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Clear Blood – MRD Surveillance for Blood-Based Contexts · OnKommon
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Clear Blood — MRD surveillance for blood-based contexts.

CLEAR · MRD SURVEILLANCE FOR BLOOD-BASED CONTEXTS

Clear Blood is molecular residual disease surveillance for blood-based and haematological contexts. After curative-intent treatment, it monitors for the molecular signals of returning disease so that follow-up can be as early and precise as possible.

Learn How It Works MRD Surveillance
What It Monitors

2 · What it monitors

Disease-specific molecular markers appropriate to the condition, tracked over time from a simple blood draw, with each result read in the context of your baseline and history.

How It Works

3 · How it works

Baseline → Scheduled monitoring → Interpretation → Clinician review

1

Baseline

Establish your molecular starting point after treatment.

2

Scheduled monitoring

Planned blood draws on a subscription cadence.

3

Interpretation

Each result is read in context by the OnKommon engine.

4

Clinician review

A changing signal triggers KPCIRC review and a plan.

Honest Limits

4 · Honest limits

We believe in transparency about what a test can and cannot do.

MRD surveillance improves the chance of catching a return early, but no test detects every recurrence, and a negative result is reassuring rather than absolute. Clear Blood complements, and does not replace, your scheduled clinical follow-up.

Terminology

TERMINOLOGY ON THIS PAGE

The words you will see, in plain language

Term / What it means
MRDMolecular residual disease — microscopic disease left after treatment, seen as trace ctDNA.
ctDNACirculating tumour DNA — tumour DNA fragments a blood test can read.
Tumour-informedAn MRD test designed from your own tumour's mutations, for higher sensitivity.
RecurrenceThe cancer returning after a period of remission.
Lead timeHow far ahead of a scan a blood test can flag returning disease.
Important information about this test

Clear Blood is a genomic (DNA-based) test offered for use by qualified healthcare professionals. It is intended to support — not replace — clinical judgement, and must be interpreted alongside your full clinical history, other investigations, and applicable guidelines.

  • • A result is not a diagnosis and does not by itself decide treatment.
  • • A “not detected” or normal result does not rule out cancer or a genetic change.
  • • Not all cancers release enough DNA into blood to be detected.
  • • The test does not guarantee access to any medicine, its regulatory approval, insurance cover, or that a therapy will work.
  • • Sample-collection kits are for use by qualified phlebotomists only — not for self-testing or self-sampling.
  • • Confirmatory testing may be required.

Regulatory status (India). OnKommon's registration of its genomic tests as in-vitro diagnostic (IVD) medical devices with the Central Drugs Standard Control Organisation (CDSCO) is in progress (IVD class pending). Sequencing and variant calling are performed by an accredited laboratory partner (College of American Pathologists — CAP-accredited; ISO 15189) following international guidelines (ACMG/AMP/ASCO/CAP) using a CE-IVD certified variant database. The OnKommon interpretation engine is provided for research and decision-support use. Marketing follows the Drugs and Magic Remedies (Objectionable Advertisements) Act, 1954 and applicable Indian advertising standards.

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