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Completed

NCT Number: NCT06059326

Multiple-dose Study to Evaluate the Safety,Tolerability, Pharmacokinetics and Pharmacodynamics of HSK7653 in T2DM

To evaluate the safety, tolerability and pharmacokinetic (PK)/pharmacodynamic (PD) characteristics of HSK7653 tablets in Type 2 Diabetes Mellitus Patients.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Peking university people's hospital

Beijing, Beijing Municipality, 100044, 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 ≤70 years
  • T2DM patients,
  • Control the blood glucose level only with diet and exercise in last 3 months;
  • BMI ≥19 and BMI ≤ 35 kg/m2 (Body Mass Index)
  • HbA1c ≥7.0% and HbA1c <10.0%
  • FPG <13.9 mmol/L

Exclusion criteria

  • Non-type 2 diabetes mellitus: Type 1 diabetes mellitus, gestational diabetes history;
  • History of acute complications of diabetes (diabetic ketoacidosis, diabetic hyperglycemia hyperosmolar syndrome or lactic acidosis);
  • History of chronic complications of severe diabetes (retinal proliferative disease, severe diabetic neuropathy or intermittent claudication confirmed by fundus examination during screening);
  • Patients who used systemic glucocorticoids within 3 months prior to screening had severe infections or major surgeries and transplants within 3 months;
  • Three or more episodes of hypoglycemia occurred in the six months prior to screening;
  • History of hyperthyroidism within 6 months before screening;
  • Severe cardiovascular disease. ;
  • Medical conditions that may significantly affect drug absorption, distribution, metabolism, and excretion within 2 weeks prior to screening;
  • Liver function tests abnormal;
  • Moderate or severe renal impairment;
  • Medical history or clinical evidence of pancreatic injury or pancreatitis, or abnormalities in lipase and amylase judged by investigators to be clinically significant;
  • Patients with a history of hypertension who regularly take antihypertensive therapy for over 4 weeks still have poor control, SBP > 160 mmHg and (or) DBP > 100 mmHg;
  • Patients with uncontrolled hyperlipidemia.

Treatment and study plan

HSK7653 10 mg

Drug

Tablet, HSK7653 10 mg Q2W, 12 weeks

HSK7653 25 mg

Drug

Tablet, HSK7653 25 mg Q2W, 12 weeks

HSK7653 50 mg

Drug

Tablet, HSK7653 50 mg Q2W, 12 weeks

Placebo

Drug

Tablet, 0 mg Q2W, 12 weeks

Primary outcomes

  1. Number of Participants With Treatment-Emergent Adverse Events (TEAEs)

    Time frame: From baseline to up to 2 weeks after last dose for a total of approximately 14 weeks

    Assessment by adverse event monitoring, 12 lead ECGs, vital signs and laboratory measurements.

Secondary outcomes

  1. Peak plasma concentration (Cmax) of HSK7653

    Time frame: Day 1 to Day 43

    Cmax of HSK7653 after first dose and multi-dose administration

  2. Area under the plasma concentration versus time curve (AUC) of HSK7653

    Time frame: Day 1 to Day 43

    AUC of HSK7653 after first dose and multi-dose administration

  3. Half-life (t1/2) of HSK7653

    Time frame: Day 1 to Day 43

    T1/2 of HSK7653 after single-dose and multi-dose administration

  4. Change from baseline in dipeptidyl peptidase-IV (DPP-4) inhibition rate

    Time frame: Day 1 to Day 84

    Change from baseline in dipeptidyl peptidase-IV (DPP-4) inhibition rate after single-dose and multi-dose administration of HSK7653

  5. Change from baseline in GLP-1

    Time frame: Day 1 to Day 84

    Change from baseline in GLP-1 after single-dose and multi-dose administration of HSK7653

  6. Change from baseline of fasting plasma glucose

    Time frame: Day 1 to Day 84

    Change from baseline in fasting plasma glucose after multi-dose administration of HSK7653

  7. Change from baseline of HbA1c

    Time frame: Day 1 to Day 84

    Change from baseline in HbA1c after multi-dose administration of HSK7653

Sponsors and collaborators

Lead sponsor

Haisco Pharmaceutical Group Co., Ltd.

Industry

Registry information

Official study title

A Multicenter, Randomized, Double-blind, Placebo Control, Dose-escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of HSK7653 in Type 2 Diabetes Mellitus Patients

Important dates

Study start
2019
Primary completion
2019
Study completion
2019
First posted
Sep 28, 2023
Registry last updated
Sep 28, 2023

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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