We help pharma enroll the right patients
and bring successful therapies to patients.
— hampers drug development, clinical monitoring, and ultimately patient care.
Dying brain cells shed molecular signals
Reflects real-time molecular signals and disease state
Profiles personalized immune responses over the longer term
Integrates multi-omic signals with clinical and biological knowledge to identify biomarkers
An AI-native path to blood diagnostics for neurology.
Scientists guide the agent step by step
Contributes its own judgement alongside the team
Trustworthy judgements, scientists sign off
Scale high-quality paired measurements while establishing clinically relevant biomarker value.
Complementary biology, patient heterogeneity and use-case utility
Biomarker trajectories linked to clinical change; reproducibility & QC
Candidate panel, locked AI model and pilot-ready assay / report
Accessible, rapid, affordable blood test to screen patients for clinical trials.
PET only confirms the shortlist.
Objective, blood-based molecular monitoring of treatment effect.
TAM is the global annual brain-disease diagnosis and monitoring market; SAM is the neurodegenerative-disease segment; the ~30% 5-year share is an NDx assumption · growth FMI · clearance FDA, May 2025 · demand signal Fortune, STAT.
An AI-native biomarker engine where commercial adoption, proprietary data and validation reinforce each other.
Study contracts + per-sample analytical fees
Reusable assays, AI models and sponsor relationships
Strengthened by pharma partnerships and repeated learning
Paid studies on existing trial samples
Longitudinal monitoring & validation
More programs, sponsors & indications
Differentiation today: signal selection + customer focus · Defensibility tomorrow: data + validation + workflow integration
Purposeful pairing of cfDNA methylation and autoantibody signals
Matched longitudinal profiles connected to disease trajectories
Evidence for stratification, progression and trial workflows
Wet lab, computational biology and ML product — with the clinical access to run the study.



