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CAR-pNK Cell Immunotherapy in CD7 Positive Leukemia and Lymphoma

Primary Purpose

Acute Myeloid Leukemia, Precursor T-Cell Lymphoblastic Leukemia-Lymphoma, T-cell Prolymphocytic Leukemia

Status
Unknown status
Phase
Phase 1
Locations
China
Study Type
Interventional
Intervention
anti-CD7 CAR-pNK cells
Sponsored by
PersonGen BioTherapeutics (Suzhou) Co., Ltd.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Myeloid Leukemia

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Male and female subjects with CD7+ malignancies in patients with no available curative treatment options who have limited prognosis (several months to < 2 year survival) with currently available therapies will be enrolled:

  1. Eligible diseases: CD7 positive relapsed or refractory Leukemia and Lymphoma. ᅳ Acute myeloid leukemia, previously identified as CD7+ ᅳ Precursor T lymphoblast leukemia/lymphoma ᅳ T-cell prolymphocytic leukemia ᅳ T-cell large granular lymphocytic leukemia ᅳ Peripheral T-cell lymphoma, NOS ᅳ Angioimmunoblastic T-cell lymphoma ᅳ Extranodal NK/T-cell lymphoma, nasal type ᅳ Enteropathy-type intestinal T-cell lymphoma ᅳ Hepatosplenic T-cell lymphoma
  2. Patients 18 years of age or older, and must have a life expectancy > 12 weeks.
  3. CD7 is expressed in malignancy tissues by immuno-histochemical (IHC) or Flow cytometry.
  4. Assessable disease as measured by laboratory and bone marrow examinations.
  5. Eastern cooperative oncology group (ECOG) performance status of 0-2 or karnofsky performance status (KPS) score is higher than 60.
  6. Females of child-bearing potential must have a negative pregnancy test and all subjects must agree to use an effective method of contraception for up to two weeks after the last infusion of CAR-pNK cells.
  7. Adequate bone marrow, liver and renal function as assessed by the following laboratory requirements: 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.
  8. Ability to give informed consent.

Exclusion Criteria:

  1. Patients with symptomatic central nervous system (CNS) involvement.
  2. Pregnant or nursing women may not participate.
  3. Known HIV, hepatitis B virus (HBV) or hepatitis C virus (HCV) infection.
  4. Serious illness or medical condition which would not permit the patient to be managed according to the protocol, including active uncontrolled infection, major cardiovascular, coagulation disorders, respiratory or immune system, myocardial infarction, cardiac arrhythmias, obstructive/restrictive pulmonary disease, or psychiatric or emotional disorders.
  5. Concurrent use of systemic steroids. Recent or current use of inhaled steroids is not exclusionary.
  6. Previously treatment with any gene therapy products.
  7. The existence of unstable or active ulcers or gastrointestinal bleeding.
  8. Patients with a history of organ transplantation or are waiting for organ transplantation.
  9. Patients need anticoagulant therapy (such as warfarin or heparin).
  10. Patients need long-term antiplatelet therapy (aspirin at a dose > 300mg/d; clopidogrel at a dose > 75mg/d).

Sites / Locations

  • PersonGen BioTherapeutics (Suzhou) Co., Ltd.Recruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

CAR-pNK Cell immunotherapy

Arm Description

Enrolled patients will receive CAR-pNK cell immunotherapy with a novel specific chimeric antigen receptor targeting CD7 antigen by infusion.

Outcomes

Primary Outcome Measures

Adverse events attributed to the administration of the anti-CD7 CAR-pNK cells
Determine the toxicity profile of the CD7 targeted CAR-pNK cells with Common Toxicity Criteria for Adverse Effects (CTCAE) version 4.0.

Secondary Outcome Measures

Clinical response to CD7 CAR-pNK cell infusions
Patients with measurable disease will be assessed for the response of their disease to CD7 CAR-pNK cell treatment.
Determine the existence of CD7-CAR-pNK in vivo

Full Information

First Posted
March 31, 2016
Last Updated
December 4, 2016
Sponsor
PersonGen BioTherapeutics (Suzhou) Co., Ltd.
Collaborators
The First People's Hospital of Hefei, Hefei Binhu Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02742727
Brief Title
CAR-pNK Cell Immunotherapy in CD7 Positive Leukemia and Lymphoma
Official Title
Chimeric Antigen Receptor-Modified pNK Cells for CD7 Positive Relapsed or Refractory Leukemia and Lymphoma
Study Type
Interventional

2. Study Status

Record Verification Date
December 2016
Overall Recruitment Status
Unknown status
Study Start Date
March 2016 (undefined)
Primary Completion Date
March 2017 (Anticipated)
Study Completion Date
March 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
PersonGen BioTherapeutics (Suzhou) Co., Ltd.
Collaborators
The First People's Hospital of Hefei, Hefei Binhu Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to evaluate the safety and effectiveness of CAR-pNK cell immunotherapy in patients with CD7 positive relapsed or refractory Leukemia and Lymphoma.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Myeloid Leukemia, Precursor T-Cell Lymphoblastic Leukemia-Lymphoma, T-cell Prolymphocytic Leukemia, T-cell Large Granular Lymphocytic Leukemia, Peripheral T-cell Lymphoma, NOS, Angioimmunoblastic T-cell Lymphoma, Extranodal NK/T-cell Lymphoma, Nasal Type, Enteropathy-type Intestinal T-cell Lymphoma, Hepatosplenic T-cell Lymphoma

