Clinical trial

A Phase 3, Randomized, Open-Label, Multicenter, Active-controlled Trial Comparing Efficacy and Safety of THDB0206 Injection With Insulin Lispro Injection Combined With Insulin Glargine Injection U-100 in Chinese Participants With Type 2 Diabetes

Name
THDB0206L02
Description
This is a 26-week randomized, open-label, multicenter, active-controlled parallel group trial. The purpose of this study is to compare efficacy and safety of THDB0206 injection with insulin lispro injection combined with insulin glargine injection U-100 in Chinese participants with T2DM.
Trial arms
Trial start
2022-05-06
Estimated PCD
2024-03-30
Trial end
2024-10-31
Status
Recruiting
Phase
Early phase I
Treatment
THDB0206 Injection
Drug: THDB0206 Injection Injected subcutaneously three times a day. Dose was individually adjusted.
Arms:
THDB0206 Injection
Insulin Lispro Injection
Drug:Insulin Lispro Injection Injected subcutaneously three times a day. Dose was individually adjusted.
Arms:
Insulin Lispro Injection
Size
805
Primary endpoint
Change in Glycosylated Haemoglobin (HbA1c) After 26 Weeks of Treatment
Week 26
Eligibility criteria
Inclusion Criteria: * Body mass index: 18.0 kg/m\^2\~35.0 kg/m\^2 (both inclusive) at the time of screening. * HbA1c: 7.0%\~10.0% (both inclusive) at the time of screening. * Diagnosed with T2DM for 6 months or longer at the time of screening based on the World Health Organization (WHO) classification. * Treated with stable insulin regimen as follow for at least 3 months with or without oral antidiabetic drug: 1. Basal insulin (neutral protamine Hagedorn \[NPH\] insulin, insulin glargine, insulin degludec, insulin detemir) in combination with at least 1 prandial injection of bolus insulin. 2. Premixed insulin at least twice daily. Exclusion Criteria: * Have other types of diabetes other than T2DM. * Have used Glucagon-Like Peptide 1 (GLP-1) receptor agonist within 3 months prior to screening. * Have had 1 or more episodes of severe hypoglycemia within the 6 months prior to screening. * Have had 1 or more episodes of acute diabetic complications (diabetic ketoacidosis, hyperglycemic hyperosmolar state, diabetic lactic acidosis, etc.) within the 6 months prior to screening. * With concomitant conditions at screening that may affect the evaluation of the study, including cardiovascular and cerebrovascular diseases, respiratory diseases, gastrointestinal diseases, liver diseases, kidney diseases, nervous system diseases, psychiatric diseases, hematological diseases, immune system diseases, endocrine system diseases, pancreatic diseases, and/or malignant tumors.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE3'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 805, 'type': 'ESTIMATED'}}
Updated at
2023-04-28

1 organization

2 products

1 indication

Indication
Type 2 Diabetes
Product
THDB0206