Clinical Study of Recombinant Anti-HER2 Humanized Monoclonal Antibody for Injection

PHASE1/PHASE2UnknownINTERVENTIONAL
Enrollment

132

Participants

Timeline

Start Date

March 28, 2014

Primary Completion Date

December 31, 2021

Study Completion Date

December 31, 2022

Conditions
HER2-positive Breast Cancer
Interventions
BIOLOGICAL

GB221,2 mg/kg

Single dose, 2mg/kg group: lyophilized powder of Coprelotamab Injection; strength 110mg/bottle; 2 mg/kg for one dose, intravenous infusion, completed for over 90 minutes

BIOLOGICAL

GB221,6 mg/kg

Single dose 6mg/kg group: lyophilized powder of Coprelotamab Injection; strength 110mg/bottle; 6 mg/kg for one dose, intravenous infusion, completed for over 90 minutes

BIOLOGICAL

Herceptin,6 mg/kg

Single dose group: lyophilized powder of Trastuzumab Injection; strength 440 mg/bottle; 6 mg/kg for one dose, intravenous infusion, completed for over 90 minutes

BIOLOGICAL

GB221,8mg/kg

Single dose 8mg/kg group: lyophilized powder of Coprelotamab Injection; strength 110mg/bottle; 8mg/kg for one dose, intravenous infusion, completed for over 90 minutes

BIOLOGICAL

GB221:2mg/kg and Capecitabi:1000mg/kg

GB221:Lyophilized powder of Coprelotamab Injection; strength 110mg/bottle; 2mg/kg, the first infusion is completed over 90 minutes. If no serious adverse reaction is observed, the subsequent infusion can be completed over 30 minutes. The administration shall be continued until disease progression or intolerable toxic reactions or ICF withdrawal of subjects. Multiple dose group; Capecitabine:1000mg/kg, orally twice daily (one dose each in the morning and evening; total daily dose of 2000 mg/m2), administration for 2 weeks followed by a 1-week rest period, as a 3-week cycle.

BIOLOGICAL

Herceptin:2mg/kg and Capecitabin:1000mg/kg

Herceptin:Lyophilized powder of Trastuzumab Injection; strength 440 mg/bottle; 2mg/kg, the first infusion is completed over 90 minutes. If no serious adverse reaction is observed, the subsequent infusion can be completed over 30 minutes. The administration shall be continued until disease progression or intolerable toxic reactions or ICF withdrawal of subjects. Multiple dose groups; Capecitabine:1000mg/kg, orally twice daily (one dose each in the morning and evening; total daily dose of 2000 mg/m2), administration for 2 weeks followed by a 1-week rest period, as a 3-week cycle.

Trial Locations (1)

100071

RECRUITING

Affiliated Hospital of Academy of Military Medical Sciences, Beijing

Sponsors
All Listed Sponsors
lead

Genor Biopharma Co., Ltd.

INDUSTRY