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Completed

NCT Number: NCT06703268

A Study on Switching From Daily DPP-4 Inhibitor to HSK7653 in Type 2 Diabetes Patients

To assess the effectiveness of HSK7653 tablets following the substitution of daily DPP-4 inhibitor (DPP-4i) over a 24-week treatment period.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Chu Hsien-I Memorial Hospital, Tianjin Medical University

Tianjin, China

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age ≥18 and Age ≤75 years
  • T2DM patients,
  • During the 12 weeks before screening, on the basis of diet control and exercise therapy, patients only regularly received daily DPP-4 inhibitors (such as sitagliptin, vildagliptin, saxagliptin, linagliptin, alogliptin and retagliptin , etc.) or combined with metformin (with a metformin dose of ≥ 1500 mg/day, or the maximum tolerated dose < 1500 mg/day but ≥ 1000 mg/day);
  • HbA1c ≥6.5% and HbA1c <8.0%
  • FPG <10.0 mmol/L
  • BMI ≥19 and BMI ≤ 35 kg/m2 (Body Mass Index)

Exclusion criteria

  • Non-type 2 diabetes: Type 1 diabetes, gestational diabetes or other special types of diabetes.
  • The presence of any of the following medical histories or conditions at the time of screening:
  • History of diabetic ketoacidosis or hyperglycemic hyperosmolar state within the recent 6 months;
  • History of ≥2 episodes of severe hypoglycemia within the last 6 months;
  • History of malignant tumors within the recent 5 years (except for cured basal cell carcinoma of the skin and cervical carcinoma in situ), or currently being evaluated for potential malignant tumors.
  • Presence of severe mental disorders or language barriers, unwilling or unable to fully understand and cooperate.
  • History of drug abuse within the past 5 years
  • Previous history or clinical evidence of acute or chronic pancreatitis.
  • Using other drugs that may affect blood glucose metabolism within 12 weeks prior to screening, including systemic glucocorticoids (except for inhaled or topical ones), growth hormones, etc.
  • Any laboratory test index meeting the following criteria:
  • Hemoglobin < 110 g/L (for males) or < 100 g/L (for females).
  • Alanine aminotransferase (ALT) and/or aspartate aminotransferase (AST) > 3 times the upper limit of the normal value.
  • Total bilirubin (TBIL) > 2 times the upper limit of the normal value.
  • Fasting triglyceride (TG) > 5.7 mmol/L.
  • Estimated glomerular filtration rate (eGFR) calculated using the CKD-EPI formula < 45 mL/min/1.73m².
  • Known to be allergic to the investigational products or related excipients.

Treatment and study plan

HSK7653 10 mg

Drug

HSK7653 10 mg Q2W

Daily DPP-4 inhibitor

Drug

Daily DPP-4 inhibitor

Primary outcomes

  1. Time in range

    Time frame: 24 weeks

    The change in time in range (TIR) of continuous glucose monitoring (CGM) relative to the baseline after 24 weeks of treatment.

Secondary outcomes

  1. HbA1c

    Time frame: 24 weeks

    Change from baseline in HbA1c after 24 weeks

  2. Fasting glucose

    Time frame: 24 weeks

    Change from baseline in fasting glucose after 24 weeks

  3. Mean glucose

    Time frame: 24 weeks

    Change from baseline in mean glucose after 24 weeks

  4. Treatment-emergent adverse events.

    Time frame: 24 weeks

    The incidence of treatment-emergent adverse events.

Sponsors and collaborators

Lead sponsor

Haisco Pharmaceutical Group Co., Ltd.

Industry

Registry information

Official study title

A Multicenter, Randomized, Open-label, Controlled Study on Evaluating the Efficacy and Safety of Switching From Daily DPP-4 Inhibitors to HSK7653 Tablets in Patients With Type 2 Diabetes Mellitus in China

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Nov 25, 2024
Registry last updated
Nov 25, 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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