUD), double-barrier method of contraception (e.g., use of a condom and spermicide), partner has undergone vasectomy and subject is in monogamous relationship. The investigator is responsible for determining whether the subject has adequate birth control for study participation.
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range
1.Histologically proven cirrhosis 2.Positive Hepatitis B or C serology 3.Positive HIV serology 4.Primary Sclerosing Cholangitis 5.Wilson?s-Disease 6.Celiac Disease (blood tests and/or oesophago-gastro-duodenoscopy with histological examination to be performed) 7.α1?anti-Trypsin-deficiency 8.Haemochromatosis 9.Autoimmune-Hepatitis (AIH; defined by an Alvarez score > 15 without treatment or ≥ 17 with treatment); Note: PBC/AIH overlap disease, treated insufficiently with UDCA monotherapy may be enrolled 10.Treatment with any of the following drugs within the last 3 months prior to inclusion: colchicine, corticosteroids, azathioprine or other immunosuppressive drugs (e.g. cyclosporine, methotrexate), chlorambucil, D-penicillamine, fibrates, or antihyperlipidemic drugs 11.Treatment with ketoconazole or other CYP3A inhibitors within the last 4 weeks before baseline; rifampicin (up to 600 mg/d) is allowed to treat pruritus until baseline 12.Sonographic or endoscopic signs of portal hypertension 13.Ascites or history of ascites 14.Hepatic encephalopathy or history of hepatic encephalopathy 15.Total bilirubin > 3.0 mg/dl (> 50 µmol/L) 16.Albumin < 36 g/L 17.Prothrombin ratio < 70% 18.Platelet count < 135.000/mm3 19.Osteoporosis proven by bone densitometry 20.Diabetes mellitus, defined as B-Glucose > 125 mg/dl on an empty stomach (even when controlled) 21.Hypertension, defined as persistent raised blood pressure > 140/90 mmHg 22.Suspected non-compliance of the patient (suspected difficulties to comply with the study period of 36 months) 23.Severe co-morbidity substantially reducing life expectancy 24.Known intolerance/hypersensitivity/resistance to study drugs or drugs of similar chemical structure or pharmacological profile 25.Existing or intended pregnancy or breast-feeding 26.Participation in another clinical trial within the last 30 days, simultaneous participation in another clinical trial, or previous participation in this trial
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Main Objective: 1) To compare the efficacy and tolerability of a combination therapy with ursodeoxycholic acid (12-16 mg/kg body weight (BW)/d) plus budesonide (9 mg/d) vs. ursodeoxycholic acid (12-16 mg/kg BW/d) plus placebo in the treatment of PBC. 2) To study safety and tolerability in the form of adverse events and laboratory parameters. 3) To assess patients? Quality of Life.;Secondary Objective: non applicable;Primary end point(s): Rate of patients without treatment failure after 3 years of treatment. Treatment failure is defined as: ·Death, or ·Registration on the liver transplant waiting list, or ·Cirrhosis defined by histology (staging according to Ludwig1), or ·Presence of esophageal varices and/or ascites
- Secondary Outcome Measures
Name Time Method