Clinical Study to Compare the Pharmacokinetics and Safety of Trastuzumab for Injection With Herceptin® in Healthy Male Volunteers

NCT05765357 | Completed Phase 1

• 1 other identifier: ZDTQ-2017-QTZDK
• Study Type: interventional
• Target: 89
• Locations: 1 country
• Sites: 1

Brief Summary

Trastuzumab for injection is a biosimilar of Herceptin ® produced by Chia Tai Tianqing Biotechnology Co., LTD, which is a humanized IgG1 monoclonal antibody produced by chinese hamster ovary (CHO) cells. A randomized, double-blind, single-dose, parallel phase I study comparing trastuzumab for injection with Herceptin ® in healthy male volunteers was conducted to evaluate the similarities in pharmacokinetics, tolerability, safety and immunogenicity of Trastuzumab for injection and Herceptin®.

Conditions

Metastatic Breast Cancer; Metastatic Gastric Cancer

Outcome Measures

Primary Outcomes (1)

• Area under drug concentration - time curve (AUC0-t)

  Area under the curve from time zero to the lowest detectable blood drug concentration

  Within 30 minutes before administration to 1344 hours after administration

Secondary Outcomes (6)

• Area under drug concentration - time curve (AUC0-∞)

  Within 30 minutes before administration to 1344 hours after administration

• Peak concentration (Cmax)

  Within 30 minutes before administration to 1344 hours after administration

• Time to reach maximum plasma (Tmax)

  Within 30 minutes before administration to 1344 hours after administration

• Clearance (CL)

  Within 30 minutes before administration to 1344 hours after administration

• half-life (T1/2)

  Within 30 minutes before administration to 1344 hours after administration

Study Arms (2)

Trastuzumab for injection

EXPERIMENTAL

4mg/kg, Single dose for intravenous infusion

Drug: Trastuzumab for injection

Herceptin

ACTIVE COMPARATOR

4mg/kg, Single dose for intravenous infusion

Drug: Herceptin

Interventions

Trastuzumab for injection DRUG

Trastuzumab for injection manufactured by Chia Tai Tianqing. Trastuzumab is a humanized IGG1-class monoclonal antibody produced by CHO cells. Its mechanism of action is to prevent the attachment of human epidermal growth factor to Her2 by attaching itself to Her2, thus blocking the growth of cancer cells. In addition, Trastuzumab can also stimulate the body's own immune cells to destroy cancer cells.

Trastuzumab for injection

Herceptin DRUG

Herceptin is the brand name of Trastuzumab for injection manufactured by Roche. Trastuzumab is a humanized IGG1-class monoclonal antibody produced by CHO cells. Its mechanism of action is to prevent the attachment of human epidermal growth factor to Her2 by attaching itself to Her2, thus blocking the growth of cancer cells. In addition, Trastuzumab can also stimulate the body's own immune cells to destroy cancer cells.

Herceptin

Eligibility Criteria

• Age: 18 Years - 65 Years
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Fully understand the purpose of the trial, and have a basic understanding of the pharmacological effects and possible adverse reactions of the drug under study; Voluntary written informed consent in accordance with the Helsinki Declaration;
• Healthy male subjects aged ≥ 18 years and ≤ 65 years;
• Body weight ≥ 50 kg ≤ 90 kg, body mass index ≥ 18 ≤ 28kg/m2;
• The system examination indicators were within the normal range, or the examination results were abnormal but the researchers judged that there was no clinical significance;
• Subjects agree to use reliable contraceptive methods for both themselves and their partners during the study period and for 6 months after the study drug infusion.

You may not qualify if:

• History of hypertension or abnormal blood pressure at screening/baseline measurement;
• A history of albuminuria or albuminuria as assessed by the investigator as clinically significant;
• Received any antibody or protein targeting Vascular Endothelial Cell Growth Factor (VEGF) or VEGF receptors in the previous 1 year;
• Study the use of any biological product or live virus vaccine within 3 months prior to drug infusion, or the use of any monoclonal antibody within 12 months;
• Have an inherited tendency to bleed or have coagulation dysfunction, or have a history of thrombosis or bleeding;
• History of digestive tract perforation or digestive tract fistula;
• Unhealed wound ulcers or fractures, or major surgery within 2 months prior to randomization or expected to be performed during the study period or within 2 months after study completion;
• Use of a prescription or over-the-counter drug or nutritional supplement within the 5 half-life of the drug or nutritional supplement or within 2 weeks prior to the study drug use;
• Positive virology test;
• Known allergy to trastuzumab;
• Known history of allergic diseases or allergic constitution;
• Study the history of blood donation 3 months before drug infusion;
• Received any other investigational drug therapy or participated in another interventional clinical trial within 2 months prior to screening
• A history of alcohol or drug abuse in the 12 months prior to screening;
• A history of mental illness;

Sponsors & Collaborators

• Chia Tai Tianqing Pharmaceutical Group Co., Ltd.: lead

Study Sites (1)

Affiliated Hospital of Changchun University of Traditional Chinese Medicine

Changchun, Jilin, 130021, China

Location

MeSH Terms

Conditions

Breast Neoplasms; Stomach Neoplasms

Interventions

Trastuzumab; Injections

Condition Hierarchy (Ancestors)

Neoplasms by Site; Neoplasms; Breast Diseases; Skin Diseases; Skin and Connective Tissue Diseases; Gastrointestinal Neoplasms; Digestive System Neoplasms; Digestive System Diseases; Gastrointestinal Diseases; Stomach Diseases

Intervention Hierarchy (Ancestors)

Antibodies, Monoclonal, Humanized; Antibodies, Monoclonal; Antibodies; Immunoglobulins; Immunoproteins; Blood Proteins; Proteins; Amino Acids, Peptides, and Proteins; Serum Globulins; Globulins; Drug Administration Routes; Drug Therapy; Therapeutics

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: QUADRUPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: March 1, 2023
• First Posted: March 13, 2023
• Study Start: July 16, 2017
• Primary Completion: October 27, 2017
• Study Completion: October 27, 2017
• Last Updated: March 13, 2023

Record last verified: 2017-04

Data Sharing

• IPD Sharing: Will not share

Locations

CN (1)