Clinical Research of ROBO1 Specific BiCAR-NK Cells on Patients With Pancreatic Cancer
Primary Purpose
Pancreatic Cancer
Status
Unknown status
Phase
Phase 1
Locations
China
Study Type
Interventional
Intervention
BiCAR-NK cells (ROBO1 CAR-NK cells)
Sponsored by
About this trial
This is an interventional treatment trial for Pancreatic Cancer
Eligibility Criteria
Inclusion Criteria:
- Histologically confirmed metastatic pancreatic adenocarcinoma
- Patients aged between 18 and 75
- ROBO1 expression in malignancy tissues detected by immuno-histochemistry (IHC)
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
- Life expectancy greater than 3 months
- Subjects must have measurable disease as defined by RECIST 1.1 criteria
- Satisfactory organ and bone marrow function: White blood cell count (WBC) ≥ 3.0×10^9/L, Platelets ≥ 70×10^9/L, Hb ≥ 9.0g/dL, lymphocyte (LY) ≥ 0.7×10^9/L, LY% ≥ 15%, Alb ≥ 2.8g/dL, serum lipase and amylase < 1.5 × upper limit of normal, serum creatinine ≤ 2.5mg/dL, aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 5×upper limit of normal, serum total bilirubin ≤ 2.0mg/dL. These tests must be conducted within 7 days prior to registration
- Karnofsky score ≥ 60
- Ability to give informed consent
Exclusion Criteria:
- Previously treated with any gene therapy products
- Patients who are receiving any other investigational agents
- Women of child-bearing potential who are pregnant or breastfeeding because of the potentially dangerous effects of the treatment on the fetus or infant
- Active systemic infections (e.g.: requiring anti-infective treatment), coagulation disorders or any other major medical illnesses
- Any form of primary immunodeficiency (such as Severe Combined Immunodeficiency Disease)
- Concurrent opportunistic infections
Sites / Locations
- Department of Radiology, Shanghai Ruijin HospitalRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
anti-tumor response of BiCAR-NK cells (ROBO1 CAR-NK cells)
Arm Description
Patients with relapsed and refractory pancreatic cancer of ROBO1 expression will be treated with BiCAR-NK cells (ROBO1 CAR-NK cells).
Outcomes
Primary Outcome Measures
Occurrence of treatment related adverse events as assessed by CTCAE v4.03
Defined as >= Grade 3 signs/symptoms, laboratory toxicities, and clinical events) that are possibly, likely, or definitely related to study treatment.
Secondary Outcome Measures
Full Information
NCT ID
NCT03941457
First Posted
May 6, 2019
Last Updated
May 6, 2019
Sponsor
Asclepius Technology Company Group (Suzhou) Co., Ltd.
1. Study Identification
Unique Protocol Identification Number
NCT03941457
Brief Title
Clinical Research of ROBO1 Specific BiCAR-NK Cells on Patients With Pancreatic Cancer
Official Title
Clinical Research of ROBO1 Specific BiCAR-NK Cells on Patients With Pancreatic Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
May 2019
Overall Recruitment Status
Unknown status
Study Start Date
May 2019 (Anticipated)
Primary Completion Date
May 2021 (Anticipated)
Study Completion Date
May 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Asclepius Technology Company Group (Suzhou) Co., Ltd.
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Immunotherapy has become the major breakthrough and the most promising treatment, with the host of development of tumor biology, molecular biology and immunology. ROBO1 is a potential target and spectacular paradigm in the treatment of solid tumors. This study is for evaluation of the safety and efficacy of ROBO1 CAR-NK cell immunotherapy for pancreatic cancer.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Cancer
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
9 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
anti-tumor response of BiCAR-NK cells (ROBO1 CAR-NK cells)
Arm Type
Experimental
Arm Description
Patients with relapsed and refractory pancreatic cancer of ROBO1 expression will be treated with BiCAR-NK cells (ROBO1 CAR-NK cells).
Intervention Type
Biological
Intervention Name(s)
BiCAR-NK cells (ROBO1 CAR-NK cells)
Intervention Description
The subject will be observed for any side effects during this time and all the adverse events will be recorded.
Primary Outcome Measure Information:
Title
Occurrence of treatment related adverse events as assessed by CTCAE v4.03
Description
Defined as >= Grade 3 signs/symptoms, laboratory toxicities, and clinical events) that are possibly, likely, or definitely related to study treatment.
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Histologically confirmed metastatic pancreatic adenocarcinoma
Patients aged between 18 and 75
ROBO1 expression in malignancy tissues detected by immuno-histochemistry (IHC)
Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
Life expectancy greater than 3 months
Subjects must have measurable disease as defined by RECIST 1.1 criteria
Satisfactory organ and bone marrow function: White blood cell count (WBC) ≥ 3.0×10^9/L, Platelets ≥ 70×10^9/L, Hb ≥ 9.0g/dL, lymphocyte (LY) ≥ 0.7×10^9/L, LY% ≥ 15%, Alb ≥ 2.8g/dL, serum lipase and amylase < 1.5 × upper limit of normal, serum creatinine ≤ 2.5mg/dL, aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 5×upper limit of normal, serum total bilirubin ≤ 2.0mg/dL. These tests must be conducted within 7 days prior to registration
Karnofsky score ≥ 60
Ability to give informed consent
Exclusion Criteria:
Previously treated with any gene therapy products
Patients who are receiving any other investigational agents
Women of child-bearing potential who are pregnant or breastfeeding because of the potentially dangerous effects of the treatment on the fetus or infant
Active systemic infections (e.g.: requiring anti-infective treatment), coagulation disorders or any other major medical illnesses
Any form of primary immunodeficiency (such as Severe Combined Immunodeficiency Disease)
Concurrent opportunistic infections
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Guangfu Li
Phone
+86 13615181959
Email
lgf@atcgcell.com
First Name & Middle Initial & Last Name or Official Title & Degree
Xianfeng Feng
Phone
+86 15157190521
Email
fxf@atcgcell.com
Facility Information:
Facility Name
Department of Radiology, Shanghai Ruijin Hospital
City
Shanghai
ZIP/Postal Code
200025
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zhongmin Wang, PhD
Email
james0722@163.com
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Clinical Research of ROBO1 Specific BiCAR-NK Cells on Patients With Pancreatic Cancer
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