Prognia
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🇪🇺EU · EMAAuthorisedATC: L01FX28

Columvi(Glofitamab)

Lymphoma, Large B-Cell, Diffuse

Marketing Authorisation Holder: Roche Registration GmbH

EMA Authorisation: 07/07/2023

INN: glofitamab

Indication

Columvi in combination with gemcitabine and oxaliplatin is indicated for the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma not otherwise specified (DLBCL NOS) who are ineligible for autologous stem cell transplant (ASCT).Columvi as monotherapy is indicated for the treatment of adult patients with relapsed or refractory diffuse large B cell lymphoma (DLBCL), after two or more lines of systemic therapy.

Official EMA Resources

View on EMA (ema.europa.eu)

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Medical disclaimer: This information is intended for qualified healthcare professionals. Always verify with the official EMA Summary of Product Characteristics (SmPC) before clinical use.