IS-001 Injection in Patients Undergoing Robotic-Assisted Gynecological Surgery

About the study

This study evaluates the safety and efficacy of intravenous injection of IS-001 to aid in intraoperative ureter structure delineation.

Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Inclusion Criteria:

Inclusion Criteria

Female subject is between the ages of 18 and 75, inclusive.
Subject is scheduled to undergo robotic-assisted gynecological procedure using a da Vinci® surgical system with Firefly® fluorescent imaging.
Subject is willing and able to provide informed consent.

EXCLUSION CRITERIA

Exclusion Criteria:

Subject is pregnant or nursing.
Subject has known active hepatitis B virus (HBV) or hepatitis C virus (HCV) infection.
Subject is already enrolled in another investigational drug or device study receiving therapeutic agents within the past 6 months
Subject has any other condition or personal circumstance that, in the judgment of the Investigator, might interfere with the collection of complete quality data or represents an unacceptable safety profile.
Subject has a known or suspected hypersensitivity to indocyanine green (ICG)
Subject has any of the following screening laboratory values:

Estimated glomerular filtration rate (eGFR) < 60 mL/min/1.73 m^2
Aspartate aminotransferase (AST) or serum glutamic oxaloacetic transaminase (SGOT) ≥ 2.5 × upper limit normal (ULN)
Alanine aminotransferase (ALT) or serum glutamic pyruvic transaminase (SGPT) ≥ 2.5 × upper limit normal (ULN).