Biotek-snakken — December 2019
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frasorterer ILD pat i deres ZW49 trial ? https://clinicaltrials.gov/ct2/show/NCT03821233?term=ZW49&rank=1
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Er der kommet et nyt kursmål på Hansa Biopharma siden oppdateringen den anden dag. Eller er det dit personlige kursmål Nadia6111. Bare for oppklaring (-:. Når man høre konferencen fra den anden dag så bliver der sagt at fase 3 forsøget i USA ikke kommer til at ender på deres finansielle guiding. Men betyder det at de ikke må hente penge ? Deres kassebeholdning ser ikke ud til at være stor nok til at køre fase 3 mm frem til 2023. Eller regner de med nok indtægter fra Europa.
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Orphazyme får amerikansk særstatus i endnu en indikation
Biotekselskabet Orphazyme kan se frem til en række regulatoriske fordele i det videre arbejde med hovedkandidaten arimoclomol, der har fået endnu en særstatus - denne gang mod muskelsvindssygdommen sIBM.
(medwatch.dk)
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Spændende år Orphazyme går ind i.
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Photocure (PHO) : Studieresultat er netop offentliggjort https://www.marketscreener.com/PHOTOCURE-ASA-1413243/news/Photocure-Reduced-recurrence-after-flexible-Blue-Light-Cystoscopy-with-Hexvix-in-surveillance-Ne-29748393/
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Hansa Biopharma: https://www.proinvestor.com/debat/80265
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U.S. Food and Drug Administration granted accelerated approval to Padcev (enfortumab vedotin-ejfv), a Nectin-4-directed antibody and microtubule inhibitor conjugate, meaning the drug specifically targets cancer cells – in this case, the cell adhesion molecule Nectin-4, which is highly expressed in urothelial cancers. https://www.fda.gov/news-events/press-announcements/fda-approves-new-type-therapy-treat-advanced-urothelial-cancer
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Interstitial lung disease is a very important side effect to monitor and be vigilant for, but KOL is concerned that practitioners are going to be hyper-vigilant and patients will be taken off a drug that's very active because of an inflated perception of interstitial lung disease
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