A Study of HS-20094 in T2DM Participants
Status and phase
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Treatments
Details and patient eligibility
About
This is a randomized, placebo and active-control, multiple-dose, phase IIa trial. Patients were randomly assigned to receive HS-20094 (12 patients), placebo (3 patients), or active control drug Semaglutide injection (3 patients) in a 4:1:1 ratio to each of four dose cohorts of 5 mg, 10 mg, 15 mg, and 20 mg. HS-20094 and placebo were administered in a double-blind design by subcutaneous injection once a week for a total of four times, and the dose was gradually increased weekly (2.5-2.5-5-5 mg, 5-510-10 mg, 5-10-15-15 mg, 5-10-15-20 mg). The active control drug semaglutide was administered by open-label, titrated subcutaneous injection once a week for a total of four times, and the dose was increased gradually every week until 1.0 mg (0.25-0.5-0.5-1.0 mg). The primary study objective was to 1) Evaluate the safety and tolerability of multiple subcutaneous injections of HS-20094 in subjects with type 2 diabetes mellitus (T2DM) with or without overweight or obesity;2) Evaluate the pharmacokinetics, pharmacodynamics and immunogenicity of multiple subcutaneous injections of HS-20094.
Enrollment
Sex
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Volunteers
Inclusion criteria
- Male or female subjects,20-65 years of age at the time of signing informed consent.
- Type 2 diabetes mellitus diagnosed for at least 3 months before the screening visit.
- Treated with conventional lifestyle intervention and stable treatment with metformin ( ≥ 1000 mg/day) at least 3 months prior to screening HbA1c 7.5-10%(both inclusive)at screening visit.
Exclusion criteria
- A history of type 1 diabetes, specific diabetes, or secondary diabetes.
- Presence of-clinically significant lab or ECG results that may affect the evaluation of the efficacy or safety of the study drug at screening visit.
- Acute or chronic pancreatitis at any time before screening, or serum lipase/amylase above the upper limit of normal at screening.
- A history of grade 2 hypoglycemia(blood glucose 3.0 mmol/L)or grade 3 hypoglycemia(hypoglycemia with a serious event of consciousness and/or physical alteration requiring assistance from another person for recovery)within 6 months before screening.
- Diabetid ketoacidosis or hyperosmolar coma or lactic acidosis requiring hospitalization occurred within 6 months before screening.
- Severe infection such as diabetic foot infection, pneumonia, or sepsis within 30 days before screening.
- Uncontrollable hypertension.
- History of acute cardiovascular and cerebrovascular diseases within 6 months prior to screening.
- Any organ-system malignancies developed within 5 years except for cured local basal cell carcinoma of the skin and carcinoma in situ of the cervix.
- Pregnant or lactating woman.
- In the investigator's judgment, there were circumstances that affected subject safety or otherwise interfered with the evaluation of results.
Trial design
Primary purpose
Allocation
Interventional model
Masking
54 participants in 4 patient groups
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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