Genmab — Maj 2020
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OPTAKT TIL GENMABS KVARTALSREGNSKAB https://lifescience.ugebrev.dk/selskabsanalyser/optakt-til-genmabs-kvartalsregnskab/
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Bispecific Antibody Market Opportunity, Drug Sales & Clinical Trials Insight 2026 https://www.openpr.com/news/2032028/bispecific-antibody-market-opportunity-drug-sales-clinical
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En gammel patient fortælling om Amivantamab https://www.inspire.com/groups/american-lung-association-lung-cancer-survivors/discussion/jnj-372-cycle-2-and-beyond/?page=11
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Heller ikke jeg
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Patienthistorien og kommentarer til Amivantamab (18:26) er interessant. Noget giftigt stads, men disse patienter har vist ikke mange andre muligheder...
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Vitus... afkast på mine bull´s i år til dato...kom ud inden den crashed og ind igen på det rigtige tidspunkt...ved ikke om det er mere held end forstand..:-D
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Jeg daytrader...
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Måske...men det sidste halve år er det gået meget godt...:-)
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Jeg har mine laaange Genmab som bare står..det andet er noget jeg leger lidt med;-)
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Fed overskift på Blood artikel: AL patients don’t dare go without dara (artiklen i Rajkumars tweet) https://twitter.com/vincentrk/status/1256213766628347907?s=21
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Congratulations to Genmab, @LUMC_Leiden, @MedicineUVA and @VUmcAmsterdam team on getting published in the Blood Cancer Journal. The study shares insight on potent anti-tumor activity exhibited by DuoHexaBody-CD37
in preclinical B-cell malignancy models. https://twitter.com/genmab/status/1256252129792217090?s=21 -
Genmab Announces U.S. FDA Approval of Subcutaneous Formulation of Daratumumab, DARZALEX FASPRO
(daratumumab and hyaluronidase-fihj), for the Treatment of Patients with Multiple Myeloma
Company AnnouncementSubcutaneous formulation of daratumumab, DARZALEX FASPRO
, approved by the U.S. FDA for the treatment of patients with multiple myeloma
Approval based on data from Phase III COLUMBA and Phase II PLEIADES studies
In the studies, the fixed-dose subcutaneous formulation reduced treatment time
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