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Completed

NCT Number: NCT04905667

Single Dose Pharmacokinetic Study of GB221 in Comparison With Herceptin ®

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 ®.

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Key information

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

The Fifth Affiliated Hospital of Guangzhou Medical University

Guangzhou, 510799, China

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 1. Signed informed consent form;
  • 2. Healthy adult volunteers aged between 18 and 45, male or female;
  • 3. 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;
  • 4. 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;
  • 2. Allergic constitution; or history of allergic to experimental drug ingredient or any drug or food or pollen; or abnormal serum immunoglobulin E (IgE) test;
  • 3. History of drug abuse, or positive urine test for drug;
  • 4. 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;
  • 5. Family history of cancer, or tumor markers (male: CEA, AFP, PSA, CA-125; Female: CEA, AFP, CA-153, CA-125) positive.
  • 6. Participated in other clinical trials of drug or used drugs harmful to major organs within 3 months;
  • 7. Blood donation within 3 months;
  • 8. Used prescription or OTC drugs within 14 days;
  • 9. Left ventricular ejection fraction (LVEF) < 60%;
  • 10. ALT or AST > 1.5 ULN, Cr > ULN;
  • 11. WBC < 0.8 LLN or > 1.2 ULN; ANC < 0.8 LLN; PLT < 0.8 LLN; HGB < 0.9LLN.
  • 12. HBs-Ag, HCV-Ab, anti-HIV or TP-Ab positive;
  • 13. Anti-drug antibody (ADA) test positive;
  • 14.History of psychosis;
  • 15. History of postural hypotension;
  • 16. More than 5 cigarettes per day;
  • 17. More than 28 units of alcohol per week; Or alcohol breath test positive within 24 hours before pre-dose;
  • 18. History of dizziness of blood or needle;
  • 19. Unsuitable for other reasons.

Treatment and study plan

GB221

Drug

6 mg/kg, single dose, intravenous infusion, 90-100 min

Herceptin

Drug

6 mg/kg, single dose, intravenous infusion, 90-100 min

Primary outcomes

  1. AUC0-t

    Time frame: Day 43

    compare the pharmacokinetic AUC0-t parameters of GB221 and Herceptin ®

  2. AUC0-∞

    Time frame: Day 43

    compare the pharmacokinetic AUC0-∞parameters of GB221 and Herceptin ®

  3. Cmax

    Time frame: Day 43

    compare the pharmacokinetic Cmax parameters of GB221 and Herceptin ®

Secondary outcomes

  1. Tmax

    Time frame: Day 43

    compare the pharmacokinetic Tmax parameters of GB221 and Herceptin ®

  2. t1/2

    Time frame: Day 43

    compare the pharmacokinetic t1/2 parameters of GB221 and Herceptin ®

  3. CL

    Time frame: Day 43

    compare the pharmacokinetic CL parameters of GB221 and Herceptin ®

  4. Vd

    Time frame: Day 43

    compare the pharmacokinetic Vd parameters of GB221 and Herceptin ®

  5. Ke

    Time frame: Day 43

    compare the pharmacokinetic Ke parameters of GB221 and Herceptin ®

  6. ADA

    Time frame: Day 43

    compare the incidence of ADA in of GB221 and Herceptin ® group

  7. Nab

    Time frame: Day 43

    compare the incidence of Nab in of GB221 and Herceptin ® group

Sponsors and collaborators

Lead sponsor

Genor Biopharma Co., Ltd.

Industry

Registry information

Official study title

A Single Center, Randomized, Blind, Parallel Controlled, Single Dose Pharmacokinetic Study of Recombinant Humanized Anti-HER-2 Monoclonal Antibody Injection GB221 in Comparison With Herceptin ® in Chinese Healthy Adult Volunteers

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
May 27, 2021
Registry last updated
May 27, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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