Clinical Study of CAR-iNKT Cells in the Treatment of Relapsed/Refractory/High-risk B-cell Tumors
Primary Purpose
Acute Lymphoblastic Leukemia, B-cell Lymphoma, Chronic Lymphocytic Leukemia
Status
Recruiting
Phase
Phase 1
Locations
China
Study Type
Interventional
Intervention
hCD19.IL15.CAR-iNKT
Sponsored by
About this trial
This is an interventional treatment trial for Acute Lymphoblastic Leukemia
Eligibility Criteria
Inclusion Criteria:
- Male or female patients aged 5-70 years;
- The patient's ECOG score was ≤2, and the expected survival time of > was 12 weeks.
- The patient was diagnosed with B-cell tumor by pathological and histological examination and had no effective treatment options, such as recurrence after chemotherapy or hematopoietic stem cell transplantation. Or the patient voluntarily chooses the infusion of CAR-INKT cells as the first treatment.
B cell tumors include the following three types:
- B-cell acute lymphocytic leukemia (B-ALL);
- Inert B-cell lymphoma (CLL, FL, MZL, LPL, HCL);
- Aggressive B-cell lymphoma (DLBCL, BL, MCL);
Subject:
- Residual lesions remain after primary treatment and are not suitable for HSCT (Auto/Allo-HSCT);
- relapse after complete response (CR1) and unsuitable for allogeneic/autologous HSCT;
- Patients with high risk factors;
- relapse or no remission after hematopoietic stem cell transplantation or cellular immunotherapy.
- having measurable or evaluable lesions;
The main tissues and organs of the patient function well:
- Liver function: ALT/AST < 3 times the upper limit of normal (ULN);
- Renal function: creatinine < 220μmol/L;
- Lung function: indoor oxygen saturation ≥95%;
- Heart function: left ventricular ejection fraction (LVEF) ≥40%.
- Patients or their legal guardians voluntarily participate and sign the informed consent.
Exclusion Criteria:
- Pregnant or lactating women, or women who plan to become pregnant within six months;
- Infectious diseases (e.g. HIV, active hepatitis B or C infection, active tuberculosis, etc.);
- GVHD;
- Abnormal vital signs and failure to cooperate with the examination;
- People with mental or mental illness who are unable to cooperate with treatment and efficacy evaluation;
- People with high allergic constitution or severe allergic history, especially those allergic to IL-2;
- Subjects with systemic infection or severe local infection need anti-infection therapy;
- Complicated with dysfunction of heart, lung, brain, liver, kidney and other important organs;
- Any unstable systemic disease: including but not limited to unstable angina pectoris, cerebrovascular accident or transient cerebral ischemia (within 6 months before screening), myocardial infarction (within 6 months before screening), congestive heart failure (NYHA classification ≥III);
- Doctors believe that there are other reasons for not being included in treatment.
Sites / Locations
- The Affiliated hospital of Xuzhou medical UniversityRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
hCD19.IL15.CAR-iNKT cells
Arm Description
Dose escalation follows the accelerated titration and the standard 3+3 dose escalation design. A total of 3 dose levels are set for subjects.
Outcomes
Primary Outcome Measures
Dose-limiting toxicity
Adverse events assessed according to NCI-CTCAE v5.0 criteria
Secondary Outcome Measures
MRD negative overall response rate (MRD- ORR)
Assessment of MRD negative overall response rate (MRD- ORR) at 3 months of treatment
Overall response rate (ORR)
Assessment of ORR (ORR = CR + CRi ) at Month 6, 12, 18 and 24
Event-free survival (EFS)
Assessment of EFS at Month 6, 12, 18 and 24
Overall survival (OS)
Assessment of OS at Month 6, 12, 18 and 24
Full Information
NCT ID
NCT04814004
First Posted
March 22, 2021
Last Updated
March 24, 2021
Sponsor
Kai Lin Xu; Jun Nian Zheng
Collaborators
North Jiangsu People's Hospital, The First People's Hospital of Changzhou, Nantong University, First Affiliated Hospital of Zhejiang University, Affiliated Hospital of Jiangsu University, Huai 'an First People's Hospital
1. Study Identification
Unique Protocol Identification Number
NCT04814004
Brief Title
Clinical Study of CAR-iNKT Cells in the Treatment of Relapsed/Refractory/High-risk B-cell Tumors
Official Title
Clinical Study of CAR-iNKT Cells in the Treatment of Relapsed/Refractory/High-risk B-cell Tumors
Study Type
Interventional
2. Study Status
Record Verification Date
March 2021
Overall Recruitment Status
Recruiting
Study Start Date
March 19, 2021 (Actual)
Primary Completion Date
April 1, 2023 (Anticipated)
Study Completion Date
April 1, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Kai Lin Xu; Jun Nian Zheng
Collaborators
North Jiangsu People's Hospital, The First People's Hospital of Changzhou, Nantong University, First Affiliated Hospital of Zhejiang University, Affiliated Hospital of Jiangsu University, Huai 'an First People's Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study aims to evaluate the safety and feasibility of hCD19.IL15.CAR-iNKT cells in treating patients with relapsed/refractory/high-risk B-cell tumors.
