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FDA accepts application for Roche's Columvi to treat advanced lymphoma, showing improved survival.
The FDA has accepted a new application for Roche's Columvi combined with other drugs to treat relapsed or refractory diffuse large B-cell lymphoma (DLBCL).
This follows study results showing the treatment significantly improved overall survival compared to existing treatments.
If approved by July 2025, it will be the first CD20xCD3 bispecific antibody to show a survival benefit in DLBCL in a phase III trial.
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La FDA acepta la aplicación de Roche's Columvi para tratar el linfoma avanzado, mostrando una mejor supervivencia.