Type 2 Diabetes
Conditions
Brief summary
To evaluate the pharmacokinetics similarity between the 14028 injection produced by Sunshine Lake Pharma Co., Ltd. and dulaglutide injection (TRULICITY®) produced by Eli Lilly and Company for single dose in healthy male subjects, as well as to evaluate the similarity of the safety and immunogenicity between 14028 Injection and TRULICITY® in Healthy Subjects
Interventions
BIOLOGICAL14028 injection
14028 injection, single dose, s.c. injection
BIOLOGICALdulaglutide injection
dulaglutide injection(TRULICITY®), single dose, s.c. injection
Sponsors
Sunshine Lake Pharma Co., Ltd.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
MALE
Age
18 Years to 45 Years
Healthy volunteers
Yes
Inclusion criteria
1. Sign the informed consent form before the trial, understand and comply with the research process, and participate the trial voluntarily 2. Healthy male subjects aged 18 to 45 (including the critical value) 3. Weight \> or = 50 kg, and 19.0 kg/m2 \< or = BMI (body mass index) \< or = 28.0 kg/m2 4. Vital signs, physical examination, laboratory examination, electrocardiogram, thyroid color Doppler ultrasound, abdominal color Doppler ultrasound and chest X-ray (anteroposterior) and other test results during screening are normal or have no clinical significance as judged by the investigator 5. Subjects agree to use effective contraceptive methods from signing the informed consent form to the end of the trial drug use within 3 months, and there is no sperm donation plan.
Exclusion criteria
1. The investigator judges that the subjects have the following clinically significant diseases (including but not limited to gastrointestinal, kidney, liver, nerve, blood, endocrine, tumor, lung, immune, mental or cardiovascular and cerebrovascular diseases) 2. Have a medical or family history of medullary thyroid cancer (grandparents, parents, brothers and sisters), or a genetic disease that lead to medullary thyroid cancer; or a history or family history of multiple endocrine neoplasia syndrome type 2 3. Past or current history of pancreatitis (chronic or acute pancreatitis) 4. Past or current history of habitual constipation or intestinal obstruction 5. Clinically significant history of drug allergy or specific allergic disease (asthma, urticaria) or known allergy to the investigational drug and any component or related excipient components 6. Those who have difficulty with venous blood collection, a history of needle sickness, haemorrhage, or a known tendency to severe bleeding 7. Positive test results for hepatitis B surface antigen (HBsAg), hepatitis C virus antibody (HCVAb), human immunodeficiency virus antibody (HIV), and Treponema pallidum antibody (TPAb) 8. Those who have used any prescription drugs, over-the-counter drugs, Chinese herbal medicines, health products (except vitamin supplements) within 2 weeks before the first dose 9. Those who have a history of vaccination with live attenuated vaccine within 3 months before screening or a history of vaccination with inactivated vaccine within 1 month before screening 10. Those who have previously received dulaglutide or any other glucagon-like peptide-1 (GLP-1) analog 11. Those who donated blood or lost blood \> or = 400 mL within 3 months before screening, or those who plan to donate blood 12. Those who smoked more than 5 cigarettes per day within 3 months before screening or who could not give up smoking during the period from signing the informed consent to the subjects leaving the group 13. Those who have a history of alcohol abuse, that is, drinking more than 14 units of alcohol per week (1 unit = 360 mL of beer or 45 mL of 40% alcohol or 150 mL of wine) , or those who have a positive alcohol breath test during the screening period 14. Those who have a history of drug abuse or poison use within 2 years before screening, or those who have a positive test results for urine drug abuse screening during the screening period 15. Participated in other clinical trials within 3 months before screening (subjects who are not randomized or not receiving treatment withdraw from the study before treatment, they can be enrolled in this study) 16. Acute illness or concomitant medication occurred from the time of signing the informed consent to the first administration 17. Those who have special requirements for diet and cannot obey the unified diet 18. Others judged by the investigator to be unsuitable to participate in this trial 19. Subjects who may not be able to complete this trial for other reasons
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Maximum (peak) plasma drug concentration(Cmax) | 0 hour (pre-dose,within 30mins) to 384 hours after administration | Maximum (peak) plasma drug concentration |
| Area under the plasma concentration-time curve from time zero to ∞ (AUC0-∞) | 0 hour (pre-dose, within 30mins) to infinity | The area under the plasma concentration curve from 0 to ∞ |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Elimination half-life (t1/2) | 0 hour (pre-dose,within 30mins) to 384 hours after administration | Elimination half-life |
| Apparent total body clearance (CL/F) | 0 hour (pre-dose,within 30mins) to 384 hours after administration | Apparent total body clearance |
| Area under the plasma concentration-time curve from time zero to time t (AUC0-t) | 0 hour (pre-dose,within 30mins) to 384 hours after administration | The area under the plasma concentration curve from 0 to 384 h |
| Elimination constants (λz) | 0 hour (pre-dose,within 30mins) to 384 hours after administration | Elimination constants |
| Apparent volume of distribution (Vd/F) | 0 hour (pre-dose,within 30mins) to 384 hours after administration | Apparent volume of distribution |
| Time to reach maximum plasma concentration following drug administration (Tmax) | 0 hour (pre-dose,within 30mins) to 384 hours after administration | Time to maximum concentration |
Countries
China
Outcome results
None listed