METHODS OF DETERMINING POTENCY OF A THERAPEUTIC CELL COMPOSITION

    公开(公告)号:US20240168012A1

    公开(公告)日:2024-05-23

    申请号:US18283434

    申请日:2022-03-21

    发明人: Neil HAIG

    IPC分类号: G01N33/50

    摘要: The present disclosure relates to methods of determining potency of a therapeutic cell compositions in connection with cell therapy. The cells of the therapeutic cell composition can express recombinant receptors such as chimeric receptors, e.g., chimeric antigen receptors (CARs) or other transgenic receptors such as T cell receptors (TCRs). The methods provide an assay for identifying the potency, including relative potency, of a therapeutic cell composition.

    METHODS OF ASSESSING OR MONITORING A RESPONSE TO A CELL THERAPY

    公开(公告)号:US20240302349A1

    公开(公告)日:2024-09-12

    申请号:US18674099

    申请日:2024-05-24

    摘要: Provided are methods and articles of manufacture for use with cell therapy for the treatment of diseases or conditions, e.g., cancer, including for predicting likelihood of the subject responding to a therapy, such as a cell therapy, e.g., a chimeric antigen receptor (CAR) T cell therapy. In some aspects, the predicting is based on detecting certain biomarkers of immune cells associated with and/or that correlate with response following administration of the therapy. The methods generally involve detecting a marker by assaying a biological sample from a subject that is a candidate for treatment, optionally with a cell therapy, to determine if the subject is likely to respond to the therapy. The present disclosure also provides methods for treating a subject having a disease or condition, in some cases involving administration of the cell therapy, based on assessment the biomarker. Also provided herein are reagents and kits for performing the methods.

    METHODS OF IDENTIFYING FEATURES ASSOCIATED WITH CLINICAL RESPONSE AND USES THEREOF

    公开(公告)号:US20230178239A1

    公开(公告)日:2023-06-08

    申请号:US17924652

    申请日:2021-05-12

    IPC分类号: G16H50/20 A61K35/17 G06N20/20

    CPC分类号: G16H50/20 A61K35/17 G06N20/20

    摘要: The present disclosure relates to methods for identifying features, such as attributes of subjects, therapeutic cell compositions, and input compositions used to produce therapeutic cell compositions, associated with clinical responses of subjects, e.g., patients, following treatment with the therapeutic cell composition in connection with a cell therapy. The cells of the therapeutic cell composition express recombinant receptors such as chimeric receptors, e.g., chimeric antigen receptors (CARs) or other transgenic receptors such as T cell receptors (TCRs). The methods provide for the identification of features associated with clinical responses. In some embodiments, the methods can be used to determine (e.g., predict) a subject's response to treatment with the therapeutic cell composition.

    METHODS FOR DOSING AND TREATMENT OF FOLLICULAR LYMPHOMA AND MARGINAL ZONE LYMPHOMA IN ADOPTIVE CELL THERAPY

    公开(公告)号:US20230071910A1

    公开(公告)日:2023-03-09

    申请号:US17794245

    申请日:2021-01-22

    发明人: Thalia FARAZI

    摘要: Provided herein are methods of administering a dose of T cells for treating subjects with indolent non-Hodgkin3 s lymphoma (NHL), and related methods, compositions, uses and articles of manufacture. The cells express a recombinant receptor such as a chimeric antigen receptor (CAR) for targeting an antigen of the lymphoma, such as CD19. In some embodiments, the methods are for treating grade 1-3 A follicular lymphoma (FL 1-3 A) or marginal zone lymphoma (MZL), including in heavily pretreated or poor-prognosis subjects, such as subjects that have relapsed after treatment with, or are refractory to treatment with, one or more prior therapies.