
Technical & Scientific
Due Diligence
Reimagining Drug Development for Good
The world of drug development must evolve to keep pace with the growing need for speed, innovation, and efficiency. Imagine Biotech leads this transformation to de-risk private biotech investors by harnessing predictive simulations, advanced data modeling, and AI solutions specifically designed for drug discovery and development.
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About
Imagine Biotech
At Imagine Biotech, we help early to mid-stage biotech teams avoid one of the industry’s most costly pitfalls, burning capital on lab and animal studies without fully understanding their molecules.
Traditional development often relies on trial and error experiments that are expensive, time consuming, and frequently fail due to unforeseen issues like poor solubility, off target toxicity, or weak drug enzyme interactions.
We offer a smarter path forward. Using advanced computational modeling, molecular simulations, and quantum chemistry, we provide a deep, predictive understanding of how compounds behave early on.
Our platform enables faster, more informed decisions, supports high value IP creation, and gives investors greater confidence by reducing technical risk.
Backed by a world class team of PhDs, Imagine Biotech delivers integrated, science driven insights at every stage of the drug discovery process.
We are building the future of drug discovery, one where clarity replaces guesswork, and data drives smarter science.
ADMET prediction with PK modeling
AnimalGAN - Simulate synthetic animal data
Mass spectrometry assets
Bioinformatics & Metabolite databases
3D protein modelling and molecular docking
Toxicology | Drug delivery & infusion
Chromatography Techniques
The Importance of Knowing Your Molecule Before you Invest Time and Capital

Approximately 30% of drug failures in clinical trials are due to unmanageable toxicity.

About 18% of drug failures are specifically due to drug-induced liver injury (DILI).

Drug toxicity can result from both off-target and on-target inhibition of molecular targets.

Toxicity issues are oftennot detected until clinicaltrials, despite rigorouspreclinical testing in animalmodels.

Many potential drugs fail due to misclassification by animal models, which may not accurately predict human toxicity.

The high failure rate due to toxicity underscores the importance of improved methods for predicting and assessing drug safety early on.

"Sometimes it is the people no one can imagine anything of, who do the things no one can imagine."
- Alan Turing
The Investor Problem
Amid economic instability and previous biotech setbacks, investors, especially Limited Partners, face declining confidence. Bottom line is that it becomes harder to close future funding rounds because of this higher historic risk profile associated to life science projects.
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Traditionally, biotech investments centred on conventional business due diligence often overlook or don’t place heavy emphasis on meticulous technical analysis due to high associated cost.
Undesirable pharmacokinetics and toxicity are major reasons for drug development failures, with safety and efficacy of major concern for project success, recognizing drug ADMET properties early reduces clinical phase failure rates.

What The Numbers Show
$6M
Average spend on pre-clinical toxicology studies
12
Drug discovery can take 12 years and cost $2.6 billion.
90%
Clinical drugs fail, costing investors & partners millions
45%
Fail because of limited pre-clinical efficacy
30%
Fail because of unmanageable toxicity
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