Efficacy and Safety Study of TUDCA Compare UDCA to Treatment Chronic Cholestatic Liver Disease-PBC

Cholestatic Liver Disease Clinical Trial

Official title:

Evaluate the Efficacy And Safety Of TUDCA Compare UDCA In The Treatment Of Cholestatic Liver Disease-PBC by A Randomized,Double-Blind,Double Dummy,Parallel-Controlled,Multicenter Trial and The Consecutive Treatment By TUDCA

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01829698
• Other study ID #: Trendful-TAU-001
• Secondary ID: 2009L05707
• Status: Completed
• Phase: Phase 3
• First received: April 9, 2013
• Last updated: March 21, 2014
• Start date: August 2009
• Est. completion date: February 2014

Study information

• Verified date: March 2014
• Source: Beijing Trendful Kangjian Medical Information Consulting Limited Company
• Contact: n/a
• Is FDA regulated: No
• Health authority: China: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

Though ursodeoxycholate acid (UDCA) is the well known effective therapy for PBC,clinical effectiveness of UDCA may be limited by its poor absorption and extensive biotransformation.The more hydrophillic bile acid tauroursodeoxycholate (TUDCA) is the active ingredients of UDCA,and has been approved by state food and drug administration in China for treatment of cholesterol stones.So it is necessary to verify the efficacy and safety of TUDCA in the treatment of adult primary biliary cirrhosis. In this randomized, double-blinded, double -dummy, parallel-controlled and multicenter clinical trial, we detect the proportion of patients who had AKP decline more than 25% as the primary outcome;decline of ALP,total bilirubin, GGT,ALT and AST as secondary outcomes after patients were treated with TUDCA or UDCA for 24 weeks.

Description:

This is a double-blind, randomized, parallel controlled, multicenter, clinical trial. Subjects inclusion by randomization after passing the screening, continuous administration the test drug (Taurolite) or control drug (Ursofalk) treatment for 24 weeks. Compare the safety and efficacy of Taurolite vs Ursofalk.

At the end of the double-blind period，enroll 100 subjects from both two group randomly ,for a consecutive treatment use TUDCA up to 24 weeks. Further evaluate the efficacy and safety of tauroursodeoxycholic acid (TUDCA) in the treatment of adult primary biliary cirrhosis (PBC) for a long time up to one year. Also evaluate the regimen's efficacy and safety that udca take placed by TUDCA in the treatment of adult primary biliary cirrhosis (PBC) for the patients who use udca treatment for 24 weeks.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 199
• Est. completion date: February 2014
• Est. primary completion date: January 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• 1 Ages Eligible for Study: 18 Years to 70 Years

2 Alkaline phosphatase (ALP) = 2 times the Upper Limits of Normal (ULN);

3 Anti mitochondrial antibody (AMA) positive and / or anti-mitochondrial antibody subtype M2 (AMA-M2) positive; if the AMA and AMA-M2 were negative, need liver biopsy confirmed pathological changes in PBC.

Exclusion Criteria:

• 1.in the 3 months before screening received UDCA, hormones, immunosuppressive therapy;

2.with extrahepatic biliary obstruction;

3.accompanied by hepatitis B virus (HBV) and hepatitis C virus (HCV) infection;

4.laboratory screening examination :

1. hemoglobin (HB): male< 11 g/dL, female <10 g/dL < g/dL;

2. the total white blood cell (WBC) count < 3000/mm3;

3. the absolute neutrophil count (ANC) <1500/mm3;

4. platelet (PLT) count <50000/mm3;

5. serum albumin <3.3g/dL;

6. alanine aminotransferase (ALT) = 10 ULN and / or aspartate aminotransferase (AST) = 10ULN;

7. ALT = 5 ULN and / or AST = 5 ULN with immunoglobulin G (IgG) = 2ULN;

8. total bilirubin (T-Bil) = 4 ULN;

9. prothrombin time (PT) prolonged = 3 seconds (limit reference value based on) or PTA = 60%;

10. the serum creatinine (Cr) = 1.5ULN.

5.patients with esophageal variceal or bleeding, ascites, hepatic encephalopathy or other evidence of hepatic decompensation;

6.diagnosed with liver cancer, suspected to have liver cancer, AFP > 100ng/ml. As the AFP in 2 times the upper limit of normal to 100ng/ml, need re-check in 2 weeks, if their AFP > 100ng/ml can not be included

7.body mass index >28 (Kg/m2);

8.alcohol or drug abusers within the recent year;

9.there is a serious heart, lung, kidney, digestive, nervous, mental disease, autoimmune diseases or malignant tumor

10.drug-induced liver injury;

11. plan to transplant or have had organ transplants;

12. are unable or unwilling to provide informed consent or fails to comply with the test requirements;

13.pregnant, lactating women.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Cholestasis
• Cholestatic Liver Disease
• Liver Diseases

Intervention

Drug:
• tauroursodeoxycholic
Testing arm: tauroursodeoxycholic acid, 750mg , divided into three times, each time 250mg, oral administration, after meal
• ursodeoxycholic acid
ursodeoxycholic acid, 750mg ,divided into three times, each time 250mg, oral administration, after meal

Locations

Country	Name	City	State
China	Liver Research Center,Beijing Friendship Hospital	Beijing	Beijing

Sponsors (1)

Lead Sponsor	Collaborator
Beijing Trendful Kangjian Medical Information Consulting Limited Company

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Efficiency is defined as the patients composition whose ALP level of serum decreased more than 25% compared to baseline at treatment for 24 weeks.	After 24 weeks of treatment, calculate the rate of patients whose ALP level of serum ALP decreased more than 25% compared to the baseline. After 48 weeks of treatment, calculate the rate of patients whose ALP level of serum ALP decreased more than 40% compared to the baseline.	48 weeks	Yes
Secondary	The change of laboratory parameters about liver function	after 24 weeks of treatment, the serum level ALP decreased compared with baseline.; after 24 weeks of treatment, the serum bilirubin level decreased compared with baseline.; after 24 weeks of treatment, the serum level of GGT decreased compared with baseline.; after 24 weeks of treatment, serum ALT, AST levels decreased compared to baseline.; after 48 weeks of treatment, the serum level ALP decreased compared with 24 weeks.; after 48 weeks of treatment, the serum level ALP decreased compared with baseline.; after 48 weeks of treatment, the serum bilirubin level decreased compared with 24 weeks.; after 48 weeks of treatment, the serum level of GGT decreased compared with 24 weeks.; after 48 weeks of treatment, serum ALT, AST levels decreased compared to 24 weeks.	48 weeks	Yes