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Tacrolimus Combined With Entecavir on HBV Associated Glomerulonephritis(HBV-GN) (TOHBVGN)

Primary Purpose

Hepatitis B Virus Associated Nephrotic Syndrome

Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Tacrolimus &entecavir
placebo & entecavir
Sponsored by
Guangdong Provincial People's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatitis B Virus Associated Nephrotic Syndrome focused on measuring Hepatitis B virus, tacrolimus,membranous nephropathy

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Male and female patients aged between 18 and 65 years with HBV-GN;
  • All HBV-GN cases with biopsy-proven;
  • Evidence of chronic HBV infection based on the presence of HBsAg, HBeAg or HBV DNA in the serum;(HBsAg, HBeAg was positive, HBV DNA ≥10*3 IU/ml). Chronic HBV infection lasted for six months, and all patients did not receive the antiviral therapy in the past six months;
  • Proteinuria more than 3.0g/24h, UPCR>3000mg/g.cr, the result will be proofed by at least two tests;
  • No glucocorticoid and immunosuppressive treatment within the previous 2 weeks.

Exclusion Criteria:

  • The diagnosis of idiopathic membranous nephropathy(MN), systemic lupus erythematosus, malignancy, diabetes mellitus, severe infections or any other systemic disease known to be associated with secondary MN;
  • eGFR<30ml/min.1.73m*2;
  • Renal pathology showed that Tubular atrophy or Interstitial fibrosis was more than 50%;
  • The participant is allergy to tacrolimus, entecavir;
  • History of diabetes mellitus;
  • History of severe heart disease or cerebrovascular diseases;
  • Other active infection such as cytomegalovirus (CMV),Tuberculosis,Hepatitis A virus (HAV),Hepatitis C virus (HCV),Hepatitis D virus (HDV); Innate or acquired immunodeficiency; liver cirrhosis, liver malignment tumor;
  • Pregnant, trying to become pregnant or breast feeding;

Sites / Locations

  • Guangdong General Hospital, Guangdong Academy of Medical SciencesRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Tacrolimus & entecavir

placebo & entecavir

Arm Description

Tacrolimus capsule, 0.5mg/capsule,1.0mg/capsule, 0.05-0.1mg/kg.d by mouth , every 12 hours for a day.Entecavir 0.5mg tablet by mouth every night.

Tacrolimus capsule, 0.5mg/capsule,1.0mg/capsule, 0.05-0.1mg/kg.d by mouth , every 12 hours for a day.Entecavir 0.5mg tablet by mouth every night.

Outcomes

Primary Outcome Measures

Remission rate of proteinuria
the number of patients who reached complete or partial remission (CR or PR) after the 25 week-treatment. CR was defined as <0.3 g/24 h proteinuria (UPCR<300mg/g.cr) or lower plus stable renal function (eGFR>50 ml/min/1.73 m2) and PR as proteinuria 0.3-3.0 g/24 h (UPCR 300-3000mg/g.cr) and 50% lower than baseline proteinuria plus stable renal function.

Secondary Outcome Measures

Remission rate of proteinuria
The number of patients who reached complete or partial remission (CR or PR) after the 13 week-treatment.
The change of Scr
SCr increased 2 times the baseline levels or 50% lower than the baseline eGFR(according to CKD-EPI)
Serum HBV DNA
Serum HBV DNA was undetectable(HBV DNA<500copies/ml) at the end of 25 week-treatment.
The rate of acute kidney injury
The number of patients who present acute kidney injury at the end of 25 week-treatment.

