A SAD Study of ZT002 Injection in Healthy Participants

NCT ID: NCT06423872

Last Updated: 2024-05-21

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 28 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-06-19
• Study Completion Date: 2023-12-08

Brief Summary

This study will comprise a randomized, parallel assignment, double blind, placebo controlled, single and multiple ascending dose, safety, tolerability and pharmacokinetic study of ZT002 in healthy participants.

Conditions

Type 2 Diabetes Mellitus

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

ZT002

Participants will be randomized to receive ZT002 injection or Placebo in 1 of 6 dose cohorts.

Group Type: EXPERIMENTAL

ZT002

Intervention Type: DRUG

Participants will receive a single subcutaneous (SC) ZT002 injection.

Placebo

Participants will be randomized to receive ZT002 injection or Placebo in 1 of 6 dose cohorts.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: OTHER

Participants will receive same volume as of the study drug.

Interventions

ZT002

Participants will receive a single subcutaneous (SC) ZT002 injection.

Intervention Type: DRUG

Placebo

Participants will receive same volume as of the study drug.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

1. Fully understand the purpose, nature, methods, and potential adverse reactions of the experiment, voluntarily participate as a participant, comply with the requirements of this study, and sign an informed consent form.

2. Healthy adults, age 18~45 years, both inclusive, at time of informed consent.

3. Body Mass Index (BMI) between 19～27.0 kg/m2 both included. Male weight>55.0kg, famale weight>50.0kg.

4. In good health, determined by no clinically significant findings from medical history, physical examination, vital signs measurements, anterior and lateral chest X-ray,12-lead ECG, and clinical laboratory evaluations(blood routine, blood biochemistry, coagulation function, and urine routine)at screening and before administration of study drug, as assessed by the Investigator.

5. Female participants are required to abstain or use two effective contraceptive methods simultaneously from 1 month before screening to 6 months after the last dose. Male participants are required to abstain or use two effective contraceptive methods simultaneously from the first dose to 6 months after the last dose: male participants are required to undergo surgical sterilization (such as vas deferens ligation) or use condoms correctly, or their spouse is required to use hormonal contraceptives approved by the National Medical Products Administration (such as contraceptive pills, patches, implantable or injectable preparations) or intrauterine devices (IUDs) or undergo surgical sterilization; Female subjects may undergo surgical sterilization (such as tubal ligation) or intrauterine devices (IUDs), or their spouses may use condoms correctly or undergo surgical sterilization. After the trial, female subjects may also use hormone contraceptives approved by the National Medical Products Administration (such as contraceptive pills, patches, implantable or injectable preparations).

Exclusion Criteria

1. History of drug allergy or allergic related diseases (allergic rhinitis, asthma, urticaria, eczema, etc.)，allergic to experimental drugs and excipients or GLP-1 class drugs.

2. Significant history or clinical manifestation of any neurological, cardiovascular, hematological, hepatic, renal, gastrointestinal, respiratory, metabolic, endocrine, immune or skeletal, as determined by the Investigator.

3. Family or personal history of medullary thyroid carcinoma (MTC).

4. Medical history of multiple endocrine neoplasia type 2(MEN2).

5. History of acute or chronic pancreatitis.

6. History of hypoglycemia.

7. Calcitonin equal or above 50 ng/L at screening.

8. The content of amylase or lipase during the screening period is higher than the upper limit of normal values and has clinical significance.

9. Screening period HbAlc (glycated hemoglobin) ≥ 6.5%.

10. According to the Fridericias formula，QTcF ≥ 450 ms for subjects in 12-lead ECG examination during screening or baseline period.

11. History of drug abuse within the previous year of screening or positive results from drug abuse screening (urine screening).

12. Have smoked ≥5 cigarettes per day in the past 3 month prior to Screening or unable to refrain from smoking during the study.

13. Screening for subjects who have consumed more than 14 units of alcohol per week within the first 3 months (1 unit of alcohol=360 mL of beer or 45 mL of 40% alcohol or 150 mL of wine), or who have taken alcoholic products within 48 hours before administration, or who cannot abstain from alcohol during the trial period.

14. Positive test for hepatitis B surface antigen (HBsAg)，hepatitis C antibody (HCV-Ab), human immunodeficiency virus (HIV-Ab) antibody, treponema pallidum(TP-Ab) antibody at screening.

15. Screening for subjects who have participated in other clinical trials and received drug therapy or medical device intervention within the first 3 months.

16. Blood donation or blood loss - more than 400 mL during the 3 months prior to screening, or received blood transfusion; or blood donation or blood loss - more than 200 mL during the 1 months prior to screening.

17. History of infectious diseases within 4 weeks before screening (judged by the investigator to affect the ability of the subject to participate in the test)

18. Cannot tolerate venous puncture blood collection or have a history of fainting or fainting

19. Received vaccination within 28 days prior to administration or plan to receive vaccination during the study period.

20. Use of prescription or non-prescription or chinese herbal medicine or discontinue medication before 1 month to screening or within 5 half-lives of the medicinal product, (whichever is longest).

21. Participant is unable to refrain from strenuous exercise during the study

22. Breastfeeding or pregnant women, or positive tests of pregnancy in screening or baseline

23. Other unsuitable conditions to participate in the clinical study judged by the investigator.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 45 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Beijing Hospital

OTHER_GOV

Sponsor Role: collaborator

Beijing QL Biopharmaceutical Co.,Ltd

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Aixin Shi, Master

Role: PRINCIPAL_INVESTIGATOR

No.1 Dahua Road, Dongdan, Dongcheng District, Beijing

Locations

Beijing Hospital

Beijing, Beijing Municipality, China

Countries

China

Other Identifiers

BJQLZT002002

Identifier Type: -

Identifier Source: org_study_id