CAR T Cells in the Treatment of Refractory and Relapsed CD19+ B Cell Neoplasms

NCT06593145 | Recruiting Phase 1

• 1 other identifier: 2021-005720-37
• Study Type: interventional
• Target: 6
• Locations: 1 country
• Sites: 2

Brief Summary

One arm, open label study to assess the clinical use of Investigational Medicinal Product FCTX-CL19-1 (scientific name: Tarcidomgen Kimleucel) containing autologous anti-CD19 CAR T cells with a preliminary determination of the safety of intravenous IMP administration in patients diagnosed with refractory and relapsed CD19 + B cell neoplasms.

Conditions

Acute Lymphoblastic Leukemia (ALL); Mantle Cell Lymphoma (MCL); Large B-cell Lymphoma

Outcome Measures

Primary Outcomes (1)

• Percentage of patients with CRS in particular degree of severity according to ASTCT neurological side effects, febrile neutropenia and infection, cytopenia, other unspecified adverse events and death

  Safety assessment of IMP administration as the percentage of patients with cytokine release syndrome (CRS) in particular degree of severity according to ASTCT, neurological side effects, febrile neutropenia and infection, cytopenia, other unspecified adverse events and death as a result of the side effects and adverse events described within a 1 month after IMP administration

  through study completion, an average of 1 year

Secondary Outcomes (2)

• Percentage of participants with response to the therapy (sum of complete remissions and partial responses in the particular malignancies)

  through study completion, an average of 1 year

• Percentage of participants with no possibility to receive the product due to the production failure

  through study completion, an average of 1 year

Study Arms (1)

FCTX-CL19-1 (Tarcidomgen Kimleucel)

EXPERIMENTAL

FCTX-CL19-1 (Tarcidomgen Kimleucel) - active IMP - consists of autologous T-cells with chimeric antigen receptor (CAR), Advanced Therapy Medicinal Product, ATMP, Gene Therapy Medicinal Product, GTMP

Biological: FCTX-CL19-1 (Tarcidomgen Kimleucel)

Interventions

FCTX-CL19-1 (Tarcidomgen Kimleucel) BIOLOGICAL

It will be administered only by Investigators during hospitalization. Each patient will receive one administration of IMP on Day 0: * administration route - intravenous * cell dose: 0,2 x 106 -2 x 106 CAR T cells per kilogram of patient body weight

FCTX-CL19-1 (Tarcidomgen Kimleucel)

Eligibility Criteria

• Age: 18 Years - 65 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Adult patients 18-65 both inclusive;
• Diagnosis of:
• Refractory B-ALL (acute lymphocytic leukemia) - relapse after hematopoietic cell transplantation, second or more relapse in patients when transplantation is contraindicated)
• Large B-cell lymphoma including DLBCL NOS, lymphoma with high level of malignancy, follicular lymphoma transformed to DLBCL and primary mediastinal lymphoma - refractory or relapse or after at least 2 lines of systemic treatment)
• Mantle cell lymphoma (MCL) - relapsing or refractory after at least 2 lines of systemic treatment; Diagnostics of individual diagnoses (criteria for complete remission and partial responses for individual disease entities) was developed on the basis of current (July 2022) recommendations of experts of the Polish Society of Clinical Oncology
• Confirmed CD19 expression on malignant cells;
• General condition measured by ECOG (Eastern Cooperative Oncology Group) ≤ 1;
• Patient's weight between 40 kg - 130 kg
• Sufficient general condition of organs on screening visit:
• ALT/AST \<2,5 of UNL and bilirubin \<1,5 mg/dl (\<4 mg/dl for patients with Gilbert syndrome)
• Ejection fraction (EF) \>50% confirmed in ECHO with no signs of exudation in pericardium during 6 weeks before screening
• Saturation of arterial blood \>93% with no oxygen insufflation, with no significant exudation in pleural cavity
• Serum creatinine clearance \>60 ml/min (by Cockcroft-Gault formula);
• Negative result for HCV, HBV, HIV, Syphilis;
• Negative test for pregnancy (serum or urine) in the screening visit and/or 7 days before leucapheresis and 7 days before lymphodepleting therapy in women in reproductive age;

You may not qualify if:

• Any significant CNS diseases that preceded and not connected with relapse (including seizures, paresis, aphasia, stroke or CNS bleeding, severe brain trauma, dementia, Parkinson's disease, any disease affecting cerebellum, psychosis and diseases involving lack of coordination or movement);
• Bulky or rapidly progressing disease;
• Less than 3 months after allo-HSCT transplantation or DLI before screening;
• The need for high-dose chemotherapy less than 4 weeks before the scheduled apheresis;
• Patient's weight below 40 kg and above 130kg
• Any active bacterial, viral or fungal infection including SARS-CoV2;
• Latent HBV/HCV/HIV/Syphilis infection;
• Any other concomitant disease which in the opinion of the investigator would be interfering with the safety of participant in the trial
• Allergic to penicillin, streptomycin and amphotericin B;
• Intolerance to cyclophosphamide or fludarabine during previous treatment with these drugs;
• Chronic systemic immunosuppression treatment (i.e. cyclosporin). Corticosteroids are allowed up to dexamethasone dose of 4 mg a day or equal of this dose;
• Systemic immunosuppression treatment of acute and/or chronic Graft-versus host disease (GvHD) connected to earlier allogeneic HSCT treatment;
• Pregnancy;
• Women in reproductive age as well as men (regardless of age) that do not agree to maintain effective method of contraception during the trial, lactated women can be included into the trial unless declaration of stopping breast feeding during the whole trial time;
• Unable to provide informed consent for this trial;

Sponsors & Collaborators

• FamiCordTx: lead

Study Sites (2)

Uniwersyteckie Centrum Kliniczne Warszawskiego Uniwersytetu Medycznego - Centralny Szpital Kliniczny

Warsaw, Ul. Banacha 1a, 02-097, Poland

RECRUITING

Uniwersyteckie Centrum Kliniczne Gdańskiego Uniwersytetu Medycznego - Katedra i Klinika Hematologii i Transplantologii

Gdansk, Ul. Smoluchowskiego 17, 80-214, Poland

RECRUITING

MeSH Terms

Conditions

Precursor Cell Lymphoblastic Leukemia-Lymphoma; Lymphoma, Mantle-Cell

Condition Hierarchy (Ancestors)

Leukemia, Lymphoid; Leukemia; Neoplasms by Histologic Type; Neoplasms; Hematologic Diseases; Hemic and Lymphatic Diseases; Lymphoproliferative Disorders; Lymphatic Diseases; Immunoproliferative Disorders; Immune System Diseases; Lymphoma, Non-Hodgkin; Lymphoma

Study Officials

• Emilian Snarski

  FamiCordTx S.A.

  STUDY DIRECTOR

Central Study Contacts

Natalia Żmijewska

CONTACT

+48 795 158 306; n.zmijewska@famicordtx.com

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: September 2, 2024
• First Posted: September 19, 2024
• Study Start: May 24, 2023
• Primary Completion: June 1, 2025
• Study Completion: June 1, 2025
• Last Updated: September 19, 2024

Record last verified: 2024-09

Locations

PL (2)