跳至主要内容
临床试验/NCT07266298
NCT07266298
招募中
1 期

A Phase I, Multicenter, Dose-escalation, Single-arm Study of PRAME Antigen-targeted TCR-T Cells(NW-101C) in the Treatment of Subjects With Advanced Solid Malignant Tumors.

Neowise Biotechnology1 个研究点 分布在 1 个国家目标入组 24 人2025年12月1日
干预措施NW-101C

概览

阶段
1 期
干预措施
NW-101C
疾病 / 适应症
未指定
发起方
Neowise Biotechnology
入组人数
24
试验地点
1
主要终点
Evaluate the Dose-limiting toxicities(DLTs) of NW-101C in patients with solid malignant tumors
状态
招募中
最后更新
4个月前

概览

简要总结

This clinical trial is a prospective, dose-escalation, multicenter, single- arm, Phase 1 clinical trial to evaluate the safety, tolerability, PK and preliminary clinical activity of PRAME Antigen-targeted TCR-T Cells (NW-101C) infusion in patients with previously heavily treated, metastatic solid malignant tumors.

详细描述

Using a classic 3+3 dose escalation design, this study will enroll \~24 subjects to characterize the safety and preliminary anti-tumor activity of NW-101C. SCREENING: Patient eligibility will be determined by protocol inclusion/exclusion criteria including HLA (human leukocyte antigen) and a biopsy (or collection of archival tumor tissue) for biomarker screening. Leukapheresis for potential manufacturing of the NW-101C cellular product may be performed,if patients are HLA-A\*02:01 positive and meet the eligibility criteria for leukapheresis. MANUFACTURING: NW-101C products will be made from the patients' white blood cells. TREATMENT: Lymphodepletion with cyclophosphamide and fludarabine will occur in the days before the NW-101C product infusion to improve the duration of time that NW-101C product stays in the body. The patient will be admitted to the hospital during the T-cell infusion until 28 days following NW-101C infusion. After the NW-101C product infusion, dose -limiting toxicities (DLT) will be assessed from the infusion of NW-101C until 28 days following the infusion of NW-101C.

注册库
clinicaltrials.gov
开始日期
2025年12月1日
结束日期
2030年12月1日
最后更新
4个月前
研究类型
Interventional
研究设计
Sequential
性别
All

研究者

发起方
Neowise Biotechnology
责任方
Sponsor

入排标准

入选标准

  • Age between 18-75 years
  • Diagnosis of pathologically or histologically confirmed unresectable or advanced solid tumors and must have no standard treatment options available or unable to tolerate the currently available standard treatments
  • For patients with ovarian caner :Patients must have confirmed diagnosis of Platinum-resistant ovarian epithelial carcinoma(PROC)
  • HLA-A\*02:01positive
  • Patient's tumor must express PRAME assessed by central lab,Retrospective testing will be required for patients that qualify.
  • Adequate organ function prior to apheresis and lymphodepleting chemotherapy
  • ECOG performance status of 0-1
  • At least one tumor lesion measurable according to RECIST 1.1
  • (Additional protocol-defined Inclusion criteria may apply)

排除标准

  • Received the following treatments: Cytotoxic chemotherapy within 2 weeks prior to apheresis and within 1 week prior to lymphodepletion; Treatment with antibodies (including but not limited to those with monoclonal antibodies and immune checkpoint inhibitors) or other biologic therapy within 2 weeks prior to apheresis and within 1 week prior to lymphodepletion; Immunosuppressive agents (e.g., calcineurin inhibitors, methotrexate or other chemotherapeutic agents, mycophenolate mofetil, rapamycin, thalidomide, immunosuppressive antibodies such as anti-TNF, anti-IL-6, or anti-IL-6 receptor) within 2 weeks prior to apheresis and within 1 week prior to lymphodepletion
  • History of allergic reactions to cyclophosphamide, fludarabine, or any other chemical or biological components of the drugs used in this study
  • History of chronic or recurrent severe autoimmune disease, or active immune disease requiring treatment with steroids or other immunosuppressive agents within 1 year prior to enrollment
  • Have symptomic CNS metastases
  • Have leptomeningeal disease or carcinomatous meningitis
  • Have ongoing or active infection
  • Active infections with HIV, HBV, HCV, or syphilis
  • Breastfeeding or pregnant
  • (Additional protocol-defined Exclusion criteria may apply)

研究组 & 干预措施

NW-101C dose 1-4

干预措施: NW-101C

结局指标

主要结局

Evaluate the Dose-limiting toxicities(DLTs) of NW-101C in patients with solid malignant tumors

时间窗: 28 days following NW-101C infusion

Type, frequency and severity of adverse events assessed by CTCAE5.0

Evaluate the Maximum Tolerated Dose (MTD) of NW-101C in patients with solid malignant tumors

时间窗: Through the study completion, an average of 2 years

Type, frequency and severity of adverse events assessed by CTCAE5.0

次要结局

  • Evaluate the AUC of NW-101C in patients with solid malignant tumors(2 years following NW-101C infusion)
  • Evaluate the Objective response rate (ORR) of NW-101C in patients with solid malignant tumors(2 years following NW-101C infusion)
  • Evaluate the Tmax of NW-101C in patients with solid malignant tumors(Through the study completion, an average of 2 years)
  • Evaluate the Cmax of NW-101C in patients with solid malignant tumors(Through the study completion, an average of 2 years)

研究点 (1)

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