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
10 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
CAR-pNK Cell immunotherapy
Arm Type
Experimental
Arm Description
Enrolled patients will receive CAR-pNK cell immunotherapy with a novel specific chimeric antigen receptor targeting CD7 antigen by infusion.
Intervention Type
Biological
Intervention Name(s)
anti-CD7 CAR-pNK cells
Other Intervention Name(s)
chimeric antigen receptor NK cells with specificity for CD7
Intervention Description
The allogeneic NK cells (NK-92 cell line for clinical use) are engineered to contain anti-CD7 attached to TCRzeta, CD28 and 4-1BB signaling domains. These modified cells are called chimeric antigen receptor NK cells with specificity for CD7.
Primary Outcome Measure Information:
Title
Adverse events attributed to the administration of the anti-CD7 CAR-pNK cells
Description
Determine the toxicity profile of the CD7 targeted CAR-pNK cells with Common Toxicity Criteria for Adverse Effects (CTCAE) version 4.0.
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Clinical response to CD7 CAR-pNK cell infusions
Description
Patients with measurable disease will be assessed for the response of their disease to CD7 CAR-pNK cell treatment.
Time Frame
Safety follow-up is 100 days from last CAR-pNK infusion
Title
Determine the existence of CD7-CAR-pNK in vivo
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male and female subjects with CD7+ malignancies in patients with no available curative treatment options who have limited prognosis (several months to < 2 year survival) with currently available therapies will be enrolled: Eligible diseases: CD7 positive relapsed or refractory Leukemia and Lymphoma. ᅳ Acute myeloid leukemia, previously identified as CD7+ ᅳ Precursor T lymphoblast leukemia/lymphoma ᅳ T-cell prolymphocytic leukemia ᅳ T-cell large granular lymphocytic leukemia ᅳ Peripheral T-cell lymphoma, NOS ᅳ Angioimmunoblastic T-cell lymphoma ᅳ Extranodal NK/T-cell lymphoma, nasal type ᅳ Enteropathy-type intestinal T-cell lymphoma ᅳ Hepatosplenic T-cell lymphoma Patients 18 years of age or older, and must have a life expectancy > 12 weeks. CD7 is expressed in malignancy tissues by immuno-histochemical (IHC) or Flow cytometry. Assessable disease as measured by laboratory and bone marrow examinations. Eastern cooperative oncology group (ECOG) performance status of 0-2 or karnofsky performance status (KPS) score is higher than 60. Females of child-bearing potential must have a negative pregnancy test and all subjects must agree to use an effective method of contraception for up to two weeks after the last infusion of CAR-pNK cells. Adequate bone marrow, liver and renal function as assessed by the following laboratory requirements: 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. Ability to give informed consent. Exclusion Criteria: Patients with symptomatic central nervous system (CNS) involvement. Pregnant or nursing women may not participate. Known HIV, hepatitis B virus (HBV) or hepatitis C virus (HCV) infection. Serious illness or medical condition which would not permit the patient to be managed according to the protocol, including active uncontrolled infection, major cardiovascular, coagulation disorders, respiratory or immune system, myocardial infarction, cardiac arrhythmias, obstructive/restrictive pulmonary disease, or psychiatric or emotional disorders. Concurrent use of systemic steroids. Recent or current use of inhaled steroids is not exclusionary. Previously treatment with any gene therapy products. The existence of unstable or active ulcers or gastrointestinal bleeding. Patients with a history of organ transplantation or are waiting for organ transplantation. Patients need anticoagulant therapy (such as warfarin or heparin). Patients need long-term antiplatelet therapy (aspirin at a dose > 300mg/d; clopidogrel at a dose > 75mg/d).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lin Yang, Ph.D.
Phone
86-512-65922190
Email
info@persongen.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lin Yang, Ph.D.
Organizational Affiliation
PersonGen BioTherapeutics (Suzhou) Co., Ltd.
Official's Role
Principal Investigator
Facility Information:
Facility Name
PersonGen BioTherapeutics (Suzhou) Co., Ltd.
City
Suzhou
State/Province
Jiangsu
ZIP/Postal Code
215123
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lin Yang, Ph.D.
Phone
86-512-65922190
Email
info@persongen.com
First Name & Middle Initial & Last Name & Degree
Yangyi Bao, MD
First Name & Middle Initial & Last Name & Degree
Xiang Sun, MD
First Name & Middle Initial & Last Name & Degree
Lin Yang, Ph.D

12. IPD Sharing Statement

Plan to Share IPD
Yes
Citations:
PubMed Identifier
28054442
Citation
Del Zotto G, Marcenaro E, Vacca P, Sivori S, Pende D, Della Chiesa M, Moretta F, Ingegnere T, Mingari MC, Moretta A, Moretta L. Markers and function of human NK cells in normal and pathological conditions. Cytometry B Clin Cytom. 2017 Mar;92(2):100-114. doi: 10.1002/cyto.b.21508. Epub 2017 Feb 12.
Results Reference
derived

Learn more about this trial

CAR-pNK Cell Immunotherapy in CD7 Positive Leukemia and Lymphoma

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