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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

2026年5月15日 更新者: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 .

研究概览

地位

尚未招聘

详细说明

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.

研究类型

介入性

注册 (估计的)

258

阶段

  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

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.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:双倍的

武器和干预

参与者组/臂
干预/治疗
实验性的: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)
有源比较器: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)

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Peak concentration (Cmax)
大体时间: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)
大体时间: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)
大体时间: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)
大体时间: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

次要结果测量

结果测量
措施说明
大体时间
Trough concentration (Ctrough)
大体时间: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)
大体时间: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)
大体时间: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)
大体时间:up to 180 days
time to peak concentration after a single dose administration
up to 180 days
Elimination half-life (T1/2)
大体时间:up to 180 days
elimination half-life after a single dose administration
up to 180 days
Total clearance (CL/F)
大体时间:up to 180 days
total clearance after a single dose administration
up to 180 days
Terminal phase distribution volume (Vz/F)
大体时间:up to 180 days
terminal phase distribution volume after a single dose administration
up to 180 days
Mean residence time (MRT)
大体时间:up to 180 days
mean residence time after a single dose administration
up to 180 days
Steady-state trough concentration (Ctrough,ss)
大体时间: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)
大体时间: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)
大体时间: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)
大体时间: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)
大体时间: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)
大体时间: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)
大体时间: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)
大体时间: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
大体时间:up to 180 days
up to 180 days
Breast pathologic complete response (bpCR) rate assessed by the investigator
大体时间:up to 180 days
up to 180 days
Objective response rate (ORR) assessed by the investigator
大体时间: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)
大体时间: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
大体时间: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
大体时间: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
大体时间: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
大体时间: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)
大体时间:up to 180 days
up to 180 days
Positivity rates of neutralizing antibodies (NAb)
大体时间:up to 180 days
up to 180 days

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年7月3日

初级完成 (估计的)

2027年4月23日

研究完成 (估计的)

2027年7月22日

研究注册日期

首次提交

2026年5月8日

首先提交符合 QC 标准的

2026年5月15日

首次发布 (实际的)

2026年5月22日

研究记录更新

最后更新发布 (实际的)

2026年5月22日

上次提交的符合 QC 标准的更新

2026年5月15日

最后验证

2026年5月1日

更多信息

与本研究相关的术语

其他研究编号

  • HLX319-BC001

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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