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Safety, Efficacy and Pharmacokinetics of ThisCART19A in Patients With Refractory or Relapsed B Cell Lymphoma

Primary Purpose

Refractory or Relapsed B Cell Lymphoma

Status
Not yet recruiting
Phase
Phase 1
Locations
China
Study Type
Interventional
Intervention
ThisCART19A
Fludarabine
Cyclophosphamide
Etoposide
Sponsored by
Chongqing University Cancer Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Refractory or Relapsed B Cell Lymphoma focused on measuring Allogeneic CAR T,B cell Lymphoma

Eligibility Criteria

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

Inclusion Criteria: 18 years ≤ age ≤ 65 years. Voluntarily sign a documented IRB-approved ICF prior to any screening procedure. Patients with histologically confirmed B-cell NHL defined by the World Health Organization (WHO) 2016, including but not limited to diffuse large B-cell lymphoma (DLBCL), follicular lymphoma transferring to DLBCL, mantle cell lymphoma (MCL), follicular lymphoma 3B (FL-3B), original Mediastinal (thymus) large B-cell lymphoma, high-grade B-cell lymphoma and AIDS-associated B-cell lymphoma. Prior therapy must have included: Anti-CD20 monoclonal antibody and Anthracycline containing chemotherapy regimen. Had available evaluation lesion. ECOG(Eastern Cooperative Oncology Group) ≤ 2 or Karnofsky ≥ 60%. Serum creatinine≤1.5×ULN or creatinine clearance>30 mL/min/1.73 m2. Alanine aminotransferase(ALT)≤5×ULN(Upper limit of normal) and total bilirubin(TBIL)<2.0 mg/dL(for patients with Gilbert heald diseases, live involvement and taking atazanavir or indinavir, TBIL<3.0 mg/dL can be enrolled.) Left ventricular ejection fraction(LVEF)≥40% Absolute neutrophile counts≥1000/mm3 Thrombocyte≥30000/mm3 Total bilirubin(TBIL) ≤ 2.0 mg/dL Confirmed Cluster of differentiation(CD)19 positive by biopsy for the patients who received CD19 target therapy before. Pregnancy tests for women of childbearing age shall be negative; Both men and women agreed to use effective contraception during treatment and during the subsequent 1 year. AIDS Related B Cell Lymphoma :HIV virus loading < 200 copy/ml and CD4+T cell counts >200 cells/mm3 within 4 weeks before screening. Patients with TBIL≤ 1.5 mg/dL, Aspartate aminotransferase(AST) and ALT ≤ 3×ULN, and hepatitis B virus(HBV) DNA <2000 IU/ml can be enrolled for HBV positive patients(defined as hepatitis B virus surface antigen(HBsAg) positive and hepatitis B core(HBc)-total positive ) and hepatitis C virus(HCV) positive patients(defined as HCV antibody positive) . Patients with cirrhosis are excluded. Hepatitis B core antibody(HBcAb) positive patients enrolled in this trial have to taking anti-HBV drugs during the whole research. Exclusion Criteria: Known for allergic to the preconditioning measures. Uncontrollable bacterial, fungal, viral infection before enrollment. Patients with pulmonary embolism within 3 months prior enrollment. Intolerable serious cardiovascular and cerebrovascular diseases and hereditary diseases. Imaging confirmed the presence of central nervous system involvement(including primary and secondary) and rapid progressing diseases. Receive allogeneic hematopoietic stem cell transplantation less than 100 days. Systemic steroid use (e.g., prednisone ≥20mg) within 3 days prior to screening. iIntermittent use of topical, inhaled or intranasal steroids recently or currently. Or systemic disease requiring long-term use of immunosuppression drugs. Excluded the patients received Influenza vaccinations within 2 weeks prior to lymphodepletion (Received Severe Acute Respiratory Syndrome-Corona virus disease(SARS-COV)19 vaccines could be included. Received inactivated, live/non-live adjuvant vaccines could be enrolled). Excluded women who are in pregnant or lactating, and female subjects or partners who plan to be pregnant within 1 year after infusion. Male subjects planning pregnancy within 1 year after infusion should be excluded.

Sites / Locations

  • Chongqing University Cancer Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

ThisCART19A cells infusion

Arm Description

In this study, allogeneic anti-CD19 CAR T cells (ThisCART19A) infusion is used to treat patients with r/r B cell Lymphoma.