Full Information

First Posted
February 20, 2017
Last Updated
February 22, 2017
Sponsor
Guangdong Provincial People's Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03062813
Brief Title
Tacrolimus Combined With Entecavir on HBV Associated Glomerulonephritis(HBV-GN)
Acronym
TOHBVGN
Official Title
The Therapy of Tacrolimus Combined With Entecavir on HBV Associated Glomerulonephritis : A Multicenter, Prospective, Randomized, Controlled, Single-blind Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
February 2017
Overall Recruitment Status
Unknown status
Study Start Date
February 1, 2017 (Actual)
Primary Completion Date
February 1, 2020 (Anticipated)
Study Completion Date
March 31, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Guangdong Provincial People's Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study was to evaluate the efficacy and safety of Tacrolimus combined with entecavir antiviral therapy for HBV-associated glomerulonephritis in china. Tacrolimus combined with entecavir rapidly and effectively induced remission of HBV-GN in Chinese adults. Meanwhile, Tacrolimus may have a synergistic antiviral effect with entecavir. The study protocol was reviewed and approved by Guangdong General Hospital's Ethic Committee, and all participants provided written informed consents. The study will be a prospective, randomized,controlled,single-blind, multi-centre, withdrawal study conducted by Guangdong general hospital, Guangdong Academy of Medical Sciences.there will be two phases, phase 1, Screening and enrolling 112 HBV-GN patients about one year,and phase 2, ongoing follow-up for 24 weeks.The data of all patients will be recorded in the HBV-GN electronic database.Before the randomisation, All patients will receive entecavir routine antiviral therapy for two weeks.And then they will be randomized to two different group,the treatment group: Tacrolimus combined with entecavir antiviral therapy,the control group: The Tacrolimus placebo and entecavir antiviral therapy. The Tacrolimus target trough concentration was 5-10 ng/mL during the therapy. The primary outcome variables were the number of patients who reached complete or partial remission (CR or PR) after the 25 week-treatment. CR was defined as <0.3 g/24 h proteinuria (UPCR<300mg/g.cr) or lower plus stable renal function (eGFR>50 ml/min/1.73 m2) and PR as proteinuria 0.3-3.0 g/24 h (UPCR 300-3000mg/g.cr) and 50% lower than baseline proteinuria plus stable renal function. Secondary outcome variables: 1) The number of patients who reached complete or partial remission (CR or PR) after the 13 week-treatment. 2) Serum creatinine (SCr) increased 2 times the baseline levels or 50% lower than the baseline eGFR(according to chronic kidney disease-EPI (CKD-EPI) )after the 25 week-treatment. 3)Serum HBV DNA was undetectable(HBV DNA<500copies/ml) at the end of 25 week-treatment. 4) The number of patients who present acute kidney injury at the end of 25 week-treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatitis B Virus Associated Nephrotic Syndrome
Keywords
Hepatitis B virus, tacrolimus,membranous nephropathy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
112 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Tacrolimus & entecavir
Arm Type
Experimental
Arm Description
Tacrolimus capsule, 0.5mg/capsule,1.0mg/capsule, 0.05-0.1mg/kg.d by mouth , every 12 hours for a day.Entecavir 0.5mg tablet by mouth every night.
Arm Title
placebo & entecavir
Arm Type
Active Comparator
Arm Description
Tacrolimus capsule, 0.5mg/capsule,1.0mg/capsule, 0.05-0.1mg/kg.d by mouth , every 12 hours for a day.Entecavir 0.5mg tablet by mouth every night.
Intervention Type
Drug
Intervention Name(s)
Tacrolimus &entecavir
Other Intervention Name(s)
FK506,Prograf, baraclude
Intervention Description
HBV-GN patients with nephrotic syndrome were randomly givenTacrolimus (0.05-0.1 mg/kg/day) combined with entecavir. Tacrolimus was divided into two daily doses at 12-hour intervals. Subsequent doses were adjusted to achieve a whole blood 12-hour trough level between 5 and 10 ng/ml.All patients will receive entecavir antiviral therapy(0.5mg/d), entecavir was taken once a day. All of HBV-GN patients were followed up to 25week.
Intervention Type
Drug
Intervention Name(s)
placebo & entecavir
Other Intervention Name(s)
baraclude
Intervention Description
