A SHR-1210 BE Study on Healthy Subjects

Advanced Tumors Clinical Trial

Official title:

A Bioequivalence Study of SHR-1210 in Healthy Subjects

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05799183
• Other study ID #: SHR-1210-I-105
• Status: Recruiting
• Phase: Phase 1
• Start date: July 4, 2023
• Est. completion date: November 25, 2023

Study information

• Verified date: September 2023
• Source: Jiangsu HengRui Medicine Co., Ltd.
• Contact: Shaorong Li, Ph.D.
• Phone: +86-180-0162-4511
• Email: shaorong.li[@]hengrui.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to assess the bioequivalence of SHR-1210 before and after process changes.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 118
• Est. completion date: November 25, 2023
• Est. primary completion date: October 25, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Male subjects aged = 18;

2. Weigh at least 50 kg, and have a body mass index (BMI) = 19 and =28 kg/m2;

3. Subjects agree to use reliable contraceptive measures (e.g., abstinence, sterilization, contraceptives, injectable contraceptives methylprogesterone or subcutaneous implantation in the duration of the study and for 4 months after the study drug infusion);

4. Sign the informed consent before the trial, and fully understand the content, process and possible adverse reactions of the trial. Must be able to communicate with the investigator, understand and comply with all study requirements.

Exclusion Criteria:

1. Those with a history of chronic liver, kidney, cardiovascular, neurological/psychiatric, digestive tract, respiratory, urinary, endocrine and other systemic diseases;

2. Those with a history of autoimmune diseases;

3. Regular drinkers in the 6 months prior to the trial had an average daily alcohol intake of more than 15 g (equivalent to 145 mL of wine, 450 mL of beer, or 43 mL of liquor with 40% alcohol content);

4. Those who are suspected or confirmed to be allergic or have had serious drug or food allergic reactions in the past, have a clear history of allergies and/or are allergic to the research drug or its ingredients;

5. Have used any drug (including Chinese medicine and vitamins) within 2 weeks before screening, or the last dose is less than 5 half-lives of the drug from the test administration date, whichever is longer;

6. Have used of anti-PD-1/PD-L1 drugs;

7. Those who have participated in other interventional clinical trials within 3 months before screening;

8. =400 ml of blood loss, blood donation or receiving any blood product transfusion within 3 months before screening;

9. Those who have undergone major surgery or hospitalized for illness within 3 months before screening;

10. Those who have received live vaccines within 6 months prior to screening, or who are expected to receive live vaccines during the study period;

11. Those with a history of drug abuse or positive drug screening results within 12 months prior to screening;

12. Those who have abnormalities in vital signs, physical examination, and laboratory tests during the screening period and are judged to be clinically significant by the study physician (Note: If there is an abnormality and the study doctor judges that it has clinical significance, if it is within the normal range after re-examination, it can also be enrolled);

13. There are abnormalities in the ECG during the screening period (such as QTcF= 450ms, shortened or prolonged PR interval, second-degree and third-degree atrioventricular block, pre-excitation syndrome, etc.) and are judged by the study doctor to have clinical significance;

14. Chest x-ray (positive and lateral position) or lung CT during the screening period is abnormal and judged by the study doctor to be clinically significant;

15. History of needle sickness and blood sickness; or those with poor vascular conditions, unable to retain implanted needles or unable to tolerate venipuncture blood collection;

16. Those that the investigator believes are not suitable to participate in this clinical trial for other reasons.

Related Conditions & MeSH terms

• Advanced Tumors

Intervention

Drug:
• SHR-1210
Subjects will receive treatment SHR-1210 before process changes 20 mg
• SHR-1210
Subjects will receive treatment SHR-1210 after process changes 20 mg

Locations

Country	Name	City	State
China	The Third Xiangya Hospital of Central South University	Changsha	Hunan

Sponsors (1)

Lead Sponsor	Collaborator
Jiangsu HengRui Medicine Co., Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pre-test: Incidence and severity of AE/SAE/AESI (rated based on CTCAE v5.0)		Day-1 to Day 46
Primary	Formal Test: Pharmacokinetics parameters of SHR-1210 before and after process changes in the fed state: AUC0-inf		Based on pre-dose, 0.25-192 hours post-dose sampling times on Day 1 ~ Day 4 and Day 6 ~ Day 9
Primary	Formal Test: Pharmacokinetics parameters of SHR-1210 before and after process changes in the fed state: the geometric mean ration		Based on pre-dose, 0.25-192 hours post-dose sampling times on Day 1 ~ Day 4 and Day 6 ~ Day 9
Primary	Formal Test: Pharmacokinetics parameters of SHR-1210 before and after process changes in the fed state: 90% confidence interval (90% CI) of AUC0-inf		Based on pre-dose, 0.25-192 hours post-dose sampling times on Day 1 ~ Day 4 and Day 6 ~ Day 9
Secondary	Pre-test: Inter-individual coefficient of variation (CV) of the AUC0-inf of SHR-1210		Based on pre-dose, 0.25-192 hours post-dose sampling times on Day 1 ~ Day 4 and Day 6 ~ Day 9
Secondary	Formal Test: Other Pharmacokinetics parameters of SHR-1210 before and after process changes in the fed state: Cmax		Based on pre-dose, 0.25-192 hours post-dose sampling times on Day 1 ~ Day 4 and Day 6 ~ Day 9
Secondary	Formal Test: Other Pharmacokinetics parameters of SHR-1210 before and after process changes in the fed state: AUC0-t		Based on pre-dose, 0.25-192 hours post-dose sampling times on Day 1 ~ Day 4 and Day 6 ~ Day 9
Secondary	Formal Test: Other Pharmacokinetics parameters of SHR-1210 before and after process changes in the fed state: Tmax		Based on pre-dose, 0.25-192 hours post-dose sampling times on Day 1 ~ Day 4 and Day 6 ~ Day 9
Secondary	Formal Test: Other Pharmacokinetics parameters of SHR-1210 before and after process changes in the fed state: t1/2		Based on pre-dose, 0.25-192 hours post-dose sampling times on Day 1 ~ Day 4 and Day 6 ~ Day 9
Secondary	Formal Test: Other Pharmacokinetics parameters of SHR-1210 before and after process changes in the fed state: CL		Based on pre-dose, 0.25-192 hours post-dose sampling times on Day 1 ~ Day 4 and Day 6 ~ Day 9
Secondary	Formal Test: Other Pharmacokinetics parameters of SHR-1210 before and after process changes in the fed state: Vss		Based on pre-dose, 0.25-192 hours post-dose sampling times on Day 1 ~ Day 4 and Day 6 ~ Day 9
Secondary	Formal Test: The incidence of anti-drug antibody (ADA) and neutralizing antibody (Nab) for SHR-1210		Based on sampling times pre-dose on Day1, post-dose on Day 9 and Day 16
Secondary	Formal Test: Incidence and severity of adverse events (rated based on CTCAE 5.0)		Day-1, Day 1 to Day 46±7