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Feasibility of Fluorescence Imaging with Bevaci-zumab-800CW During Bronchoscopy in Patients with a Pulmonary Lesion Considered to Be Malignant
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.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Start Date
June 1, 2025
Primary Completion Date
June 1, 2026
Completion Date
December 1, 2026
Last Updated
February 20, 2025
20
ESTIMATED participants
injection with 15 mg bevacizumab-800CW before bronchoscopy
DRUG
injection with 25 mg bevacizumab-800CW before bronchoscopy
DRUG
Lead Sponsor
University Medical Center Groningen
NCT07143110
NCT06885697
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT04577599