FDA Accepts Roche's Columvi sBLA for Expanded Use in Lymphoma
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The FDA has accepted Roche's supplemental Biologics License Application (sBLA) for Columvi, aiming to expand its use for treating second-line relapsed or refractory diffuse large B-cell lymphoma (R/R DLBCL).
December 05, 2024 | 2:45 pm
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Roche's sBLA for Columvi has been accepted by the FDA, which could expand its use for treating second-line R/R DLBCL, potentially boosting Roche's market position in oncology.
The FDA's acceptance of the sBLA is a positive regulatory development for Roche, indicating potential future revenue growth if the expanded use is approved. This could enhance Roche's competitive position in the oncology market.
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