Biotek-snakken — December 2020
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Norske Bergenbio har data readout på AML indikation, med positive resultater. Abstract tilgængelig for præsentation 6/12: https://ash.confex.com/ash/2020/webprogram/Paper136566.html
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OncLive. : Zanidatamab. https://www.onclive.com/view/fda-grants-zanidatamab-breakthrough-status-in-her2-biliary-tract-cancer?utm_source=sfmc&utm_medium=email&utm_campaign=11-30-20_JAN-19-OGD0730_OncLiveSS_MCL CC eNews_Imbruvica,Janssen_NON_US_Send&eKey=amFuYm9ydXAxOTc4QGdtYWlsLmNvbQ== Til dem der ikke har adgang til Sukkers link.

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"This is a really good drug. It has received the orphan designation [in Europe]. We have [also] worked with zanidatamab and you will see some data from us at the ASCO GI [The Gastrointestinal Cancers Symposium, January 15-17, 2021]. It's a multi-institutional trial. We get a lot of responses with this drug. It's also targeting the HER2-positive population. And certainly, it is not as toxic as Enhertu, which is a pretty toxic drug."
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"In fact this molecule is going to go into Phase III first-line and they're working with a Chinese company called BeiGene. So BeiGene is partnering with Zymeworks. In terms of the trial design it should be compared to Herceptin plus chemotherapy versus zanidatamab plus chemotherapy. And that will be a third arm, which will be zanidatamab and BeiGene's own PD-1 inhibitor, tislelizumab and chemotherapy.
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Paa Placeras Immunovia forum skriver de at denne artikel er skylden: https://www.di.se/live/diagnostikbolagets-aktie-pressas-efter-di-s-granskning/
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