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Efficacy and Safety of Cofrogliptin Tablets as Sequential Therapy Following Intensive Treatment Achievement in Type 2 Diabetes Mellitus

Efficacy and Safety of Cofrogliptin Tablets as Sequential Therapy Following Intensive Treatment Achievement in Type 2 Diabetes Mellitus

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106205
Enrollment
Unknown
Registered
2025-07-21
Start date
2025-07-21
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Type 2 Diabetes Mellitus

Interventions

Control group:lifestyle intervention
Treatment group:Cofrogliptin tablets

Sponsors

The Second Clinical Medical College of Jilin University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age 18 years old or above; 2. Meets the diagnostic criteria for type 2 diabetes; 3. After the patient achieves the target of intensified treatment (normalization of blood sugar (fasting or pre-meal blood glucose < 6.5 mmol/L, and 2-hour post-meal blood glucose < 8.0 mmol/L)), screening will be conducted immediately. 4. Capable of understanding and voluntarily signing the written informed consent form.

Exclusion criteria

Exclusion criteria: 1. Exclude those with progressive central nervous system diseases, severe heart, lung, liver or kidney disorders; 2. Those who are allergic to the active ingredients or any excipients contained in repaglinide are prohibited from using it. 3. Excluding pregnant or lactating women; 4. Excluding patients who participated in another clinical study within 30 days prior to the baseline visit (using any investigational drugs or medical devices), participation in observational studies is permitted. 5. Exclude situations where the researchers make judgments about other factors that might affect the conduct of the clinical study and the interpretation of the research results.

Design outcomes

Secondary

MeasureTime frame
2-hour postprandial blood glucose (2hPG);fasting blood glucose (FBG);Fasting C-peptide (FCP);Fasting insulin (FINS);

Primary

MeasureTime frame
glycated hemoglobin (GHB);

Countries

China

Contacts

Public ContactWang Yanjun

The Second Clinical Medical College of Jilin University

yj_wang@jlu.edu.cn+86 138 4308 8777

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026