Les jumeaux numériques promettent de mettre l’anatomie humaine en équation pour évaluer des scénarios thérapeutiques, guider le geste du chirurgien ou tester de nouveaux médicaments. Les premiers cas d’usage sortent des laboratoires.
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Novadiscovery prémodélise les essais cliniques pour gagner en efficacité – Les Echos
Jusqu’ici, la recherche pharmaceutique était in vitro ou in vivo. Il existe un nouveau modèle, in silico , dans le monde immatériel de l’informatique…
La recherche in silico en plein développement – Le Quotidien du Médecin
La recherche in silico reste toutefois très déterministe. « Il faut définir la question posée et ne simuler que les systèmes et les mécanismes qui permettent d’y répondre », ajoute le Pr Jean-Pierre Boissel, Novadiscovery.
Quand les essais cliniques plongent dans le virtuel – Les Echos
Beaucoup d’arguments militent en faveur du in silico en complément et en renforcement mais non en remplacement des recherches in vitro et in vivo.
Totem HealthTech organisé par BpifranceHub : Dans quelle mesure intégrer l’IA dans le parcours de soin ?
François-Henri BOISSEL est invité lors du Totem HealthTech de BpifranceHub aux côtés de @therapixel et du Dr Jean Sébastien Hulot
Députée Françoise GROSSETÊTE: Europe supports innovation and in silico trials
It is now important for the European Medicines Agency to recognize and integrate into its regulatory processes these new methods of in silico simulation and prediction.
François-Henri BOISSEL at Refresh 2017
François-Henri BOISSEL introducing NOVA at Labiotech Refresh 2017, Berlin.
Prof. Jean-Pierre BOISSEL: The impact of in silico assays on drug R&D
Specify the optimal duration which helps to obtain the target effect, the dose that has to be used to maximize this effect. In other words, it’s to help us do the operations that are done today by a rather theoretical approach.
Dr David PEROL: The impact of in silico assays in oncology
With the help of in silico models we can integrate the right patients in clinical trials and reduce the size of these trials.
Prof. Marc HOMMEL: The Effect Model methodology
The Effect Model enables us -according to the indicators that you have, either clinical, genetic, imaging or biomarkers, – to go down to the patient and to go much further in an individual prescription.
François-Henri BOISSEL at 17th Biotech in Europe Forum – Sachs Associates
François-Henri BOISSEL introducing NOVA at 17th Biotech in Europe Forum – Sachs Associates
François-Henri BOISSEL: Introduction to NOVADISCOVERY
The human body contains 10 000 potential targets. that means that we are just at the begining and there is a huge of fields to be explored with the right tools to investigate in a capital efficient maner.
Dr Claudio MONTEIRO-SOUSA: The mechanism of action of the drug-candidate
Our work is to really get to the bottom of these mechanisms. To identify step-by-step the sequences that lead to the disease and to the treatment that can be given.
Prof. Jean-Pierre BOISSEL: Models and methodology
In itself, the virtual population, irrespective of its important role in the use of models, has other qualities. The first quality is to be able to collect data that are today stored in various dispersed databases…
Dr Adriano HENNEY, Avicenna Alliance: Building bridges to deliver predictive medicine
Let’s think the human body as a machine and start to look at it as engineers look at machines. In a normal state and at time of dysfunction.
Dr David PEROL: The impact of in silico assays in immuno-oncology
Anything that will contribute upstream to better mechanistic knowledge and to improved selection of responder patients will be welcome. I think that there is a whole avenue opening up for in silico modeling in oncology today.
Députée Françoise GROSSETÊTE: In silico clinical trials view from the European Union
In silico is truly a new method of medical research investigation. Digital technology is used to be able to reduce as much as possible the experiments to be performed: animal testing and of course trials in patients.
Prof. Jean-Pierre BOISSEL: In silico clinical trials view from regulatory authorities
There was a fundamental stage that we weren’t expecting, that is the integration by the FDA then by the EMA of the potential importance of in silico in the clinical research of new therapies.
Prof. Marc HOMMEL: Transposability from animal to human studies: the stroke example
The result demonstrated that with the molecule we were using, the way that finally proved to be promising, it was not effective, even deleterious. This result was important as it allowed this molecule to not be used.
Eulalie LANDÈCHE: The impact of in silico assays on drug R&D
Clearly the model enables us to learn more about the mechanism of action of the therapy and this is unprecedented compared with «small aspects» that we were concerned about through in vitro and in vivo trials.