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Clinical study of GLP-1 receptor agonist (Exenatide) for type 2 diabetes patients with diabetic nephropathy

Clinical study of GLP-1 receptor agonist (Exenatide) for type 2 diabetes patients with diabetic nephropathy - Clinical study of exenatide for type 2 diabetes patients with diabetic nephropathy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000037106
Enrollment
30
Registered
2019-06-19
Start date
2015-12-01
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

Interventions

Administer GLP-1 receptor agonist (Exenatide) 1. In principle, this drug is administered within 60 minutes before morning supper and not after meals. 2. The administration of this drug starts with

Sponsors

Kagawa University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with type 2 diabetes who meet the criteria below 1) HbA1c (NGSP): 7.0% or more and less than 10% 2) Patients aged 20 years or older and less than 80 years regardless of gender 3) Diabetic nephropathy stage 2-3 (diagnostic criteria attached) 4) Patients who can obtain written consent to participate in this clinical research

Exclusion criteria

Exclusion criteria: Patients who fall under any of the following are excluded from this clinical study. 1) Patients who fall under the contraindication for GLP-1 receptor agonist 2) Patients participating in other clinical research 3) Pregnant women, pregnant women, lactating women or women who may have pregnancy 4) Patients with other serious complications 5) Patients judged to be unsuitable as a target by the judgment of other doctors

Design outcomes

Primary

MeasureTime frame
Rate of change of delta eGFR at 12 weeks before and after administration

Countries

Japan

Contacts

Public ContactKensaku Fukunaga

Kagawa University Hospital Department of Endocrinology and Metabolism

labmed@med.kagawa-u.ac.jp0878985111

Outcome results

None listed

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