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Recruiting Phase 2 NCT06662097

A Study of Bevonescein in Patients Undergoing Abdominopelvic Surgery

Trial Parameters

Condition Surgery
Sponsor Alume Biosciences, Inc.
Study Type INTERVENTIONAL
Phase Phase 2
Enrollment 64
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2024-10-16
Completion 2025-06
Interventions
Bevonescein

Brief Summary

Feasibility study of Bevonescein to highlight Nerves and Ureter in patients undergoing Minimally Invasive Surgery

Eligibility Criteria

Inclusion Criteria: * Must be a minimum of 18 years of age * Study participant is planning to proceed with surgery * Willing to provide informed consent * Sexually active patients must be willing to use an acceptable form of contraceptive while participating and 30 days after. * Females of childbearing potential must have a negative pregnancy test at screening and during the study. Exclusion Criteria: * Patient has had prior surgery at the intended surgical site. * Patient has abnormal cardiac rhythm not controlled by medication. * Patient has moderate to severe renal impairment. * Patient has a history of fluorescein allergy. * Patient has a history of drug-related anaphylactic. * Presence of a concurrent disease or condition that may interfere with study participation. * Presence or history of any condition that, in the view of the investigator, places the patient at high risk of treatment compliance. * Use of any Investigational Product or investigational medial device within 30 day

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