Dual Anti-CD22/CD19 Chimeric Antigen Receptor-directed T Cells (CART2219.1) for Relapsed Refractory B-Lineage Leukaemia

Lymphoblastic Leukemia Clinical Trial

Official title:

Dual Anti-CD22/CD19 Chimeric Antigen Receptor-directed T Cells (CART2219.1) for Relapsed Refractory B-Lineage Leukaemia

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05429905
• Other study ID #: CART2219-1.0
• Status: Recruiting
• Phase: Phase 1/Phase 2
• Start date: July 18, 2022
• Est. completion date: December 2025

Study information

• Verified date: March 2023
• Source: KK Women's and Children's Hospital
• Contact: Michaela Seng, MD
• Phone: +65 6394 1989
• Email: michaela.seng[@]singhealth.com.sg
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to deliver dual-targeting CAR-T cell therapy (CART 2219.1) as a salvage treatment to patients with relapsed/refractory B-lineage leukaemia in place of stem cell transplant or irradiation.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 48
• Est. completion date: December 2025
• Est. primary completion date: December 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 2 Years to 75 Years

Eligibility

Inclusion Criteria:

All Cohorts:

• Age 2 to 75 years
• Absolute blood CD3+ T cell count =100/µl
• ECOG performance score of =2 if >16 years old, or Lansky performance score of >50 if =16 years old at screening
• Patients and/or parents must give their written informed consent/assent.
• Patients have relapsed/refractory B-lineage acute lymphoblastic leukaemia, includes persistent minimal residual disease (MRD) Cohort 1 (Phase I): Relapsed/Refractory B-ALL
• Patients must have relapsed/refractory (r/r) B-lineage ALL meeting one of the

following disease-specific criteria:

• Patients with r/r ALL with >5% blasts in BM (M2 or M3) after at least one standard chemotherapy and one salvage regimen who are ineligible for allogeneic stem cell transplant (alloSCT) or have refractory disease activity (e.g. persistent MRD in bone marrow) precluding alloSCT, or
• Patients with Ph+ ALL if they are intolerant to tyrosine kinase inhibitor (TKI) therapy, or if they have r/r disease after treatment including TKI, or
• Patients who have relapsed post-allogeneic HSCT and are at least 100 days post-transplant, with no evidence of active GVHD, > 6 weeks post donor lymphocyte infusion (DLI) and no longer taking immunosuppressive agents for at least 30 days prior to enrolment.
• Patients who have relapsed after prior CAR-T therapy who are not eligible for stem cell transplant and have < 5% circulating CAR-T prior to apheresis
• Patients with refractory/relapsed combined extramedullary ALL are eligible. This includes patients with combined CNS-2 (<5 WBC/µl CSF, with blasts on cytospin) or CNS-3 (>5 WBC/ul CSF, with blasts on cytospin) disease and patients with combined testicular relapse. Cohort 2 (Phase II): B-ALL with persistent MRD (High Risk B-ALL)
• Patients must have persistent MRD >0.1% blasts after frontline induction chemotherapy or >0.01% blasts after consolidation therapy. Cohort 3 (Phase II): Relapsed/Refractory Extramedullary B-ALL
• Patients with testicular leukaemia confirmed on biopsy
• Patients with CNS-3 B-ALL or Leptomeningeal disease
• Patients with combined bone marrow and extramedullary relapse (as defined in Cohort 1) are eligible. Exclusion Criteria:

All Cohorts:

