Overview
A Study of IBI362 in Participants With Type 2 Diabetes
Status:
Not yet recruiting
Not yet recruiting
Trial end date:
2025-02-28
2025-02-28
Target enrollment:
0
0
Participant gender:
All
All
Summary
This trial is conducted in China. The aim of the trial is to evaluate efficacy and Safety of IBI362 Versus dulaglutide as add-on to Metformin and/or SGLT2 inhibitor or TZD in Subjects With Type 2 Diabetes.Phase:
Phase 3Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Innovent Biologics (Suzhou) Co. Ltd.Treatments:
Dulaglutide
Criteria
Inclusion Criteria:1. T2D was diagnosed according to WHO standards in 1999 for
2. Age ≥ 18 when signing the informed consent form
3. After used stable-dose metformin (≥1500 mg/day) or stable-dose metformin (≥1500
mg/day) combined with SGLT2 inhibitors (empagliflozin 10 mg/day, dapagliflozin 10
mg/day, canagliflozin 100 mg/day, Henagliflozin 5 mg/day) for 2 months before
screening, or stable-dose metformin (≥1500 mg/day) combined with daily fixed-dose
sulfonylureas (half the maximum dose on the drug label), the blood sugar was still
poorly controlled, the local laboratory test at the time of screening was
7.5%≤HbA1c≤11.0%.
4. BMI≥23 kg/m2 at screening.
5. Subjects voluntarily signed the informed consent form and agreed to strictly follow
the requirements of this protocol
Exclusion Criteria:
1. Subjects who the investigator thinks may be allergic to the components in the study
drug or similar drugs
2. Weight change>5% within 12 weeks before screening (chief complaint)
3. Oral hypoglycemic drugs other than background therapy drugs have been used within 2
months before screening.
4. Previous diagnosis of type 1 diabetes (including adult latent autoimmune diabetes),
special type diabetes or gestational diabetes
5. There are active or untreated malignant tumors within 5 years before screening, or
patients are in remission of clinical malignant tumors (except patients with skin
basal cell carcinoma and squamous cell carcinoma, cervical carcinoma in situ, prostate
carcinoma in situ or papillary thyroid carcinoma who have no recurrence after surgery)
6. Mental illness existed in the past or at the time of screening, and the researcher
thinks it is not suitable to participate in this study
7. Pregnant or lactating women, or men or women who are fertile and unwilling to use
contraception throughout the study period
8. The investigator believes that the subject has any other factors that may affect the
efficacy or safety evaluation of this study and is not suitable to participate in this
study