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OpenTrials
Completed

NCT Number: NCT03723252

Dapagliflozin Efficacy and Action in NASH

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Nanfang Hospital of Southern Medical University

Guangzhou, Guangdong, 510515, China

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Dapagliflozin

Drug

Participants will receive dapagliflozin 10mg po qd

Placebo

Drug

Participants will receive placebo po qd

Primary outcomes

  1. Improvement in scored liver histological improvement over 12 months

    Time frame: Baseline to 12 months

Secondary outcomes

  1. Resolution of NASH

    Time frame: Baseline to 12 months

    defined as a hepatocellular ballooning score of 0, and lobular inflammation score of 0 or 1) without worsening of fibrosis

  2. Improvement of fibrosis

    Time frame: Baseline to 12 months

    defined as reduction in fibrosis of at least 1 stage) without worsening of NASH

  3. Change in fibrosis score

    Time frame: Baseline to 12 months

  4. Change in each component score in the NAS

    Time frame: Baseline to 12 months

  5. Change in body weight

    Time frame: Baseline to 12 months

  6. Change in waist circumference

    Time frame: Baseline to 12 months

  7. Change in visceral fat

    Time frame: Baseline to 12 months

  8. Change in liver fat

    Time frame: Baseline to 12 months

  9. Change in HbA1C

    Time frame: Baseline to 12 months

  10. Change in blood pressure

    Time frame: Baseline to 12 months

  11. Change in serum lipids

    Time frame: Baseline to 12 months

  12. Change in insulin resistance

    Time frame: Baseline to 12 months

  13. Change in inflammatory markers of NASH

    Time frame: Baseline to 12 months

  14. Change in health related quality of life scores (SF-36)

    Time frame: Baseline to 12 months

Sponsors and collaborators

Lead sponsor

Nanfang Hospital, Southern Medical University

Other

Registry information

Official study title

Efficacy and Safety of Dapagliflozin in Non-alcoholic Steatohepatitis: a Multicentre, Randomized, Placebo-controlled Trial

Acronym: DEAN

Important dates

Study start
2019
Primary completion
2024
Study completion
2024
First posted
Oct 29, 2018
Registry last updated
Mar 29, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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