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NCT Number: NCT07623473

Non-Invasive Malignancy Classifiers Using Blood-Biomarkers for Lung Nodule Evaluation

The goal of the NIMBLE study is to evaluate blood-based biomarkers for lung cancer risk prediction in patients referred with a lung nodule.

Each blood biomarker will be evaluated for descriminating malignant from benign lung nodules alone and in combination with other blood biomarkers, patient characteristics and radiological features.

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

Gentofte Hospital

Gentofte Municipality, Denmark

Location status: Recruiting

Location contact

Søren Egstrand, MD, PhD

CONTACT

[email protected]

0045 21682147

About this study

Lung nodules are frequent findings on chest CT scans. The majority of nodules are benign, but a substantial fraction will be malignant. The decision to pursue invasive diagnostics currently rely on a risk estimate based on patient characteristics and radiological features of the nodule.

Accurate risk estimation is crucial as invasive diagnostics comes with a significant risk of severe complications such as collapsed lung, bleeding, infections and in rare cases death. The NIMBLE project seeks to improve the early risk assessment by incorporation of blood biomarkers in the risk algorithm. The study will include 1,200 patients with a nodule when patients are referred to the dept. of pulmonology and perform an addition blood draw. The blood will be analyzed using a wide range of blood tests. These will include standard blood tests, novel protein tumor markers specifically targeting lung cancer, an epigenetic smoking marker (AHRR methylation), and combined fragmentome, mutational and methylome analysis of cell-free tumor DNA.

Blood tests will be evaluated following REMARK guidelines in terms of lung cancer predictive performance but also in terms of feasibility in implementation in daily routine testing at a Dept. of Clinical Biochemistry.

The study will perform all tests on patient material collected at baseline when patients are referred to work-up and use machine learning to optimally combine blood tests with patient characteristics and radiological features.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with a newly detected IPN suspected of lung cancer referred to the infiltrate unit
  • Having signed informed consent

Exclusion criteria

  • Active cancer, excluding non-melanoma skin cancer
  • Comorbidities that exclude the patient from clinical follow-up and final diagnosis

Treatment and study plan

Blood tests

Diagnostic Test

Standard blood tests, Novel protein tumor markers specifically targeting lung cancer, Epigenetic smoking marker (AHRR methylation), Combined fragmentome, mutational and methylome analysis of cell-free tumor DNA

Primary outcomes

  1. Lung cancer diagnosis during work-up

    Time frame: At least two years of followup

Study contacts

Contact information is provided by the study sponsor or research team.

Søren Egstrand, MD, PhD

CONTACT

[email protected]

0045 21682147

Sponsors and collaborators

Lead sponsor

Herlev and Gentofte Hospital

Other

Collaborators

  • Beckett Foundation
  • Direktør Michael Hermann Nielsens mindelegat, afd B
  • Grosserer L. F. Foghts Fond Denmark
  • NEYE Foundation
  • P. A. Messerschmidt & hustrus Fond
  • Toyota Foundation Denmark

Registry information

Official study title

NIMBLE | Non-Invasive Malignancy Classifiers Using Blood-Biomarkers for Lung Nodule Evaluation

Acronym: NIMBLE

Important dates

Study start
2024
Primary completion
2028
Study completion
2028
First posted
Jun 3, 2026
Registry last updated
Jun 3, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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