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CD19 Targeted CAR T Cell Therapy in Patients With Relapsed/ Refractory B Cell Acute Lymphoblastic Leukaemia (ALL)

Primary Purpose

Relapsed B Cell Acute Lymphoblastic Leukemia (ALL), Refractory B Cell Acute Lymphoblastic Leukemia (ALL)

Status
Not yet recruiting
Phase
Phase 1
Locations
Iran, Islamic Republic of
Study Type
Interventional
Intervention
CD19 CAR engineered autologous T-cells
Cyclophosphamide
Fludarabine
Mesna
Sponsored by
Sabz Biomedicals
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Relapsed B Cell Acute Lymphoblastic Leukemia (ALL) focused on measuring CD19+ B-cell Acute Lymphoblastic Leukemia, CAR T cell, Relapsed/Refractory B cell acute lymphoblastic leukemia

Eligibility Criteria

undefined - 25 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

CD19+ ALL patients with any of the following:

  1. Relapsed or Refractory CD19 positive B-cell acute lymphoblastic leukemia (R/R B-ALL) A. Primary refractory disease despite at least 2 cycles of an intensive chemotherapy regimen designed to induce remission B. Refractory disease despite salvage therapy C. 2nd or greater relapse D. Any relapse after allogeneic hematopoietic stem cell transplantation
  2. Informed consent explained to and signed by patient/parents or legal guardian.
  3. The Karnofsky (age ≥10 years)/Lansky (age <10 years) performance status score over 50 points.
  4. Expected to survive for more than 3 months.
  5. Patients with a history of prior allogeneic hematopoietic stem cell transplant (HSCT) must be at least 3 months from HSCT at the time of CD19 CAR-T cells infusion and also have not received a donor lymphocyte infusion (DLI) within the 28 days prior to apheresis.
  6. Important organ function is satisfied: Heart ultrasound indicates cardiac ejection fraction ≥ 50%, no obvious abnormality in ECG; Adequate pulmonary function defined as forced vital capacity (FVC) ≥ 50% of predicted value; or pulse oximetry ≥ 92% on room air if the patient is unable to perform pulmonary function testing; creatinine clearance calculated by Cockcroft-Gault formula ≥ 50 ml/min/1.73m2; Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) ≤ 5 times the upper limit of normal for age; Total Bilirubin ≤ 3 times the upper limit of normal for age.
  7. Absolute lymphocyte count ≥ 0.5 x 10⁹/L.
  8. Hemoglobin ≥ 8 g/dl (can be transfused).
  9. Platelet count ≥ 20,000/μL (can be transfused).
  10. Meets eligibility criteria to undergo autologous apheresis.

Exclusion Criteria:

  1. Isolated extra-medullary disease relapse.
  2. Active CNS involvement of ALL (CNS Grade 3 per National Comprehensive Cancer Network guidelines).
  3. Severe, uncontrolled bacterial, fungal or viral infections (Active hepatitis B or C, history of HIV infection)
  4. Pre-existing significant neurological disorder.
  5. Active significant acute graft versus host disease (GVHD) or moderate/severe chronic GVHD requiring systemic steroids or other immunosuppressants within 4 weeks of enrolment.
  6. Pregnant or lactating female.
  7. The patient did not agree to use effective contraception during the treatment period and for the following 1 year.
  8. A history of other malignant tumors.
  9. Receiving systemic steroids therapy exceeding the equivalent of 0.5 mg/ kg/day of methylprednisolone, in the 7 days prior to CAR T-cell infusion
  10. Receiving systemic immunosuppressive therapy in the 14 days prior to CAR T-cell infusion
  11. Receiving intrathecal chemotherapy in the 7 days prior to CAR T-cell infusion

Sites / Locations

  • Gene therapy research center, Shariati hospital, Tehran university of medical sciences, Iran
  • Research Institute for Oncology- Hematology and Cell Therapy (RIOHCT), Tehran University of Medical Sciences

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

CD19 CAR-T cells

Arm Description

Pediatric or adolescent/young adult patients with CD19+ relapsed or refractory B cell acute lymphoblastic leukemia (R/R B-ALL)

Outcomes

Primary Outcome Measures

Maximum Tolerated Dose (MTD) and Dose-limiting Toxicities (DLT) of CD19 CAR-T cells
Patients will be continually assessed for unexpected adverse events using the NCI CTCAE (version 5.0) or unexpected early mortality 30 days post-infusion. The primary objectives for the Phase I study portion are to determine the maximum tolerated dose (MTD) and characterize the safety profile and dose-limiting toxicities (DLTs) of treatment with CD19 CAR-T cells in pediatric, adolescent and young adult patient's ≤ 25 years of age, with relapsed/refractory CD19+ ALL.

