- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07591649
Adapt NK for High Risk Myeloid Diseases as Bridge to Allo HSCT
Safety and Efficacy of Expanded KIR-HLA Mismatched Natural Killer Cell Immunotherapy (AdaptNK) for High-Risk Myeloid Diseases as Bridge to Allogeneic Hematopoietic Stem Cell Transplantation
Descripción general del estudio
Estado
Intervención / Tratamiento
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 2
- Fase 1
Contactos y Ubicaciones
Ubicaciones de estudio
-
-
Minnesota
-
Minneapolis, Minnesota, Estados Unidos, 55455
- Reclutamiento
- Mark Juckett, MD
-
Contacto:
- Mark Juckett, MD
- Número de teléfono: 612-676-4200
- Correo electrónico: juck0001@umn.edu
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- 18-74 years with Karnofsky score ≥ 70%
- 75 years and older: KPS ≥ 70%, HCT-CI < 5 (excluding history of solid tumor), AND not frail by Fried frailty criteria (see Appendix III)
- HLA type C1/C1 or C2/C2
Note: For easy determination, the definition of HLA-C ligand group assigments is included below:
HLA-C1 group alleles are defined as HLA-C01, C03, C07, C08, C12, C14, C16 HLA-C2 group alleles are defined as HLA-C02, C04, C05, C06, C15, C17, C18
- adequate liver, renal, pulmonary and cardiac function
- ability to be off glucocorticoids and other immunosuppressive medications indicated for acute or chronic GVHD for at least 28 days prior to the AdaptNK cell infusion
- There must be sufficient time between the most recent therapy and the screening bone marrow as delineated below:
- anti-leukemic systemic cytotoxic chemotherapy - 2 weeks
- Targeted anti-leukemic agents (FLT-3, IDH, menin inhibitors) - 3 half-lives of the medication
- Radiotherapy - 1 week
- donor lymphocyte infusions - 6 weeks
- hematopoietic growth factors (filgrastim, TPO agonists, EPO) - 1 week
- biologic therapy (monoclonal antibodies, T-cell engagers) - 2 weeks
- Immune effector cellular therapy - 4 weeks
- Intrathecal chemotherapy for treatment of active CNS leukemia - there must be at least two CSF samples negative for leukemia separated by one week before enrollment.
- WBC shall be < 25,000 before infusion. Hydroxyurea is permitted until day -3 to control excess blast proliferation. No other systemic treatment is allowed after the screening bone marrow is performed for inclusion in protocol
- All prior treatment related toxicities should have resolved to ≤ grade 1 prior to study enrollment
- agrees to use of adequate contraception from study enrollment to 4 months after cell infusion
- voluntary written consent
Exclusion Criteria:
- Myeloid neoplasms with known or strongly suspected germline background, except DDX41, TP53, or RUNX1.
- Acute promyelocytic leukemia (APL)
- myocardial infarction (MI) within previous 6 months of study enrollment
- pregnant or breastfeeding
- Active CNS involvement with AML
- new or progressive pulmonary infiltrates
- active autoimmune disease requiring immunosuppressive therapy
- Preexisting inflammatory disease requiring immunosuppressive therapy
- history of severe asthma and currently on chronic systemic medications
- HIV-1/2 positivity or hepatitis C/B
- active systemic infections requiring anti-infective treatment
- received any investigational agent within the 14 days before the start of study treatment (1st dose of fludarabine)
- Patients with second malignancies are excluded if they have required systemic cytotoxic chemotherapy within 1 year or if they are not in remission
- Exception: patients that are on stable dosing of hormonal therapy (e.g. aromatase inhibitor or antiandrogen therapy) for active breast or prostate cancer for 1 year are eligible.
- Patients with excised basal cell or squamous cell carcinoma of the skin are eligible.
- Patients with excised carcinoma in situ of the cervix or breast are eligible.
- Patients with untreated T1a or T1b prostate cancer are eligible.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: No aleatorizado
- Modelo Intervencionista: Asignación Secuencial
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Dose Level Cohort -1
Safety dose level.
< 1 x 10^8 Total Nucleated Cells (TNC) of AdaptNK product administered intravenously (IV).
|
The NK cell product is comprised of peripheral blood (PB) leukocytes sourced from a cryopreserved pool. of third-party donors that are seropositive for cytomegalovirus (CMV+), have NK cells expressing >20% NKG2C and >30% single-self KIR and depleted from CD3+ (T-lymphocytes) and CD19+ (B-lymphocytes) cells.
25 mg/kg administered on days -6, -5, -4, -3 and -2.
Part of Lymphodepleting conditioning chemotherapy regimen.
60 mg/kg administered on days -5 and -4.
Part of Lymphodepleting conditioning chemotherapy regimen.
