echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Medical News > Medicines Company News > Data from the obutinib combined with RCHOP treatment with primary extranodal initial treatment non-GCB subtype DLBCL were selected for the 2022 ESMO Oral Report

    Data from the obutinib combined with RCHOP treatment with primary extranodal initial treatment non-GCB subtype DLBCL were selected for the 2022 ESMO Oral Report

    • Last Update: 2022-09-14
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com

    From September 9 to 13, 2022, the 2022 European Society of Oncology (ESMO) Annual Conference will be held


    Selected Study: Osbutinib plus RCHOP in patients with extranodal non-proliferative center B-cell-like (non-GCB) diffuse large B-cell lymphoma (DLBCL) with primary extranodal treatment

    Orelabrutinib Plus RCHOP for Previously Untreated Non-Germinal Center B-Cell-like (GCB) Diffuse Large B-Cell Lymphoma (DLBCL) Patients with Extranodal Disease

    Presentation format: Short oral presentation

    Abstract code: 627MO

    Report Author: Wang Mingyue (Affiliated Cancer Hospital of Guangxi Medical University)

    Corresponding Author: Cen Hong (Affiliated Cancer Hospital of Guangxi Medical University)

    Reporting time: 12 September, 15:15 - 15:20 (CST)

    At present, Nuocheng Jianhua has a deep layout


    A registration study of the first-line treatment of oboutinib with DLBCL MCD subtypes has been initiated


    2022 The American Society of Clinical Oncology (ASCO) publishes a real-world study of oboutinib for the treatment of DLBCL, and for patients with the MCD subtype of DLBCL, the olibutinib combination therapy regimen has shown encouraging efficacy and good tolerability


    From first-line to second-line and above treatment of DLBCL, the company has a combination of multiple drugs including osbutinib, tafasitamab, ICP-B02, and ICP-490 to provide more and better treatment options


    About obertinib

    Olibutinib is a class 1 new drug developed by Noble Jianhua, which is a highly selective new BTK inhibitor designed to be used in the treatment of lymphoma and autoimmune diseases


    Obutinib was conditionally approved in China on 25 December 2020 for the treatment of relapsed/refractory chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL) and relapsed/refractory sleeve lymphoma (MCL).


    In addition, multicenter, multi-indication clinical trials


    Opoutinib also conducts clinical trials


    Obutinib was awarded Breakthrough Therapy Designation by the U.


    A global Phase II clinical study of osbutinib for multiple sclerosis (MS) and a clinical trial in China for the treatment of systemic lupus erythematosus (SLE), primary immune thrombocytopenia (ITP) and neuromyelitis optic disease (NMOSD) are being evaluated


    From September 9 to 13, 2022, the 2022 European Society of Oncology (ESMO) Annual Conference will be held


    Selected Study: Osbutinib plus RCHOP in patients with extranodal non-proliferative center B-cell-like (non-GCB) diffuse large B-cell lymphoma (DLBCL) with primary extranodal treatment

    Selected Study: Osbutinib plus RCHOP in patients with extranodal non-proliferative center B-cell-like (non-GCB) diffuse large B-cell lymphoma (DLBCL) with primary extranodal treatment

    Orelabrutinib Plus RCHOP for Previously Untreated Non-Germinal Center B-Cell-like (GCB) Diffuse Large B-Cell Lymphoma (DLBCL) Patients with Extranodal Disease

    Presentation format: Short oral presentation

    Abstract code: 627MO

    Report Author: Wang Mingyue (Affiliated Cancer Hospital of Guangxi Medical University)

    Corresponding Author: Cen Hong (Affiliated Cancer Hospital of Guangxi Medical University)

    Reporting time: 12 September, 15:15 - 15:20 (CST)

    At present, Nuocheng Jianhua has a deep layout


    A registration study of the first-line treatment of oboutinib with DLBCL MCD subtypes has been initiated


    2022 The American Society of Clinical Oncology (ASCO) publishes a real-world study of oboutinib for the treatment of DLBCL, and for patients with the MCD subtype of DLBCL, the olibutinib combination therapy regimen has shown encouraging efficacy and good tolerability


    From first-line to second-line and above treatment of DLBCL, the company has a combination of multiple drugs including osbutinib, tafasitamab, ICP-B02, and ICP-490 to provide more and better treatment options


    About obertinib

    About obertinib

    Olibutinib is a class 1 new drug developed by Noble Jianhua, which is a highly selective new BTK inhibitor designed to be used in the treatment of lymphoma and autoimmune diseases
    .

    Obutinib was conditionally approved in China on 25 December 2020 for the treatment of relapsed/refractory chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL) and relapsed/refractory sleeve lymphoma (MCL).

    At the end of 2021, olibutinib was included in national health insurance to benefit more lymphoma patients
    .

    In addition, multicenter, multi-indication clinical trials
    with olibutinib as a stand-alone or combination are being conducted in China and the United States.

    Opoutinib also conducts clinical trials
    in China for the treatment of marginal lymphoma (MZL), central nervous system lymphoma (CNSL), fahrenhet macroglobulinemia (WM), and diffuse large B-cell lymphoma (DLBCL).

    Obutinib was awarded Breakthrough Therapy Designation by the U.
    S.
    Food and Drug Administration (FDA) for the treatment of relapsed/refractory studdle lymphoma (R/R MCL
    ).

    A global Phase II clinical study of osbutinib for multiple sclerosis (MS) and a clinical trial in China for the treatment of systemic lupus erythematosus (SLE), primary immune thrombocytopenia (ITP) and neuromyelitis optic disease (NMOSD) are being evaluated
    .

    This article is an English version of an article which is originally in the Chinese language on echemi.com and is provided for information purposes only. This website makes no representation or warranty of any kind, either expressed or implied, as to the accuracy, completeness ownership or reliability of the article or any translations thereof. If you have any concerns or complaints relating to the article, please send an email, providing a detailed description of the concern or complaint, to service@echemi.com. A staff member will contact you within 5 working days. Once verified, infringing content will be removed immediately.

    Contact Us

    The source of this page with content of products and services is from Internet, which doesn't represent ECHEMI's opinion. If you have any queries, please write to service@echemi.com. It will be replied within 5 days.

    Moreover, if you find any instances of plagiarism from the page, please send email to service@echemi.com with relevant evidence.