Dapagliflozin Efficacy and Action in NASH (DEAN)
Primary Purpose
Nonalcoholic Steatohepatitis
Status
Recruiting
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
Dapagliflozin
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Nonalcoholic Steatohepatitis focused on measuring Nonalcoholic Steatohepatitis, SGLT-2 inhibitor
Eligibility Criteria
Inclusion Criteria:
- Men or women aged≥18 years;
- Non-alcoholic steatohepatitis as determined by liver biopsies within 6 months;
- Patients with T2DM at screening had to have stable glycaemic control (HbA1c <9.5%) .
Exclusion Criteria:
- Significant alcohol consumption in the past six months (Consumed more than 20 g/day for women or 30 g/day for men);
- A history of alcoholic liver disease, chronic viral hepatitis, drug-induced hepatitis, autoimmune hepatitis, cirrhosis, and liver cancer;
- Obstructive biliary disease;
- Having any medical condition that would affect metabolism (i.e. Cushing syndrome, known hyperthyroidism or hypothyroidism);
- Poor glucose control (defined as HbA1C≤ 9.5% within 3 months) if diagnosed with T2DM, or taking any antidiabetic medication that would affect metabolism or weight loss (i.e. TZD, GLP-1, DPP-4i or initially using insulin in the past 3 months);
- Taking any medication (i.e. cortisol, methotrexate)that would affect steatohepatitis for more than two weeks in the past year;
- Chronic kidney disease or severe impaired renal function (serum creatinine≥ 2.0mg/dl);
- Serum alanine aminotransferase (ALT) greater than 300U/L
- A history of Type 1 diabetes;
- A history of bladder cancer;
- Women who are pregnant or plan to become pregnant;
- Serious medical disease with likely life expectancy less than 5 years;
- Patients who cannot be followed for 24 months (due to a health situation or migration);
- Participation in other clinical trial in the 30 days before randomization;
- Patients who are unwilling or unable to give informed consent.
Sites / Locations
- Nanfang Hospital of Southern Medical UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Dapagliflozin group
Placebo group
Arm Description
Participants will receive dapagliflozin 10mg po qd.
Participants will receive placebo po qd.
Outcomes
Primary Outcome Measures
Improvement in scored liver histological improvement over 12 months
Secondary Outcome Measures
Resolution of NASH
Change in fibrosis score
Change in each component score in the NAS
Change in body weight
Change in waist circumference
Change in visceral fat
Change in liver fat
Change in HbA1C
Change in blood pressure
Change in serum lipids
Change in insulin resistance
Change in inflammatory markers of NASH
Change in health related quality of life scores (SF-12)
Full Information
NCT ID
NCT03723252
First Posted
October 23, 2018
Last Updated
October 21, 2022
Sponsor
Nanfang Hospital, Southern Medical University
1. Study Identification
Unique Protocol Identification Number
NCT03723252
Brief Title
Dapagliflozin Efficacy and Action in NASH
Acronym
DEAN
Official Title
Efficacy and Safety of Dapagliflozin in Non-alcoholic Steatohepatitis: a Multicentre, Randomized, Placebo-controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
March 20, 2019 (Actual)
Primary Completion Date
November 1, 2023 (Anticipated)
Study Completion Date
November 30, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Nanfang Hospital, Southern Medical University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
5. Study Description
Brief Summary
This is a multicentre, randomized, placebo-controlled trial to assess the efficacy and safety of dapagliflozin on improving non-alcoholic steatohepatitis as determined by liver biopsies and metabolic risk factors.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nonalcoholic Steatohepatitis
Keywords
Nonalcoholic Steatohepatitis, SGLT-2 inhibitor
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Dapagliflozin group
Arm Type
Experimental
Arm Description
Participants will receive dapagliflozin 10mg po qd.
Arm Title
Placebo group
Arm Type
Placebo Comparator
Arm Description
Participants will receive placebo po qd.
Intervention Type
Drug
Intervention Name(s)
Dapagliflozin
Intervention Description
Participants will receive dapagliflozin 10mg po qd
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Participants will receive placebo po qd
Primary Outcome Measure Information:
Title
Improvement in scored liver histological improvement over 12 months
Time Frame
Baseline to 12 months
Secondary Outcome Measure Information:
Title
Resolution of NASH
Time Frame
Baseline to 12 months
Title
Change in fibrosis score
Time Frame
Baseline to 12 months
Title
Change in each component score in the NAS
Time Frame
Baseline to 12 months
Title
Change in body weight
Time Frame
Baseline to 12 months
Title
Change in waist circumference
Time Frame
Baseline to 12 months
Title
Change in visceral fat
Time Frame
Baseline to 12 months
Title
Change in liver fat
Time Frame
Baseline to 12 months
Title
Change in HbA1C
Time Frame
Baseline to 12 months
Title
Change in blood pressure
Time Frame
Baseline to 12 months
Title
Change in serum lipids
Time Frame
Baseline to 12 months
Title
Change in insulin resistance
Time Frame
Baseline to 12 months
Title
Change in inflammatory markers of NASH
Time Frame
Baseline to 12 months
Title
Change in health related quality of life scores (SF-12)
Time Frame
Baseline to 12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Men or women aged≥18 years;
Non-alcoholic steatohepatitis as determined by liver biopsies within 6 months;
Patients with T2DM at screening had to have stable glycaemic control (HbA1c <9.5%) .
Exclusion Criteria:
Significant alcohol consumption in the past six months (Consumed more than 20 g/day for women or 30 g/day for men);
A history of alcoholic liver disease, chronic viral hepatitis, drug-induced hepatitis, autoimmune hepatitis, cirrhosis, and liver cancer;
Obstructive biliary disease;
Having any medical condition that would affect metabolism (i.e. Cushing syndrome, known hyperthyroidism or hypothyroidism);
Poor glucose control (defined as HbA1C≤ 9.5% within 3 months) if diagnosed with T2DM, or taking any antidiabetic medication that would affect metabolism or weight loss (i.e. TZD, GLP-1, DPP-4i or initially using insulin in the past 3 months);
Taking any medication (i.e. cortisol, methotrexate)that would affect steatohepatitis for more than two weeks in the past year;
Chronic kidney disease or severe impaired renal function (serum creatinine≥ 2.0mg/dl);
Serum alanine aminotransferase (ALT) greater than 300U/L
A history of Type 1 diabetes;
A history of bladder cancer;
Women who are pregnant or plan to become pregnant;
Serious medical disease with likely life expectancy less than 5 years;
Patients who cannot be followed for 24 months (due to a health situation or migration);
Participation in other clinical trial in the 30 days before randomization;
Patients who are unwilling or unable to give informed consent.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Huijie Zhang, MD.PhD.
Phone
+86-020-61641635
Email
Huijiezhang2005@126.com
First Name & Middle Initial & Last Name or Official Title & Degree
Jinjun Chen, MD.PhD.
Phone
+86-020-62787310
Email
chjj@smu.edu.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Huijie Zhang, MD.PhD.
Organizational Affiliation
Nanfang Hospital, Southern Medical University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Nanfang Hospital of Southern Medical University
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510515
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Huijie Zhang, MD,PhD
Phone
+86-020-61641635
Email
Huijiezhang2005@126.com
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Dapagliflozin Efficacy and Action in NASH
We'll reach out to this number within 24 hrs