Secondary Outcome Measures

Number of patients who achieve complete morphological remission
Number of patients who achieve complete morphological remission (Complete Response (CR) or Complete Response with Incomplete count recovery (CRi) in the bone marrow)

Full Information

First Posted
November 22, 2020
Last Updated
March 17, 2021
Sponsor
Sabz Biomedicals
Collaborators
Gene Therapy Research Center, Shariati Hospital, Tehran University of Medical Sciences, Iran, Research Institute for Oncology- Hematology and Cell Therapy (RIOHCT), Tehran University of Medical Sciences, Iran
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1. Study Identification

Unique Protocol Identification Number
NCT04653493
Brief Title
CD19 Targeted CAR T Cell Therapy in Patients With Relapsed/ Refractory B Cell Acute Lymphoblastic Leukaemia (ALL)
Official Title
Phase I Clinical Trial Evaluating Safety of CD19 CAR-T Cells in Patients With Relapsed or Refractory Acute B-cell Lymphoblastic Leukemia (R/R B-ALL)
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Not yet recruiting
Study Start Date
August 2021 (Anticipated)
Primary Completion Date
August 2024 (Anticipated)
Study Completion Date
August 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sabz Biomedicals
Collaborators
Gene Therapy Research Center, Shariati Hospital, Tehran University of Medical Sciences, Iran, Research Institute for Oncology- Hematology and Cell Therapy (RIOHCT), Tehran University of Medical Sciences, Iran

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 is a single-arm, open-label, phase I study (safety and dose escalation) of autologous Chimeric Antigen Receptor (CAR) T-cells targeting CD19 in patients with relapsed/refractory B cell acute lymphoblastic leukemia (ALL).
Detailed Description
In this single-center, open-label, nonrandomized, no control, prospective clinical trial, pediatric or adolescent/young adult patients with CD19+ relapsed or refractory B cell acute lymphoblastic leukemia (R/R B-ALL) will be enrolled. Eligible patients will receive CAR T product intravenously as a single or split dose following pre-conditioning by a lymphodepleting chemotherapeutic regimen and will then enter a 30-day follow-up period to monitor adverse events using the NCI CTCAE (version 5.0).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Relapsed B Cell Acute Lymphoblastic Leukemia (ALL), Refractory B Cell Acute Lymphoblastic Leukemia (ALL)
Keywords
CD19+ B-cell Acute Lymphoblastic Leukemia, CAR T cell, Relapsed/Refractory B cell acute lymphoblastic 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
22 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
CD19 CAR-T cells
Arm Type
Experimental
Arm Description
Pediatric or adolescent/young adult patients with CD19+ relapsed or refractory B cell acute lymphoblastic leukemia (R/R B-ALL)
Intervention Type
Biological
Intervention Name(s)
CD19 CAR engineered autologous T-cells
Intervention Description
Given IV Following preconditioning with lymphodepleting chemotherapy (cyclophosphamide and fludarabine) patients will be treated with CD19 Chimeric Antigen Receptor (CAR) T cells as a single or split dose (day 0, 1 and 2, CAR cells will be intravenously infused at the 10%, 30% and 60% ratio respectively). Dosing of CD19 CAR-T cells will follow a dose-escalation schema, with dose changes based on dose-limiting toxicities.
Intervention Type
Drug
Intervention Name(s)
Cyclophosphamide
Intervention Description
Given IV
Intervention Type
Drug
Intervention Name(s)
Fludarabine
Intervention Description
Given IV
Intervention Type
Drug
Intervention Name(s)
Mesna
Intervention Description
Given IV
Primary Outcome Measure Information:
Title
Maximum Tolerated Dose (MTD) and Dose-limiting Toxicities (DLT) of CD19 CAR-T cells
Description
Patients will be continually assessed for unexpected adverse events using the NCI CTCAE (version 5.0) or unexpected early mortality 30 days post-infusion. The primary objectives for the Phase I study portion are to determine the maximum tolerated dose (MTD) and characterize the safety profile and dose-limiting toxicities (DLTs) of treatment with CD19 CAR-T cells in pediatric, adolescent and young adult patient's ≤ 25 years of age, with relapsed/refractory CD19+ ALL.
Time Frame
Within 30 days after the last dose of CD19 CAR-T cells
Secondary Outcome Measure Information:
Title
Number of patients who achieve complete morphological remission
Description
Number of patients who achieve complete morphological remission (Complete Response (CR) or Complete Response with Incomplete count recovery (CRi) in the bone marrow)
Time Frame
Within 30 days post CD19 CAR-T cells

