IR Pharma company logo
  • Company overview
  • Technology - The drug development process at IRP, The Drug Evaluation Process, Model systems
  • Contact us
  • IR Pharma capability is based on four main pre-clinical stages
    975 Cornforth Drive
    Kent Science Park
    Sittingbourne, Kent ME9 8PX
    T 01795 437426
    F 01795 423440
    E info@irpharma.co.uk
    National Heart & Lung Institute
    Sir Alexander Fleming Building
    Imperial College, London SW7 2AZ
    T 01795 437426
    F 01795 423440
    E info@irpharma.co.uk

    The Drug Evaluation Process

    IR Pharma capability is based on four main pre-clinical stages that taken together, represent an integrated drug discovery approach.

    Target Validation Models

    Models provide the means to determine, or confirm, target location and function in rodent tissue, human tissue and cells. This includes:

    • Immuno-localisation at tissue and cellular level
    • Evaluation of gene expression profiles
    • Disease model assessment using knock-out and transgenic animals.

    In Vitro Profiling (in rodent and human tissue)

    Methodologies to map compound function at a tissue, cellular and molecular level for both human and rodent include:

    • Isolated tissue bioassay
    • Cellular assays
    • Biochemical assays

    In Vivo Profiling

    Undertaken in both mechanistic and disease models, includes:

    • Cellular inflammation and histology
    • Functional physiology
    • Pharmacodynamic models to establish effective dosing regimens

    Clinically relevant biomarkers

    Linking laboratory to clinical trials through comparison of control and disease samples in both animal and human studies, utilising:

    • Imaging
    • Exhaled biomarkers