Study Investigating the Safety of CD19 CAR-T Cells in Relapsed/Refractory AML Expressing CD19 (CARLA-M19)

Prospective Non-randomized Phase I Study Investigating the Safety of CD19 CAR-T Cells in Patients With Refractory/Relapsed AML Expressing CD19.

Refractory/Relapsed (R/R) acute myeloid leukemia (AML) is associated with a dis-mal prognosis.

In some subsets of AML such as AML driven by the t(8;21) translocation, leading to the RUNX1-RUNX1T1 (AML1-ETO) fusion transcript expression, CD19 B-cell antigen is aberrantly expressed on malignant blasts in around 80 % of cases. Interestingly, the expression of the CD19 antigen is also detected in the CD34+ CD38-population leukemic stem cells.

t(8;21) AML subtype has a rather good prognosis with an intensive chemotherapy regimen, but relapses occur in around 40 % of the patients and new therapeutic options are needed for these patients.

Plesa et al, reported a successful treatment of a refractory t(8;21) AML with bispecific monoclonal antibodies that targets CD19. More recently, Danylesko et al, have reported long-term remission following CD19 CAR-T cells in a heavily pre-treated patient with t(8;21) AML(1). The same group has just submitted an abstract of 6 treated patients to the European Haematology Association (EHA) 2023 meet-ing: Six patients (adults-5, child-1) with t(8; 21) AML (confirmed by cytogenetic and FISH) and aberrant CD19 expression were included. One patient had a complex karyotype. Molecular analysis for CKIT, NPM1, IDH1, IDH2, and CBPa were nega-tive in all pts. One pt harbors the FLT3 ITD and TKD mutations. Median number of previous chemotherapy (CT) lines was 4 (3-8). Four patients were with chemo re-sistant relapse post allo-HCT (MSD-1, 10/10 MUD -3) 5-18 months before CAR T-cell infusion. All patients developed CRS (grade 1-3) and were treated with i.v tocili-zumab and dexamethasone. 2/6 patients suffered from ICANS and were treated with steroids. In 4/6 patients, day 28 BM aspiration disclosed normal hematopoie-sis with no excess blasts and lack of t(8;21) by FISH confirming clinical and cyto-genetic remission, while 2/6 pts with progressive AML had no response (Danylesko etal. Abstract EHA 2023, submitted).

Interestingly, other subsets of AML display an aberrant expression of CD19. These observations indicate that CD19 can be a target of choice for CAR-T cells in patients with R/R AML expressing this antigen.

In this study, we plan to offer anti-CD19 CAR-T cell therapy to patients with re-lapsed/refractory AML expressing CD19 for whom no curative alternatives are available.

To this end, CAR-T cells will be manufactured using closed semi-automated bioreactor CliniMACS Prodigy (Miltenyi Biotec) in academic setting.

Study Overview

• Status: Recruiting
• Conditions: Relapsed Adult AML
• Intervention / Treatment: Drug: CAR-T cell therapy

• Study Type: Interventional
• Enrollment (Estimated): 5
• Phase: Phase 1

Contacts and Locations

• Study Contact: Name: Ibrahim Yakoub-Agha, MD,PhD; Phone Number: +33 0320445962; Email: ibrahim.yakoubagha@chru-lille.fr

Study Locations

• France
  • Lille, France, 59000
    • Recruiting
    • CHU de LILLE
    • Contact: Ibrahim Yakoub-Agha, Prof

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• Subject is ≥ 18 years of age at the time of signing the informed consent form,
• Patient with AML that expresses CD19 by Flow-cytometry, (CD19 expression ≥ 70% of AML blasts)

• Patients with R/R AML defined as:

  • Primary refractory: absence of remission after two courses of induction chemotherapy,
  • Secondary refractory: absence of remission after salvage treatment in relapsing patients,
  • Post-transplant relapse in patients having had allo-HCT.
• Lack of accessible targeted therapy that has not been previously utilized.
• Eastern Cooperative Oncology Group (ECOG) performance status of < 2,
• Estimated life expectancy of > 2 months,
• Magnetic resonance imaging (MRI) of the brain showing no evidence of central nervous system (CNS) involvement,
• Toxicities due to prior therapy must be stable and recovered to ≤ Grade 1 (except for clinically non-significant toxicities, such as alopecia),
• Platelet count ≥ 30000/uL,
• Absolute lymphocyte count ≥ 200/uL,
• Creatinine clearance (as estimated by Cockcroft Gault) ≥ 40 mL/min,
• Serum ALT/AST ≤ 2.5 upper limit of normal (ULN),
• Total bilirubin ≤ 1.5 mg/dl, except in subjects with Gilbert's syndrome,
• Cardiac ejection fraction ≥ 45 %,
• No clinically significant electrocardiogram (ECG) findings,
• No clinically significant pleural effusion,
• Baseline oxygen saturation > 92 % on room air,

• Female patients of childbearing potential must:

