Phase Ⅰ Clinical Trial of Gerilimzumab Injection in Healthy Subjects

NCT ID: NCT04178070

Last Updated: 2019-11-27

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE1
• Total Enrollment: 58 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-11-06
• Study Completion Date: 2021-04-30

Brief Summary

The primary objectives of this study are to evaluate the safety, tolerability and pharmacokinetic (PK) profiles of single-dose, dose-escalated, abdominal subcutaneous injection of GB224 in Chinese healthy adult subjects. The secondary objectives are to preliminarily understand the immunogenicity and pharmacodynamic variable (IL-6) of single abdominal subcutaneous injection of GB224 in Chinese healthy adult subjects.

Conditions

Rheumatoid Arthritis

Study Design

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

Study Groups

GB224 2mg

single dose

Group Type: EXPERIMENTAL

GB224 2mg

Intervention Type: BIOLOGICAL

2mg (100μL), single dose, abdominal subcutaneous injection

GB224 5mg

single dose

Group Type: EXPERIMENTAL

GB224 5mg

Intervention Type: BIOLOGICAL

5mg (250μL), single dose, abdominal subcutaneous injection

GB224 10mg

single dose

Group Type: EXPERIMENTAL

GB224 10mg

Intervention Type: BIOLOGICAL

10mg (500μL), single dose, abdominal subcutaneous injection

GB224 15mg

single dose

Group Type: EXPERIMENTAL

GB224 15mg

Intervention Type: BIOLOGICAL

15mg (750μL), single dose, abdominal subcutaneous injection

GB224 20mg

single dose

Group Type: EXPERIMENTAL

GB224 20mg

Intervention Type: BIOLOGICAL

20mg (1mL), single dose, abdominal subcutaneous injection

GB224 30mg

single dose

Group Type: EXPERIMENTAL

GB224 30mg

Intervention Type: BIOLOGICAL

30mg (1.5mL), single dose, abdominal subcutaneous injection

Placebo, 30mg

Intervention Type: OTHER

30mg (1.5mL), single dose, abdominal subcutaneous injection

Placebo 2mg

single dose

Group Type: PLACEBO_COMPARATOR

Placebo, 2mg

Intervention Type: OTHER

2mg (100μL), single dose, abdominal subcutaneous injection

Placebo 5mg

single dose

Group Type: PLACEBO_COMPARATOR

Placebo, 5mg

Intervention Type: OTHER

5mg (250μL), single dose, abdominal subcutaneous injection

Placebo 10mg

single dose

Group Type: PLACEBO_COMPARATOR

Placebo, 10mg

Intervention Type: OTHER

10mg (500μL), single dose, abdominal subcutaneous injection

Placebo 15mg

single dose

Group Type: PLACEBO_COMPARATOR

Placebo, 15mg

Intervention Type: OTHER

15mg (750μL), single dose, abdominal subcutaneous injection

Placebo 20mg

single dose

Group Type: PLACEBO_COMPARATOR

Placebo, 20mg

Intervention Type: OTHER

20mg (1mL), single dose, abdominal subcutaneous injection

Placebo 30mg

single dose

Group Type: PLACEBO_COMPARATOR

Placebo, 30mg

Intervention Type: OTHER

30mg (1.5mL), single dose, abdominal subcutaneous injection

Interventions

GB224 2mg

2mg (100μL), single dose, abdominal subcutaneous injection

Intervention Type: BIOLOGICAL

GB224 5mg

5mg (250μL), single dose, abdominal subcutaneous injection

Intervention Type: BIOLOGICAL

GB224 10mg

10mg (500μL), single dose, abdominal subcutaneous injection

Intervention Type: BIOLOGICAL

GB224 15mg

15mg (750μL), single dose, abdominal subcutaneous injection

Intervention Type: BIOLOGICAL

GB224 20mg

20mg (1mL), single dose, abdominal subcutaneous injection

Intervention Type: BIOLOGICAL

GB224 30mg

30mg (1.5mL), single dose, abdominal subcutaneous injection

Intervention Type: BIOLOGICAL

Placebo, 2mg

2mg (100μL), single dose, abdominal subcutaneous injection

Intervention Type: OTHER

Placebo, 5mg

5mg (250μL), single dose, abdominal subcutaneous injection

Intervention Type: OTHER

Placebo, 10mg

10mg (500μL), single dose, abdominal subcutaneous injection

Intervention Type: OTHER

Placebo, 15mg

15mg (750μL), single dose, abdominal subcutaneous injection

Intervention Type: OTHER

Placebo, 20mg

20mg (1mL), single dose, abdominal subcutaneous injection

Intervention Type: OTHER

Placebo, 30mg

30mg (1.5mL), single dose, abdominal subcutaneous injection

Intervention Type: OTHER

Other Intervention Names

Gerilimzumab injection; Gerilimzumab injection; Gerilimzumab injection; Gerilimzumab injection; Gerilimzumab injection; Gerilimzumab injection

Eligibility Criteria

Inclusion Criteria

1. Understand the study procedures and contents, and voluntarily sign the informed consent form;

2. Chinese healthy adult volunteers aged 18 to 45 years, males and females;

3. The subjects have qualified physical examination within 30 days before the study, the body mass index (BMI) is within the range of 19~24 and the body weight is within the range of 45~75kg;

4. Males or females agree to adopt medically confirmed effective contraceptive measures during the entire study period and within 6 months after the end of this study.

