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临床试验/NCT07583953
NCT07583953尚未招募1 期

An Exploratory Study of Personalized Cancer Vaccine (ABO2109) in Adjuvant Therapy of Solid Tumors

Suzhou Abogen Biosciences Co., Ltd.0 个研究点目标入组 50 人开始时间: 2026年4月17日最近更新:

试验速览

阶段
1 期
状态
尚未招募
入组人数
50

研究概览

简要总结

The purpose of this study is to evaluate the safety and tolerability of ABO2109 in combination with toripalimab, and to evaluate the immunogenicity, pharmacokinetics, pharmacodynamics, as well as biomarker characteristics of the investigational cancer vaccine. In addition, the antitumor activity of ABO2109 will be assessed during both dose exploration and expansion stages, the accumulative data will support the clinical development of ABO2109.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Key inclusion criteria:
  • ≥18 years of age at time of informed consent
  • Eastern Cooperative Oncology Group (ECOG) performance status score of 0-1
  • Life expectancy of ≥6 months
  • Patient diagnosed with solid tumors and is receiving perioperative and/or adjuvant anti-cancer therapy.
  • Sufficient organ function
  • Female patients must meet both of the criteria: a) Surgically sterile, or postmenopausal for ≥2 years, or women of childbearing potential with a negative pregnancy test and willing to use effective contraception during the study and for at least 90 days after the last study dose. Use of progesterone-containing contraceptives is not permitted. b) Agree not to breastfeed during the study and for at least 90 days after the last study dose.Male patients must meet the following criteria:If not surgically sterile and potentially engaging in sexual activity that could lead to pregnancy, agree to use effective contraception during the study and for at least 90 days after the last study dose.

排除标准

  • Key Exclusion Criteria:
  • For perioperative or adjuvant therapy setting, participants have received systemic anti-tumor treatment previously
  • Any other prior malignancy active within the previous 5 years, except for skin basal cell cancer that has been cured, or superficial bladder cancer, carcinoma in situ of the breast, carcinoma in situ of the cervix, thyroid cancer
  • Active or prior history of interstitial lung disease, tuberculosis, or any other condition known to compromise pulmonary function.
  • Active infections
  • History of severe cardiovascular or cerebrovascular diseases occurring within 6-month prior to study treatment
  • Known hypersensitivity to the active ingredients or excipients of ABO2109 or toripalimab
  • Positive pregnancy test or lactating women

研究者

申办方类型
Industry
责任方
Sponsor

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