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  • ​Empowering Drug Discovery Towards Successful Clinical Outcomes.

    SynLaia provides novel mechano-biological insights into candidate drug efficacy and mode-of-action through the use of virtual tissues.

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​Overcoming High Costs of Clinical Failures

The average success rate for new drugs to be approved is a mere 10.8%. With the estimated average cost of developing a new drug at £173 million, this equates to an average of £1.6 billion for securing one approved drug amidst nine unsuccessful ones.


The majority of clinical failures stem from a lack of efficacy (50%), followed by toxicity (30%). Drug efficacy is rigorously tested during the target validation process, yet it remains challenging to correlate these in vitro and in vivo studies with human biology and clinical outcomes. The poor translation of in vitro and in vivo model data to human biology is a major cause of clinical failures, with inaccuracies in disease modelling technologies being the primary obstacle.

PROVE Platform

SynLaia is developing PROVE (Patient-centric Research Optimisation and Validation Engine) platform, designed to optimise and validate research by incorporating patient variability using personalised in silico tissues. We combine physics, biology and spatial awareness, to validate new compound efficacy across scale and across patient population.

Get in touch with our team!

If you would like any further information please get in touch with our team by clicking the button below or email agata@synlaia.com

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In association with

We are part of a Venture Builder (Zinc VC) and AI in Health accelerator (Pioneer).

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