10. Eligibility

Sex
All
Maximum Age & Unit of Time
25 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: CD19+ ALL patients with any of the following: Relapsed or Refractory CD19 positive B-cell acute lymphoblastic leukemia (R/R B-ALL) A. Primary refractory disease despite at least 2 cycles of an intensive chemotherapy regimen designed to induce remission B. Refractory disease despite salvage therapy C. 2nd or greater relapse D. Any relapse after allogeneic hematopoietic stem cell transplantation Informed consent explained to and signed by patient/parents or legal guardian. The Karnofsky (age ≥10 years)/Lansky (age <10 years) performance status score over 50 points. Expected to survive for more than 3 months. Patients with a history of prior allogeneic hematopoietic stem cell transplant (HSCT) must be at least 3 months from HSCT at the time of CD19 CAR-T cells infusion and also have not received a donor lymphocyte infusion (DLI) within the 28 days prior to apheresis. Important organ function is satisfied: Heart ultrasound indicates cardiac ejection fraction ≥ 50%, no obvious abnormality in ECG; Adequate pulmonary function defined as forced vital capacity (FVC) ≥ 50% of predicted value; or pulse oximetry ≥ 92% on room air if the patient is unable to perform pulmonary function testing; creatinine clearance calculated by Cockcroft-Gault formula ≥ 50 ml/min/1.73m2; Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) ≤ 5 times the upper limit of normal for age; Total Bilirubin ≤ 3 times the upper limit of normal for age. Absolute lymphocyte count ≥ 0.5 x 10⁹/L. Hemoglobin ≥ 8 g/dl (can be transfused). Platelet count ≥ 20,000/μL (can be transfused). Meets eligibility criteria to undergo autologous apheresis. Exclusion Criteria: Isolated extra-medullary disease relapse. Active CNS involvement of ALL (CNS Grade 3 per National Comprehensive Cancer Network guidelines). Severe, uncontrolled bacterial, fungal or viral infections (Active hepatitis B or C, history of HIV infection) Pre-existing significant neurological disorder. Active significant acute graft versus host disease (GVHD) or moderate/severe chronic GVHD requiring systemic steroids or other immunosuppressants within 4 weeks of enrolment. Pregnant or lactating female. The patient did not agree to use effective contraception during the treatment period and for the following 1 year. A history of other malignant tumors. Receiving systemic steroids therapy exceeding the equivalent of 0.5 mg/ kg/day of methylprednisolone, in the 7 days prior to CAR T-cell infusion Receiving systemic immunosuppressive therapy in the 14 days prior to CAR T-cell infusion Receiving intrathecal chemotherapy in the 7 days prior to CAR T-cell infusion
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Tahereh Rostami, M.D
Phone
+9821-88004140
Email
trostami@sina.tums.ac.ir
First Name & Middle Initial & Last Name or Official Title & Degree
Naser Ahmadbeigi, PhD
Phone
+9821-82415103
Email
n-ahmadbeigi@sina.tums.ac.ir
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tahereh Rostami, M.D
Organizational Affiliation
Research Institute for Oncology- Hematology and Cell Therapy (RIOHCT), Tehran University of Medical Sciences, Tehran, Iran
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Naser Ahmadbeigi, PhD
Organizational Affiliation
Gene Therapy Research Center, Shariati hospital, Tehran University of Medical Sciences, Tehran, Iran
Official's Role
Study Director
Facility Information:
Facility Name
Gene therapy research center, Shariati hospital, Tehran university of medical sciences, Iran
City
Tehran
Country
Iran, Islamic Republic of
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Naser Ahmadbeigi, Phd
Phone
+9821-82415103
Email
n-ahmadbeigi@sina.tums.ac.ir
Facility Name
Research Institute for Oncology- Hematology and Cell Therapy (RIOHCT), Tehran University of Medical Sciences
City
Tehran
Country
Iran, Islamic Republic of
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tahereh Rostami, M.D
Phone
+982188004140
Email
trostami@sina.tums.ac.ir

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

CD19 Targeted CAR T Cell Therapy in Patients With Relapsed/ Refractory B Cell Acute Lymphoblastic Leukaemia (ALL)

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