  1. have a negative pregnancy test (blood) at screening visit.
  2. either commit to true abstinence from heterosexual contact or agree to use, and be able to comply with, effective measures of contraception without interruption, from screening through 1 year following the CAR-T cell infusion. A highly effective method of contraception or birth control (failure rate less than 1% per year when used consistently and correctly) must be practiced. The patient should be informed of the potential risks associated with becoming pregnant while enrolled in this clinical trial. Reliable methods for this trial are: combined (estrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation (oral, intravaginal, transdermal), progestogen-only hormonal contraception associated with inhibition of ovulation (oral, injectable, implantable), intrauterine device, intrauterine hormone-releasing system, bilateral tubal occlusion, sexual abstinence or vasectomized sexual partner. Abstinence is only accepted as true abstinence: when this is in line with the preferred and usual lifestyle of the patient. (Periodic abstinence [e.g. calendar, ovulation, symptothermal, post-ovulation methods and withdrawal] are not acceptable methods of contraception.) Postmenopausal (no menses for at least 1 year without alternative medical cause) or surgically sterile female patients (tubal ligation, hysterectomy or bilateral oophorectomy) may be enrolled.
  3. Agree to abstain from breast feeding during the study participation and for 1 year after the CAR-T cell infusion.
• Male patients must practice true abstinence or agree to use a condom during sexual contact with a pregnant female or a female of childbearing potential for at least 1 year after the CAR-T cell infusion, even if he has undergone a successful vasectomy.

Exclusion Criteria:

• Patient unable to sign the informed consent,
• Patient with R/R AML that does not expresses CD19,
• History of malignancy other than nonmelanoma skin cancer or carcinoma in situ (e.g. cervix, bladder, breast) unless disease-free and without anticancer therapy for at least 3 years,
• Prior CD19 targeted therapy,
• Prior CAR therapy or other genetically modified T cell therapy,
• Presence or suspicion of fungal, bacterial, viral, or other infection that is uncontrolled or requiring intravenous (IV) antimicrobials for management,
• History of human immunodeficiency virus (HIV) or HTLV1,
• Infection or acute or chronic active hepatitis C infection,
• Infection or acute or chronic active hepatitis (Hep) B. Subjects with history of Hep B or Hep C infection must have cleared their infection as determined by standard serological and genetic testing per current Infectious Diseases Society of America (IDSA) guidelines,
• Subjects with detectable cerebrospinal fluid malignant cells or known brain metastases or with a history of cerebrospinal fluid (CSF) malignant cells or brain metastases,
• History or presence of non-malignant CNS disorder, such as seizure disorder, cerebrovascular ischemia/hemorrhage, dementia, cerebellar disease, or any autoimmune disease with CNS involvement,
• Patient placed under guardianship or curatorship,
• Females either pregnant/breast-feeding or planning to become pregnant,
• Any contraindication due to hypersensitivity to the active substance or to any of the excipients,
• Contraindication to the lymphodepleting chemotherapy,
• Absence of medical insurance cover.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Other: Experimental group	Drug: CAR-T cell therapy; cyclophosphamide and fludarabin conditioning , followed by a target dose of 1 x 10exp6 of autologous, genetically modified, anti-CD19 CAR-T cells per kg of body weight.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of patients deceased without progression one month after CAR-T cell infusion	Non-progression mortality (NPM), type and frequency of adverse events. NPM is defined as death occurred in patients without evidence of AML progression. Absence of response, progression or relapse of AML define progression status	at 1 month

Secondary Outcome Measures

Outcome Measure	Time Frame
Number of patients with manufacturing failure and out of specification (OOS) deviation	Througth study completion, an average of 2 years
Duration of CAR-T cell persistence in blood after infusion evaluated by flow-cytometry and PCR,	Througth study completionan, average of 2 years
Number of patients with overall response	at 1 month
Response duration	at 3 months, 6 months and 12 months
Number of patients alive	at 3 months, 6 months and 12 months
Number of patients alive without relapse	at 3 months, 6 months and 12 months
Number of deaths without progression	at 3 months, 6 months and 12 months
Number of patients with complete remission (CR)	at 1 month and 3 months

Collaborators and Investigators

• Sponsor: University Hospital, Lille
• Collaborators: University Hospital, Rouen; Ministry of Health, France; Miltenyi
• Investigators: Principal Investigator: Ibrahim Yakoub-Agha, MD,PhD, University Hospital, Lille

Study record dates

Study Major Dates

• Study Start (Actual): July 10, 2025
• Primary Completion (Estimated): July 10, 2029
• Study Completion (Estimated): July 10, 2030

Study Registration Dates

• First Submitted: October 15, 2024
• First Submitted That Met QC Criteria: October 17, 2024
• First Posted (Actual): October 18, 2024

Study Record Updates

• Last Update Posted (Actual): December 5, 2025
• Last Update Submitted That Met QC Criteria: November 27, 2025
• Last Verified: November 1, 2025

More Information

Terms related to this study

• Keywords: AML; CD19; CAR-T cells; Relapsed/refractory AML expressing CD19
• Additional Relevant MeSH Terms: Pathologic Processes; Neoplasms; Disease Attributes; Neoplasms by Histologic Type; Hematologic Diseases; Leukemia, Myeloid; Leukemia; Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases; Recurrence; Leukemia, Myeloid, Acute; Investigative Techniques; Therapeutics; Biological Therapy; Immunologic Techniques; Immunomodulation; Adoptive Transfer; Immunization, Passive; Immunization; Immunotherapy; Immunotherapy, Adoptive
• Other Study ID Numbers: 2021_0578; 2023-509212-29-01 (Ctis)

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No