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    Home > Active Ingredient News > Blood System > The complete remission rate of refractory patients exceeds 30% CD37 targeted ADC combination Phase 2...

    The complete remission rate of refractory patients exceeds 30% CD37 targeted ADC combination Phase 2...

    • Last Update: 2021-06-22
    • Source: Internet
    • Author: User
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    On June 14, 2021, Debiopharm announced that its CD37-targeted antibody conjugate (ADC) naratuximab emtansine, combined with rituximab (anti-CD20 antibody), is used in the treatment of relapsed/refractory (R/R) diffuse Positive results were obtained in a phase 2 clinical trial of large B-cell lymphoma (DLBCL)


    The latest results presented at the European Hematology Association (EHA) annual meeting on June 12 showed that among refractory patients who have previously received more than two treatments, naratuximab emtansine combined with rituximab can be evaluated The objective response rate (ORR) among the patients (N=76) was 44.


    In terms of safety, the safety characteristics of the combination therapy are predictable and manageable, the rate of treatment discontinuation due to adverse events is low (8%), and the incidence of severe febrile neutropenia is low (4%)


    Naratuximab emtansine is a potentially innovative method for the treatment of patients with B-cell malignancies


    Image source: Bioconjugator, CC BY-SA 4.


    Image source: Bioconjugator, CC BY-SA 4.


    Note: The original text has been deleted

    Reference materials:

    Reference materials:

    [1] Debiopharm's CD37 Antibody Drug Conjugate Shows Promising Phase II Results for the Treatment of B-Cell Malignancies.


    [1] Debiopharm's CD37 Antibody Drug Conjugate Shows Promising Phase II Results for the Treatment of B-Cell Malignancies.


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