Valuation framework

Scientific de-risking creates economic value.

A primary, transparent and evolving methodology to estimate the indicative economic value of the scientific assets structured on AXIOM — measuring how evidence, validation, intellectual property and technological maturity turn a research project into a structured asset.

AXIOM Scientific Asset Valuation Framework — Version 1.0

  1. Science
  2. Evidence
  3. Asset
  4. De-risking
  5. Value
  6. Capital

Scientific assets

19

Development phase assigned

19

Assets with AXIOM Asset Score

19

A score requires all six dimensions documented.

Indicative ranges published

19

Remaining assets read “under assessment”.

Terminology

What a valuation is — and is not

Projected Indicative Valuation

A model-based estimate of the economic value of one specific scientific asset, expressed as a range, with a confidence level and a valuation date. It is indicative and subject to update as new evidence and milestones arrive.

It is not a guaranteed price, book value, offering price, return promise, guaranteed future value, investment recommendation or certified independent valuation.

Market Opportunity

The economic dimension of the market or problem related to the asset — TAM, SAM, SOM, prevalence, unmet need — published only with a verifiable source and date.

A US$ 10 billion market does not mean the asset is worth US$ 10 billion. Market opportunity is one variable of the model, weighted at 15%.

  • Market sizeAsset value
  • Scientific viabilityProbability of financial return
  • ValuationOffering price
  • Token priceScientific asset valuation

Methodology

Six weighted dimensions

Each dimension is assessed from 0 to 100 against documented inputs. Where the inputs do not exist, the dimension is not scored.

A25%

Scientific Evidence

Scientific rationale, quality and reproducibility of the evidence base.

  • Scientific rationale
  • Quality of evidence
  • Reproducibility
  • Existing studies
  • Proof of concept
  • Experimental data
  • Human studies, where applicable
  • Related publications
B20%

Technology Readiness

Based primarily on TRL and the actual development stage of the asset.

  • Concept
  • Prototype
  • Validation
  • Pilot
  • Scale-up
  • Integration
  • Market readiness
C15%

IP & Defensibility

Documented protection and difficulty of replication. No legal protection is asserted beyond what is filed or granted.

  • Patent / patent application
  • Know-how, trade secret
  • Proprietary formulation
  • Software, database, proprietary protocol
  • Exclusivity
  • Difficulty of replication
  • Freedom to operate, when documented
D15%

Market Opportunity

Economic dimension of the problem. Market size alone never determines valuation.

  • Problem size
  • TAM / SAM / SOM, when available
  • Prevalence and demand
  • Economic cost of the problem
  • Market growth
  • Potential buyers
  • Unmet need
E15%

Regulatory & Development Risk

Inverted scale: lower assessed risk produces a higher score.

  • Regulatory complexity
  • Additional studies required
  • Estimated development time
  • Technical, clinical and industrial risk
  • Validation requirements
  • Critical dependencies
F10%

Commercial & Licensing Potential

Licensing routes, industrial integration and capacity to generate future revenue.

  • Licensing possibility
  • B2B / B2G / B2C
  • Industrial integration
  • Scalability
  • Potential partners and channels
  • International applicability
  • Future revenue capacity

AXIOM Asset Score

25% · 20% · 15% · 15% · 15% · 10% → 0–100

The score is a multidimensional assessment of an asset's stage and potential. It does not represent a probability of success, and it does not represent a financial return: a score of 76/100 is not a 76% chance of success or a 76% return.

Development phases

Four macro-phases

01

Phase 1 — Concept / Prototype

Scientific rationale, concept, initial IP, initial formulation, prototype, exploratory research.

High risk. Valuation must reflect substantial uncertainty.

02

Phase 2 — Validated Prototype

Proof of concept, laboratory validation, technical testing, stability, functionality, optimisation, pre-clinical evidence where applicable.

Reduced risk relative to Phase 1.

03

Phase 3 — Pilot / Clinical Validation

Pilot, field study, human or clinical study where applicable, operational validation, prospective data in a relevant environment.

Material reduction of scientific and/or operational risk.

04

Phase 4 — Market Validated

Advanced scientific validation, industrial scale-up, regulatory and manufacturing readiness where applicable, commercial validation, licensing, contracts, market entry.

A finished prototype alone never qualifies an asset as Phase 4.

