Genmab — April 2019
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- Supplemental new drug application (sNDA) submitted in Japan for
daratumumab in combination with lenalidomide and dexamethasone as
treatment for patients newly diagnosed with multiple myeloma who are
not candidates for high-dose chemotherapy and autologous stem cell
transplant - Submission based on data from Phase III MAIA study
- Supplemental new drug application (sNDA) submitted in Japan for
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Ja men det kræver også at der vitterlig er så mange muligheder i Genmab præklinik, hvilket vi helt konkret ikke ved ret meget om - vi ved blot løst at der er >20 prækliniske kandidater inklusive partnernes kandidater. Det kan være hvad som helst i princippet
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De fleste af disse fase I studier er open label, så det er jeg også overbevist om at han gør - og generelt så synes jeg markedet undervurderer en smule, at bare det at studierne skrider rimeligt hurtigt fremad er af stor værdi. Stofferne er så potente at det mest af alt er safety siden man skal være nervøs for i første omgang
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