
Medical Device R&D and Manufacturer
Johnson & Johnson asMMThe leader in the field has almost monopolized the relevant therapies in this area, but Johnson & Johnson is not satisfied with the status quo and has begun to expand into other hematological tumors.2023Year5Month2Day,Johnson & Johnson andCBMG Reaches Global Exclusive Cooperation to Jointly Develop and Commercialize Next-Generation NovelCAR-TCell Therapy ProductsC-CAR039(TargetedCD19/CD20) andC-CAR066(TargetedCD20), used for the treatment of non-Hodgkin lymphoma(NHL)。In this year'sEHAAt the meeting, Johnson & Johnson disclosedJNJ-90014496(C-CAR039) TreatmentR/R LBCLClinical data.
C-CAR039For the new second generation4-1BBDual-targetCAR-TProducts that can act simultaneously onCD19AndCD20Dual targets, can continuously clear in vivoCD19/CD20Single-positive or double-positive tumor cells. In China,C-CAR039InLBCLIn the treatment of,4The annual follow-up results showed a complete remission rateCRFor86%,4Year'sOSFor67%,4Year'sPFSFor53%。

Johnson & Johnson's disclosure this time isC-CAR039TreatmentR/R LBCLGlobal1bPhase Clinical Study, Globally8Country31A total of clinical centers recruited51Conduct research on different doses and drug efficacy for patients.The three dose groups are respectively2 M(Million)/kg,150 MAnd75 M, and it has been confirmed so far75 MForRP2DDose。
In terms of safety,All patients experienced treatment-related side effects, among which inRP2DIn the dosage group,84%Patients experience3-4Grade side effects, with the main side effect being neutropenia,CRS,Thrombocytopenia, anemia, fatigue, diarrhea, infection, etc. ForCRSSide effects,RP2DIn the dose group88%The incidence rate, but all are1~2Level
Neurotoxicity,16%Occurred in patientsICANSSide effects, among which8%For3Level reaction; and inRP2DIn the dose group8%Patients experienceICANSSide effects, including4%For3Grade reaction.
In terms of efficacy: All patients,OverallORRFor91%, among which75%of patients reachedCR, and inRP2DIn the dose group, overallORRFor100%, among which77%of patients reachedCR.RP2DFurther analysis of the treatment effects in the dose group patients who had previously received1Among patients undergoing line therapy, overallORRFor100%,CRRate is80%, and have received ≥2Among patients receiving line therapy,ORRFor92%,CRFor75%。
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