Genmab — Juni 2022
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Man vurderer, at markedet skal informeres om væsentlige forhold
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Da man ansøgte Tisotumab Vedotin kom selskabsmeddelelsen først da FDA havde accepteret ansøgningen.
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Fedt.
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Genmab to Submit Biologics License Application to U.S. Food and Drug Administration for Epcoritamab (DuoBody
-CD3xCD20) for the https://www.proinvestor.com/investornyt/844797/genmab-to-submit-biologics-license-application-to-us-food-and-drug-administration-for-epcoritamab-duobody-cd3xcd20-for-the -
FDA warns about possible increased risk of death and serious side effects with cancer drug Copiktra (duvelisib) https://www.healio.com/news/hematology-oncology/20220630/fda-warns-about-potential-elevated-risk-for-death-with-blood-cancer-therapy-durvelisib
https://www.fda.gov/drugs/drug-safety-and-availability/fda-warns-about-possible-increased-risk-death-and-serious-side-effects-cancer-drug-copiktra#:~:text=The U.S. Food and Drug,found in the lymph nodes.
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