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CD7 CAR-T in the Treatment of CD7 Positive Refractory Relapsed Acute Leukemia

Primary Purpose

T-ALL

Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
T cell injection targeting CD7 chimeric antigen receptor
Sponsored by
PersonGen BioTherapeutics (Suzhou) Co., Ltd.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for T-ALL

Eligibility Criteria

12 Years - 65 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 12-65
  • Sign informed consent
  • Expected survival time ≥ 3 months
  • CD7 positive refractory and relapsed acute leukemia
  • Karnofsky score≥60
  • ECOG score ≤ 2
  • Have not received other immunotherapy within 3 months
  • The CD7 expression rate on the surface of leukemia cells detected by flow cytometry is greater than 30%

Exclusion Criteria:

  • Uncontrolled active infection
  • Active viral hepatitis B or C
  • HIV test positive
  • Congenital immunodeficiency patients
  • Pregnant and breastfeeding patients
  • Patients with central nervous system tumors or central nervous system leukemia
  • The patient and/or family members do not agree to the treatment plan

Sites / Locations

  • The First Affiliared Hospital Of SOOCHOW UniversityRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

T cell injection targeting CD7 chimeric antigen receptor

Arm Description

Outcomes

Primary Outcome Measures

DLT
Dose-limiting toxicity

Secondary Outcome Measures

Safety results
Number of adverse events
PK
The maximum concentration (Cmax)
PD
Absolute value of CD7 Positive Cells in peripheral blood at each time point

Full Information

First Posted
March 3, 2021
Last Updated
March 3, 2021
Sponsor
PersonGen BioTherapeutics (Suzhou) Co., Ltd.
Collaborators
The First Affiliated Hospital of Soochow University
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1. Study Identification

Unique Protocol Identification Number
NCT04785833
Brief Title
CD7 CAR-T in the Treatment of CD7 Positive Refractory Relapsed Acute Leukemia
Official Title
A Prospective, Open, Single-arm Clinical Study on the Efficacy and Safety of CD7 CAR-T in the Treatment of CD7-positive Refractory Relapsed Acute Leukemia
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Recruiting
Study Start Date
March 4, 2021 (Anticipated)
Primary Completion Date
April 30, 2022 (Anticipated)
Study Completion Date
February 4, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
PersonGen BioTherapeutics (Suzhou) Co., Ltd.
Collaborators
The First Affiliated Hospital of Soochow University

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
Patients with acute leukemia derived from T lymphocytes have the characteristics of high expression of CD7 antigen, such as acute T lymphocyte leukemia (T-ALL).CAR-T therapy is to genetically modify the patient's T lymphocytes to target and eliminate tumor cells in a major histocompatibility complex-independent manner. CAR-T cells are costimulatory molecules that include single-chain antibodies (scFv) that recognize tumor-specific antigens, hinge regions, transmembrane regions, intracellular signaling regions (immunoreceptor tyrosine activation motif ITAM), and intracellular signaling regions. The chimeric antigen receptor of CD28 or CD137(4-1BB) conduction domain is expressed in a lentiviral vector, and the vector is transfected into autologous T cells, so that the modified CAR-T cells have targeting and specificity Recognizes and kills cancer cells expressing tumor antigens, and can proliferate and activate in vivo, but has no effect on cells that do not express the antigen

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
T-ALL

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
T cell injection targeting CD7 chimeric antigen receptor
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
T cell injection targeting CD7 chimeric antigen receptor
Intervention Description
Drug name: T cell injection targeting CD7 autologous chimeric antigen receptor. Package specification: 10-50ml bag, 1-4 bags / person, which is determined according to the body weight of the subject and the effective content of cell preparation
Primary Outcome Measure Information:
Title
DLT
Description
Dose-limiting toxicity
Time Frame
Up to 2 years
Secondary Outcome Measure Information:
Title
Safety results
Description
Number of adverse events
Time Frame
Up to 2 years
Title
PK
Description
The maximum concentration (Cmax)
Time Frame
Up to 2 years
Title
PD
Description
Absolute value of CD7 Positive Cells in peripheral blood at each time point
Time Frame
Up to 2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 12-65 Sign informed consent Expected survival time ≥ 3 months CD7 positive refractory and relapsed acute leukemia Karnofsky score≥60 ECOG score ≤ 2 Have not received other immunotherapy within 3 months The CD7 expression rate on the surface of leukemia cells detected by flow cytometry is greater than 30% Exclusion Criteria: Uncontrolled active infection Active viral hepatitis B or C HIV test positive Congenital immunodeficiency patients Pregnant and breastfeeding patients Patients with central nervous system tumors or central nervous system leukemia The patient and/or family members do not agree to the treatment plan
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
xiaowen tang
Phone
13913538266
Email
xwtang1020@163.com
First Name & Middle Initial & Last Name or Official Title & Degree
huimin meng
Phone
18896802149
Email
huimin.meng@persongen.com.cn
Facility Information:
Facility Name
The First Affiliared Hospital Of SOOCHOW University
City
Suzhou
State/Province
Jiangsu
ZIP/Postal Code
215006
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
xiaowen tang
Phone
13913538266
Email
xwtang1020@163.com

12. IPD Sharing Statement

Learn more about this trial

CD7 CAR-T in the Treatment of CD7 Positive Refractory Relapsed Acute Leukemia

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