Genmab — September 2020
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Genmab, in partnership with BioNTech, has begun clinical development of an investigational therapy, GEN1042 (DuoBody
-CD40x4-1BB), for solid tumors. GEN1042 is a first-in-class bispecific agonistic antibody targeting CD40 and 4-1BB for priming and activation of a tumor-specific immune response. The key aim of InSysBio in this collaboration is to develop a quantitative system pharmacology (QSP) model that allows exploration of the relationships between dose, schedule, and tumor response in -
in patients treated with this novel agent. These advantages of QSP modeling are enabled by the fact that such models are virtual representations of the disease based on experimental data and biological knowledge.
InSysBio's great expertise in QSP modeling in oncology and immuno-oncology settings, allows to increase the efficiency of new drug development. -
Moreover, to perform such projects more efficiently InSysBio has developed internal tools and software facilitating the process of model development, several of which will be applied during this project. The Immune Response Template (IRT) is a tool for development of QSP models/platforms of different diseases associated with the immune response in humans. Application of the IRT allows simplification of the model development process by using pre-defined sub-models as building blocks.
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Another InSysBio tool, the CYTOCON DB, will assist in the estimation of remaining unknown factors and translation of in vitro data to in vivo situations.
Oleg Demin, CEO of InSysBio, highlights: "The project with Genmab represents ideal case for application of QSP modeling approach. The choice of the technique is supported by complexity of biological system, needs in mechanistic understanding of the data available and importance of the project deliverables for the drug development program. -
Genmab and BioNTech are jointly developing GEN1042 using the DuoBody
technology, which is a revolutionary new approach in the oncology treatment. We are proud to be part of this process."
It should be outlined that the project absolutely coincides with InSysBio mission which is to take part in drug development thus bringing hope to patients. -
Ja jeg tænker, at det på aftaletidspunktet var klart at BigPharma arbejder med alle kneb for at forlænge patent på et drug. Mens det nok har været mere overraskende at dara pludselig blev sc-version ved hjælp at et andet stof. Så derfor er mit gæt at det højst er HALOs betalinger er i spil grundet uklarhed i aftalen omkring dette issue.
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Link til GB´s nyhed.
Insysbio-announces-its-collaboration-with-genmab: https://www.proinvestor.com/boards/86995 -
Hexa-cd38 har ikke brug for HALOs teknologi. Hvis antager at Jan har ret, og Hexa-cd38 er 10x bedre end Darzalex, så "sparer" JNJ de 5% til HALO hvsi de opter in på hexa-ce38
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Jeg mener de valgte at sælge sc til samme pris som iv
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nok pga Sanofi valgte at lægge prisen på Sarclisa lidt under Darzalex
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