Outcomes

Primary Outcome Measures

Dose limited toxicity(DLT) observation in patient with r/r B cell Lymphoma
DLT was defined as CAR T cells-related events with onset within first 28 days following infusion.
The incidence of all grade TEAEs and ≥3 grade TEAEs
Incidence of treatment-emergent adverse events (TEAEs) and ≥3 grade TEAEs
Objective Response Rate
the incidence of complete response (CR), partial response (PR), stable disease (SD), progressive disease (PD), or unevaluable (UE) as best response to treatment.
Duration of response (DOR)
DOR is defined as the date of their first CR or PR (which is subsequently confirmed) to PD assessed by investigators and based on the Lugano 2014 assessment criterion for r/r B cell Lymphoma, or death regardless of cause.
Progress-free survival (PFS)
PFS is defined as the time from the ThisCART19A infusion date to the date of disease progression assessed by investigators and based on the Lugano 2014 assessment criterion, or death any cause.

Secondary Outcome Measures

TTR (Time to response)
TTR is defined as the time from ThisCART19A infusion to first assessed CR or PR based on the Lugano 2014 assessment criterion.
OS (Overall survival)
Overall survival (OS) is defined as the time from the date of lymphodepletion until death from any cause.

Full Information

First Posted
March 8, 2023
Last Updated
March 8, 2023
Sponsor
Chongqing University Cancer Hospital
Collaborators
Fundamenta Therapeutics, Ltd.
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1. Study Identification

Unique Protocol Identification Number
NCT05776407
Brief Title
Safety, Efficacy and Pharmacokinetics of ThisCART19A in Patients With Refractory or Relapsed B Cell Lymphoma
Official Title
A Single Dose-escalation and Dose-expansion Study to Evaluate the Safety, Efficacy and Pharmacokinetics of Allogeneic CAR-T Targeting CD19 in Patients With Refractory or Relapsed B Cell Lymphoma.
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
May 2023 (Anticipated)
Primary Completion Date
May 2024 (Anticipated)
Study Completion Date
November 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Chongqing University Cancer Hospital
Collaborators
Fundamenta Therapeutics, 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
This is a phase 1/2, open-label study to assess the efficacy, safety and pharmacokinetics of ThisCART19A (Allogeneic Anti CD19 CAR-T) in patients with refractory or relapsed CD19 positive B cell Lymphoma.
Detailed Description
This is a phase 1/2, single-center, nonrandomized, open-label, dose-escalation and dose-expansion study to evaluate the efficacy, safety and pharmacokinetics of ThisCART19A in patients with r/r CD19 positive B cell Lymphoma and identify a treatment regimen most likely to result in clinical efficacy while maintaining a favorable safety profile. AIDS-related B-cell lymphoma were not excluded from this clinical trial. Before initiating ThisCART19A infusion, subjects will be administered lymphodepletion chemotherapy composed of fludarabine、cyclophosphamide and VP-16. At Day 0 of the Treatment Period, subjects will receive an intravenous (IV) infusion of ThisCART19A. All subjects are monitored during the treatment period through Day 42. All subjects who receive a dose of ThisCART19A will be followed up to 2 years.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Refractory or Relapsed B Cell Lymphoma
Keywords
Allogeneic CAR T,B 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
12 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
ThisCART19A cells infusion
Arm Type
Experimental
Arm Description
In this study, allogeneic anti-CD19 CAR T cells (ThisCART19A) infusion is used to treat patients with r/r B cell Lymphoma.
Intervention Type
Drug
Intervention Name(s)
ThisCART19A
Other Intervention Name(s)
Allogeneic Anti-CD19 CAR T cells
Intervention Description
Single dose of Allogeneic Anti-CD19 CAR T cells (ThisCART19A) will be infused after the lymphodepletion conditioning of Fludarabine, Cyclophosphamide and Etoposide.
Intervention Type
Drug
Intervention Name(s)
Fludarabine
Intervention Description
Fludarabine is used for lymphodepletion.
Intervention Type
Drug
Intervention Name(s)
Cyclophosphamide
Intervention Description
Cyclophosphamide is used for lymphodepletion.
Intervention Type
Drug
Intervention Name(s)
Etoposide
Other Intervention Name(s)
VP-16
Intervention Description
Etoposide is used for lymphodepletion.
Primary Outcome Measure Information:
Title
Dose limited toxicity(DLT) observation in patient with r/r B cell Lymphoma
Description
DLT was defined as CAR T cells-related events with onset within first 28 days following infusion.
Time Frame
28 days
Title
The incidence of all grade TEAEs and ≥3 grade TEAEs
Description
Incidence of treatment-emergent adverse events (TEAEs) and ≥3 grade TEAEs
Time Frame
Up to 2 years after ThisCART19A infusion
Title
Objective Response Rate
Description
the incidence of complete response (CR), partial response (PR), stable disease (SD), progressive disease (PD), or unevaluable (UE) as best response to treatment.
Time Frame
Up to 2 years after ThisCART19A infusion
Title
Duration of response (DOR)
Description
DOR is defined as the date of their first CR or PR (which is subsequently confirmed) to PD assessed by investigators and based on the Lugano 2014 assessment criterion for r/r B cell Lymphoma, or death regardless of cause.
Time Frame
Up to 2 years after ThisCART19A infusion
Title
Progress-free survival (PFS)
Description
PFS is defined as the time from the ThisCART19A infusion date to the date of disease progression assessed by investigators and based on the Lugano 2014 assessment criterion, or death any cause.
Time Frame
Up to 2 years after ThisCART19A infusion
Secondary Outcome Measure Information:
Title
TTR (Time to response)
Description
TTR is defined as the time from ThisCART19A infusion to first assessed CR or PR based on the Lugano 2014 assessment criterion.
Time Frame
Up to 2 years after ThisCART19A infusion
Title
OS (Overall survival)
Description
Overall survival (OS) is defined as the time from the date of lymphodepletion until death from any cause.
Time Frame
Up to 2 years after lymphodepletion

