- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT06541405
Sécurité et efficacité du NK520 pour traiter la leucémie myéloïde aiguë récidivante/réfractaire pédiatrique
Une étude exploratoire ouverte et monocentrique pour évaluer l'innocuité et l'efficacité du NK520 chez les patients pédiatriques atteints de leucémie myéloïde aiguë récidivante/réfractaire
This study will evaluate the safety and efficacy of NK520 in the treatment of pediatric relapsed/refractory acute myeloid leukemia. NK520 will be administered by intravenous injection. The safety and efficacy of this treatment will be evaluated.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
This open label, single-arm study aims to evaluate the efficacy and safety of allogenic natural killer (NK) cells in pediatric relapsed/refractory acute myeloid leukemia. Allogenic NK cells will be infused once a week. After infusion, the investigators will observe the characteristics of dose limited toxicity (DLT), and determine the maximum tolerable dose(MTD). To provide basis for the dosage and treatment plan of cell products in follow-up clinical trials.
Type d'étude
Inscription (Réel)
Phase
- Première phase 1
Contacts et emplacements
Lieux d'étude
-
-
Shanghai Municipality
-
Shanghai, Shanghai Municipality, Chine, 200127
- Shanghai Children Medical Center
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
- Participants must be between 6 and 18 years;
- Diagnostic Criteria: Meet the 2022 World Health Organization (WHO) diagnostic criteria for acute myelocytic leukemia (AML), unsuitable for current treatments or patients with relapsed/refractory AML after ≥2 lines of therapy. The definition of relapsed/refractory acute myeloid leukemia is based on the 2017 Chinese Guidelines for Diagnosis and Treatment: a. Relapsed AML: Diagnosis is confirmed when leukemia cells reappear in the peripheral blood or bone marrow blast cells exceed 5% after complete remission (CR) (excluding reasons such as bone marrow regeneration post-consolidation chemotherapy) or there is extramedullary infiltration by leukemia cells; b. Refractory AML: Initial cases unresponsive after two cycles of standard regimen treatment; recurrence within 12 months after CR and consolidation therapy; recurrence beyond 12 months with ineffectiveness of conventional chemotherapy; those who have relapsed twice or more; or persistent extramedullary leukemia;
- For participants under 16 years old, Lansky performance status must be ≥50%; for participants aged 16 or older, Karnofsky performance status must be ≥50%;
- Expected survival of at least 12 weeks;
- Normal Organ Function.
Exclusion Criteria:
-
Acute promyelocytic leukemia, chronic myeloid leukemia, acute mixed lineage leukemia, or known central nervous system leukemia;
-
AML associated with congenital syndromes, such as Down syndrome, Fanconi anemia, Bloom syndrome, Kostmann syndrome, or congenital aplastic anemia;
-
Severe bleeding tendency or coagulation disorders, or currently receiving thrombolytic therapy;
-
Human immunodeficiency virus (HIV)-infected individuals, or individuals with known active syphilis infection;
-
Receipt of live attenuated vaccines within 2 weeks before the first dose or planned during the study period;
-
Participation in another clinical trial and receipt of investigational drug within 4 weeks prior to the first dose;
-
Receipt of immune-modulatory drugs (including thymosin, interferons, except for local use to manage conditions like pleural or ascites fluid) within 2 weeks before the first dose;
-
At screening, positive hepatitis B or C viral markers as follows:
- Hepatitis B surface antigen (HBsAg) positive with serum hepatitis B virus-deoxyribonucleic acid (HBV-DNA) level ≥1×10^3 copies/mL or above normal range;
- Positive for hepatitis C virus (HCV) antibodies;
-
Any other condition or situation in which the investigator deems the patient unsuitable for participation in this study.
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: Group A(low-dose group)
NK520: 5x10^7 NK/kg |
The number of NK520 cell infused for each dosing should be calculated base on the body weight of subject. NK520 will be administered through intravenous infusion.
Autres noms:
|
|
Expérimental: Group B(medium-dose group)
NK520: 1.5×10^8NK/kg |
The number of NK520 cell infused for each dosing should be calculated base on the body weight of subject. NK520 will be administered through intravenous infusion.
Autres noms:
|
|
Expérimental: Group C(high-dose group)
NK520: 3×10^8NK/kg |
The number of NK520 cell infused for each dosing should be calculated base on the body weight of subject. NK520 will be administered through intravenous infusion.
Autres noms:
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Dose-Limiting Toxicity
Délai: From the first infusion of NK520 to 4 weeks after last infusion of NK520
|
To evaluate the DLT during N520 treatment |
From the first infusion of NK520 to 4 weeks after last infusion of NK520
|
|
Complete Response Rate (CRR)
Délai: from the date of first infusion of NK510 up to 104 weeks
|
Effectiveness Metrics |
from the date of first infusion of NK510 up to 104 weeks
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Overall response rate (ORR)
Délai: from the date of first infusion of NK510 up to 104 weeks
|
Effectiveness Metrics |
from the date of first infusion of NK510 up to 104 weeks
|
|
Duration of Response (DOR)
Délai: From the date of enrollment up to 104 weeks
|
Effectiveness Metrics |
From the date of enrollment up to 104 weeks
|
|
Event-Free Survival (EFS)
Délai: From date of enrollment up to 104 weeks, or progression, or date of death, whichever came first.
|
Effectiveness Metrics |
From date of enrollment up to 104 weeks, or progression, or date of death, whichever came first.
|
|
Overall Survival (OS)
Délai: From date of enrollment up to 104 weeks, or date of death, whichever came first.
|
Effectiveness Metrics |
From date of enrollment up to 104 weeks, or date of death, whichever came first.
|
Collaborateurs et enquêteurs
Parrainer
Collaborateurs
Les enquêteurs
- Chercheur principal: wenting Hu, Shanghai children's medical center
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
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
Autres numéros d'identification d'étude
- NK520-01
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
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
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .