20-22 February 2017 the 10th ISBM Enclosed Conference was held. For ten years the employees annually have been meeting together to share their scientific results and talk over future plans. ISBM did a great job in this working year.
Seven big projects with international pharmaceutical companies were completed. Two research papers co-authored with colleagues from other organizations were published in PLOS Computational Biology and CPT: Pharmacometrics & Systems Pharmacology.
ISBM took part in 2 exhibitions and 4 important conferences, the employees presented their reports and posters on The International Liver Congress 2016, Population Approach Group in Europe 2016 Meeting (PAGE 2016), American Society for Clinical Pharmacology and Therapeutics 2016 Meeting (ASCPT 2016) and 6th American Conference on Pharmacometrics (ACoP6). And ISBM CEO, Oleg Demin, won the Quality Award for his oral presentation at the ACoP6.
We released an updated version of the Immune Response Template (IRT), a platform for Quantitative Systems Pharmacology modeling in the immune oncology field. It’s a big step for further QSP platform solutions development.
A new working year starts from the very important event – ASCPT 2017 Meeting. ISBM presents 8 posters and the IRT stand at the Exhibition. We will write about it in more details soon.
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06 Nov 2018 17:27
Investigation of amyloid pathology mechanisms and prediction of clinical trial results using QSP model
InSysBio presents the video of Tatiana Karelina’s talk in framework of session “From translational PKPD models to quantitative system pharmacology in neurodegeneration drug development” at the 9th American Conference on Pharmacometrics (ACoP9):
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26 Nov 2018 14:03
InSysBio updates Immune Response Template online
InSysBio, a pioneer in Quantitative Systems Pharmacology (QSP) modeling and simulation for drug development, today announced a release of updated version of Immune Response Template (IRT) online. The main update in new 2.1.0 version is myeloid-derived suppressor cells (MDSCs). Published human in vitro and in vivo data were analyzed to reconstruct monocytic MDSCs (Mo-MDSCs) and granulocytic MDSCs (Gr-MDSCs) life cycles, derive equations and identify parameters.
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