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Smart health, simplified

Medication decisions, screened against your proteins.

Every prescription is tested on an average patient who does not exist. Navi8 uploads your sequence once, then answers every medication question your family has — side-effect risk, dosage, interactions, alternatives — against your own molecular biology.

Structure-based, not population-based Sequence uploaded once, reused forever One account for the whole household
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Treatments
Navi8 app: Treatments list with RxNorm-matched medications
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Medication screening
Navi8 app: Medication screening — choose same-class alternatives, side-effect mode or multi-drug panel
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Navi8 app: Today view with schedule and reminders
$528Bwasted every year on prescriptions that do not work for the person taking them
>50%of patients carry a gene variant that changes how they respond to a drug
2–3medication changes before many patients find one that works
1sequence upload with Navi8 — then every question is answered against you

Sources: FDA, JAMA, NIH Clinical Pharmacogenetics.

What Navi8 answers

Five questions every family asks about a prescription. One engine that answers them from your sequence.

How it works

From a saliva sample to a ranked answer — without ever seeing a sequence editor, a configuration file or a GPU.

01

Your sequence

Upload whole-genome, exome or a targeted panel. Navi8 keeps only the protein-changing variants that matter.

02

Your proteins

Variants become patient-specific protein structures — folded once, cached, and reused across every future question.

03

Your medications

Each drug resolves to a canonical molecule and expands into same-class, research and natural candidates.

04

Your answer

Structure-based screening ranks alternatives, side-effect risk and multi-drug interactions against your proteins.

Schematic of a structure-based screen: a ligand posed in a kinase active site with the hinge, N-lobe and C-lobe labelled
Schematic of a structure-based screen. Not a live Navi8 result.
Why it is affordable

The expensive step happens once. The tenth question is essentially free.

Navi8 folds only what changed in your proteins — not a whole proteome. That is the difference between four figures of compute per person and single digits, and it is why the second question a family asks costs a fraction of the first.

Oncesequence upload, reused for every later question
Minutesfrom request to a ranked, provenance-complete result
~$9of compute per newly modeled user at the target structure count

Read the science →

Navi8 family management: a member workspace showing 30-day medication adherence, symptom changes and review flags (synthetic preview)
Household member workspace · synthetic preview, not live patients
Family management

A household, not a single patient.

Medication management is a family job. One household manager links spouses, children and parents, and sees adherence, symptoms and review flags for all of them on one review range — with each member’s screening run against their own sequence.

  • Link existing Navi8 accounts by email; each member keeps their own login and data.
  • 30-day adherence and symptom timelines for every medication, every member, side by side.
  • Rule-based review flags — adherence gaps, supplement overlaps, timing drift — that are display-only, never diagnostic.
  • The same view a clinician sees, so a visit starts from shared facts.
Investors

We are raising a $500K SAFE to reach two observable milestones.

$100K committed so far. The round funds compute capacity, production engineering and a third clinical pilot site.

$100K raised$500K target