Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 7:45 PM
Ignite Modification Date:
2025-12-24 @ 7:45 PM
NCT ID:
NCT04959903
Eligibility Criteria:
Inclusion Criteria:
Group A (adults):
1. Adult patients affected by:
* Acute leukemia (AML, ALL) defined as:
* Acute Myeloid Leukemia (AML):
* High risk AML in CR1; any adverse genetic abnormality, secondary or therapy related AML excluding good risk genetic abnormalities
* Chemo-refractory relapse (MRD+)
* ≥ CR2
* Acute Lymphoblastic Leukemia (ALL):
* Chemo-refractory relapse (MRD+)
* High risk ALL in CR1; Philadelphia (like) or any poor risk feature
* ≥ CR2
* Acute leukemia of ambiguous lineage:
* ≥ CR1 with a minimal residual disease (MRD) \<5% (flow cytometry, molecular and/or cytogenetics accepted)
* Myelodysplastic Syndrome (MDS) with least one of the following:
* Revised International Prognostic Scoring System risk score of intermediate or higher at the time of transplant evaluation.
* Life-threatening cytopenia.
* Karyotype or genomic changes that indicate high risk for progression to acute myelogenous leukemia, including abnormalities of chromosome 7 or 3, mutations of TP53, or complex or monosomal karyotype.
* Therapy related disease or disease evolving from other malignant processes.
2. Patient eligible for a T-depleted allogeneic HSCT
3. Age ≥ 18y and clinical condition compatible with allogeneic stem cell transplantation
4. Karnofsky index ≥ 70% prior to conditioning regimen
5. Patients with normal organ function prior to conditioning regimen
Group B (pediatrics):
1. Pediatric patients affected by acute leukemia defined as:
* Acute Myeloid Leukemia (AML):
* High risk AML in CR1; any adverse genetic abnormality, secondary or therapy related AML excluding good risk genetic abnormalities,
* Chemo-refractory relapse (MRD+)
* ≥ CR2
* Acute Lymphoblastic Leukemia (ALL):
* Chemo-refractory relapse (MRD+)
* High risk ALL in CR1; Philadelphia (like) or any poor risk feature
* ≥ CR2
* Acute leukemia of ambiguous lineage:
* ≥ CR1 with a minimal residual disease (MRD) \<5% (flow cytometry, molecular and/or cytogenetics accepted)
2. Patient eligible for a T-depleted allogeneic HSCT
3. Age \< 18y at the time of inclusion
4. Absence of a matched sibling donor (MSD)
5. Lansky ≥ 70% / Karnofsky performance status ≥ 70% prior to conditioning regimen
6. Patients with normal organ function prior to conditioning regimen
Exclusion Criteria:
Groups A and B:
1. Use of an HLA matched Cord Blood (8/8 allele matched) or haploidentical donor
2. Prior therapy with allogeneic stem cell transplantation
3. Treatment with another cellular therapy within one month before inclusion
Healthy Volunteers:
False
Sex:
ALL
Study:
NCT04959903
Study Brief:
Protocol Section:
NCT04959903