OncoMatch/Clinical Trials/NCT07039526
Single Dose Investigator Initiated Pilot Study to Investigate CYTALUX (Pafolacianine) for Intraoperative Detection of Malignant Tissue in Subjects Undergoing Surgical Resection for Cancer.
Is NCT07039526 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies CYTALUX™ (pafolacianine) for esophageal cancer.
Treatment: CYTALUX™ (pafolacianine) — 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.
Check if I qualifyExtracted eligibility criteria
Cancer type
Esophageal Carcinoma
Colorectal Cancer
Gastric Cancer
Hepatocellular Carcinoma
Pancreatic Cancer
Cholangiocarcinoma
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- Clemments University Hospital · Dallas, Texas
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