5. The investigator considers that the patients have good health condition according to the physical examination, medical history, vital signs and ECG etc.

6. Patients have good compliance, can receive follow-up visits as scheduled, are able to well communicate with the investigators and complete the study as required by the study.

Exclusion Criteria

1. Any of the following is met: allergic constitution; known allergic to the components of the investigational product or allergy history to any drug or food or pollen; subjects who have medical history of skin allergy such as physical urticaria; subjects who have abnormal serum immunoglobulin E (IgE) test;

2. Any of the current symptoms, signs or laboratory test abnormalities indicating the possible presence of acute or subacute infection (e.g., pyrexia, cough, urgent micturition, urodynia, abdominal pain, diarrhea, cutaneous infected wound etc.)

3. Patients with active pulmonary tuberculosis; patients who previously had medical history of active pulmonary tuberculosis;

4. Subjects who have medical history of drug addiction or drug abuse;

5. Subjects who have clear medical history of central nervous system, cardiovascular, renal, hepatic, gastrointestinal, respiratory, metabolic system or subjects with other significant diseases; subjects with medical history of hypertension or screening systolic blood pressure ≥ 140mmHg and/or diastolic blood pressure ≥ 90mmHg, which are clinically significant at the discretion of the investigators; subjects who have medical history of orthostatic hypotension;

6. Subjects who have medical history of malignant tumors;

7. Subjects who participated in other clinical studies within 3 months before enrollment, or subjects who received drugs which are known to injure the major organs within 3 months before enrollment;

8. Subjects who used prescription drugs or non-prescription drugs within 14 days before enrollment;

9. Subjects who have blood donation history within 3 months before enrollment;

10. Subjects who meet any of the following criteria: alanine aminotransferase (ALT) or aspartate aminotransferase (AST) >1.5 times the upper limit of normal (ULN), serum creatinine (Cr) > the upper limit of normal (ULN);

11. Abnormal routine blood tests: any of the following is met: white blood cells (WBC)<3.0×109/L or >9.5×109/L, neutrophil count (ANC)<1.5×109/L, platelet count (PLT)<100×109/L, hemoglobin (HGB)<104g/L;

12. Any of the following is positive: hepatitis B surface antigen (HBsAg), hepatitis C antibody (HCV-Ab), acquired immunodeficiency syndrome antibody (Anti-HIV) and anti-treponema pallidum antibody (TP-Ab);

13. Subjects who have positive tuberculosis skin test (5 units of dosage, induration of not less than 5 millimeters (mm) within 48 ~ 72 hours);

14. Subjects with positive anti-nuclear antibody (ANA), anti-double stranded DNA antibody (ds-DNA) and anti-extractable nuclear antigens (ENA);

15. Subjects with positive anti-drug antibody (ADA);

16. Subjects with positive tumor markers (CEA, AFP, PSA and CA-125);

17. Subjects with abnormal coagulation function, which is clinically significant at the discretion of the investigators;

18. Subjects with medical history of psychiatric disorders;

19. Smoking more than 5 cigarettes/day or equivalent tobacco;

20. Weekly alcohol consumption more than 28 units (1 unit = 285 mL of beer or 25 mL of spirits or a glass of wine); or subjects who have positive breath alcohol test within 24 hours before the use of investigational drug;

21. Subjects who have clinically significant abnormal laboratory test values at screening;

22. Female subjects who have positive serum/urine pregnancy tests at screening or lactating women;

23. Patients who have insufficient communication, understanding and cooperation; or patients who have poor compliance and cannot guarantee to strictly follow the study protocol;

24. Subjects who are considered unsuitable for participating in this study for various reasons at the discretion of the investigator.

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

Sponsors

Genor Biopharma Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Yi Fang, Ph.D

Role: PRINCIPAL_INVESTIGATOR

Peking University People's Hospital

Locations

Peking University People's Hospital

Beijing, Beijing Municipality, China

Site Status: RECRUITING

Countries

China

Central Contacts

Shawn Yu, Master

Role: CONTACT

Shawn.Yu@genorbio.com

010-65260820

Facility Contacts

Yi Fang, Ph.D

Role: primary

010-66583834

Other Identifiers

GENOR GB224-001; V1.4

Identifier Type: -

Identifier Source: org_study_id