HBV-GN patients with nephrotic syndrome were randomly givenTacrolimus placebo (0.05-0.1 mg/kg/day) combined with entecavir.Tacrolimus placebo was divided into two daily doses at 12-hour intervals. All patients will receive entecavir antiviral therapy(0.5mg/d), entecavir was taken once a day. All of HBV-GN patients were followed up to 25week.
Primary Outcome Measure Information:
Title
Remission rate of proteinuria
Description
the number of patients who reached complete or partial remission (CR or PR) after the 25 week-treatment. CR was defined as <0.3 g/24 h proteinuria (UPCR<300mg/g.cr) or lower plus stable renal function (eGFR>50 ml/min/1.73 m2) and PR as proteinuria 0.3-3.0 g/24 h (UPCR 300-3000mg/g.cr) and 50% lower than baseline proteinuria plus stable renal function.
Time Frame
25 weeks
Secondary Outcome Measure Information:
Title
Remission rate of proteinuria
Description
The number of patients who reached complete or partial remission (CR or PR) after the 13 week-treatment.
Time Frame
13 weeks
Title
The change of Scr
Description
SCr increased 2 times the baseline levels or 50% lower than the baseline eGFR(according to CKD-EPI)
Time Frame
25 weeks
Title
Serum HBV DNA
Description
Serum HBV DNA was undetectable(HBV DNA<500copies/ml) at the end of 25 week-treatment.
Time Frame
25 weeks
Title
The rate of acute kidney injury
Description
The number of patients who present acute kidney injury at the end of 25 week-treatment.
Time Frame
25 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male and female patients aged between 18 and 65 years with HBV-GN; All HBV-GN cases with biopsy-proven; Evidence of chronic HBV infection based on the presence of HBsAg, HBeAg or HBV DNA in the serum;(HBsAg, HBeAg was positive, HBV DNA ≥10*3 IU/ml). Chronic HBV infection lasted for six months, and all patients did not receive the antiviral therapy in the past six months; Proteinuria more than 3.0g/24h, UPCR>3000mg/g.cr, the result will be proofed by at least two tests; No glucocorticoid and immunosuppressive treatment within the previous 2 weeks. Exclusion Criteria: The diagnosis of idiopathic membranous nephropathy(MN), systemic lupus erythematosus, malignancy, diabetes mellitus, severe infections or any other systemic disease known to be associated with secondary MN; eGFR<30ml/min.1.73m*2; Renal pathology showed that Tubular atrophy or Interstitial fibrosis was more than 50%; The participant is allergy to tacrolimus, entecavir; History of diabetes mellitus; History of severe heart disease or cerebrovascular diseases; Other active infection such as cytomegalovirus (CMV),Tuberculosis,Hepatitis A virus (HAV),Hepatitis C virus (HCV),Hepatitis D virus (HDV); Innate or acquired immunodeficiency; liver cirrhosis, liver malignment tumor; Pregnant, trying to become pregnant or breast feeding;
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Zhiming Ye, PHD
Phone
86-13826161678
Email
13826161678@139.com
First Name & Middle Initial & Last Name or Official Title & Degree
Lifen Wang, PHD
Phone
86-18022392896
Email
15010942109@139.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zhiming Ye, PHD
Organizational Affiliation
Guangdong General Hospital, Guangdong Academy of Medical Sciences
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Lifen Wang, PHD
Organizational Affiliation
Guangdong General Hospital, Guangdong Academy of Medical Sciences
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Lixia Xu, PHD
Organizational Affiliation
Guangdong General Hospital, Guangdong Academy of Medical Sciences
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Xinling Liang, PHD
Organizational Affiliation
Guangdong General Hospital, Guangdong Academy of Medical Sciences
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Wei Shi, PHD
Organizational Affiliation
Guangdong General Hospital, Guangdong Academy of Medical Sciences
Official's Role
Study Director
Facility Information:
Facility Name
Guangdong General Hospital, Guangdong Academy of Medical Sciences
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510080
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Liming Yao, bachelor
Phone
86-83827812-20894

12. IPD Sharing Statement

Plan to Share IPD
Undecided
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Tacrolimus Combined With Entecavir on HBV Associated Glomerulonephritis(HBV-GN)

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