Genmab — Juli 2019
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Tak EL. Jeg noterede også 10% flad royalties på ofa. Er det ikke lavere end hvad de fleste analytikere har estimeret? Det er transitionen fra GSK der har kostet på royalties. Gsk vil naturligvis forsøge at få en del af deres mange udgifter tilbage
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The U.S. Food and Drug Administration (FDA) has accepted for review the Biologics License Application (BLA) for isatuximab for the treatment of patients with relapsed/refractory multiple myeloma (RRMM). The target action date for the FDA decision is April 30, 2020. Isatuximab is an investigational monoclonal antibody that targets a specific epitope on the CD38 receptor of a plasma cell.
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Hvornår forventer vi de sidste resultater for SC der skal anvendes som dokumentation til FDA?
bispecific technology platform to further the development of HMBD-004A.Hello! It looks like you're interested in this conversation, but you don't have an account yet.
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