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 years ≤ age ≤ 65 years. Voluntarily sign a documented IRB-approved ICF prior to any screening procedure. Patients with histologically confirmed B-cell NHL defined by the World Health Organization (WHO) 2016, including but not limited to diffuse large B-cell lymphoma (DLBCL), follicular lymphoma transferring to DLBCL, mantle cell lymphoma (MCL), follicular lymphoma 3B (FL-3B), original Mediastinal (thymus) large B-cell lymphoma, high-grade B-cell lymphoma and AIDS-associated B-cell lymphoma. Prior therapy must have included: Anti-CD20 monoclonal antibody and Anthracycline containing chemotherapy regimen. Had available evaluation lesion. ECOG(Eastern Cooperative Oncology Group) ≤ 2 or Karnofsky ≥ 60%. Serum creatinine≤1.5×ULN or creatinine clearance>30 mL/min/1.73 m2. Alanine aminotransferase(ALT)≤5×ULN(Upper limit of normal) and total bilirubin(TBIL)<2.0 mg/dL(for patients with Gilbert heald diseases, live involvement and taking atazanavir or indinavir, TBIL<3.0 mg/dL can be enrolled.) Left ventricular ejection fraction(LVEF)≥40% Absolute neutrophile counts≥1000/mm3 Thrombocyte≥30000/mm3 Total bilirubin(TBIL) ≤ 2.0 mg/dL Confirmed Cluster of differentiation(CD)19 positive by biopsy for the patients who received CD19 target therapy before. Pregnancy tests for women of childbearing age shall be negative; Both men and women agreed to use effective contraception during treatment and during the subsequent 1 year. AIDS Related B Cell Lymphoma :HIV virus loading < 200 copy/ml and CD4+T cell counts >200 cells/mm3 within 4 weeks before screening. Patients with TBIL≤ 1.5 mg/dL, Aspartate aminotransferase(AST) and ALT ≤ 3×ULN, and hepatitis B virus(HBV) DNA <2000 IU/ml can be enrolled for HBV positive patients(defined as hepatitis B virus surface antigen(HBsAg) positive and hepatitis B core(HBc)-total positive ) and hepatitis C virus(HCV) positive patients(defined as HCV antibody positive) . Patients with cirrhosis are excluded. Hepatitis B core antibody(HBcAb) positive patients enrolled in this trial have to taking anti-HBV drugs during the whole research. Exclusion Criteria: Known for allergic to the preconditioning measures. Uncontrollable bacterial, fungal, viral infection before enrollment. Patients with pulmonary embolism within 3 months prior enrollment. Intolerable serious cardiovascular and cerebrovascular diseases and hereditary diseases. Imaging confirmed the presence of central nervous system involvement(including primary and secondary) and rapid progressing diseases. Receive allogeneic hematopoietic stem cell transplantation less than 100 days. Systemic steroid use (e.g., prednisone ≥20mg) within 3 days prior to screening. iIntermittent use of topical, inhaled or intranasal steroids recently or currently. Or systemic disease requiring long-term use of immunosuppression drugs. Excluded the patients received Influenza vaccinations within 2 weeks prior to lymphodepletion (Received Severe Acute Respiratory Syndrome-Corona virus disease(SARS-COV)19 vaccines could be included. Received inactivated, live/non-live adjuvant vaccines could be enrolled). Excluded women who are in pregnant or lactating, and female subjects or partners who plan to be pregnant within 1 year after infusion. Male subjects planning pregnancy within 1 year after infusion should be excluded.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yao Liu, MD
Phone
13228684685
Email
liuyao77@cqu.edu.cn
First Name & Middle Initial & Last Name or Official Title & Degree
Jun Li, Ph.D
Phone
+86 18662604088
Email
jli@ctigen.com
Facility Information:
Facility Name
Chongqing University Cancer Hospital
City
Chongqing
State/Province
Chongqing
ZIP/Postal Code
400030
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No

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Safety, Efficacy and Pharmacokinetics of ThisCART19A in Patients With Refractory or Relapsed B Cell Lymphoma

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