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Completed

NCT Number: NCT06553248

A Trial Investigating the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of GZR4 in Subjects With Type 2 Diabetes

This trial is conducted in China. The aim of the trial is to investigate the safety, tolerability, pharmacokinetics and pharmacodynamics of mutiple-dose GZR4 in subjects with type 2 diabetes

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Gan & Lee Pharmaceuticals Co., Ltd

Beijing, Beijing Municipality, 100000, China

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Male or female at the age of 18-65 (inclusive) at the time of informed consent
  • Body mass index (BMI) between 18.5 and 35 kg/m2 (inclusive) at screening
  • Diagnosis of type 2 diabetes mellitus for over 3 months
  • Hemoglobin A1c (HbA1c) ≥ 6.5% and ≤ 10.0% at screening.

Exclusion criteria

  • History of drug abuse within 1 year before screening, or positive drug abuse screening results during the screening period or at baseline
  • Malignancy or increased risk of malignancy before screening: any suspected and/or diagnosed malignancy or documented history of malignancy
  • Confirmed or suspected type 1 diabetes mellitus, gestational diabetes mellitus, or specific types of diabetes mellitus from other causes (monogenic diabetes syndrome, cystic fibrosis, pancreatitis, drug-induced or chemically induced diabetes mellitus, etc.) prior to screening
  • Presence of the following diseases within 6 months prior to screening: diabetic ketoacidosis, diabetic lactic acidosis, or hyperosmolar nonketotic diabetic coma; proliferative retinopathy or maculopathy that is unstable or requiring treatment; symptomatic diabetic neuropathy, intermittent claudication or diabetic foot
  • Severe hypoglycaemic events (Level 3 hypoglycaemia) within 6 months prior to screening, or 3 or more hypoglycaemic events (blood glucose ≤ 3.9 mmol/L) within 1 month prior to screening, or recurrent hypoglycaemia-related symptoms

Treatment and study plan

GZR4

Drug

Administered once weekly subcutaneously (s.c., under the skin) for 6 weeks

insulin degludec

Drug

Administered once daily subcutaneously (s.c., under the skin) for 6 weeks

Primary outcomes

  1. Incidence of TEAE

    Time frame: Baseline to Week 6

Secondary outcomes

  1. AUC0-inf

    Time frame: Week 6

  2. AUC0-last

    Time frame: Week 6

  3. AUC0-168h

    Time frame: Week 1, Week 6

  4. Tmax,GZR4

    Time frame: Week 1, Week 6

  5. ADA of GZR4

    Time frame: Baseline to Week 10

Sponsors and collaborators

Lead sponsor

Gan and Lee Pharmaceuticals, USA

Industry

Registry information

Official study title

A Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multiple Doses of GZR4 in Chinese Patients With Type 2 Diabetes Mellitus

Important dates

Study start
2023
Primary completion
2023
Study completion
2023
First posted
Aug 14, 2024
Registry last updated
Aug 14, 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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