
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.
One platform, four seats at the table

Patient-granted records, structured pre-visit context, one-page summaries.
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Live public-data assistant, simulators, and de-identified CSV/JSON/FHIR export.
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Track your journey, prep for visits, share on your terms.
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Log on their behalf under access they grant — and can revoke.
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Running a clinic or health system? Organizations are provisioned automatically on first Microsoft work-account sign-in — start with the care-team overview or read the admin docs.
Why teams choose Teloma
Clinics and research teams bring Teloma in; patients and caregivers keep the record alive. Everyone works from the same consented, structured source of truth.
Symptoms, treatments, labs, imaging, documents, and questions on a single chronological timeline — for any cancer type.
A deterministic one-page summary, serial lab trends, and a research-use-only tumor-state view — organized signal, not raw notes.
A conversational assistant wired into ClinicalTrials.gov, PubMed, cBioPortal, and NCI GDC — plus simulators, cohort insights, and de-identified CSV/JSON/FHIR export.
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
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
Access control, de-identification, and auditability are enforced in the platform itself — not promised in the fine print.
Safety & scope →Patient, caregiver, clinician, researcher, and admin roles with per-patient, revocable grants.
Every view, export, and denial recorded in an append-only audit log.
Researchers never see identity — names, DOBs, MRNs, and exact dates are stripped by architecture, not policy.
Records live in encrypted storage; access happens through short-lived signed links only.
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.