Projection model

What generates the projection: global problem size versus viability

The projected range of each Scientific Asset is generated from the documented global size of the problem and the data available in the literature, weighed against AXIOM's viability of building and delivering the solution. It is a projection, never an offering price.

01

Addressable market (SAM)

Economic magnitude of the problem addressed by the asset, taken from public literature and market research, with the source disclosed per asset.

02

Licensable capture band

Conservative share attributable to a single licensable asset: 0.4% to 1.6% of the addressable market.

03

Phase probability

Probability-of-success factor by development phase: Phase 1 5%, Phase 2 12%, Phase 3 28.000000000000004%, Phase 4 55.00000000000001%.

04

AXIOM viability

Technical, regulatory and industrial capacity to build and deliver the solution, expressed as the asset viability index (0–100).

projection = SAM × capture band × phase probability × viability

Valuation basis

A hybrid approach, never a single multiplier

Valuation is not market opportunity multiplied by the AXIOM Asset Score. Approaches are combined according to the data actually available for each asset, and only the approaches used are disclosed.

Cost Approach

Historical investment and estimated cost of reproducing or developing the asset.

Market Approach

Licensing, M&A and venture comparables for similar technologies or scientific assets — used only where reliable data exists.

Risk-Adjusted Income Approach

Potential revenue, royalties, licensing fees, margins, probability of success, time to market, future costs and discount rate. Architected for rNPV in later versions.

Early-Stage Composite

For very early assets where DCF/rNPV is not defensible: replacement/development cost, IP & knowledge premium, market attractiveness, scientific evidence and development stage, adjusted for technical, regulatory and commercial risk.

No universal multiples are invented. Parameters are to be calibrated against real comparable transactions, and rNPV modelling is reserved for assets — typically pharmaceutical, biotech or milestone-driven technologies — where such data can be sustained.

Ranges & confidence

Uncertainty is stated, not hidden

Valuations are published as ranges — for example US$ 1.8M – US$ 2.4M — rather than a single precise figure, because a precise figure would misrepresent the underlying uncertainty.

A high valuation does not imply high confidence. They are different dimensions: confidence depends on the quality of the data used.

  • Low

    Preliminary data, limited evidence, no comparables or wide uncertainty.

  • Moderate

    Reasonable scientific data, a defined stage and some verifiable assumptions.

  • High

    Robust evidence, advanced stage, relevant commercial/regulatory data and/or reliable comparables.

Milestone-based revaluation

Value creation through de-risking

Each valuation carries a version, date, methodology, main assumptions, confidence level and change history, under an auditable identifier such as AXV-001-V1.

Material events

  • Patent filed
  • Patent granted
  • Prototype validated
  • Study completed
  • Scientific publication
  • Ethics approval
  • Clinical result
  • Pilot completed
  • TRL increase
  • Industrial validation
  • Licensing agreement
  • Industrial partner
  • Regulatory approval
  • Market entry

Possible outcomes of a revaluation

  • Up
  • Unchanged
  • Down
  • Under review

A new milestone does not automatically increase a valuation. Negative results may keep, reduce, suspend or invalidate the previous estimate. A new publication is assessed for relevance and quality of evidence — it is never an automatic uplift.

Valuation history — interface structure (illustrative labels, no asset values)

  1. ConceptUnder assessment
  2. Prototype validatedUnder assessment
  3. Pilot completedUnder assessment
  4. Industrial validationUnder assessment

Current state

What is calculated today

The infrastructure is in place and the existing data is classified. No asset receives a fabricated score or range: dimensions without documented inputs remain unscored, and each asset carries a list of the data still required.

  • Development phase and TRL are derived from documented stage data for all assets.
  • Technology Readiness is scored from TRL; the remaining five dimensions await documented inputs.
  • Without all six dimensions there is no AXIOM Asset Score and no indicative range.
  • Market figures are published only with a verifiable source and date.

Planned for later versions

  • Sector-specific models
  • Biotech rNPV
  • Pharma probability-of-success models
  • Licensing comparables
  • Patent valuation
  • Software / SaaS valuation
  • Industrial technology valuation
  • Monte Carlo simulations
  • External independent valuation
  • Transaction comparables

Model-based projection derived from the global size of the problem and data available in the literature, weighed against AXIOM's viability of building and delivering the solution. Indicative estimate based on the AXIOM methodology and information available as of the valuation date. It does not constitute an independent valuation, offering price, investment recommendation, or guarantee of future value.