IL-2 at 6 million IU subcutaneously (SC) every other day (EOD) for 3 doses with Dose 1 on Day 0 (no sooner than 4 hours post cell infusion) with the last dose no later than Day +8.
|
|
Experimental: Dose Level Cohort 1
2.4 - 3 x 10^8 Total Nucleated Cells (TNC) of AdaptNK product administered intravenously (IV).
|
The NK cell product is comprised of peripheral blood (PB) leukocytes sourced from a cryopreserved pool. of third-party donors that are seropositive for cytomegalovirus (CMV+), have NK cells expressing >20% NKG2C and >30% single-self KIR and depleted from CD3+ (T-lymphocytes) and CD19+ (B-lymphocytes) cells.
25 mg/kg administered on days -6, -5, -4, -3 and -2.
Part of Lymphodepleting conditioning chemotherapy regimen.
60 mg/kg administered on days -5 and -4.
Part of Lymphodepleting conditioning chemotherapy regimen.
IL-2 at 6 million IU subcutaneously (SC) every other day (EOD) for 3 doses with Dose 1 on Day 0 (no sooner than 4 hours post cell infusion) with the last dose no later than Day +8.
|
|
Experimental: Dose Level Cohort 2
0.8 - 1 x 10^9 Total Nucleated Cells (TNC) of AdaptNK product administered intravenously (IV).
|
The NK cell product is comprised of peripheral blood (PB) leukocytes sourced from a cryopreserved pool. of third-party donors that are seropositive for cytomegalovirus (CMV+), have NK cells expressing >20% NKG2C and >30% single-self KIR and depleted from CD3+ (T-lymphocytes) and CD19+ (B-lymphocytes) cells.
25 mg/kg administered on days -6, -5, -4, -3 and -2.
Part of Lymphodepleting conditioning chemotherapy regimen.
60 mg/kg administered on days -5 and -4.
Part of Lymphodepleting conditioning chemotherapy regimen.
IL-2 at 6 million IU subcutaneously (SC) every other day (EOD) for 3 doses with Dose 1 on Day 0 (no sooner than 4 hours post cell infusion) with the last dose no later than Day +8.
|
|
Experimental: Dose Level Cohort 3
2.4 - 3 x 10^9 Total Nucleated Cells (TNC) of AdaptNK product administered intravenously (IV).
|
The NK cell product is comprised of peripheral blood (PB) leukocytes sourced from a cryopreserved pool. of third-party donors that are seropositive for cytomegalovirus (CMV+), have NK cells expressing >20% NKG2C and >30% single-self KIR and depleted from CD3+ (T-lymphocytes) and CD19+ (B-lymphocytes) cells.
25 mg/kg administered on days -6, -5, -4, -3 and -2.
Part of Lymphodepleting conditioning chemotherapy regimen.
60 mg/kg administered on days -5 and -4.
Part of Lymphodepleting conditioning chemotherapy regimen.
IL-2 at 6 million IU subcutaneously (SC) every other day (EOD) for 3 doses with Dose 1 on Day 0 (no sooner than 4 hours post cell infusion) with the last dose no later than Day +8.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Maximum tolerated dose (MTD)
Periodo de tiempo: 1 year
|
The primary objective of the study is to assess the safety and determine the maximum tolerated dose (MTD) of AdaptNK administered as a single infusion intravenously (IV) to KIR-HLA mismatched patients with relapsed or refractory AML.
|
1 year
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Objective response (OR)
Periodo de tiempo: Day 42
|
includes complete remission with or without hematologic recovery (CR or CRi) or partial remission (PR)
|
Day 42
|
|
Safety of AdaptNK
Periodo de tiempo: Day 42
|
measured by rate of treatment related mortality (TRM)
|
Day 42
|
Otras medidas de resultado
Medida de resultado |
Periodo de tiempo |
|---|---|
|
Sobrevivencia promedio
Periodo de tiempo: 1 año
|
1 año
|
|
Sobrevivencia promedio
Periodo de tiempo: 2 años
|
2 años
|
|
Leukemia free survival (LFS)
Periodo de tiempo: 1 year
|
1 year
|
|
Leukemia free survival (LFS)
Periodo de tiempo: 2 year
|
2 year
|
Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
- Neoplasias
- Neoplasias por tipo histológico
- Enfermedades hematológicas
- Leucemia Mieloide
- Leucemia
- Enfermedades hemic y linfáticas
- Leucemia Mieloide Aguda
- Péptidos
- Aminoácidos, péptidos y proteínas
- Proteínas
- Químicos orgánicos
- Hidrocarburos
- Factores biológicos
- Mostaza de fosforamida
- Compuestos de mostaza de nitrógeno
- Compuestos de mostaza
- Hidrocarburos, halogenados
- Fosforamidas
- Compuestos organofosforados
- Péptidos de señalización intercelular y proteínas
- Citocinas
- Interleucina
- Linfocinas
- Ciclofosfamida
- Interleucina-2
- fludarabina
Otros números de identificación del estudio
- 2023LS005
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .