研究项目库 / NCT07070232

BNT326用于晚期实体瘤的I 期 / II 期研究

这是一项关于晚期实体瘤的I 期 / II 期研究,登记的药物或干预包括BNT326;Pumitamig;Itraconazole;Paroxetine,当前状态为招募中。登记地点显示中国杭州、天津、武汉有研究中心记录。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。

一分钟看懂

这是一项关于晚期实体瘤的I 期 / II 期研究,登记的药物或干预包括BNT326;Pumitamig;Itraconazole;Paroxetine,当前状态为招募中。登记地点显示中国杭州、天津、武汉有研究中心记录。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

BNT326;Pumitamig;Itraconazole;Paroxetine · I 期 / II 期

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。

  • Sir Run Run Shaw Hospital, Zhejiang University, School of Medicine · 杭州
  • The Second Affiliated Hospital of Zhejiang University School of Medicine · 杭州
  • Tianjin Medical University Cancer Institute & Hospital · 天津
  • Hubei Cancer Hospital · 武汉

公开的入选条件

  • (applicable to all participants and all parts unless otherwise specified):
  • * Aged ≥18 years at the time of giving informed consent. Local laws will be followed if the age of consent is older.
  • * Have histologic or cytologic documented advanced disease, either at relapse or upon diagnosis of metastatic disease. This requirement may be considered met when advanced disease derives from unequivocal progression of a previously biopsied site of disease (e
  • * Have measurable disease defined by RECIST v1.1.
  • * Have ECOG performance status of 0 or 1.
  • * Have adequate organ and bone marrow function (as specified in the protocol) within 7 days before randomization/enrollment.
  • * Cohort 1A:
  • Have histologically or cytologically confirmed diagnosis of unresectable or metastatic cutaneous melanoma not amenable to local therapy.

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:NCT07070232;登记信息更新于 2026-09-02。

查看原始登记记录