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Clinical Study of Recombinant Anti-HER2 Humanized Monoclonal Antibody (GB221) for Injection

14 de novembro de 2019 atualizado por: Genor Biopharma Co., Ltd.

A Randomized, Double-blind, Multi-center Phase Ⅲ Clinical Study to Evaluate the Recombinant Anti-HER2 Humanized Monoclonal Antibody or Placebo in Combination With Capecitabine for the Treatment of HER-2-positive Advanced Breast Cancer

The primary objective of this trial is to compare the progression-free survival (PFS) in two groups of combined therapy of GB221/ capecitabine tablets versus combined therapy of placebo/capecitabine tablets; the secondary objective is to evaluate the objective response rate (ORR),time to progression (TTP) from treatment period to week 12; overall survival (OS), safety, immunogenicity (anti-drug antibody), PFS of subjects during continued treatment period.

Visão geral do estudo

Status

Desconhecido

Tipo de estudo

Intervencional

Inscrição (Antecipado)

336

Estágio

  • Fase 3

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

    • Beijing
      • Beijing, Beijing, China, 100071
        • Recrutamento
        • People's Liberation Army General Hospital The Fifth Medical Center
        • Investigador principal:
          • Ze Fei Jiang, Ph.D

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

18 anos a 70 anos (Adulto, Adulto mais velho)

Aceita Voluntários Saudáveis

Não

Gêneros Elegíveis para o Estudo

Tudo

Descrição

Inclusion Criteria

  1. Aged 18 to 70 years;
  2. Pathologically confirmed as advanced breast cancer and there is at least one measurable target lesion (based on RECIST V1.1):

    l According to Response Evaluation Criteria in Solid Tumors, the target lesions must be accurately measured in at least one dimension; l No previous radiotherapy, intervention for target lesions;

  3. HER-2 positive [definition: including IHC (+++) or ISH positive; if IHC (++), HER-2 gene amplification detection should be further performed through fluorescence in situ hybridization (FISH) or chromogenic in situ hybridization (CISH),silver-enhanced in situ hybridization (SISH) and other methods. The test reports of the clinical study site associated with the subject should be provided];
  4. The relapsed or metastatic patients who failed respond to the previous taxanes and/or anthracyclines, previous first-line chemotherapy for the metastatic lesion is acceptable;
  5. The expected survival is 3 months or longer;
  6. The function of major organs such as heart, liver and kidney are basically normal;
  7. ECOG score ≤2;
  8. Understand and voluntarily sign the written informed consent form;

2 Exclusion Criteria

  1. Pregnant or breastfeeding females; or women of childbearing potential who have positive serum/urine pregnancy tests; females of childbearing potential and their partners are unwilling to adopt effective contraceptive methods during the clinical study period and within 6 months after the end of the study;
  2. Received radiotherapy or chemotherapy within 4 weeks before randomization;
  3. Received anti-tumor endocrine therapy within 2 weeks before randomization;
  4. Previously received the standard anti-HER-2 treatment;
  5. Previously received capecitabine treatment;
  6. Subjects who previously received no taxanes; or subjects who respond to taxanes (no disease progression or intolerable toxic reactions);
  7. The major organ function of subjects is abnormal. The laboratory test results are presented below:

Hematology test:

l Absolute neutrophil count (ANC) < 1.5×109/L; l Platelet count (PLT) <100×109/L; l Hemoglobin (Hb) < 90 g/L (no blood transfusion within 14 days);

Hepatic and renal function tests:

l Bilirubin (TBIL)>1.5×ULN (upper limit of normal); l Alanine aminotransferase (ALT) and aspartate aminotransferase (AST)>2.5×ULN; if there is any hepatic metastasis, ALT and AST >5×ULN; l Serum creatinine (Cr) >1.5×ULN; 8. Left ventricular ejection fraction ( LVEF)<50%; 9. The organ system status of subjects:

1 Subjects with known or suspected brain metastasis: subjects with evidence indicating signs or symptoms of brain metastasis are not allowed to participate in this study unless such brain metastasis is excluded by CT or MRI. However, subjects whose brain metastasis lesions have been controlled can be enrolled (no progression within at least 4 weeks after radiotherapy and/or no neurological symptom or sign after surgical resection, treatment with dexamethasone or mannitol is not necessary);

1 Evidence showing severe or uncontrolled systemic diseases (e.g. unstable or non-compensated respiratory, cardiac, hepatic or renal disease);

