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A Study to Evaluate the Pharmacokinetics, Efficacy, and Safety of HLX319 vs. EU-Phesgo® in the Neoadjuvant Therapy of HER2-Positive Early or Locally Advanced Breast Cancer

15 de maio de 2026 atualizado por: Shanghai Henlius Biotech

A Multicenter, Randomized, Double-Blind, Parallel-Controlled Phase I Clinical Study to Evaluate the Pharmacokinetics, Efficacy, and Safety of Phesgo® Biosimilar HLX319 vs. EU-Phesgo® in the Neoadjuvant Therapy of HER2-Positive Early or Locally Advanced Breast Cancer

This is a study to compare the similarity in Pharmacokinetics (PK) profile of HLX319 vs. EU-Phesgo® in patients with HER2-positive early or locally advanced breast cancer .

Visão geral do estudo

Status

Ainda não está recrutando

Descrição detalhada

This is a randomized, double-blind, parallel-controlled, multi-center Phase I equivalence study to compare the similarity in PK profile of HLX319 vs. EU-Phesgo® in patients with HER2-positive early or locally advanced breast cancer with a primary tumor > 2 cm or nodes-positive.

Tipo de estudo

Intervencional

Inscrição (Estimado)

258

Estágio

  • Fase 1

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.

Contato de estudo

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

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

Inclusion Criteria:

  • Voluntary participation in the clinical study and signed the Informed Consent Form (ICF).
  • Male or female aged ≥ 18 years old at the time of signing the ICF;
  • Histologically confirmed invasive breast cancer, stage II-IIIC, Human Epidermal Growth Factor Receptor 2 (HER2) positive confirmed by central laboratory.
  • Participants agree to undergo surgery while meeting the criteria for surgery after neoadjuvant therapy.
  • Left ventricular ejection fraction (LVEF) at baseline ≥ 55%.
  • An Eastern Cooperative Oncology Group (ECOG) performance status (PS) score of 0-1.
  • Adequate major organ functions.
  • Women with child-bearing potential have a negative result of serum pregnancy test at screening period (within 7 days prior to the first dose) or if they are infertile, non- lactating, reproduction-age men and women following highly effective contraceptive measures until 7 months after last dose.

Exclusion Criteria:

  • Stage IV breast cancer, bilateral breast cancer, or multicentric breast cancer.
  • History of other malignancy within 5 years.
  • Prior systemic therapy for breast cancer treatment or radiotherapy.
  • Patients with a history of ductal carcinoma in situ (DCIS) or lobular carcinoma in situ (LCIS) who have received systemic therapy or radiotherapy to the ipsilateral breast.
  • Patients who have undergone excision biopsy of the primary tumor and/or axillary lymph nodes or lymph node dissection.
  • Have severe heart disease or medical conditions.
  • Participants with viral hepatitis or those with autoimmune hepatitis, sclerosing cholangitis, or liver cirrhosis.
  • Human Immunodeficiency Virus (HIV) infection, HIV antibody positive.
  • Daily use of corticosteroid treatment is required.
  • Sensitivity to any study medications or any of its ingredients or excipients.
  • Participants who underwent any major surgery within 28 days prior to the first dose. Or participants who have received local radiotherapy, radiofrequency ablation, or interventional therapy within 2 weeks prior to the first dose.
  • Received another interventional clinical trial therapy within 4 weeks prior to enrollment in the study, or intentionally participated in another interventional clinical trial during the entire study period.
  • Severe, uncontrolled systemic diseases that may currently interfere with the therapeutic plan.
  • Any other conditions which are inappropriate for the study in the opinion of the investigator.

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: Dobro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: HLX319
The regimen in the experimental group is HLX319 in combination with docetaxel and carboplatin.
HLX319 is a biosimilar of pertuzumab-trastuzumab monoclonal antibody injection (subcutaneous injection)
Comparador Ativo: EU-Phesgo®
The regimen in the control group is EU-Phesgo® in combination with docetaxel and carboplatin.
EU-Phesgo® is an original marketed drug product, with the generic name pertuzumab-trastuzumab monoclonal antibody injection (subcutaneous injection)

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Peak concentration (Cmax)
Prazo: up to 180 days
Peak concentration after a single drug administration in Cycle 1.
up to 180 days
Area under the serum drug concentration-time curve from 0 to 21 days (AUC0-21d)
Prazo: up to 180 days
Area under the serum drug concentration-time curve from 0 to 21 days after a single drug administration in Cycle 1.
up to 180 days
Steady-state peak concentration (Cmax,ss)
Prazo: up to 180 days
The steady-state peak concentration after multiple doses administration in Cycle 4.
up to 180 days
Steady-state area under the serum drug concentration-time curve within a dosing interval (AUCss)
Prazo: up to 180 days
Steady-state area under the serum drug concentration-time curve within a dosing interval after multiple doses administration in Cycle 4.
up to 180 days

