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CompletedNCT03389035CARCIKUpdated May 6, 2023

Transposon-manipulated Allogeneic CARCIK-CD19 Cells in Pediatric and Adult Patients With r/r ALL Post HSCT

A Phase 1/2 interventional study of CARCIK-CD19 in Acute Lymphoblastic Leukemia, in Relapse, sponsored by Fondazione Matilde Tettamanti Menotti De Marchi Onlus. Completed at 2 sites in Italy. Open to participants aged 1 Year to 75 Years. Per ClinicalTrials.gov, last updated 2023-05-06.

Sponsored by Fondazione Matilde Tettamanti Menotti De Marchi Onlus · Phase 1/2, Interventional, and Treatment

Phase
Phase 1/2
Study type
Interventional
Enrollment
21
Allocation
Not applicable
Ages
1 Year to 75 Years
Sex
All
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Study summary

This is a single arm, open-label, multi-center, phase 1-2a study to determine the Maximum Tolerated Dose and/or the Recommended Phase 2 Dose and the safety of CARCIK-CD19 in adult and pediatric patients with relapsed or refractory B-cell precursor acute lymphoblastic leukemia.

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Conditions studied

  • Acute Lymphoblastic Leukemia, in Relapse

Keywords

  • Acute Lymphoblastic Leukemia
  • CAR-T
  • CARCIK
  • Transposon
03

In context

Precursor Cell Lymphoblastic Leukemia-Lymphoma

2,584 studies on the registry are indexed under Precursor Cell Lymphoblastic Leukemia-Lymphoma; 473 are open to participants now.

This study's enrollment of 21 is below the median of 40 across 1,952 interventional studies indexed under Precursor Cell Lymphoblastic Leukemia-Lymphoma.

Browse Precursor Cell Lymphoblastic Leukemia-Lymphoma studies →

Lead sponsor

Fondazione Matilde Tettamanti Menotti De Marchi Onlus is the lead sponsor of 5 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
1 Year to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Children (1-17) and adults (18-75 years old);
  • adult and pediatric B-cell precursor ALL after ;
  • Evidence of CD19 tumor expression in bone marrow and/or peripheral blood by flow cytometry;
  • Bone marrow with ≥ 5% lymphoblasts by morphologic assessment at screening;
  • No evidence of overall aGVHD > Grade I or chronic (cGVHD) greater than mild at time of enrollment and in the previous 30 days;
  • No longer taking agents for at least 30 days prior to enrollment;

Exclusion criteria

Exclusion Criteria:

  • Patients with Grades II-IV;
  • Any cell therapy in the last 30 days;
Terms in these criteria, in plain language(4)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Relapsed and refractory

Relapsed: the illness came back after treatment had worked. Refractory: it did not respond to treatment, or stopped responding while still on it.

Allogeneic and autologous transplant

Stem cell (bone marrow) transplants. Allogeneic uses cells from a donor; autologous uses your own cells, collected earlier and given back.

GVHD (graft-versus-host disease)

After a transplant from a donor, the donor’s immune cells attack the recipient’s body, often the skin, gut or liver.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

05

Study design

Phase
Phase 1 / Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Sequential assignment
Masking
None (open label)
Enrollment
21 participants (actual)

Study arms

  • Experimental
    CARCIK-CD19

    Biological: CARCIK-CD19

Interventions

  • BiologicalCARCIK-CD19

    Allogeneic (donor-derived) Cytokine Induced Killer (CIK) cells transduced with a transposon CD19 Chimeric Antigen Receptor (CAR) gene

06

What researchers measure

Primary outcomes

  1. Dose Limiting Toxicities (DLT):

    rate and severity of the cytokine release syndrome (CRS)

    Time frame: 1 month

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Study locations

2 sites
  • Ospedale PG23
    Bergamo, BG 24127, Italy
  • Fondazione MBBM
    Monza, MB 20900, Italy
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References and documents

Publications

  • Magnani CF, Gaipa G, Lussana F, Belotti D, Gritti G, Napolitano S, Matera G, Cabiati B, Buracchi C, Borleri G, Fazio G, Zaninelli S, Tettamanti S, Cesana S, Colombo V, Quaroni M, Cazzaniga G, Rovelli A, Biagi E, Galimberti S, Calabria A, Benedicenti F, Montini E, Ferrari S, Introna M, Balduzzi A, Valsecchi MG, Dastoli G, Rambaldi A, Biondi A. Sleeping Beauty-engineered CAR T cells achieve antileukemic activity without severe toxicities. J Clin Invest. 2020 Nov 2;130(11):6021-6033. doi: 10.1172/JCI138473. PubMed 32780725 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 6, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03389035
Lead sponsor
Fondazione Matilde Tettamanti Menotti De Marchi Onlus
Responsible party
Sponsor
First posted
Jan 3, 2018
Start date
Dec 20, 2017
Primary completion
Mar 31, 2021
Completion
Dec 30, 2022
Last update
May 6, 2023

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2023. You cannot join it, but the record below documents what was studied.

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