Pharma & clinical development · Real-world evidence
Real-world data shows what happened. Biological outcomes show what changed.
Longitudinal biomarkers, multi-omic diagnostics and real-world data to measure biological change and intervention outcomes in the populations who actually use your therapy.

Why biological outcomes strengthen real-world evidence
For prevention, longevity and chronic-disease interventions, hard endpoints can take a decade to accrue. Repeated multi-omic measurement provides objective intermediate evidence now.
- 01
Earlier read-outs
Biological-age and multi-omic trajectories shift within months, long before morbidity or mortality data mature. - 02
Objective measurement
Lab-measured outcomes reduce reliance on coded or self-reported endpoints prone to misclassification in routine-care data. - 03
Response heterogeneity
Individual trajectories reveal who responds, who does not, and the biology behind the difference. - 04
Stronger causal inference
Measured baseline biology becomes a covariate for matching, weighting and adjustment in observational designs.
From real-world events to real biological change
Real-world data is rich in events but poor in biology. Adding a biological outcomes layer turns observational data into evidence of how a therapy changes the body under real conditions of adherence, comorbidity and co-medication.
We combine epigenomic, proteomic and metabolomic measurement with claims, EHR and registry data, so real-world studies capture objective biological response years before hard endpoints mature.
- Claims
- EHR
- Registries
- PROs & devices
Linked at participant level
- DNA methylation · biological age at the organ-system level
- Circulating protein signatures · organ health & inflammation
- Metabolic state, resilience & disease risk
- + Immune ageing & glycans
- + Microbiome
- + NAD+
- + Clinical biomarkers
- + Brain health
- Baseline: genetics & PGx
Change · Durability · Heterogeneity
Real-world data
- Diagnoses & prescriptions
- Hospitalisations & events
- Treatment persistence
- Patient-reported outcomes
- Costs & utilisation
Biological outcomes
- Whole-body biological age
- Organ/system-specific age
- ProteoAge & hallmarks of ageing
- Metabolic Age & disease risk
- Immune & inflammatory ageing
- Longitudinal trajectories
Evidence of what actually changed
Objective, mechanistic and longitudinal proof of effect in real-world populations.
- Clinical development
- Translational medicine
- Real-world evidence
- Market access
- Lifecycle management
A multi-omic portfolio built for repeated measurement
Our portfolio combines dynamic layers that change with intervention and a stable genetic layer that helps explain who responds. Real-world studies need both: one to measure change, the other to understand it.
Core longitudinal outcome layers
- Epigenomics
Advanced Biological Age & Epigenetics
How fast is the body ageing, and where?
RWE roleprimary or key secondary endpoint; baseline covariate for matching
What it measures
DNA methylation records the cumulative biological impact of disease, treatment and environment. Repeated measurement shows whether an intervention slows, halts or reverses ageing, and in which organ systems.
- 460+ biomarkers across 21 physiological systems
- Whole-body and organ-system biological age
- Ageing patterns and epigenetic health
Sample: at-home collection kit or in-clinic blood draw
- Proteomics
Advanced Proteomics
Which biological processes respond?
RWE rolemechanism, responder signatures, highly scalable repeat sampling
What it measures
Proteins are the functional read-out of biology. Mapping change onto the hallmarks of ageing links what a therapy does in real-world patients to its mechanism of action.
- ProteoAge: protein-based biological age
- Hallmarks of Aging profile
- Functional protein insights
Sample: non-invasive cheek swab, at home or in clinic
- Metabolomics
Metabolic Resilience
What is the metabolic state, resilience and risk?
RWE roleearly pharmacodynamic signal; links biology to risk for HEOR
What it measures
Metabolites move fastest of all layers, capturing the combined effect of therapy, diet, lifestyle and co-medication, and translating biology into future disease risk.
- Metabolic health and Metabolic Age
- 10-year risk for five chronic diseases
- Targeted metabolomics, cardiometabolic panel, amino acids & energy metabolism
Sample: one finger-prick, at home or in clinic
Complementary layers
Immune Ageing & Glycan Biology
IgG glycan biological age with pro- and anti-inflammatory indexes. Finger-prick at home.Inflammatory response to treatmentMicrobiome Blueprint
Gut composition, diversity, dysbiosis and metabolic function. Stool sample.Gut-host mediation of responseNAD+ Levels
NAD+ status and cellular energy. Minimally invasive blood test.Target engagement for NAD+ interventionsClinical Blood Biomarkers
Cardiometabolic, hormonal, nutritional and organ-function markers.Bridge to EHR lab values and safetyBrain Health & Cognitive Resilience
Brain health biomarkers, cognitive assessment and fatty acid profile.Cognitive outcomes over time
Baseline layer · measured once
Genetics & Pharmacogenetics
Polygenic risk assessment and pharmacogenetic panel from one saliva sample.
In real-world data, drug response varies for reasons the record cannot see. Pharmacogenetic genotype and inherited risk make that variation measurable: as effect modifiers when analysing heterogeneity, as covariates for confounding control, and as a basis for defining subgroups.
Five collection routes, designed for decentralised studies
Most layers can be collected at home
- Genetics & pharmacogenetics
- Advanced Proteomics
- Metabolic Resilience, Immune Ageing
- Microbiome Blueprint
- Biological Age, NAD+, Clinical Biomarkers
Six real-world study designs. One measurement layer.
- 01
Post-authorisation effectiveness
Measure biological response in older, multimorbid and diverse populations under-represented in pivotal trials. Supports label expansion and post-marketing commitments. - 02
External & synthetic control arms
Match comparators on measured biological status, not only diagnosis codes, to reduce residual confounding when randomisation is impractical. - 03
Pragmatic & decentralised studies
Add objective biological endpoints without adding site burden, with standardised collection across large, dispersed cohorts. - 04
Responder stratification
Combine pharmacogenetic genotype with multi-omic baselines to find signatures that predict benefit, for enrichment of the next interventional trial and precision positioning. - 05
Durability & persistence
Follow biological change after discontinuation, dose change or switching, to show whether effects last in routine care. - 06
HEOR & market access
Link measured biological change to utilisation and cost in linked datasets, strengthening HTA submissions and outcomes-based agreements.
Real-world questions across therapeutic areas
Examples of questions a biological outcomes layer can answer in real-world programmes.
Obesity & metabolic health
Does biological benefit extend beyond weight loss, and does it persist after treatment stops?Cardiometabolic disease
Which organ systems respond, in which patients, under real-world adherence?MASH & liver disease
Can liver-specific and systemic change be followed without repeated biopsy?Healthy ageing & geroscience
Does an intervention slow the pace of biological ageing where disease endpoints are too rare to power a study?Regenerative medicine
Is systemic biological recovery durable over years of follow-up?Oncology survivorship
How does treatment burden affect long-term biological ageing and resilience in survivors?
From protocol to analysis-ready data
- 01
Endpoint strategy
Fit-for-purpose omic layers, endpoints and sample size. - 02
Sampling cadence
Timepoints aligned with each layer’s biology and the exposure window. - 03
Collection & logistics
Home or in-clinic, with standardised pre-analytics and chain of custody. - 04
Integration & delivery
Quality-controlled data, ready for linkage with EHR, claims or registries.
Add a biological outcomes layer to your real-world programme
Tell us about your intervention, population and data sources. Our scientific team will propose an endpoint and sampling strategy.
Scientific rigour
Documented precision and locked assay versions for the life of a study.Implementation ready
Infrastructure for study-size observational and pragmatic programmes.Privacy by design
Pseudonymised, GDPR-compliant data flows with consent for linkage.