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Trough concentration (Ctrough)
Prazo: up to 180 days
Trough concentration after a single dose administration
up to 180 days
Area under the serum drug concentration-time curve from time 0 to infinity (AUC0-inf)
Prazo: up to 180 days
Area under the serum drug concentration-time curve from time 0 to infinity after a single dose administration
up to 180 days
Percentage of extrapolated area in the total AUC (%AUCex)
Prazo: up to 180 days
Percentage of extrapolated area in the total AUC after a single dose administration
up to 180 days
Time to peak concentration (Tmax)
Prazo: up to 180 days
time to peak concentration after a single dose administration
up to 180 days
Elimination half-life (T1/2)
Prazo: up to 180 days
elimination half-life after a single dose administration
up to 180 days
Total clearance (CL/F)
Prazo: up to 180 days
total clearance after a single dose administration
up to 180 days
Terminal phase distribution volume (Vz/F)
Prazo: up to 180 days
terminal phase distribution volume after a single dose administration
up to 180 days
Mean residence time (MRT)
Prazo: up to 180 days
mean residence time after a single dose administration
up to 180 days
Steady-state trough concentration (Ctrough,ss)
Prazo: up to 180 days
steady-state trough concentration after multiple doses administration in Cycle 4
up to 180 days
Average steady-state concentration (Caverage,ss)
Prazo: up to 180 days
average steady-state concentration after multiple doses administration in Cycle 4
up to 180 days
Steady-state time to peak concentration (Tmax,ss)
Prazo: up to 180 days
steady-state time to peak concentration after multiple doses administration in Cycle 4
up to 180 days
Elimination half-life (T1/2,ss)
Prazo: up to 180 days
elimination half-life after multiple doses administration in Cycle 4
up to 180 days
Steady-state volume of distribution (Vss/F)
Prazo: up to 180 days
steady-state volume of distribution after multiple doses administration in Cycle 4
up to 180 days
Steady-state total clearance (CLss/F)
Prazo: up to 180 days
steady-state total clearance after multiple doses administration in Cycle 4
up to 180 days
accumulation ratio based on Cmax (RCmax)
Prazo: up to 180 days
accumulation ratio based on Cmax after multiple doses administration in Cycle 4
up to 180 days
Accumulation ratio based on AUC (RAUC)
Prazo: up to 180 days
accumulation ratio based on AUC after multiple doses administration in Cycle 4
up to 180 days
The total pathological complete response (tpCR) rate assessed by the investigator
Prazo: up to 180 days
up to 180 days
Breast pathologic complete response (bpCR) rate assessed by the investigator
Prazo: up to 180 days
up to 180 days
Objective response rate (ORR) assessed by the investigator
Prazo: up to 180 days
according to Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 criteria
up to 180 days
Incidence and severity of adverse events (AEs)
Prazo: up to 180 days
severity determined according to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version 6.0
up to 180 days
Number of participants with abnormal vital signs
Prazo: up to 180 days
Detailed Outcome Measure will be defined in the Statistical Analysis Plan
up to 180 days
Number of participants with abnormal physical examination findings
Prazo: up to 180 days
Detailed Outcome Measure will be defined in the Statistical Analysis Plan
up to 180 days
Number of participants with abnormal Laboratory tests results
Prazo: up to 180 days
Detailed Outcome Measure will be defined in the Statistical Analysis Plan
up to 180 days
Number of participants with abnormal 12-lead ECG readings
Prazo: up to 180 days
Detailed Outcome Measure will be defined in the Statistical Analysis Plan
up to 180 days
Positivity rates of anti-drug antibodies (ADA)
Prazo: up to 180 days
up to 180 days
Positivity rates of neutralizing antibodies (NAb)
Prazo: up to 180 days
up to 180 days

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 (Estimado)

3 de julho de 2026

Conclusão Primária (Estimado)

23 de abril de 2027

Conclusão do estudo (Estimado)

22 de julho de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

8 de maio de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

15 de maio de 2026

Primeira postagem (Real)

22 de maio de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

22 de maio de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

15 de maio de 2026

Última verificação

1 de maio de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • HLX319-BC001

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

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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