Phase I Study of CD19-CAR-T2 Cells for Patients With Chemotherapy Resistant or Refractory CD19+ Acute Leukemia
Primary Purpose
Acute Leukemia
Status
Unknown status
Phase
Phase 1
Locations
China
Study Type
Interventional
Intervention
CD19-CAR-T2 Cells
Sponsored by
About this trial
This is an interventional treatment trial for Acute Leukemia focused on measuring Leukemia, CART CD19, Chemotherapy Resistant, Chemotherapy Refractory, CD19 +, Lymphoma
Eligibility Criteria
Inclusion Criteria:
- Patient with relapsed and/or refractory CD19 positive B-cell acute leukemia
- Eastern Cooperative Oncology Group (ECOG) performance status 《 3
- ALT/ AST 《 3x normal
- Bilirubin < 2.0 mg/dl
- Creatinine < 2.5 mg/dl and less than 2.5x normal for age
- LVEF》 45%
- Accept white blood cell collection
- Provide informed consent
Exclusion Criteria:
- Previous treatment with investigational gene or cell therapy medicine products
- Solitary extramedullary relapse
- Active hepatitis B , hepatitis C or HIV infection
- Uncontrolled active infection
- Presence of grade 2-4 acute or extensive chronic GVHD
- Active CNS involvement: epilepsy, paresis, aphasia, stroke, severe head trauma,
- Dementia, Parkinson's disease, cerebellar disease, organic brain syndrome, uncontrolled mental illness, etc.
- Any uncontrolled active medical disorder that would preclude participation as outlined.
- Received non-diagnostic purposes major surgery within the past 4 weeks
- Participated in any other clinical study within the past 4 weeks
- Used murine biological products (except blinatumomab), unless it is proved no anti-mouse antibodies exist.
- Pregnancy or breast-feeding women
- Use of prohibited drugs:
- Steroids: Therapeutic doses of steroids must be stopped > 72 hours prior to CD19-CAR-T2 Cells infusion
- Allogeneic cellular therapy: Any donor lymphocyte infusions (DLI) must be completed > 4 weeks prior to CD19-CAR-T2 Cells infusion
- GVHD therapies: Any drug used for GVHD must be stopped > 4 weeks prior to CD19-CAR-T2 Cells infusion
- Chemotherapy: i. The following drugs must be stopped > 1 week prior to CTL019 infusion and should not be administered concomitantly or following lymphodepleting chemotherapy: hydroxyurea, vincristine, 6-mercaptopurine, 6-thioguanine, methotrexate <25 mg/m2, cytosine arabinoside < 10 mg/m2/day, asparaginase; ii. The following drugs must be stopped > 4 weeks prior to CTL019 infusion: salvage chemotherapy (e.g. clofarabine, cytosine arabinoside > 100 mg/m2, anthracyclines, cyclophosphamide), excluding the required lymphodepleting chemotherapy drugs
- Any situation that may increase the risk of the test or interfere with the test results
Sites / Locations
- Guangdong General HospitalRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
CD19-CAR-T2 T Cells
Arm Description
The subject's T cells will be modified to those which could identify and kill the tumor cells (CD19+ cells). These CD19-CAR-T2 T cells will be infused over 10-15 minutes on days Day 1, 2 and 3 tentatively according to the response to infusion.
Outcomes
Primary Outcome Measures
The maximum tolerated dose(MTD) of CD19 positive relapsed/ refractory acute leukimia treated wtih CD19-CAR-T2 cells
Secondary Outcome Measures
Number of Participants With Abnormal Laboratory Values and/or Adverse Events That Are Related to Treatment
Adverse events and laboratory abnormalities (type, frequency and severity)
Overall Response Rate
Overall Response Rate (ORR), which includes Complete Remission (CR) and Complete Remission with Incomplete Blood Count Recovery (CRi), as determined by assessments of peripheral blood, bone marrow, CNS symptoms, physical exam (PE) and CSF. The primary endpoint will be based on the IRC assessment. The local investigator's assessed results will be used for sensitivity analysis.
Full Information
NCT ID
NCT02822326
First Posted
June 28, 2016
Last Updated
September 8, 2017
Sponsor
Guangdong Provincial People's Hospital
Collaborators
Chinese Academy of Sciences, Guangdong Zhaotai InVivo Biomedicine Co. Ltd.
1. Study Identification
Unique Protocol Identification Number
NCT02822326
Brief Title
Phase I Study of CD19-CAR-T2 Cells for Patients With Chemotherapy Resistant or Refractory CD19+ Acute Leukemia
Official Title
CD19-CAR-T2 Cells for Relapse/Refractory CD19 Positive Acute Leukemia-a Phase I Trial
Study Type
Interventional
2. Study Status
Record Verification Date
September 2017
Overall Recruitment Status
Unknown status
Study Start Date
January 2016 (undefined)
Primary Completion Date
September 2019 (Anticipated)
Study Completion Date
September 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Guangdong Provincial People's Hospital
Collaborators
Chinese Academy of Sciences, Guangdong Zhaotai InVivo Biomedicine Co. Ltd.
