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NOT YET RECRUITING
NCT06809946
PHASE2

Feasibility of Fluorescence Imaging With Bevacizumab-800CW During Bronchoscopy

Sponsor: University Medical Center Groningen

View on ClinicalTrials.gov

Summary

In this feasibility study, bronchoscopy will be combined with fluorescence molecular imaging using the near-infrared fluorescence (NIRF) tracer bevacizumab-800CW for assessment of pulmonary lesions and/or lymph nodes considered to be malignant.

Official title: Feasibility of Fluorescence Imaging With Bevacizumab-800CW During Bronchoscopy in Patients With a Pulmonary Lesion Considered to be Malignant - DEFLECT I

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

20

Start Date

2026-08-17

Completion Date

2028-08-17

Last Updated

2026-03-30

Healthy Volunteers

No

Interventions

DRUG

injection with 15 mg bevacizumab-800CW before bronchoscopy

Patients will receive an intravenous administration of 15 mg bevacizumab-800CW before the bronchoscopy procedure. The bronchoscopy will start with high-definition white light bronchoscopy, followed by fluorescence molecular bronchoscoy to observe the fluorescence signal and MDSFR-SFF spectroscopy to quantify the fluores-cence signal in vivo.

DRUG

injection with 25 mg bevacizumab-800CW before bronchoscopy

Patients will receive an intravenous administration of 15 mg bevacizumab-800CW before the bronchoscopy procedure. The bronchoscopy will start with high-definition white light bronchoscopy, followed by fluorescence molecular bronchoscoy to observe the fluorescence signal and MDSFR-SFF spectroscopy to quantify the fluores-cence signal in vivo.

Locations (1)

University Medical Center Groningen

Groningen, Netherlands