NCT04959903PHASE1, PHASE2Recruiting
Safety and Efficacy of SMART101 in Pediatric and Adult Patients With Hematological Malignancies After T Cell Depleted Allo-HSCT
Smart Immune SAS
Start Date
3/31/2022
Completion Date
5/1/2027
Summary
The purpose of this study is to evaluate the safety and the efficacy of SMART101 (Human T Lymphoid Progenitor (HTLP)) injection to accelerate immune reconstitution after T cell depleted allogeneic hematopoietic stem cell transplantation (HSCT) in adult and pediatric patients with hematological malignancies.
Eligibility Criteria
Age Range: No minimum to No maximum
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
Interventions
BIOLOGICAL
Allogeneic T cell progenitors, cultured ex-vivo
Conditions
Hematological Malignancies
Locations
Memorial Sloan Kettering Cancer Center (MSKCC)
New York, New York 10065
United States