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to evaluate the safety and efficacy of chimeric antigen receptor 19 (CD19-CAR-T2 Cells) infusions in patients with chemotherapy resistant or refractory CD19+ acute Leukemia.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Leukemia
Keywords
Leukemia, CART CD19, Chemotherapy Resistant, Chemotherapy Refractory, CD19 +, Lymphoma
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
CD19-CAR-T2 T Cells
Arm Type
Experimental
Arm Description
The subject's T cells will be modified to those which could identify and kill the tumor cells (CD19+ cells). These CD19-CAR-T2 T cells will be infused over 10-15 minutes on days Day 1, 2 and 3 tentatively according to the response to infusion.
Intervention Type
Biological
Intervention Name(s)
CD19-CAR-T2 Cells
Primary Outcome Measure Information:
Title
The maximum tolerated dose(MTD) of CD19 positive relapsed/ refractory acute leukimia treated wtih CD19-CAR-T2 cells
Time Frame
24 weeks
Secondary Outcome Measure Information:
Title
Number of Participants With Abnormal Laboratory Values and/or Adverse Events That Are Related to Treatment
Description
Adverse events and laboratory abnormalities (type, frequency and severity)
Time Frame
12 months
Title
Overall Response Rate
Description
Overall Response Rate (ORR), which includes Complete Remission (CR) and Complete Remission with Incomplete Blood Count Recovery (CRi), as determined by assessments of peripheral blood, bone marrow, CNS symptoms, physical exam (PE) and CSF. The primary endpoint will be based on the IRC assessment. The local investigator's assessed results will be used for sensitivity analysis.
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
14 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient with relapsed and/or refractory CD19 positive B-cell acute leukemia
Eastern Cooperative Oncology Group (ECOG) performance status 《 3
ALT/ AST 《 3x normal
Bilirubin < 2.0 mg/dl
Creatinine < 2.5 mg/dl and less than 2.5x normal for age
LVEF》 45%
Accept white blood cell collection
Provide informed consent
Exclusion Criteria:
Previous treatment with investigational gene or cell therapy medicine products
Solitary extramedullary relapse
Active hepatitis B , hepatitis C or HIV infection
Uncontrolled active infection
Presence of grade 2-4 acute or extensive chronic GVHD
Active CNS involvement: epilepsy, paresis, aphasia, stroke, severe head trauma,
Dementia, Parkinson's disease, cerebellar disease, organic brain syndrome, uncontrolled mental illness, etc.
Any uncontrolled active medical disorder that would preclude participation as outlined.
Received non-diagnostic purposes major surgery within the past 4 weeks
Participated in any other clinical study within the past 4 weeks
Used murine biological products (except blinatumomab), unless it is proved no anti-mouse antibodies exist.
Pregnancy or breast-feeding women
Use of prohibited drugs:
Steroids: Therapeutic doses of steroids must be stopped > 72 hours prior to CD19-CAR-T2 Cells infusion
Allogeneic cellular therapy: Any donor lymphocyte infusions (DLI) must be completed > 4 weeks prior to CD19-CAR-T2 Cells infusion
GVHD therapies: Any drug used for GVHD must be stopped > 4 weeks prior to CD19-CAR-T2 Cells infusion
Chemotherapy: i. The following drugs must be stopped > 1 week prior to CTL019 infusion and should not be administered concomitantly or following lymphodepleting chemotherapy: hydroxyurea, vincristine, 6-mercaptopurine, 6-thioguanine, methotrexate <25 mg/m2, cytosine arabinoside < 10 mg/m2/day, asparaginase; ii. The following drugs must be stopped > 4 weeks prior to CTL019 infusion: salvage chemotherapy (e.g. clofarabine, cytosine arabinoside > 100 mg/m2, anthracyclines, cyclophosphamide), excluding the required lymphodepleting chemotherapy drugs
Any situation that may increase the risk of the test or interfere with the test results
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xin Du, Dr.
Phone
+86 20 83827812
Ext
62122
Email
miyadu@hotmial.com
First Name & Middle Initial & Last Name or Official Title & Degree
Peng Li, Dr.
Phone
+86 20 32015300
Email
li_peng@gibh.ac.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jianyu Weng, Dr.
Organizational Affiliation
Guangdong Provincial People's Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Peilong Lai, Dr.
Organizational Affiliation
Guangdong Provincial People's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Guangdong General Hospital
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510080
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xin Du, Dr.
Phone
+86 20 83827812
Email
miyadu@hotmail.com
12. IPD Sharing Statement
Plan to Share IPD
No
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Phase I Study of CD19-CAR-T2 Cells for Patients With Chemotherapy Resistant or Refractory CD19+ Acute Leukemia
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