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VarSee clinical validation study

Multicentre prospective & retrospective remnant Biospecimen collection program for study and future biomedical research

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/03/105171
Enrollment
100
Registered
2026-03-02
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: C349- Malignant neoplasm of unspecifiedpart of bronchus or lung

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil

Sponsors

BioMarkIQ Scientific Technologies Private Limited
Lead Sponsor
BioMarkIQ Scientific Technologies Private Limited
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: newly diagnosed lung cancer patients with confirmed tissue biopsy and CT scan and no treatment or surgery before enrollment. Inclusion criteria for cancer cohort

Exclusion criteria

Exclusion criteria: Pediatric lung cancer patients, patients with history of previous cancers.

Design outcomes

Primary

MeasureTime frame
To identify the panel of most sensitive and specific biomarkers amongst the 12 candidate protein biomarkers that can yield a sensitivity of more than 90%. To assess the sensitivity, specificity, positive predictive value, negative predictive value, and area under the receiver operating characteristic curve (AUC-ROC) of the biomarker panel for lung cancer diagnosis. To compare the diagnostic performance of individual biomarkers within the shortlisted panel and compare them with the entire panel. Timepoint: At the baseline

Secondary

MeasureTime frame
To assess the correlation between biomarker levels and tumor characteristics, such as tumor size, histological subtype, or stage of lung cancer.Timepoint: At the baseline

Countries

India

Contacts

Public ContactDr Snahlata Singh

BioMarkIQ Scientific Technologies Private Limited

snahlata.singh@biomarkiq.com7499159787

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Apr 4, 2026