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Residual Disease Driven Strategy for CARCIK (CD19) in Adults/Pediatric BCP-ALL

Measurable Residual Disease Driven Strategy for One or Two Infusions of Non- Viral, Transposon-manipulated CARCIK (CD19) Cells: A Phase II Study in Pediatric and Adult Patients With Relapsed/Refractory B Cell Precursor ALL (BCP-ALL)

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05252403
Enrollment
35
Registered
2022-02-23
Start date
2021-12-01
Completion date
2025-03-31
Last updated
2023-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Lymphoblastic Leukemia

Keywords

ALL

Brief summary

This is a single arm, open-label, multi-center, phase II study to determine the activity and the safety of a therapeutic strategy that allows a second CARCIK-CD19 cells infusion, driven by the status of disease from one month after the first infusion, in adult and pediatric patients with r/r BCP- ALL.

Interventions

PTG-CARCIK-CD19 cells is a gene therapy medicinal product (GTMP) composed of genetically modified allogeneic T lymphocytes formulated as cell suspension in normal saline solution and freezing media

Sponsors

Fondazione Matilde Tettamanti Menotti De Marchi Onlus
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
1 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

Children (1-17) and adults (18-75 years old); * Relapsed or refractory adult and pediatric B- ALL as defined for the presence of bone marrow with ≥ 5% lymphoblasts by morphologic assessment, or if \<5%, with at least 1% of molecular disease at PCR; * Evidence of CD19 tumor expression in bone marrow and/or peripheral blood by flow cytometry; * Diagnosis of CD19 positive ALL in the bone marrow, and/or peripheral blood and/or extramedullary sites with the exclusion of Central Nervous System (CNS) if CNS-3 disease.

Exclusion criteria

* GVHD Grades II-IV for patients who had previously been transplanted; 2. Any cell therapy in the previous 30 days; * Patient with concomitant life-threatening infectious disease; * Lansky/Karnofsky score \<60; * Patients with hepatic or renal disease as specific above; * Pregnant or breast-feeding females; * Rapidly progressive disease that in the estimation of the investigator and sponsor would compromise ability to complete study therapy;

Design outcomes

Primary

MeasureTime frameDescription
To evaluate the overall response rate: change from baseline at day 28 after the first CARCIK-CD19 infusionBaseline and day 28At baseline and at Day 28 after infusion: lymphoblasts \< 5% at morphological evaluation of bone marrow aspirate
To evaluate the duration of response of patients treated with CARCIK - CD19 cells. Change from day 28 at month 2, 3, 4, 5, 6, 9 and 12Day 28 and month 2, 3, 4, 5, 6, 9 and 12Day 28 and month 2, 3, 4, 5, 6, 9 and 12: lymphoblasts \< 5% at morphological evaluation of bone marrow aspirate

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026