Summary

Eligibility
for people ages 18 years and up (full criteria)
Healthy Volunteers
healthy people welcome
Location
at UCSD
Dates
study started
completion around

Description

Summary

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

Official Title

Multicenter Open-Label Feasibility Study of Intraoperative Nerve and Ureter Visualization With Bevonescein in Patients Undergoing Minimally Invasive Abdominopelvic Surgery

Details

This study will evaluate the safety, tolerability and efficacy of Bevonescein administered as an intravenous (IV) infusion to patients undergoing minimally invasive surgery. This study will also characterize the pharmacokinetic of Bevonescein in this subject population and determine the dose of Bevonescein needed to generate a fluorescence signal in nerve and ureter tissue to enable fluorescence recordings and image analysis with an imaging system.

Keywords

Surgery, Nerve Injury, Imaging, Bevonescein

Eligibility

You can join if…

Open to people ages 18 years and up

  • 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.

You CAN'T join if...

  • 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 days prior to screening.

Location

  • University of California San Diego accepting new patients
    San Diego California 92037 United States

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Alume Biosciences, Inc.
ID
NCT06662097
Phase
Phase 2 research study
Study Type
Interventional
Participants
Expecting 64 study participants
Last Updated