Single Dose Investigator Initiated Pilot Study to Investigate CYTALUX (Pafolacianine) for Intraoperative Detection of Malignant Tissue in Subjects Undergoing Surgical Resection for Cancer.

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorJohn Waters

About this trial

The goal of clinical trial is to test an FDA approved drug called Pafolacianine that attaches to cancer cells and lights up when seen through a special camera system in adults with a suspected primary diagnosis, or a high clinical suspicion of gastrointestinal, fore gut, pancreatic, hepatobiliary, esophageal malignancies and gyn malignancies planned for HIPEC/debulking, warranting surgery. The main question it aims to answer is:

• Can CYTALUX™ (pafolacianine) injection used with near-infrared (NIR) fluorescent imaging improve the detection of malignant tissue in subjects undergoing surgical resection for cancer? Participants taking part in this study will receive the study medication. Then, during the surgery the investigator team will turn on the camera to evaluate if the tumor is visible with the help of the study medication. Taking part in this study will last about 2 months.

Eligibility criteria

Qualifiers

Male and Female patients 18 years of age and older

Have a primary diagnosis, or a high clinical suspicion, of gastrointestinal, fore gut, pancreatic, hepatobiliary, esophageal malignancies and gyn malignancies planned for HIPEC/debulking, warranting surgery.

Are scheduled to undergo surgical intervention for tumor resection or diagnostic laparoscopy for assessment of disease burden.

Willingness to stop the use of folate, folic acid, or folate-containing supplements within 48 hours before administration of Cytalux

Disqualifiers

Any medical condition that in the opinion of the investigators could potentially jeopardize the safety of the subject

History of anaphylactic reactions to products containing indocyanine green for near infrared imaging. Subjects with a medical history of 'idiopathic anaphylaxis' will require evaluation.

History of allergy to any of the components of CYTALUX™ (pafolacianine) injection

Presence of any psychological, familial, sociological condition or geographical challenges potentially hampering compliance with the study protocol or follow-up schedule

Trial design

Treatments tested in this trial

  • CYTALUX™ (pafolacianine) injection preoperatively

Treatment groups

50 Participants
are divided into 1 treatment group

Sponsors and collaborators

John Waters

Lead sponsor

University of Texas Southwestern Medical Center

Sponsor institution

On Target Laboratories, LLC

Collaborator