LIFE OS / Early access 2026

Medicine is about to become continuous.LIFE OS is the model that makes it possible.

Your drug acts every hour. You see the patient every twelve weeks. LIFE OS keeps a live model of that patient's biology and of what your asset is doing inside it.

What it is

A live model of patient biological state, running around a drug in trials, expanded access and post-launch.

What you get

Response, tolerability, adherence and the mechanism behind them — weekly, per patient.

What it is not

Not a survey app, not a claims database, not a dashboard on old data.

Continuous biological telemetrylive
HRVGLUCOSESLEEPINFLAMMATIONMICROBIOMESYMPTOMSNOW
Illustrative channels · sampled continuously · aligned on one timeline
·biosensor · heart rate variability·cgm · glucose variance·sleep architecture·blood panel · inflammation·shotgun metagenomics·human dna · polygenic risk·symptom report·medication & dose timing·nutrition log·activity load·clinical events
·biosensor · heart rate variability·cgm · glucose variance·sleep architecture·blood panel · inflammation·shotgun metagenomics·human dna · polygenic risk·symptom report·medication & dose timing·nutrition log·activity load·clinical events
50,000+
biological signals per patient
24/7
observation, not visits
1
runtime across indications
Nov 2026
estimated availability
Request early access

Pharma · biotech · CRO · clinical research

01 — The gap

Drug design is only the beginning.The patient is the harder system.

The asset acts continuously. Biology reacts continuously. Trials and care still observe through visits, isolated biomarkers and endpoints — and between those checkpoints the system keeps moving.

You cannot control what you cannot observe.

Continuous vs. observedlive
ASSETcontinuously actingBIOLOGYcontinuously reactingOBSERVEDvisit · lab · endpointBETWEEN CHECKPOINTS, THE SYSTEM KEEPS MOVING
The asset acts continuously. Observation is sparse.

02 — The model

Data is not the product.State is.

A lab value is a coordinate; a diagnosis is not a trajectory. LIFE OS reconstructs how the biological system moves — from what was measured, what happened, what was done and how the patient responded.

Core modellive
PERIODICblood · omics · imagingCONTINUOUSbiosensors · symptoms · foodSEMANTIC LAYERCORE BIOLOGY MODEL Z(t)TRAJECTORY
Z(t) is the estimated biological state at time t

Four different objects, tracked separately.

I(t)

Immune state — what is activated

P(t)

Biological pressure — what the system is experiencing now

D(t)

Damage / dysfunction — what has accumulated

R(t)

Repair / resilience — capacity to recover

Trajectory forecastlive
FORECASTOBSERVEDSTATE Z(t) · CONFIDENCE BAND 50% / 90%
Observed state, projected scenarios and confidence bands

03 — Your asset, observed

Watch your asset work.Answers while they still matter.

What you ask todayHow you find out todayWith LIFE OS
Is the drug working in this patient?Endpoint at week 12 or 24Weekly change in the biology that drives the endpoint
Why did this patient not respond?Post-hoc subgroup analysisTheir own baseline: genetics, microbiome, inflammation, metabolism
Is a side effect starting?The patient reports it, or a lab flags itPhysiological drift days before it is reported
Is the patient still taking it?Pill counts and self-reportDose timing plus the biological signature of a taken dose
What should we combine it with?A new study, a few more yearsWhich biological gap stays open in non-responders
Response distributionlive
Responders42%Partial response31%Non-responders19%Discontinued8%THE QUESTION IS NOT THE SPLIT · IT IS THE BIOLOGY BEHIND IT
LIFE OS models the biology behind each group

For non-responders, LIFE OS measures the distance between current state and the state associated with the desired outcome: what changed, what did not, and what is blocking full response.

04 — The loop

Medicine becomes a loop.Observe → Understand → Act → Measure → Learn.

Every measured response re-enters the model, so asset understanding improves with every treated patient.

The care looplive
PATIENTOBSERVATIONLIFE OSUNDERSTANDINGACTIONRESPONSEEVERY RESPONSE CORRECTS THE MODEL

05 — Scale

The largest biological model will not come from static datasets.It will come from trajectories.

One patient builds a Patient Biology Model. Many patients around one asset build an Asset Biology Model.

Cohort trajectorieslive
LIFE OSASSET INTELLIGENCE
Each line is one patient's evolving biological state feeding one model
Where does this asset work best?And for which biological state
What predicts early response?Baseline state + first-weeks drift
What predicts non-response or toxicity?The bottleneck, not the subgroup label
Which combinations repeatedly emerge?Across patients, indications and assets

06 — Three surfaces, one runtime

Simple for the patient. Integrated in the clinic.Real-time for the asset builder.

For the patient

One action at a time.

What to eat, when to dose, what to monitor, when to call the clinician. No graphs to decode.

  • App, account and activation code in ~2 minutes
  • Sampling and data refresh handled automatically

For clinics & hospitals

Inside existing care.

The physician links the patient by QR, sets the objective, and sees the reasoning behind every action delivered between visits.

  • Patient linked in one scan — no new workflow
  • Structured exports, GDPR and MDR-aligned governance

For the asset builder

Real-time biology.

Consented, de-identified biological state around your asset as it evolves.

  • Continuous cohort state, not quarterly extracts
  • API and secure data room, audit trail and consent scope
One runtime · three surfaceslive
LIFE OS RUNTIME Z(t)PATIENT APPwhat to do todayCLINIC CONSOLEobjective + reasoningASSET INTERFACEreal-time biologyOBSERVE ↺
Every surface feeds observation back into the same model
Drug-design platformsWork before the patient
RWE playersStructure historical data
SensorsObserve narrow streams
LIFE OSConnects observation, biological state, action, response and learning

06b — Clinical evidence

Clinically proven

Medical device · Clinical research

Clinically proven. CE-marked.

1,000+
Patients in clinical studies
5
Clinical studies conducted
4
Published results
>70%
Patients much improved at three months

07 — Questions

LIFE OS, answered directly.

What is LIFE OS?+

A continuous biology runtime. It combines periodic measurements (blood, genomics, microbiome, imaging) with continuous signals (wearables, symptoms, dose timing, food, activity) to keep a live estimate of a patient's biological state Z(t) while a therapeutic asset is acting.

How is it different from real-world evidence platforms?+

RWE structures data that was already recorded. LIFE OS measures biology as it happens and reconstructs state between visits, so response, tolerability and adherence are visible while they can still be acted on.

What can a pharma team see?+

Per-patient and cohort response trajectory, immune shift, biological pressure, accumulated dysfunction, repair capacity, response gap and the bottlenecks limiting response — consented, de-identified, with full audit trail.

What does the patient see?+

One action at a time: what to eat, what to avoid, when to take the dose, what to monitor, when to call the clinician. The modeling stays behind the interface.

Which data does LIFE OS use?+

Shotgun metagenomic microbiome sequencing, human DNA and polygenic risk, blood panels, wearables and biosensors, medication and dose timing, nutrition, activity, sleep, symptoms and clinical events — on one patient timeline.

When is it available?+

The patient companion and clinic console are live today. The asset-facing interface enters early access with selected pharma, biotech and CRO partners, estimated November 2026.

08 — Request access

LIFE OS

Understand life while it is happening.

Send your name, company, role, work email, therapeutic area and asset stage, and what you want LIFE OS to understand around your asset.

Request early access