Clinical Research of Adoptive BCMA CAR-NK Cells on Relapse/Refractory MM
Primary Purpose
Multiple Myeloma
Status
Unknown status
Phase
Phase 1
Locations
China
Study Type
Interventional
Intervention
BCMA CAR-NK 92 cells
Sponsored by
About this trial
This is an interventional treatment trial for Multiple Myeloma
Eligibility Criteria
Inclusion Criteria:
- 18 years to 80 years, expected survival > 3 months
- Confirmed diagnosis of active MM as defined by IMWG. BCMA expression of the malignant cells must be detected by immunohistochemistry or by flow cytometry
- BCMA-expressing B cell malignancy must be assured and must be relapsed or refractory disease
- ECOG performance status of 0 - 1
- Cardiac function: 1 - 2 levels; Liver: TBIL ≤ 3ULN,AST ≤ 2.5 ULN,ALT ≤ 2.5ULN; kidney: Cr ≤ 1.25ULN
- No serious allergic constitution
- No other serous diseases that conflicts with the clinical program
- No other cancer history
- Female participants of reproductive potential must have a negative serum pregnancy test
- Subjects must have signed written, informed consent
Exclusion Criteria:
- Pregnant or lactating women
- Uncontrolled active infection, HIV infection, syphilis serology reaction positive
- Active hepatitis B or hepatitis C infection
- Recent or current use of glucocorticoid or other immunosuppressor
- Serious mental disorder
- With severe cardiac, liver, renal insufficiency, diabetes and other diseases
- Participate in other clinical research in the past three months
- Previously treatment with any gene therapy products
Sites / Locations
- Department of Hematology, Wuxi People's Hospital, Nanjing Medical UniversityRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
anti-tumor response of BCMA CAR-NK-92
Arm Description
Patients with relapsed and refractory MM of BCMA expression will be treated with BCMA CAR-NK 92 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
NCT03940833
First Posted
May 5, 2019
Last Updated
May 5, 2019
Sponsor
Asclepius Technology Company Group (Suzhou) Co., Ltd.
1. Study Identification
Unique Protocol Identification Number
NCT03940833
Brief Title
Clinical Research of Adoptive BCMA CAR-NK Cells on Relapse/Refractory MM
Official Title
Clinical Research of Adoptive BCMA CAR-NK Cells on Relapse/Refractory MM
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
The purpose of this study is to infuse BCMA CAR-NK 92 cells to the patients with relapsed and refractory multiple myeloma (MM), to assess the safety and feasibility of this strategy. The CAR enables the NK-92 cells to recognize and kill the MM cells by targeting of BCMA, a protein expressed of the surface of the malignant plasma cells in MM patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Myeloma
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
20 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
anti-tumor response of BCMA CAR-NK-92
Arm Type
Experimental
Arm Description
Patients with relapsed and refractory MM of BCMA expression will be treated with BCMA CAR-NK 92 cells.
Intervention Type
Biological
Intervention Name(s)
BCMA CAR-NK 92 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
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
18 years to 80 years, expected survival > 3 months
Confirmed diagnosis of active MM as defined by IMWG. BCMA expression of the malignant cells must be detected by immunohistochemistry or by flow cytometry
BCMA-expressing B cell malignancy must be assured and must be relapsed or refractory disease
ECOG performance status of 0 - 1
Cardiac function: 1 - 2 levels; Liver: TBIL ≤ 3ULN,AST ≤ 2.5 ULN,ALT ≤ 2.5ULN; kidney: Cr ≤ 1.25ULN
No serious allergic constitution
No other serous diseases that conflicts with the clinical program
No other cancer history
Female participants of reproductive potential must have a negative serum pregnancy test
Subjects must have signed written, informed consent
Exclusion Criteria:
Pregnant or lactating women
Uncontrolled active infection, HIV infection, syphilis serology reaction positive
Active hepatitis B or hepatitis C infection
Recent or current use of glucocorticoid or other immunosuppressor
Serious mental disorder
With severe cardiac, liver, renal insufficiency, diabetes and other diseases
Participate in other clinical research in the past three months
Previously treatment with any gene therapy products
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 Hematology, Wuxi People's Hospital, Nanjing Medical University
City
Wuxi
State/Province
Jiangsu
ZIP/Postal Code
214000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xin Zhou, PhD
Email
13358111962@qq.com
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
34471234
Citation
Ng YY, Du Z, Zhang X, Chng WJ, Wang S. CXCR4 and anti-BCMA CAR co-modified natural killer cells suppress multiple myeloma progression in a xenograft mouse model. Cancer Gene Ther. 2022 May;29(5):475-483. doi: 10.1038/s41417-021-00365-x. Epub 2021 Sep 1.
Results Reference
derived
Learn more about this trial
Clinical Research of Adoptive BCMA CAR-NK Cells on Relapse/Refractory MM
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