Dual-Targeting CAR-NK Cells for Recurrent Ovarian Cancer (MSLN, FRα, MUC16) pt2 (DUAL-OV-CAR-NK)
A Phase 1/2, Open-Label, Biomarker-Assigned Study of Dual-Targeting CAR-NK Cells Directed Against Mesothelin (MSLN), Folate Receptor Alpha (FRα/FOLR1), and/or MUC16 (CA125) in Patients With Recurrent or Refractory High-Grade Serous Ovarian, Primary Peritoneal, or Fallopian Tube Cancer
研究概览
地位
详细说明
The study has two parts: (1) dose escalation using a standard 3+3 design within each antigen-pair cohort to determine safety and a recommended Phase 2 dose (RP2D), and (2) dose expansion at the RP2D to explore preliminary efficacy and translational biomarkers.
Target selection (biomarker assignment): Tumor tissue (archival or fresh biopsy) is evaluated by immunohistochemistry (IHC) and/or flow cytometry for MSLN, FRalpha, and MUC16.
Eligibility requires expression of at least two of the three targets above a pre-specified threshold. If all three are positive, a Target Selection Committee assigns the participant to the dual-target pair with the highest combined expression (e.g., H-score or percent positive cells) and acceptable normal-tissue risk.
Treatment schema: Participants receive lymphodepleting chemotherapy (cyclophosphamide and fludarabine) followed by CAR-NK administration. In this example, CAR-NK cells are given intraperitoneally via an implanted port to maximize exposure to peritoneal disease, with optional intravenous dosing per investigator judgment. Participants are monitored closely for cytokine release syndrome (CRS), neurotoxicity (ICANS), cytopenias, infections, and other adverse events.
Response assessments are performed by RECIST v1.1 at regular intervals, with CA 125 trends collected as supportive disease activity data. Follow-up: Participants are followed for adverse events through 12 months and for survival for up to 24 months. Long-term follow-up for gene-modified cell therapy safety may be required per local regulations.
研究类型
注册 (估计的)
阶段
- 阶段2
- 阶段1
联系人和位置
学习联系方式
- 姓名:Seni S Lu, Phd
- 电话号码:+86 13076790030
- 邮箱:Seni-Lu@beijing-biotech.com
学习地点
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Guangdong
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Shenzhen、Guangdong、中国、518036
- 招聘中
- Peking University Shenzhen Hospital
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接触:
- Zhen J Peng, Phd
- 电话号码:+86 13076790039
- 邮箱:Zhen-Peng@beijing-biotech.com
-
-
参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
- Histologically confirmed epithelial ovarian, fallopian tube, or primary peritoneal carcinoma (high-grade serous preferred).
- Recurrent or refractory disease after at least 2 prior systemic treatment lines (including a platinum-based regimen unless contraindicated).
- Measurable disease per RECIST v1.1.
- Tumor expresses at least two of the following targets above protocol-defined threshold: MSLN, FRalpha (FOLR1), MUC16 (CA 125) (archival or fresh biopsy).
- ECOG performance status 0-1.
- Adequate organ function : ANC >= 1.0 x 10^9/L; platelets >= 75 x 10^9/L; hemoglobin >= 8 g/dL; AST/ALT <= 3 x ULN (<= 5 x ULN with liver metastases); total bilirubin <= 1.5 x ULN; creatinine clearance >= 50 mL/min.
- Negative pregnancy test for women of childbearing potential; agreement to use effective contraception through 12 months post-infusion (or per local gene-therapy guidance).
- Able to comply with study procedures and follow-up schedule; written informed consent.
Exclusion Criteria:
- Prior gene-modified cellular therapy (e.g., CAR-T, CAR-NK) within 6 months (or any prior therapy directed to the same target, per protocol).
- Active central nervous system (CNS) metastases or carcinomatous meningitis requiring therapy.
- Uncontrolled infection, including active tuberculosis; or clinically significant, uncontrolled viral infection.
- Known HIV infection with uncontrolled viremia; active hepatitis B or hepatitis C with detectable viral load (testing required at screening).
- Clinically significant cardiovascular disease (e.g., recent myocardial infarction, uncontrolled arrhythmia, NYHA Class III/IV heart failure).
- Active autoimmune disease requiring systemic immunosuppression within 30 days (physiologic steroid replacement allowed).
- Concurrent anti-cancer therapy (chemotherapy, targeted therapy, radiotherapy) not permitted within a protocol-defined washout period.
- Major surgery within 4 weeks prior to lymphodepletion (except minor procedures)
- Pregnant or breastfeeding.
- Any condition that, in the investigator's judgment, would increase risk (e.g., severe pulmonary disease) or interfere with study interpretation.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:非随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:EB-NK-MF
Dual-target CAR-NK cells recognizing Mesothelin (MSLN) and Folate Receptor alpha (FRalpha/FOLR1).
Assigned to participants whose tumors express MSLN and FRalpha above threshold
|
EB-NK-MF CAR-NK cells (dose levels 1-3)
Cyclophosphamide + Fludarabine lymphodepletion
Standard supportive care (e.g., antimicrobial prophylaxis) per institutional practice.
|
|
实验性的:EB-NK-MM
Dual-target CAR-NK cells recognizing Mesothelin (MSLN) and MUC16 (CA 125).
Assigned to participants whose tumors express MSLN and MUC16 above threshold.
|
EB-NK-MF CAR-NK cells (dose levels 1-3)
Cyclophosphamide + Fludarabine lymphodepletion
Standard supportive care (e.g., antimicrobial prophylaxis) per institutional practice.
|
|
实验性的:EB-NK-FM
Dual-target CAR-NK cells recognizing FRalpha (FOLR1) and MUC16 (CA 125).
Assigned to participants whose tumors express FRalpha and MUC16 above threshold.
|
EB-NK-MF CAR-NK cells (dose levels 1-3)
Cyclophosphamide + Fludarabine lymphodepletion
Standard supportive care (e.g., antimicrobial prophylaxis) per institutional practice.
|
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
|
剂量限制性毒性(DLT)发生率
大体时间:28天
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28天
|
|
Incidence and severity of treatment-emergent adverse events (TEAEs) graded by CTCAE v5.0
大体时间:12 months
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12 months
|
次要结果测量
结果测量 |
大体时间 |
|---|---|
|
应答者的应答持续时间 (DOR)
大体时间:12个月
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12个月
|
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Objective response rate (ORR) by RECIST v1.1
大体时间:6 months
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6 months
|
合作者和调查者
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- EB-CARNK-OV-110
药物和器械信息、研究文件
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研究美国 FDA 监管的设备产品
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