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Know-how and skills

             Pheno-genotyping: natural history, phenotypic                          KEY FIGURES
           and genomic characterisation of patients,
           phenotype/genotype correlation, cohort studies                       164
           and stratifications, bioinformatics, single cell
           RNAseq analysis, identification of new relevant                      Permanent staff
           therapeutic targets.                                                 (full-time equivalent)

              Preclinical research:  creation of cellular                       92
           and animal models (iPSC, CRISPR-Cas9),
           characterisation of cellular and molecular                           PhD students
           mechanisms, cell and gene therapies,
           establishment of preclinical and clinical proof of                   2 242 K€
           concepts.                                                            Partnership incomes
             Clinical research: setting up clinical projects                    with industry
           (including clinical trials and orphan drug
           designations), interaction with regulatory                           324 K€
           authorities, operational and logistical support                      Collaborative research
           during studies, decision support (databases,
           clinical expertise) to identify targeted patient                     1 918 K€
           recruitment.
                                                                                Services


          Partnerships are at the heart of

          our strategy                                         Objectives

             Research collaborations and services, creation        Improve our knowledge to better target the
           and support of start-ups, on preclinical,             pathophysiological mechanisms of rare genetic
           translational or clinical projects.                   diseases
             Molecule discovery, repositioning, gene and           Accelerate the transformation of know-how into
           cell therapy in partnership with small and large      therapeutic and diagnostic solutions for the benefit
           pharmaceutical, biotechnology and diagnostic          of the patient as quickly as possible
           companies.
                                                                   Increase the number of innovative therapeutic
             Institut Carnot Imagine’s offer is available on:    studies (gene and cell therapies) and the number
           https://techtransfer.institutimagine.org              of patients participating in these studies
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