Genmab — Juni 2017
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actelion var et nicheproduktsfirma. No problem med at fokusere på nicheprodukter...
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Der har været noget stille på analytikerfronten siden asco. Mon de venter på pdufa?
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jep - formentlig indenfor de næste 3 amerikanske arbejdsdage
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In addition, the FDA has granted a Standard Review period for the use of daratumumab in combination with pomalidomide and dexamethasone for the treatment of patients with relapsed or refractory multiple myeloma who have received at least two prior therapies, with a proteasome inhibitor and an immunomodulatory agent. The PDUFA date for the combination of daratumumab with pomalidomide/dexamethasone is June 17, 2017.
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Til os der ikke er helt skarpe på PDUFA: https://www.fool.com/knowledge-center/what-is-a-pdufa-date.aspx
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Er denne kommenteret? http://www.medscape.com/viewarticle/881376 Måske Ofatumumab klarer sig bedre, men det må fase 3 jo vise.
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Jan var ekstrem positiv omkring ofas muligheder i MS i går. Han gav udtryk får at ofa kunne være bedre end det tilsvarende medikament fra Roche. Roche er dog først mover. Så der har de en klar fordel.
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Some education on PD-L1 , the 2nd little video is a must watch - really funny
https://medivizor.com/blog/2017/05/26/quick-guide-understanding-importance-fdas-keytruda-approval/
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