Feasibility of Fluorescence Imaging With Bevacizumab-800CW During Bronchoscopy
NCT06809946 · Status: NOT_YET_RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 20
Last updated 2026-03-30
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.
Conditions
- Lung Neoplasms
- Pulmonary Neoplasms
- Lymph Node Involvement
- Pulmonary Nodule
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.
Sponsors & Collaborators
-
University Medical Center Groningen
lead OTHER
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- DIAGNOSTIC
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-08-17
- Primary Completion
- 2028-08-17
- Completion
- 2028-08-17
Countries
- Netherlands
Study Locations
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