- ICH GCP
- Registre américain des essais cliniques
- Essai clinique 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
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Estimé)
Phase
- Phase 2
- La phase 1
Contacts et emplacements
Lieux d'étude
-
-
Minnesota
-
Minneapolis, Minnesota, États-Unis, 55455
- Recrutement
- Mark Juckett, MD
-
Contact:
- Mark Juckett, MD
- Numéro de téléphone: 612-676-4200
- E-mail: juck0001@umn.edu
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
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 d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Non randomisé
- Modèle interventionnel: Affectation séquentielle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: 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.
|
|
Expérimental: 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.
|
|
Expérimental: 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.
|
|
Expérimental: 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.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Maximum tolerated dose (MTD)
Délai: 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
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Objective response (OR)
Délai: Day 42
|
includes complete remission with or without hematologic recovery (CR or CRi) or partial remission (PR)
|
Day 42
|
|
Safety of AdaptNK
Délai: Day 42
|
measured by rate of treatment related mortality (TRM)
|
Day 42
|
Autres mesures de résultats
Mesure des résultats |
Délai |
|---|---|
|
La survie globale
Délai: 1 année
|
1 année
|
|
La survie globale
Délai: 2 ans
|
2 ans
|
|
Leukemia free survival (LFS)
Délai: 1 year
|
1 year
|
|
Leukemia free survival (LFS)
Délai: 2 year
|
2 year
|
Collaborateurs et enquêteurs
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Tumeurs
- Tumeurs par type histologique
- Maladies hématologiques
- Leucémie myéloïde
- Leucémie
- Maladies hémiques et lymphatiques
- Leucémie, myéloïde, aiguë
- Peptides
- Acides aminés, peptides et protéines
- Protéines
- Produits chimiques organiques
- Hydrocarbures
- Facteurs biologiques
- Moutards phosphoramides
- Composés de moutarde d'azote
- Composés moutarde
- Hydrocarbures, halogénés
- Phosphoramides
- Composés organophosphores
- Peptides de signalisation intercellulaire et protéines
- Cytokines
- Interleukins
- Lymphokines
- Cyclophosphamide
- Interleukine-2
- fludarabine
Autres numéros d'identification d'étude
- 2023LS005
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
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