• Blasts are negative for both CD22 and CD19 on flow cytometry or immunohistochemistry, defined as < 10% of blasts staining positive for CD22 and CD19 respectively [IBFM 2016 Consensus Guidelines].
• Current autoimmune disease, or history of autoimmune disease with potential CNS involvement
• Active clinically significant CNS dysfunction (including but not limited to uncontrolled seizure disorders, cerebrovascular ischemia or hemorrhage, dementia, paralysis)
• History of an additional malignancy other than non-melanoma skin cancer or carcinoma in situ unless disease free for =3 years.
• Pulmonary function: Patients with pre-existing severe lung disease (FEV1 or FVC < 65%) or an oxygen requirement of >28% O2 supplementation or active pulmonary infiltrates on chest X-ray at the time scheduled for T cell infusion
• Cardiac function: Fractional shortening <28% or left ventricular ejection fraction <50% by echocardiography
• Renal function: Creatinine clearance <50 mL/min/1.73 m2
• Liver function: Patients with a serum bilirubin >3 times upper limit of normal or an AST or ALT > 5 times upper limit of normal, unless due to leukemic liver infiltration in the estimation of the investigator
• Rapidly progressive disease that in the estimation of the investigator would compromise ability to complete study therapy
• Active Hepatitis B (HBsAg positive) or Hepatitis C (PCR positive), or known infection with human immunodeficiency virus (HIV)
• Pregnant or nursing (lactating) women
• In relation to prior therapy:
• Use of immunotherapy, cell-based or other investigational treatment within 30 days of CAR-T infusion

Related Conditions & MeSH terms

• Acute Disease
• CAR
• Leukemia
• Leukemia, Lymphoid
• Lymphoblastic Leukemia
• Lymphoblastic Leukemia in Children
• Lymphoblastic Leukemia, Acute Adult
• Lymphoblastic Leukemia, Acute, Childhood
• Precursor Cell Lymphoblastic Leukemia-Lymphoma

Intervention

Biological:
• Phase I
Dose level 0: CAR+CD3+ 0.4 x 10e6/kg (de-escalation dose) Dose level 1: CAR+CD3+ 1 x 10e6/kg (starting dose) Dose level 2: CAR+CD3+ 2.5 x 10e6/kg. Dose-escalations for adults and paediatrics will be performed in 2 independent strata for determination of RP2D.
• Phase II
RP2D will be determined in Phase I

Locations

Country	Name	City	State
Singapore	KK Women's and Children's hospital	Singapore

Sponsors (3)

Lead Sponsor	Collaborator
KK Women's and Children's Hospital	National University Hospital, Singapore, Singapore General Hospital

Country where clinical trial is conducted

Singapore, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Recommended Phase II Dose (Phase I, Cohort 1)	The RP2D will be the dose level at which < 1 DLT in 3 patients or < 2 DLT in 6 patients is observed in both the adult and paediatric dose escalation stratas.	30 days
Primary	Number of patients with dose-limiting toxicities (Phase I, Cohort 1)	To be DLTs, adverse events must be suspected to be secondary to CAR-T cell infusion, occur during the first 30 days after infusion and meet at least one of the following criteria: Grade = 3 non-hematologic toxicities, with the following exceptions: Laboratory abnormalities without associated symptomatology or clinical consequence that resolve in less than 7 days; Grade = 2 cytokine release syndrome; Grade 3 cytokine release syndrome that improves to grade = 2 within 3 days of intervention; Grade 3 neurotoxicity that resolves to grade 2 or less within 3 days.; Laboratory abnormalities compatible with tumor lysis syndrome; Grade = 4 hematologic toxicities that persist at a grade = 3 for >21 days.; Cytokine release syndrome and immune-effector cell associated neurotoxicity syndrome (ICANS) are graded according to ASTCT consensus grading. Adverse events are graded according to CTCAE version 5.0.	30 days
Primary	12-month Leukaemia Free Survival (Phase II, Cohort 2 and 3)	Survival with Marrow MRD <0.01% by flow cytometry	12 months
Secondary	Overall Survival Rate (OS)	Percentage of patients in the study who are alive 12 months after CAR-T infusion.	12 months
Secondary	Overall Response Rate (ORR)	Percentage of patients in the study who have a partial or complete response to the treatment within 3 months.	3 months
Secondary	Duration of Response (DOR)	Duration of complete remission (CR or CR with partial/incomplete haematological recovery)	Up to 24 months
Secondary	Duration of CAR-T persistence	Duration of measurable CAR-T above detection limits in peripheral blood and/or marrow	Up to 24 months