Target Validation
We offer multi-validation solutions for preclinical targets across numerous therapeutic fields
Target validation evaluates the druggability of an identified target. It does this by assessing key biological features of a target to estimate whether an investigational drug is likely to elicit a therapeutic benefit within an acceptable safety window. Having a well-researched target reduces the risk of failure during the later stages of development.
Several important features will determine whether a target is druggable. This includes a target’s regular function in maintaining cell physiology, its involvement and modulation in disease pathophysiology, as well as its localization and distribution across tissues or cells.
Ultimately, target validation provides researchers with a biologically sound, and clinically relevant, rationale that warrants further investigation and investment. Through our integrated program, InnoSer scientists continuously relay insights towards the later stages of drug development. This helps to minimize risks and to have the most seamless and efficient experience possible.
Our Approach
We provide (custom) assay development, execution, analysis and reporting.
If needed, we can source and validate your specific required research models at our facilities. Having established close connections to many (academic) hospitals and academic research groups in the Benelux, we can source primary patient materials on demand for made-to-measure, co-development projects.
These methods are important to help provide trust in your compounds throughout the development process. With InnoSer’s combination of readout possibilities and expertise we allow drug developers to build an insightful dossier and mitigate development risks early on.
Partner with an Expert to Advance Your Therapeutic Discovery.
Work with our team to evaluate your drug and target for therapeutic effects with precision and expertise
Our Capabilities
Pharmacometrics tools can help assess the feasibility of targets and drugs. By integrating data from various pharmaceutical databases we can help to extrapolate pharmacokinetic profiles of prospective approaches across in-vitro and in-vivo situations (IVIVE).
InnoSer can co-validate your target in relevant biological contexts.
Through our access to primary clinical samples from our clinical network, we can help you to investigate your target in healthy and diseased clinical subjects. In addition, we support you in validating and selecting the most suitable preclinical disease models that provide excellent translatability of pathophysiology.
Target validation models
- Cell lines of health and disease
- Transgenic lines
- Primary cell material of health and disease
- Ex vivo models of health and disease
- In vivo models
- Custom model development
Readouts
- In silico modelling
- Gene and protein expression
- Histopathology
- Blood biomarker analysis
- Immune cell profiling via flow cytometry
- High content cellular imaging
- Ex vivo imaging
- Multi-immune fluorescence
- Biomarker identification and validation
- Multiplex assays (Meso-Scale Discovery)
Navigate The Drug Development Pipeline
AAALAC Accreditation
InnoSer has earned the AAALAC accreditation, demonstrating our commitment to responsible animal care and use. AAALAC International is a nonprofit organization that promotes the humane treatment of animals in science through voluntary accreditation and assessment programs. Our accreditation is valid for three years, incl. 2023. Read more about the AAALAC accreditation programme here.
Animal Welfare
The 3Rs impact everything from policy and regulatory change to the development and uptake of new technologies and approaches. This is why InnoSer has ongoing commitment and monitoring of these processes. The steps we practice maximize our ability to replace, reduce and refine animal involvement and facilitate our commitment to these principles when it comes to research and drug development.
info@innoserlaboratories.com