Detailed Description
CD19 CAR-T has been shown to treat a variety of refractory or recurrent B-cell tumors. Because most CAR-T cells are generated from the patient's own T cells and are individualized products, and there are individual differences between patients, the generation of customized CAR-T cells is an expensive and time-consuming process. Universal CAR- iNKT cells are an ideal product for cell therapy. In this study, we prepared universal iNKT cells expressing hCD19 CAR and IL-15 to treat refractory, relapsed, or high-risk B-cell tumors.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Lymphoblastic Leukemia, B-cell Lymphoma, Chronic Lymphocytic Leukemia
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
hCD19.IL15.CAR-iNKT cells
Arm Type
Experimental
Arm Description
Dose escalation follows the accelerated titration and the standard 3+3 dose escalation design. A total of 3 dose levels are set for subjects.
Intervention Type
Drug
Intervention Name(s)
hCD19.IL15.CAR-iNKT
Intervention Description
Universal hCD19.IL15.CAR-iNKT cells by a single infusion intravenously will be given in escalating doses.
Primary Outcome Measure Information:
Title
Dose-limiting toxicity
Description
Adverse events assessed according to NCI-CTCAE v5.0 criteria
Time Frame
Baseline up to 28 days after T cell infusion
Secondary Outcome Measure Information:
Title
MRD negative overall response rate (MRD- ORR)
Description
Assessment of MRD negative overall response rate (MRD- ORR) at 3 months of treatment
Time Frame
3 months
Title
Overall response rate (ORR)
Description
Assessment of ORR (ORR = CR + CRi ) at Month 6, 12, 18 and 24
Time Frame
Month 6, 12, 18 and 24
Title
Event-free survival (EFS)
Description
Assessment of EFS at Month 6, 12, 18 and 24
Time Frame
Month 6, 12, 18 and 24
Title
Overall survival (OS)
Description
Assessment of OS at Month 6, 12, 18 and 24
Time Frame
Month 6, 12, 18 and 24
10. Eligibility
Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Male or female patients aged 5-70 years;
The patient's ECOG score was ≤2, and the expected survival time of > was 12 weeks.
The patient was diagnosed with B-cell tumor by pathological and histological examination and had no effective treatment options, such as recurrence after chemotherapy or hematopoietic stem cell transplantation. Or the patient voluntarily chooses the infusion of CAR-INKT cells as the first treatment.
B cell tumors include the following three types:
B-cell acute lymphocytic leukemia (B-ALL);
Inert B-cell lymphoma (CLL, FL, MZL, LPL, HCL);
Aggressive B-cell lymphoma (DLBCL, BL, MCL);
Subject:
Residual lesions remain after primary treatment and are not suitable for HSCT (Auto/Allo-HSCT);
relapse after complete response (CR1) and unsuitable for allogeneic/autologous HSCT;
Patients with high risk factors;
relapse or no remission after hematopoietic stem cell transplantation or cellular immunotherapy.
having measurable or evaluable lesions;
The main tissues and organs of the patient function well:
Liver function: ALT/AST < 3 times the upper limit of normal (ULN);
Renal function: creatinine < 220μmol/L;
Lung function: indoor oxygen saturation ≥95%;
Heart function: left ventricular ejection fraction (LVEF) ≥40%.
Patients or their legal guardians voluntarily participate and sign the informed consent.
Exclusion Criteria:
Pregnant or lactating women, or women who plan to become pregnant within six months;
Infectious diseases (e.g. HIV, active hepatitis B or C infection, active tuberculosis, etc.);
GVHD;
Abnormal vital signs and failure to cooperate with the examination;
People with mental or mental illness who are unable to cooperate with treatment and efficacy evaluation;
People with high allergic constitution or severe allergic history, especially those allergic to IL-2;
Subjects with systemic infection or severe local infection need anti-infection therapy;
Complicated with dysfunction of heart, lung, brain, liver, kidney and other important organs;
Any unstable systemic disease: including but not limited to unstable angina pectoris, cerebrovascular accident or transient cerebral ischemia (within 6 months before screening), myocardial infarction (within 6 months before screening), congestive heart failure (NYHA classification ≥III);
Doctors believe that there are other reasons for not being included in treatment.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jiang Cao, Ph.D
Phone
86-516-85802007
Email
zimu05067@163.com
First Name & Middle Initial & Last Name or Official Title & Degree
Ming Shi, Ph.D
Phone
86-516-85802635
Email
sm200@sohu.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kailin Xu, Ph.d
Organizational Affiliation
The Affiliated Hospital of Xuzhou Medical University
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Junnian Zheng, Ph.D
Organizational Affiliation
Xuzhou Medical University
Official's Role
Study Director
Facility Information:
Facility Name
The Affiliated hospital of Xuzhou medical University
City
Xuzhou
State/Province
Jiangsu
ZIP/Postal Code
221000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jiang Cao, M.D., Ph.D.
Phone
86-516-85802007
Email
zimu05067@163.com
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Clinical Study of CAR-iNKT Cells in the Treatment of Relapsed/Refractory/High-risk B-cell Tumors
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