Pharmacokinetic, Safety and Immunogenicity Study of CMAB809 and Herceptin in Healthy Volunteers

Mabpharm

Status and phase

Completed

Phase 1

Conditions

Healthy Volunteers

Treatments

Drug: Trastuzumab

Drug: CMAB809

Study type

Interventional

Funder types

Industry

Identifiers

NCT04049409

CMAB809HV-I

Details and patient eligibility

About

This is a randomized, double-blinded, controlled Phase I study of CMAB809 administered by intravenous infusion. This study will characterize the pharmacokinetic, safety and immunogenicity of CMAB809 versus Trastuzumab(Herceptin) in healthy male subjects after a single dose.

Enrollment

72 patients

Sex

Male

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Healthy male volunteers, age ranged 18 to 45 years (both inclusive)
A subject with body weight be equal or greater than 50 kg (inclusive) and body mass index (BMI) between 19 and 26 kg/m2 (both inclusive)
Findings within the range of clinical acceptability in medical history and physical examination, and laboratory results within the laboratory reference ranges for the relevant laboratory tests (unless the investigator considers the deviation to be irrelevant for the purpose of the study)
Left ventricular ejection fraction (LVEF) within the normal range by echocardiogram (ECHO) at 2 weeks prior to randomization
The subjects have the ability to understand the full characteristics and objectives of the study, including the possible risks and side effects of the study; Moreover, the subjects can communicate well with researchers and complete the research according to the regulations
Subjects must voluntarily sign ICF prior to the study

Exclusion criteria

Any clinical signs and symptoms (including blood pressure, pulse, and electrocardiogram) found during medical examination; And those who underwent surgery within 4 weeks before screening; Or plans to operate during the trial period
Diagnosed with any clinical history of serious illness or any other disease or physiological conditions which can interfere with the test results
Prescription or over-the-counter drugs with a long half-life (greater than 24h) within 1 month prior to administration. Take any other medication that the investigator considers may affect the subject's enrollment within 2 weeks prior to administration. A subject who has participated in any other clinical trial within 3 months before the study drug administration
Have used or are using biological products such as monoclonal antibodies or fusion proteins
Patients who have or have had chronic hepatitis b, c, syphilis or HIV infection, or who have tested positive for the above infection were deemed unsuitable to participate in this study
Those who had been vaccinated within 30 days prior to screening or who needed to be vaccinated between screening and the end of the trial
Drug abusers, or those who used soft drugs (e.g., marijuana) 3 months before screening, or took hard drugs (e.g., cocaine, phenyclohexidine, etc.) 1 year before the test, or drank excessive amounts of tea, coffee and/or caffeinated beverages (more than 8 cups, 1 cup =250ml) every day, or those who showed positive urine drug screening
Blood donation (containing component blood) or lost more than 400 mL of blood within 3 months before screening, or blood transfusion; Blood donation (containing component blood) or blood loss of more than 200 mL within 1 month before screening
Related allergies (including allergy to any mouse\human protein or immunoglobulin products, rubber or latex)
Those who smoked more than 10 cigarettes per day within 6 months before screening; And those who could not quit during the study period
Alcoholics (who drink more than 14 standard units per week), or who have positive result in breath-test of alcohol
Vigorous activity for 72h before drug administration; and cannot be avoided within 7 days after drug administration
Unable to accept clinical trial center diet
Fertile men who were unwilling to use highly effective contraceptives during the trial and for five months after administration
The investigator judges the subject not eligible for the study after reviewing clinical laboratory results or other reasons