When to Choose Aura-O™?

High risk women— with Polycystic Ovarian Syndrome (PCOS)

Avoid unnecessary treatment and protect fertility️

Distinguish non-cancerous conditions (Endometriosis & Fibroids) from early signs of malignancy

Monitor your health

after during treatment

Irregular Periods or Unusual Bleeding after Menopause

Family History

of Cancers

Aura-O™ Ovarian Cancer Screening Process (Minimally Invasive)

Step 01

Schedule Screening and Get ID

Book your appointment and receive an activation ID for secure tracking and results access.

Attend your scheduled screening appointment at the facility.

A small 5ml blood sample will be gently collected for a quick and easy experience.

Your sample will be analysed for ovarian cancer biomarkers.

Why Aura-O™ is a Game-Changer for Women’s Health?

Non-Invasive Sample Collection

Uses ctDNA from a small venous

blood draw with no surgery, no

biopsy and no discomfort.

Early Detection of FIGO Stages

84.6%
88.9%
84.8%
91.7%

Detection Sensitivity (%)

DNA Methylation-Based Assay

Targets clinically validated

markers (CDO1 and HOXA9)

for high sensitivity and,

specificity.

High Accuracy

89.7%
97.5%
High Accuracy
Aura-O Packaging

Efficient Triage Tool

CE IVD

CE-IVD Certified

Approved for clinical use. More accurate and cost-effective than CA125, HE4,

and ROMA Index.

Aura-O™ Outperforms
Traditional Ovarian Cancer Detection Methods

Sensitivity
Specificity

Percentage (%)

Clinical Trials Insights

Validated in 6,600+ patients, showing >90% accuracy and superior early-stage

ovarian cancer detection vs. CA125, HE4, and ROMA; CE-IVD marked.

Clinical Studies

What You Receive

Results Online

Access your test results securely

via our portal using your

activation ID.

Gynecology Consultation

Get a personalised consultation with a

gynecologist to discuss your results

and next steps.

Further Screening or Treatment

If needed, you’ll receive recommendations

for additional screening or

treatment.