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TERMINATED
NCT02676050
EARLY_PHASE1

Visualising c-MET and Activated Neutrophils in Lung Cancer

Sponsor: University of Edinburgh

View on ClinicalTrials.gov

Summary

Lung cancer is currently a major health problem in the UK. Despite being one of the most common cancers, lung cancer has a poor prognosis compared to other types of cancer and is the leading cause of cancer death in the world. As opposed to other organs, the lung is highly susceptible to inflammatory insults, for example from bacterial infection-induced and tobacco-induced inflammation. It has long been known that the cellular microenvironment that nurtures tumour growth and development is linked to sites of chronic inflammation but molecular insights into how external inflammation boosts or inhibits cancer in the lungs remains unclear. This study aims to directly visualise the expression of a well known marker of cancerous tissue, c-MET, and the activity of neutrophils in human lung cancer in vivo in situ using fibre-based endomicroscopy.

Official title: Exploratory Study to Optically Visualise Activated Neutrophils and the Proto-oncogene, c-MET, in Lung Cancer Using DUAL Colour Fibre-based Endomicroscopy

Key Details

Gender

All

Age Range

16 Years - Any

Study Type

INTERVENTIONAL

Enrollment

5

Start Date

2019-10-04

Completion Date

2022-03-20

Last Updated

2026-06-03

Healthy Volunteers

No

Conditions

Interventions

OTHER

Optical Imaging Agents (EMI-137, NAP)

Both optical imaging agents (NAP and EMI-137) will be administered to each patient during a bronchoscopy procedure. A novel delivery catheter (to deliver both agents), imaging fibre and endomicroscopy system with viewer software will be used to detect c-MET and activated neutrophil signal in the human lung.

DEVICE

Delivery Device Cathetar and Miniaturised imaging fibre

Both optical imaging agents (NAP and EMI-137) will be administered and imaged simultaneously during a bronchoscopy procedure using the devices mentioned above.

DEVICE

Optical endomicroscopy system

The signal emitted by both optical imaging agents (NAP and EMI-137) will be visualised using a novel endomicroscopy system.

Locations (1)

Royal Infirmary of Edinburgh

Edinburgh, United Kingdom