Genmab — Januar 2024
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@Bulder Da de også er listet i USA, så er det vel de 4 uger der trumfer Genmab's egne vedtægter (som de derfor bør ændre), og derfor gælder?
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Spørgsmålet om deres udmeldinger i denne periode kommer op hvert eneste år her på chatten, så nu har jeg spurgt dem inde på IR. Det vil jo i givet fald forklare hvorfor vi ikke har hørt noget.
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Isn’t this in line with common GEN IR practise? Since Rachel left GEN has shown precious little interest (bordering to sweet FA) for retail investors.
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Let's see JV. If I get
a reply I will of course share. -
Thx
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Jo fase 3 forsøgene er jo en nødvendighed, særligt nu da voldgiften er tabt og burde blive belønnet som et fremskridt. Gmab skal jo bare huske at highlighte deres succesrate. Så bliver det jo så godt som money in the bank
Men guidance skal helst bekræfte den fortsat kraftige vækst -
from
Scancell Interim Results for the six months ended 31 October 2023- Antibodies:
• Development of SC129, out licensed to Genmab, continues on track towards potential clinical
development.
https://www.scancell.co.uk/Data/Sites/1/media/publications/rns/2024/scancell-interim-results-31-october-2023.pdf -
Novel Cervical Cancer Treatments in Clinical Trial https://news.med.miami.edu/novel-cervical-cancer-treatments-in-clinical-trial/ “The antibody drug conjugate tisotumab vedotin-tftv has also gained approval and became a standard-of-care therapy this year. This therapy extends survival significantly,” said Dr. Sinno.
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Pfizer skriver at FDA har accepteret Tivdak sBLA ansøgning om konvertering fra "accelerated approval" til fuld godkendelse med priority review og PDUFA dato d. 9 maj, se link side 8. 2024.https://s28.q4cdn.com/781576035/files/doc_financials/2023/q4/Q4-2023-PFE-Earnings-Release.pdf
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Svar fra Andrew Carlsen angående stilleperioden "Our quiet period before earnings is still 2 weeks and has not been extended to 4 weeks with the US listing."
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