A Phase 1-2 Study to Evaluate the Safety and Efficacy of IM19 CAR-T Cells in Patients With Relapsed and Refractory (R/R) B-cell Acute Lymphoblastic Leukemia
IM19 CAR-T cells
Lymphome de Burkitt+16
+ Infections par virus ADN
+ Maladies Hématologiques
Étude thérapeutique
Résumé
Date de début de l'étude : 1 avril 2022
Date à laquelle le premier participant a commencé l'étude.This is a phase I/II, open-label, multicenter study to assess the efficacy and safety of IM19 CAR-T cells in R/R B-cell Acute Lymphoblastic Leukemia
Protocole
Cette section fournit des détails sur le plan de l'étude, y compris la manière dont l'étude est conçue et ce qu'elle évalue.58 participants à inclure
Nombre total de participants que l'essai clinique vise à recruter.Traitement
Éligibilité
Les chercheurs recherchent des patients correspondant à une certaine description appelée critères d'éligibilité : état de santé général ou traitements antérieurs du patient.Tout sexe
Le sexe biologique des participants éligibles à s'inscrire.De 3 à 25 ans
Tranche d'âge des participants éligibles à participer.Volontaires sains non autorisés
Indique si les individus en bonne santé et ne présentant pas la condition étudiée peuvent participer.Conditions
Pathologie
Critères
Inclusion Criteria: * Relapsed or refractory B-ALL, defined as: 1. Not chieving a CR after 1 cycle of standard chemotherapy for relapsed leukemia. 2. Any relapse after HSCT and must be ≥ 6 months from HSCT at the time of IM19 CAR-T cells infusion. 3. Primary refractory as defined by not achieving a CR after 2 cycles of a standard chemotherapy regimen. * Patients with Ph+ ALL are eligible if they are intolerant to or have failed two lines of TKI ± chemotherapy ;Ph + all patients with T315I mutation are not required to receive at least two TKI ± chemotherapy in the absence of effective TKI therapy; * Morphological evidence of disease in bone marrow (at least 5% blasts). * Aged 3 to 25 years, either sex; * Estimated life expectancy \>3 months; * ECOG performance status of 0 or 1(age ≥ 16 years) or Lansky (age \< 16 years) performance status ≥ 50; * Women of childbearing age who had a negative blood pregnancy test before the start of the trial and agreed to take effective contraceptive measures during the trial period until the last follow-up; male subjects with fertility partners agreed to take effective contraceptive measures during the trial period until the last follow-up; * Adequate organ function; * Volunteer to participate in this trial and sign on the informed consent. Exclusion Criteria: * Isolated extramedullary disease relapse; * Burkitt's lymphoma; * Patient has obvious symptoms of central nervous system invasion and needs targeted treatment; * Patient has previously received gene product therapy; * Patients have graft-versus-host response(GVHD) and need to use immunosuppressants; Or GVHD ≥ grade 2 or being treated with anti GVHD; Or suffering from autoimmune diseases; * Patient received chemotherapy or radiotherapy within 3 days before leukapheresis * Patient used systemic steroids within 5 days before leucapheresis, except those who were recently or currently using inhaled steroids; * Patients who used drugs to stimulate the production of bone marrow hematopoietic cells within 5 days before leucapheresis; * Patients have participated in other clinical studies within 1 month before screening or plan to participate in other drug clinical trials during this study; * Patient received allogeneic cell therapy within 6 weeks before CAR-T cell infusion, such as donor lymphocyte infusion(DLI); * History or presence of CNS disorder, such as epilepsy, epileptic seizures, cerebrovascular disease (ischemia / hemorrhage / cerebral infarction), brain edema, reversible posterior white matter encephalopathy, paralysis, aphasia, stroke, severe brain injury, dementia, Parkinson's disease, cerebellar disease, cerebral organic syndrome or mental disease; * Patients has HBV, HCV, HIV ,EBV,ECV or syphilis infection at the time of screening; * Pregnant or lactating, or planning pregnancy within 180 days after the end of CAR-T cells infusion, or male patients whose partners plan pregnancy 180 days after their CAR-T cell infusion; * Patients with other tumors in the past 5 years; * Within 14 days before enrollment, there were active or uncontrollable infections requiring systemic treatment.
Plan de l'étude
Découvrez tous les traitements administrés dans cette étude, leur description détaillée et ce qu'ils impliquent.Un seul groupe d'intervention est désigné dans cette étude
Cette étude ne comporte pas de groupe placebo.
Groupes de traitement
Groupe I
ExpérimentalObjectifs de l'étude
Objectifs principaux
Objectifs secondaires