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Glofitamab
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    Glofitamab

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    Glofitamab
    Monoclonal antibody
    Type Whole antibody
    Source Humanized
    Target CD20 and CD3
    Clinical data
    Trade names Columvi
    Other names RO7082859
    Routes of
    administration
    Intravenous
    Drug class Antineoplastic
    ATC code
    • None
    Legal status
    Legal status
    Identifiers
    CAS Number
    DrugBank
    UNII
    KEGG
    Chemical and physical data
    Formula C8632H13326N2296O2701S58
    Molar mass 194344.41 g·mol−1

    Glofitamab, sold under the brand name Columvi is a bispecific monoclonal antibody used for the treatment of diffuse large B-cell lymphoma.

    It was approved for medical use in Canada in March 2023.

    Society and culture

    Legal status

    On 26 April 2023, the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) adopted a positive opinion, recommending the granting of a conditional marketing authorization for the medicinal product Columvi, intended for the treatment of diffuse large B‑cell lymphoma (DLBCL). The applicant for this medicinal product is Roche Registration GmbH.

    Names

    Glofitamab is the international nonproprietary name.

    Further reading

    External links

    • Clinical trial number NCT03075696 for "A Dose Escalation Study of Glofitamab (RO7082859) as a Single Agent and in Combination With Obinutuzumab, Administered After a Fixed, Single Pre-Treatment Dose of Obinutuzumab in Participants With Relapsed/Refractory B-Cell Non-Hodgkin's Lymphoma" at ClinicalTrials.gov



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