Skip to content

Ipragliflozin for type 2 DM with NAFLD

Study of ipragliflozin effect on type 2 diabetes with nonalcoholic fatty liver disease - Study of ipragliflozin effect on type 2 diabetes with nonalcoholic fatty liver disease

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs071180069
Enrollment
54
Registered
2019-03-20
Start date
2015-08-10
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 2 diabetes with nonalcoholic fatty liver disease

Interventions

Oral administration of ipragliflozin (50mg tablet) once a day after meal

Sponsors

Anzai Keizo
Lead Sponsor
Astellas Pharma Inc.
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Type 2 diabetes patients who received diet+exercise therapy or diet+ exercise + medication for 12 weeks or longer 2)Patients with HbA1c is 6.0% or higher 3)Patients with liver nonalcoholic fatty liver disease diagnosed with liver biopsy which was performed within past 6 months before study inclusion. 4)Age between 20 and 80 years 5)Patients who understand the contents of informed consent form and who can voluntarily sign informed consent form

Exclusion criteria

Exclusion criteria: 1)Patients with severe diabetic complication except simple diabetic retinopathy 2)Patients with history of severe cardiovascular event 3)Patients with history of allergic response to ipragliflozin 4)Patients who requires insulin treatment including diabetic ketoacidosis, severe diabetic ketoacidosis, diabetic coma, pre-diabetic coma, type 1 diabetes, severe infection disease, severe trauma and/or indication of emergency surgery 5)Patients with severe liver and/or renal disfunction 6)Patients with viral hepatitis C and/or viral hepatitis B infection 7)Patients who the investigator determined difficult to participate in the study 8)Patients who had medication with SGLT2 inhibitor and/or thiazolidinedione within 12 weeks before enrollment.

Design outcomes

Primary

MeasureTime frame
Decrease in HbA1c after interventions for 72 weeks

Secondary

MeasureTime frame
1. Changes in HbA1c after 12 week, 24 week and 48 week of intervention. 2. Changes in bodyweight after 24 week and 72 week of intervention. 3. Changes in the parameters described below after 12 week, 24 week, 48 week and 72 week of intervention. Serum liver function test, imaging analysis, serum inflammatory marker, liver histology, serum biochemistry exams, blood counts and adverse events.

Contacts

Public ContactHirokazu Takahashi

Saga University Hospital

takahas2@cc.saga-u.ac.jp+81-952-31-6511

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026