INVENTRO.

Biological evidence for
oncology drug discovery.

Our AI models prioritise drug hypotheses. Our laboratory tests them. We bring both together to help oncology teams decide what to advance, retest or stop.

01 / FROM AI TO EVIDENCE

More hypotheses. Limited capacity to test them.

AI can propose more drug hypotheses than a team can test. The bottleneck is deciding which deserve an experiment and establishing whether the predictions hold in a biological model.

RESEARCH / SCOPE

Start with your question.

From finding compounds for a target and exploring a compound's targets to investigating combinations and drug responses across tumour types or individual samples. We shape the first study around your question and the available evidence.

Start with computational prioritisation, a standalone laboratory study or an integrated project. The scope follows the question.

AI / PREDICTION

Choose what to test.

We develop our own AI models to predict molecular targets and biological activity. They rank candidates for experimental follow-up. We also draw on external computational tools where appropriate.

A prediction alone cannot establish how a compound behaves in cells, its toxicity or its clinical efficacy.

LABORATORY / EXPERIMENT

Test the hypothesis.

We design experiments to measure compound activity and cellular responses, with methods and controls chosen for the research question.

The evidence applies to the model and conditions tested. An in vitro result does not establish efficacy in patients. Patient-derived ex vivo assays are in development.

SCIENTISTS / INTERPRETATION

Determine the next step.

Our scientists compare predictions with observations, assess uncertainty and recommend what to advance, retest or stop.

The recommendation comes from scientific review, not an automated AI verdict. Your team makes the research decision.

Schematic research workflow. Microscopy from the Inventro image archive.

One team connects the prediction and the result.

Seeing both lets us identify where models hold and where they fail, then refine the next hypothesis or experiment. This is the value of combining AI and experimental biology around one research question.

02 / WHAT WE DO

A target. A compound. A question to resolve.

For biotech, drug discovery and AI teams that need biological evidence. Start with a computational question, a laboratory study or a project that connects both.

COMPOUND PRIORITISATION

Which compounds hit my target?

Use our AI models to rank candidates for a defined protein target and design a focused experimental follow-up.

Typical outputA compound shortlist, supporting evidence and a validation plan.

TARGET EXPLORATION

What is my compound's target?

Investigate possible protein targets using Inventro AI predictions, activity data and the scientific literature.

Typical outputRanked target hypotheses, their limitations and experiments to test them.

COMBINATION RESEARCH

Which partners synergise with mine?

Explore potential combination partners and design experiments to assess whether their combined effects are synergistic.

Typical outputCombination hypotheses and a plan for experimental testing.

TUMOUR RESPONSE

Which tumour types will respond?

Investigate tumour contexts that may be sensitive to a compound, using available evidence and relevant preclinical models.

Typical outputResponse hypotheses and a model-selection plan for experimental follow-up.

SAMPLE RESPONSE

For this sample, which drugs work?

Explore responses in patient-derived material through our ex vivo programme.

Typical outputA proposed sample-specific study, subject to model validation and sample availability.

These questions guide our research. We agree feasibility and scope for each project. This work supports preclinical research, not treatment decisions.

How we do it

03 / HOW WE DO IT

One question. The evidence your decision needs.

Computational predictions and laboratory measurements address the same research question. We agree the scope with you, from a focused shortlist to experimental evidence for a preclinical decision.

AI / COMPUTATIONAL APPROACHES

Predict targets. Prioritise compounds.

Start with a protein target or a compound. Our in-house AI models predict target interactions and bioactivity to identify hypotheses worth testing.

Our own models, complemented by selected external tools.

We combine our predictions with literature and databases, adding external structure- or affinity-prediction tools where they help answer the question. Our scientists assess the evidence and decide what is worth testing.

  1. Candidate space

  2. Models and evidence

  3. Ranked hypotheses

Observed hit rates

Public-library shortlist
29.6%8 of 27 compounds active
Novel-compound shortlist
9.1%6 of 66 compounds active

AI-prioritised compounds tested in two CLK1 biochemical studies. Study-specific hit rates, not overall model accuracy.

Benchmarked on unseen data

We evaluate predictions against drug-target relationships published after the historical data used to fit the model, alongside experimental reference data.

Computational-only work delivers a ranked shortlist and a validation plan.

Explore the AI research demo

BIOLOGY / EXPERIMENTAL APPROACHES

Measure activity. Resolve cellular responses.

Biochemical assays, cellular models and quantitative imaging test selected hypotheses. We choose the measurements and controls to match the question.

Biochemical and cellular assays

Measure compound activity, cell viability, cytotoxicity and apoptosis, with functional readouts for a closer look at the response.

High-content and live-cell imaging

Measure individual cells, distinguish populations and follow changes in proliferation, protein localisation and response over time.

Patient-derived ex vivo

A single viability result can hide different cellular responses. We are developing assays on patient-derived tumour material to distinguish how tumour cells and surrounding cell populations respond to the same compound.

  1. Patient material extraction

  2. Proprietary processing protocols

  3. Sequential microscopy imaging

Multiple cellular features, measured within their biological context.

Images from Inventro in-house imaging experiments.

Original combined image of marker A-positive and marker B-positive cells, with nuclei in blue.
Original marker A-positive population panel, with identified green-stained cells and nuclei.
Original marker B-positive population panel, with identified red-stained cells and nuclei.

Identify each population before measuring its response.

Separate co-culture method example. A+/B+ are marker labels, not identities assigned to the ex vivo images.

Original figure
Drug A
Drug A dose-response: normalised cell counts for All, Type X and Type Y across increasing compound concentrations on a logarithmic scale.
Drug B
Drug B dose-response: Type Y cell counts decline more steeply than Type X as concentration increases; the All curve lies between them.

Different cell populations. Different compound responses.

Experimental data: normalised cell counts. Separate study from the A+/B+ example.

Original figure

What you receive

Translational Evidence Package (TEP)

Experimental evidence, interpreted for your next research decision.

For projects that include laboratory validation. Computational-only prioritisation remains a separate deliverable.

The answer

A recommendation on what to advance, retest or stop, supported by the evidence gathered.

Confidence and limits

An interpreted report explaining how far to trust the findings and what remains unresolved.

The next experiment

A recommended next step to address the uncertainty that matters to your decision.

Results you can work with.

Study-specific data, such as dose-response measurements or cell-population response analyses, with documented methods, controls and scientific interpretation. The contents are agreed before work begins.

04 / OUR TEAM

The people behind the evidence.

Our team brings together expertise in medicine, systems biology, molecular modeling and experimental research.

Tomasz Nowowiejski

Chief Executive Officer

MD and MBA with experience in healthcare, medical technology and biotechnology ventures.

Professional profile

Michał Komorowski

Chief Scientific Officer

Systems biologist trained in Warsaw, Warwick and at Imperial College London. Established the Inventro laboratory.

Professional profile

Piotr Setny

Head of AI

Medical doctor with a DSc in physics from the University of Warsaw. Specializes in computer-aided drug design and molecular modeling.

Jarosław Walczak

Head of Biology

PhD in biological sciences from the Nencki Institute, Polish Academy of Sciences. Designs and runs in vitro assays in cellular models.

Professional profile

Paweł Burzyński

Finance & Business Development

Entrepreneur and strategic advisor with more than 20 years of experience in finance and technology.

LET’S TALK SCIENCE

What is your next research decision?

Know what merits the next experiment before committing to the next stage of development. Tell us about your target, compound or research question.

contact@inventro.co