Teloma — cancer observability and research platform
Cancer Observability & Research Platform · all cancer types

The most advanced way to observe a cancer journey.

Teloma gives care teams a structured, patient-consented view of everything that happens between visits, gives researchers a live, de-identified engine wired into the world's public oncology data — and gives patients real ownership of their own record.

Teloma does not provide medical advice, diagnosis, treatment recommendations, or emergency care. If this is an emergency, call your local emergency number.

Why teams choose Teloma

Adopted by care teams, powered by patients, built for research

Clinics and research teams bring Teloma in; patients and caregivers keep the record alive. Everyone works from the same consented, structured source of truth.

One structured record

Symptoms, treatments, labs, imaging, documents, and questions on a single chronological timeline — for any cancer type.

Clinician-ready output

A deterministic one-page summary, serial lab trends, and a research-use-only tumor-state view — organized signal, not raw notes.

A live research engine

A conversational assistant wired into ClinicalTrials.gov, PubMed, cBioPortal, and NCI GDC — plus simulators, cohort insights, and de-identified CSV/JSON/FHIR export.

Consent at the core

Patients grant and revoke every access. Research participation is a separate, explicit opt-in. Every action lands in an append-only audit log.

The core idea

Cancer, treated as an observability problem

The same signal shape software teams use to keep complex systems alive — logs, metrics, events, system state, outcomes — maps cleanly onto a cancer journey. Teloma applies it end to end.

logs

Symptoms

metrics

Labs & vitals

events / traces

Diagnosis · biopsy · treatment · imaging · adverse events

system state

Pathology · genomics · imaging

outcomes

Treatment response & recurrence

analytics layer

Research engine

Trust, by architecture

Health data deserves more than a privacy policy

Access control, de-identification, and auditability are enforced in the platform itself — not promised in the fine print.

Safety & scope →

Role-based access

Patient, caregiver, clinician, researcher, and admin roles with per-patient, revocable grants.

Audited end to end

Every view, export, and denial recorded in an append-only audit log.

De-identified research plane

Researchers never see identity — names, DOBs, MRNs, and exact dates are stripped by architecture, not policy.

Encrypted document vault

Records live in encrypted storage; access happens through short-lived signed links only.

See it with real signal

The demo environment loads sample patients across several cancers so you can explore the timeline, clinician views, research workspace, and export tools — no setup required.