研究项目库 / NCT05884398

Apalutamide用于前列腺癌的III 期研究

这是一项关于前列腺癌的III 期研究,登记的药物或干预包括Apalutamide;Androgen-deprivation Therapy (ADT),当前状态为研究进行中,已停止招募。登记地点显示中国北京、长春、成都、广州等城市有研究中心记录。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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这是一项关于前列腺癌的III 期研究,登记的药物或干预包括Apalutamide;Androgen-deprivation Therapy (ADT),当前状态为研究进行中,已停止招募。登记地点显示中国北京、长春、成都、广州等城市有研究中心记录。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

Apalutamide;Androgen-deprivation Therapy (ADT) · III 期

登记条件中文摘要

登记的基本范围为男性,年龄18 岁;另列出8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6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 First Hospital · 北京
  • The First Hospital of Jilin University · 长春
  • West China School of Medicine/West China Hospital, Sichuan University · 成都
  • The First Affiliated Hospital Sun Yat sen University · 广州
  • Nanfang Hospital of Southern Medical Hospital · 广州
  • Shandong Provincial Hospital · 济南
  • Ningbo First Hospital · 宁波
  • Shengjing Hospital Of China Medical University · 沈阳
  • TongJi Hospital of TongJi Medical College of Huazhong University of Science & Technology · 武汉
  • The First Affiliated Hospital of Xian Jiaotong University · 西安

公开的入选条件

  • * Diagnosis of prostate cancer prior to screening with histologically or cytologically confirmed adenocarcinoma of the prostate
  • * For participants not undergoing Gender-affirming care: Metastatic prostate cancer disease documented by conventional imaging (example, computed tomography \[CT\], magnetic resonance imaging \[MRI\], or bone scan) and/or next-generation imaging \[NGI\] demons
  • * For participants undergoing Gender-affirming care: No evidence of metastasis by either conventional imaging (example, CT, MRI, or bone scan) and/or NGI is also acceptable
  • * For participants not undergoing gender-affirming care: testosterone levels \> 50 (ng/dL) nanograms per deciliter at screening, except for those who may have received ADT prior to screening. Participants are allowed to have received up to 3 months of (ADT) an
  • * For participants undergoing Gender-affirming care: There is no testosterone level requirement for inclusion
  • * Have an Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 0 or 1. Participants with ECOG PS 2 or 3 are eligible for the study if the ECOG PS score is related to stable physical limitations (example, wheelchair-bound due to prior spinal cord
  • * A participant must agree not to plan to conceive a child while enrolled in this study or within 3 months after the last dose of study treatment
  • * Must be able to take whole apalutamide tablets by swallowing alone or with another vehicle (example, applesauce)

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:NCT05884398;登记信息更新于 2026-09-25。

查看原始登记记录