Single Dose Pharmacokinetic Study of GB221 in Comparison With Herceptin ®

Genor Biopharma

Status and phase

Completed

Phase 1

Conditions

Breast Cancer

Treatments

Drug: GB221

Drug: Herceptin

Study type

Interventional

Funder types

Industry

Identifiers

NCT04905667

221-005

Details and patient eligibility

About

This is a single center, randomized, blind, parallel controlled clinical trial. The primary objective is to evaluate the single dose pharmacokinetics of recombinant Humanized anti-HER-2 monoclonal antibody injection GB221 in comparison with Herceptin ® in Chinese healthy adult volunteers. The main aim is to study the pharmacokinetic similarity between GB221 and Herceptin ®.

Full description

Subjects will enroll in random order, and be divided into two groups, then receive a single dose (6 mg/kg) of GB221 or Herceptin ®, and accept observation for 42 days. Throughout the course, safety data will be collected.

Enrollment

87 patients

Sex

All

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

1. Signed informed consent form;
1. Healthy adult volunteers aged between 18 and 45, male or female;
1. Medical examination as required within 28 days, body mass index (BMI) 19.0 ~ 24.0, weight≥50 kg for men, ≥45 kg for women, and≤ 75 kg for both;
1. Agreed with taking reliable contraceptive measures, and no fertility planning from the beginning to the end of the study within 6 months;
5.Subject can communicate well with the investigators and complete the study according to the study regulations.

Exclusion criteria

1. Pregnant or lactating women, or positive in either blood or urine pregnancy test; or unwilling to take effective contraceptive measures during the trial and within 6 months after the end of the trial at fertile age;
1. Allergic constitution; or history of allergic to experimental drug ingredient or any drug or food or pollen; or abnormal serum immunoglobulin E (IgE) test;
1. History of drug abuse, or positive urine test for drug;
1. History of the central nervous system, cardiovascular system, kidney, liver, digestive system, respiratory system, metabolic system or other significant diseases. History of high blood pressure, or clinically significant systolic blood pressure≥140 mmHg/diastolic blood pressure≥90 mmHg;
1. Family history of cancer, or tumor markers (male: CEA, AFP, PSA, CA-125; Female: CEA, AFP, CA-153, CA-125) positive.
1. Participated in other clinical trials of drug or used drugs harmful to major organs within 3 months;
1. Blood donation within 3 months;
1. Used prescription or OTC drugs within 14 days;
1. Left ventricular ejection fraction (LVEF) < 60%;
1. ALT or AST > 1.5 ULN, Cr > ULN;
1. WBC < 0.8 LLN or > 1.2 ULN; ANC < 0.8 LLN; PLT < 0.8 LLN; HGB < 0.9LLN.
1. HBs-Ag, HCV-Ab, anti-HIV or TP-Ab positive;
1. Anti-drug antibody (ADA) test positive;
14.History of psychosis;
1. History of postural hypotension;
1. More than 5 cigarettes per day;
1. More than 28 units of alcohol per week; Or alcohol breath test positive within 24 hours before pre-dose;
1. History of dizziness of blood or needle;
1. Unsuitable for other reasons.