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Global Innovation Summit 2026

6 May 2026 | Basel, Switzerland

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5 Prime Sciences

SME

5primesciences.com/Montreal, Canada
20 profile visits

About

Drug development fails at a ~90% rate because fundamental biology fails to translate to humans. 5Prime Sciences is a global leading expert that acts as the computational radar for the pharmaceutical industry, replacing guesswork with definitive genetic evidence to solve this root cause.

We develop advanced multi-omics tools—powered by our proprietary Centromere™ platform and PRIMEVault™ — to act as an extension of your R&D team.

We bring essential information to our partners by answering four critical questions before major capital is deployed:

  • Does the target truly drive disease?

  • Will modulating it change outcomes?

  • Are there safety risks?

  • Are we selecting the right patients?

By validating human biology, we multiply your probability of clinical success up to 4x . Trusted by top-tier pharma with an 80% partner return rate, our evidence-driven approach delivers concrete results: enabling 190M biotech fundraises, halting>100M late-stage trial failures, and de-risking >$600M pharma acquisitions.

The best medicines start with the best targets. We provide the evidence to stop weak programs early and the confidence to accelerate the right ones.

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What is your business/industry sector?

Biotech, Pharma and Cosmetics

Representatives

Elin Thysell

CBO

5 Prime Sciences

Brent Richards

CEO

5 Prime Sciences

Marketplace (4)

  • Expertise

    Does this target truly drive disease in humans?

    Association is not causation. The majority of late-stage failures trace back to a target that appeared relevant in preclinical data but never causally drove disease in humans. This is the question human genetics was designed to answer.

    • Biotech, Pharma and Cosmetics
    Author

    Elin Thysell

    CBO at 5 Prime Sciences

    Montreal, Canada

  • Expertise

    Will modulating this target change patient outcomes?

    A target can cause a disease without having any effect on how it progresses once established. The distinction determines whether an asset belongs in prevention, treatment, or both — and what a Phase II trial actually needs to show.

    • Biotech, Pharma and Cosmetics
    Author

    Elin Thysell

    CBO at 5 Prime Sciences

    Montreal, Canada

  • Expertise

    What are the safety risks of modulating this target in humans?

    Animal models miss a significant proportion of adverse events that emerge in human trials. Genetic variants that naturally alter target activity offer a different read — one that reflects what target perturbation does across a human population.

    Author

    Elin Thysell

    CBO at 5 Prime Sciences

    Montreal, Canada