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Clear Blood
Molecular residual disease surveillance for blood-based and haematological contexts, so follow-up is as early and precise as possible.
01Clear Blood
MRD surveillance for blood-based contexts
After curative-intent treatment, Clear Blood monitors for the molecular signals of returning disease in blood-based and haematological contexts, so follow-up can be as early and precise as possible.
It tracks disease-specific molecular markers over time from a simple blood draw, with each result read against your baseline and history.
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How it works
- Step 1Baseline
Establish your molecular starting point after treatment.
- Step 2Scheduled monitoring
Planned blood draws on a subscription cadence.
- Step 3Interpretation
Each result is read in context by the engine.
- Step 4Clinician review
A changing signal triggers KPCIRC review and a plan.
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Honest limits
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 your scheduled clinical follow-up. It does not replace it.
Being clear about our limits
What we do and do not do
What we DO
- Watch for returning disease after curative-intent treatment
- Often flag recurrence earlier than routine imaging
- Trigger a KPCIRC clinician review on a changing signal
- Personalise how closely follow-up is done
What we DON’T do
- Diagnose recurrence on its own, findings are confirmed
- Detect every recurrence, since some tumours shed little ctDNA
- Replace your scheduled scans and specialist follow-up
- Guarantee that acting earlier will change the outcome
Plain-language glossary (5 terms)
| Term | What it means |
|---|---|
| MRD | Molecular residual disease, microscopic disease left after treatment. |
| ctDNA | Circulating tumour DNA, tumour fragments a blood test can read. |
| Tumour-informed | An MRD test built from your own tumour’s mutations, for higher sensitivity. |
| Recurrence | The cancer returning after a period of remission. |
| Lead time | How far ahead of a scan a blood test can flag returning disease. |
Important information and regulatory status
Clear Blood is a genomic (DNA-based) test for use by qualified healthcare professionals. It supports clinical judgement, it does not replace it, and it must be read alongside your full clinical history and applicable guidelines.
- A result is not a diagnosis and does not by itself decide treatment.
- A “not detected” result does not rule out cancer or a genetic change.
- Not all cancers release enough DNA into blood to be detected.
- We cannot guarantee that a medicine will be available, approved, covered or effective.
- Collection kits are for qualified phlebotomists. They are not for self-testing.
- Confirmatory testing may be required.
Regulatory status (India). Registration of our genomic tests as in-vitro diagnostic (IVD) medical devices with CDSCO is in progress, with the IVD class pending. Sequencing and variant calling are done by an accredited laboratory partner (CAP-accredited, ISO 15189) following ACMG/AMP/ASCO/CAP guidelines and 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.
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