Biotek-snakken — September 2021
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How Moderna Stock Can Double From Herehttps://www.proinvestor.com/investornyt/706476/how-moderna-stock-can-double-from-here
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Teknisk status for aktierne i C25: https://www.proinvestor.com/index.php?p=debat_1&postid=97148
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San Antonio Breast Cancer Symposium® | SABCS 2026
The San Antonio Breast Cancer Symposium® (SABCS) is the world’s largest breast cancer research meeting, where leading scientists and clinicians share the latest breakthroughs advancing breast cancer research and patient care. Join the global breast cancer community in San Antonio, December 8–11, 2026.
San Antonio Breast Cancer Symposium - The San Antonio Breast Cancer Symposium® is designed to provide state-of-the-art information on the experimental biology, etiology, prevention, diagnosis, and therapy of breast cancer and premalignant breast disease to an international audience of academic and private physicians and researchers. (www.sabcs.org)
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Entasis: markedet for etx0462 ser ud til at være pænt stort, ifølge CDC var der i 2019 400K US tilfælde i ESKAPE pathogen gruppen. Det må i det mindste give lidt plus på BO prisen - tvivler på, at vi når at se resultater i klinikken før det siger haps
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Tror vi har snakket om det før, men ville Novartis ikke være oplagt partner til Zani og ZW49? Nu når de har rettighederne til tislelizumab i US, EU og Japan og endnu ikke er i HER2 gamet
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Breakthrough AstraZeneca Breast Cancer Drug Massively Reduces Disease and Fatalities in Trialhttps://www.proinvestor.com/investornyt/707066/breakthrough-astrazeneca-breast-cancer-drug-massively-reduces-disease-and-fatalities-in-trial
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Nyhed fra igår:
XBRANE: BIOGEN FÅTT USA-GODKÄNT FÖR BIOSIMILAR TILL LUCENTIS -
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Cantargia AB: Cantargia: FDA tilldelar särläkemedelsstatus (Orphan Drug Designation) till nadunolimab för behandling av bukspottkörtelcancer
Cantargia AB meddelade idag att den amerikanska läkemedelsmyndigheten, Food and Drug Administration (FDA), har beviljat särläkemedelsstatus i USA till nadunolimab (CAN04) för behandling av bukspottkörtelcancer. Detta ger möjlighet att utnyttja flertal incitament vid den fortsatta kliniska utvecklingen av nadunolimab i bukspottkörtelcancer
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