Diabetes drug liraglutide may fight fatty liver, but trial halted early
NCT ID NCT02721888
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study looked at whether liraglutide, a diabetes drug, can reduce liver fat and improve cholesterol in people with type 2 diabetes. It involved 127 patients who took liraglutide for 6 months, with liver fat measured by MRI. However, the trial was terminated early, so the full results are not available.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- liraglutide
- What this could lead to
- If successful, this could show that liraglutide helps reduce liver fat and improve cholesterol levels in people with type 2 diabetes.
- What could go wrong
- The trial was terminated early, so results are incomplete. It was also a small, single-center study, so findings may not apply broadly.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
127 people
The number who actually took part.
- Started
-
Jul 2012
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients with type 2 diabetes * Patients treated by metformin and/or sulfonylureas (or glinides) and/or acarbose and/or insulin, * HbA1C \>= 7 %, * Patients who gave their written consent. For the kinetic substudy: * Patients who have the typical features of diabetic dyslipidemia (triglycerides \>= 1.50 g/l and/or HDL\<0.50 g/l \[women\], 0.40 g/l \[men\]) Exclusion Criteria: * Treatment with thiazolidinediones or other Glucagon-like peptide-1(GLP1) agonist. * No treatment with a Dipeptidyl peptidase-4 (DPP4) inhibitor during the 3 previous months, * Renal or hepatic failure, * Contra-indication for proton-spectroscopy (pacemaker, implantable prosthesis,..), * Pregnancy. For the kinetic substudy: * Patients on hypolipidemic agents
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
CHU de Dijon
Dijon, 21079, France
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