Genmab — April 2024
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Din mening, kan jo meget vel, være lige så rigtig som min. Synes dog, at kursudviklingen støtter min udlægning g.
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HexaBody-CD38
trial dates still unchanged, so seems on track still for read out later in the year, but i wonder if the changes in recruitment centers indicate that it may not be an easy process...
https://classic.clinicaltrials.gov/ct2/history/NCT04824794?A=12&B=13&C=Side-by-Side#StudyPageTop -
Hvad tænker i om prisen på profoundbio? Jeg tænker, at GEN må se en hel del mere, end blot de kliniske programmer, for at få regnestykket til at hænge sammen
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På dit spørgsmål om anvendelse af ADC på duobody m.fl: ADCs developed may also be applied to other antibody-related therapeutics, including bi-specific antibodies, antibodies, or antibody fragments fused with a toxin (immunotoxins) with new avenues utilizing naturally derived cytotoxins, chimeric antigen receptors, and radiolabeled antibodies (radioimmunoconjugates) https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8628511/
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https://aacrjournals.org/cancerres/article/84/6_Supplement/6580/738361/Abstract-6580-A-Novel-EGFR-x-cMET-bispecific-ADC Konkurrent til Amivantamab ligger også i den tidlige pipeline hos ProfoundBio
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@Sukkeralf oplyser rigtigt at DAR er 8 på deres stof Rina-S. Altså 8 toxinmolekyler pr antistof. Læst at 2-4 er normalt. Profound oplyser at det er linkerne (dem der hæfter toxin til antistoffet) der skjuler toxinet og derved mindsker bivirkningerne (som jeg forstår det) og dermed vil der kunne fremføres mere toxin end normalt til canceren.
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