Model the cost-to-value path of your drug asset.

Model the cost-to-value path of your drug asset. Alt

AssetLens estimates development costs, commercial potential, and NPV across go-alone and outlicensing scenarios.

How much revenue could this asset generate?

  • Market size & patient population
  • Pricing assumptions & therapy positioning
  • Market share & adoption scenarios
  • Year-by-year revenue forecast
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What kind of licensing deal could this asset support?

  • Comparable licensing deals
  • Upfront, milestones & royalties
  • Stage-based deal logic
  • Negotiation evidence for BD teams
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How much will it cost to move this asset forward?

  • Clinical development cost by phase
  • Manufacturing & launch investment
  • Commercialization cost assumptions
  • Cost timeline & capital planning
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Which path creates the strongest business case: develop, license, or wait?

  • Go-alone scenario
  • Outlicense-at-IND scenario
  • Outlicense after Phase 1 / Phase 2 scenario
  • Risk-adjusted business case
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Real implementations of OmicsLayer™ – adapted to each client’s data, infrastructure, and operational needs.

Based on our clients’ experience, OmicsLayer™ saves around €40k–120k/year in avoided manual internal effort.

Secure on-prem/private cloud installation process

Discovery & data audit

  • 1–2 weeks

    Workshops with scientific, data, IT, and compliance teams. We define systems, datasets, permissions, and the first high-value use case.

Data & architecture mapping

  • 2–3 weeks

    We map data flows, metadata, access logic, pipeline dependencies, and integration points.

Build & integration

  • 4–8 weeks

    We connect priority systems, build ingestion/QC workflows, configure the semantic layer, and prepare the AI query interface.

Pilot validation

  • 2–4 weeks

    We test the first use case on real data, validate answer quality, review traceability, and tune workflows with domain experts

Scale & optimization

  • Ongoing

    Add new systems, cohorts, data modalities, dashboards, partner workspaces, and additional AI-assisted workflows.

Who it is for

Built for companies where biomedical data already exists

1 Molecular diagnostics companies

Connect variant, assay, phenotype, and evidence data into faster interpretation workflows.

2 Modality-specific design modules

Unify multi-omics and clinical metadata to support discovery, validation, and translational proof-of-concept.

3 Clinical genomics labs

Reduce manual interpretation and reporting burden with traceable, reviewable AI-assisted workflows.

4 Biobanks and research hospitals

Make biospecimen, cohort, omics, and clinical data queryable under strict governance.

5 Pharma translational medicine teams

Move from scattered datasets to reusable biomarker and patient stratification intelligence.

6 CROs and lab networks

Integrate LIMS/ELN, QC, assay outputs, and reporting workflows into one operational intelligence layer.

Start with a free demo on your own data

See how the solution works in practice before committing to deployment or integration.

No-charge initial demo

Get in touch with us.

We’re here to assist you.

Andrew Markov

Delivery Director

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