研究项目库 / NCT07844018

HER2 target therapy用于乳腺癌的II 期研究

这是一项关于乳腺癌的II 期研究,登记的药物或干预包括HER2 target therapy,当前状态为尚未开始招募。登记地点显示中国北京有研究中心记录。是否仍有名额以及是否值得进一步询问,需要向研究中心确认。

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这是一项关于乳腺癌的II 期研究,登记的药物或干预包括HER2 target therapy,当前状态为尚未开始招募。登记地点显示中国北京有研究中心记录。是否仍有名额以及是否值得进一步询问,需要向研究中心确认。

药物或干预

HER2 target therapy · II 期

登记条件中文摘要

年龄范围:18岁及以上

登记的基本范围为女性,年龄18岁及以上;以下仅摘录1项专业入选条件,需结合英文原文并由研究团队确认。

登记记录列出1项主要排除条件,具体医学含义需结合英文原文并由研究团队确认。

中国哪些地方有记录

以下地点来自登记信息,不代表此刻仍有名额;请向研究中心确认最新情况。

  • Peking University People's Hospital · 北京

入选条件原文摘录

以下为摘录,请打开原始登记查看完整入排标准。

  • * 1.18 years or older and be treatment-naïve breast cancer patients 2.histology confirmed invasive breast carcinoma.HER2-positive defined by our pathology department, defined as IHC 3+ or IHC 2+ with fluorescence/chromogenic in situ hybridization (FISH/CISH) confirming HER2 gene amplification; 3.Clinically staged as Stage II or III according to AJCC 8th edition 4.Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 5.Adequate function of major organs to meet study safety and tolerability requirements 6.Agree to provide tissue biopsies and/or blood samples at specified study timepoints (baseline, after cycle 4, after cycle 8, and at surgical resection) for translational research purposes 7.No contraindication to breast-enhanced MRI (no contraindications to breast MRI enhancement 8.Reproductive-age women must have a negative serum pregnancy test within 7 days prior to enrollment and agree to use an effective form of contraception recognized clinically during the study and for 3 months after the last study drug administration 9.agrees to participate in this study and signs the informed consent form

联系前需要确认

请继续确认中心是否启动、疾病分型、既往治疗、检查费用和知情同意安排。

查看登记信息

登记号:NCT07844018;登记信息更新于 2026-10-02;本站同步于 2026-10-08。

查看原始登记记录