1 Uncontrolled active infection (≥CTCAE grade 2); l Any other malignant tumor within 5 years, excluding patients with completely cured cervical in situ carcinoma or basal cell or squamous epithelial cell skin cancer);

1 Subjects who have any of the following cardiac conditions:

  • Unstable angina pectoris;
  • Medical history of congestive heart failure;
  • Previous medical history of myocardial infarction, coronary artery bypass grafting or coronary stent implantation;
  • Clinically significant pericardial diseases and valvular heart diseases;
  • Cardiac arrhythmias requiring therapeutic intervention;
  • Any other cardiac diseases which may cause safety risks for subjects if they are enrolled in this study; 1 Uncontrolled hypertension (defined as screening systolic blood pressure ≥ 180mmHg and/or diastolic blood pressure ≥110mmHg); 10. Immunodeficiency medical history, including positive HIV detection; 11. Positive hepatitis B surface antigen (HBsAg) and hepatitis B virus DNA of peripheral blood is not within the normal range; Positive hepatitis C virus antibody (HCV); 12. Subjects with drug abuse history or alcohol addiction history; 13. Participated in clinical study with drug intervention within one month before screening; 14. Subjects who are unsuitable for participation in this study at the discretion of the investigators.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Triplo

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: GB221+ Capecitabine tablets
test drug+capecitabine

GB221:Lyophilized powder for injection; strength 110mg/bottle; the first administration of 8 mg/kg, intravenous drip for over 90 minutes; subsequently, the administration shall be given once every 3 weeks (one cycle), the dose is 6 mg/kg, intravenous drip for 30~90 minutes; The administration shall be continued until disease progression or presence of intolerable toxic reactions or subject's active withdrawal from clinical study.

Capecitabine:Tablets; 500mg/tablet, 12 tablets/box; Total daily dose 2000 mg/m2, orally twice daily, one dose each in the morning and evening, administration for 2 weeks followed by a 1-week rest period, as a 3-week cycle. The administration shall be continued until disease progression or presence of intolerable toxic reactions or subject's active withdrawal from clinical study.

Outros nomes:
  • Capecitabina
Comparador de Placebo: Placebo control + capecitabine tablets
placebo+capecitabine

Placebo control:Lyophilized powder for injection; strength 110mg/bottle; the first administration of 8 mg/kg, intravenous drip for over 90 minutes; subsequently, the administration shall be given once every 3 weeks (one cycle), the dose is 6 mg/kg, intravenous drip for 30~90 minutes; The administration shall be continued until disease progression or presence of intolerable toxic reactions or subject's active withdrawal from clinical study.

Capecitabine:Tablets; 500mg/tablet, 12 tablets/box; Total daily dose 2000 mg/m2, orally twice daily, one dose each in the morning and evening, administration for 2 weeks followed by a 1-week rest period, as a 3-week cycle. The administration shall be continued until disease progression or presence of intolerable toxic reactions or subject's active withdrawal from clinical study.

Outros nomes:
  • capecitabina

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Progression-free survival, PFS
Prazo: through study completion, an average of 2 year
To evaluate the efficacy of GB221 as defined by progression-free survival in patients with breast cancer.
through study completion, an average of 2 year

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Objective Response Rate, ORR
Prazo: through study completion, an average of 2 year
To evaluate the efficacy of GB221 as defined by overall response rate, in patients with breast cancer.
through study completion, an average of 2 year
Antidrug antibody, ADA
Prazo: through study completion, an average of 2 year
Antidrug antibody, ADA
through study completion, an average of 2 year
Overall survival, OS
Prazo: through study completion, an average of 2 year
To evaluate the duration from the first administration to death because of any reason in patients with breast cancer.
through study completion, an average of 2 year
PFS in the extended treatment phase
Prazo: through study completion, an average of 2 year
PFS in the extended treatment phase
through study completion, an average of 2 year

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

24 de novembro de 2016

Conclusão Primária (Antecipado)

1 de julho de 2020

Conclusão do estudo (Antecipado)

1 de novembro de 2020

Datas de inscrição no estudo

Enviado pela primeira vez

13 de novembro de 2019

Enviado pela primeira vez que atendeu aos critérios de CQ

14 de novembro de 2019

Primeira postagem (Real)

15 de novembro de 2019

Atualizações de registro de estudo

Última Atualização Postada (Real)

15 de novembro de 2019

Última atualização enviada que atendeu aos critérios de controle de qualidade

14 de novembro de 2019

Última verificação

1 de novembro de 2019

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

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