CD19 CAR and PD-1 Knockout Engineered T Cells for CD19 Positive Malignant B-cell Derived Leukemia and Lymphoma

Acute Lymphoblastic Leukemia Clinical Trial

Official title:

CD19 Chimeric Antigen Receptor (CAR) and PD-1 Knockout Engineered T Cells for CD19 Positive Malignant B-cell Derived Leukemia and Lymphoma

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT03298828
• Other study ID #: TMMU-CAR-001
• Status: Not yet recruiting
• Phase: Phase 1
• First received: July 24, 2017
• Last updated: September 26, 2017
• Start date: November 2017
• Est. completion date: October 2022

Study information

• Verified date: September 2017
• Source: Third Military Medical University
• Contact: Xiaoyun Shang, Dr.
• Phone: +8618580607020
• Email: shangxiaoyun[@]gmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the safety, efficacy and blood kinetics of autologous T cells genetically modified to express CD19 Chimeric Antigen Receptor and PD-1 knockout engineered T cells in patients with relapsed or refractory B-Cell Non-Hodgkin Lymphoma and Leukaemia.

Description:

This is a multi-centre, non-randomised, open label Phase I clinical trial of an Advanced Therapy Investigational Medicinal Product named CD19 Chimeric Antigen Receptor (CAR) and PD-1 knock out engineered T-cells (CD19 CAR and PD-1 knock out engineered T-cells) in children and adults (age <70 years) with high risk, relapsed CD19+ haematological malignancies (Acute Lymphoblastic Leukemia and Burkitt's lymphoma). Following informed consent and registration to the trial, patients will undergo an unstimulated leukapheresis for the generation of the CD19 CAR T-cells. Patients will receive the CD19 CAR and PD-1 knock out engineered T-cells following lymphodepleting chemotherapy. The study will evaluate the safety, efficacy and duration of response of the CD19 CAR and PD-1 knock out engineered T-cells in children with high risk relapsed CD19+ malignancies.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 30
• Est. completion date: October 2022
• Est. primary completion date: October 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A to 70 Years

Eligibility

Inclusion Criteria:

• 1.Children and adults (age 70 years or younger) with high risk/relapsed CD19+ haematological malignancy:

1. Resistant disease (>25% blasts) at end of UKALL 2011 or equivalent induction

2. ALL with persistent high level MRD at 2nd time point of frontline national protocol (currently > 5 x 10-3 at week 14 UKALL2011 or equivalent)

3. High risk infant ALL (age < 6 months at diagnosis with MLL gene rearrangement and either presenting white cell count > 300 x 109/L or poor steroid early response (i.e circulating blast count >1x109/L following 7 day steroid pre- phase of Interfant 06)

4. Intermediate risk infant ALL with MRD > 10-3 at end of Interfant06 induction

5. Very early (< 18 months from diagnosis) bone marrow or extramedullary relapse of acute lymphoblastic leukaemia (ALL)

6. Early (within 6 months of finishing therapy) bone marrow, or combined extramedullary relapse of ALL with bone marrow minimal residual disease (MRD) > 10-3 at end of re-induction

7. Any on therapy relapse of ALL in patients age 16-70

8. Any relapse of infant ALL

9. ALL post = 2nd relapse

10. Any refractory relapse of ALL

11. ALL with MRD >10-4 prior to planned stem cell transplant

12. Any relapse of ALL eligible for stem cell transplant but no available HLA matched donor or other contraindication to transplant

13. Any relapse of ALL after stem cell transplant

14. Any relapse of Burkitt's or other CD19+ lymphoma

• 2.Agreement to have a pregnancy test, use adequate contraception (if applicable)

• 3.Written informed consent

Exclusion Criteria:

• Exclusion Criteria for registration:

1. CD19 negative disease

2. Active hepatitis B, C or HIV infection

3. Oxygen saturation = 90% on air

4. Bilirubin > 3 x upper limit of normal

5. Creatinine > 3 x upper limit of normal

6. Women who are pregnant or lactating

7. Stem Cell Transplant patients only: active acute graft-versus-host disease (GVHD) overall Grade = II (Seattle criteria) or moderate/severe chronic GVHD (NIH consensus criteria) requiring systemic steroids

8. Inability to tolerate leucapheresis

9. Karnofsky (age = 10 years) or Lansky (age < 10) score = 50%

• Exclusion criteria for CD19CAR T-cell infusion:

1. Severe intercurrent infection at the time of scheduled CD19 CAR and PD-1 Knockout Engineered T Cells infusion

2. Requirement for supplementary oxygen or active pulmonary infiltrates at the time of scheduled CD19 CAR and PD-1 Knockout Engineered T Cells infusion

3. Allogeneic transplant recipients with active acute GVHD overall grade >2 or moderate/severe chronic GVHD requiring systemic steroids at the time of scheduled CD19 CAR and PD-1 Knockout Engineered T Cells infusion

Related Conditions & MeSH terms

• Acute Lymphoblastic Leukemia
• Burkitt Lymphoma
• Leukemia
• Leukemia, Lymphoid
• Lymphoma
• Precursor Cell Lymphoblastic Leukemia-Lymphoma

Intervention

Biological:
• CD19 CAR and PD-1 knock out engineered T-cells
A single dose of 1 x 10^6/kg CD19 CAR transduced and PD-1 knock out engineered T-cells will be given as an intravenous injection through a Hickman line or PICC line(peripherally inserted central catheter) on day 0.
• CD19 CAR T-cells
A single dose of 1 x 10^6/kg CD19 CAR transduced T-cells will be given as an intravenous injection through a Hickman line or PICC line(peripherally inserted central catheter) on day 0.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Third Military Medical University

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Molecular remission	Efficacy will be assessed by determining Minimal Residual Disease in the bone marrow aspirate using immunoglobulin heavy chain (IgH) quantitative polymerase chain reaction (qPCR) and/or Next Generation Sequencing in all patients. The proportion of patients achieving molecular remission at 1 month post CD19 CAR and PD-1 Knockout Engineered T-cell infusion will be determined.	1 month
Secondary	Long term molecular remission	Number of patients in molecular remission without further therapy at 2 years	2 years
Secondary	Frequency of circulating CD19 CAR and PD-1 Knockout Engineered T-cells	Persistence and frequency of circulating CD19 CAR and PD-1 Knockout Engineered T-cells in the peripheral blood by flow cytometry and qPCR analyses.	2 years
Secondary	Incidence of hypogammaglobulinaemia	Incidence and duration of hypogammaglobulinaemia.	2 years
Secondary	Relapse rate	Relapse rate monitored during interventional phase and long term follow up for a total of 10 years post cell infusion. Number of patients who relapsed can be summarized as a percentage (for all patients registered to the trial, and also only for those who received the cell infusion).	10 years
Secondary	Overall Survival	Overall survival is monitored during interventional phase and long term follow up for 10 years post-CD19 CAR and PD-1 Knockout Engineered T-cell infusion. Number of patients alive can be summarized as a percentage (for all patients registered to the trial, and also only for those who received the cell infusion).	10 years