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Fixed-Duration Glofitamab Approved in Europe for Relapsed/Refractory DLBCL

The European Commission has granted conditional marketing authorization to glofitamab for fixed-duration administration in adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) following 2 or more lines of systemic treatment. ....

Michael Dickinson , Genentech Columvi , European Commission , Peter Maccallum Cancer Centre , Royal Melbourne Hospital ,

Columvi Approved for Relapsed or Refractory DLBCL or LBCL

Columvi (glofitamab) has accelerated approval for relapsed/refractory DLBCL not otherwise specified or LBCL arising from follicular lymphoma. ....

Genentech Columvi , Drug Administration , Accessed June ,

FDA approves off-the-shelf bispecific antibody cancer therapy

The US Food and Drug Administration (FDA) has approved the first bispecific antibody with a fixed-duration treatment in DLBCL. ....

Genentech Columvi , Levi Garraway , Drug Administration , Head Of Global Product Development , Chief Medical Officer , Global Product Development , New England Journal ,