A Phase I Clinical Trial of CART Cell Therapy for Refractory/ Relapsed Acute Lymphoblastic Leukemia With Unmet Needs in Children, Adolescents and Young Adults: Feasibility and Safety Study (REALL_CART).

Status: Recruiting
Location: See location...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

The goal of this clinical trial is to test the feasibility and safety of an academic production of two different anti-CD19 chimeric antigen receptor T cells (CART) products according to the different biomarkers of the disease in children and young adults with relapsed/refractory CD19+ B cell acute lymphoblastic leukemia (r/r B-ALL) or relapsed/refractory T-cell acute lymphoblastic leukemia (r/r T-ALL). The main questions it aims to answer are: 1. The safety and feasibility of autologous CART-19/22 in children, adolescents and young adults with a CD19+/- CD22+ relapse/ refractory disease for a r/r B-ALL. 2. The safety and feasibility of allogeneic CART-NKG2D (chimeric-antigen receptor Natural-killer group 2, member D) in children, adolescents and young adults with r/r T-ALL.

Eligibility
Participation Requirements
Sex: All
Maximum Age: 30
Healthy Volunteers: f
View:

• ARM A: CD19+/- CD22+ B-ALL with relapsed or refractory disease not responding to conventional chemotherapy and with no other curative therapy available. Treatment with previous CART CD19 therapy is permitted, but is not mandatory, OR:

• ARM B: T-ALL with relapsed or refractory disease not responding to conventional chemotherapy and with no other curative therapy available.

• Patients diagnosed with ALL must be suitable for allogeneic HSCT and willing to proceed to transplant if the CART treatment induces complete remission and the investigator believes it is the best option.

• For ARM B there must be a suitable haploidentical donor (following local standard operating procedures).

• Lansky (age \<16 years) or Karnofsky (age ≥16 years) score of 50 or greater.

• Life expectancy greater than 12 weeks.

• Absolute neutrophil count (ANC) ≥ 500/μL unless, in the opinion of the investigator, cytopenia is due to underlying leukemia and is potentially reversible with leukemia therapy.

• Platelet count ≥ 50,000/μL unless, in the opinion of the investigator, cytopenia is due to underlying leukemia and is potentially reversible with leukemia therapy.

• Absolute lymphocyte count ≥ 100/μL.

• Adequate renal, hepatic, pulmonary, and cardiac function.

• Adequate venous access and absence of contraindications for lymphoapheresis

• Patients with a seizure disorder may be enrolled if well controlled with anticonvulsants.

• Patients or patients' legal representative, parent(s), or guardian able to provide written informed consent.

Locations
Other Locations
Spain
Hospital Universitario La Paz
RECRUITING
Madrid
Contact Information
Primary
Antonio Pérez Martínez, MD
aperezmartinez@salud.madrid.org
917 27 75 76
Time Frame
Start Date: 2025-07-08
Estimated Completion Date: 2030-12-01
Participants
Target number of participants: 10
Treatments
Experimental: Arm A
Children and young adults with CD19+/- CD22+ B-ALL with relapsed or refractory disease not responding to conventional chemotherapy and with no other curative therapy available.
Experimental: Arm B
Children and youn adults with T-ALL with relapsed or refractory disease not responding to conventional chemotherapy and with no other curative therapy available.
Sponsors
Leads: Instituto de Investigación Hospital Universitario La Paz

This content was sourced from clinicaltrials.gov

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