Genmab — April 2019
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hmmm. so they are already creating Dara bispecifics… this is the article link btw https://sci-hub.tw/10.1016/j.bmc.2018.12.024
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I princippet 10mdr efter ansøgning. Men der er ikke rigtigt noget "senest" med RTOR-ordningen. Hele formålet er at speede processen op, så det formoder vi at de gør. Efter den vejledende tidsplan for RTOR skulle det være i denne uge. Men den kan der afviges fra. Det er hændt før. Så for at citere Poul Nyrup: Vi ved det ikkøø.
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Hvor er vi på linjen? Startede den 22. jan. https://www.fda.gov/AboutFDA/CentersOffices/OfficeofMedicalProductsandTobacco/OCE/ucm612927.htm
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