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An expert panel hosted by
Customizing first-line BTK inhibitors for CLL
with Gilles Salles, Paolo Ghia, and Francesc Bosch
Wednesday, October 23, 2024
18:30-19:30 BST
This independent educational activity is supported by Pharmacyclics LLC, an AbbVie Company and Janssen Biotech. All content is developed independently by the faculty. The funder is allowed no influence on the content of this activity.
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The Biologics License Application (BLA) submitted for tafasitamab (MOR208), an anti-CD19 antibody, in combination with lenalidomide, will be given Priority Review by the United States Food & Drug Administration (FDA). The BLA is specifically for the treatment of patients with relapsed/refractory diffuse large B-cell lymphoma (DLBCL).1 The FDA previously granted tafasitamab and lenalidomide breakthrough therapy designation for R/R DLBCL in 2017. The submission was based on the results from the L-MIND trial and the RE-MIND trial1,2
Results of the L-MIND trial in R/R DLBCL
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