Genmab — November 2018
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Kan være vi får nyt allerede på onsdag. Om morgenen offentliggøres LBA-titler. Hvis Maia (og Cassiopeia) er med, udsender Genmab sikkert en meddelelse herom. I den meddelelse kunne de passende oplyse om Janssen har søgt RTOR, og muligvis ved de allerede nu om det er bevilget.
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Hvor meget hjælper d
et reelt hvis der er bevilget RTOR? Der er jo stadig mangel på infusionsstole! -
På CC talte han om split dosing som en overgang til sc, som allerede har hjulpet en del, og vil fortsætte at gøre det når det godkendes. infusion chair availability, Wimal, right now is a bottleneck for daratumumab. And then to bridge the time between now and the subcu co-formulation with high (inaudible) days, don't forget that Janssen has also filed for a split dosing of the first infusion.
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that process is now going quite rapidly both in Europe and in the U.S., so we hope that we actually get quite quickly a label for the split dosing, and that's already helped, I think, to further boost the use of daratumumab, but the subcu will be a game changer, we believe.
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Om accellereret infusion: What we understand is that in some centers, like the bigger medical centers in the U.S., they are using for the third infusion and further the very quick 90-minute infusion rate. Janssen can, of course, not promote for that because it's not in the label. But we understand that only in the largest centers, James, it's being used as we speak, but not in the community health care centers, where actually the majority of the multiple myeloma patients are treated in the US.
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