About this trial
This study is to evaluate whether intraoperative fluorescence imaging targeting GPC3 can aid improve the surgical accuracy of hepatocellular carcinoma.
The main purposes of this study include:
① To raise the detection rate of hepatocellular carcinoma intraoperatively using the novel NIR-II fluorescence molecular imaging and the GPC-3 targeted fluorophore.
② To validate the safety and effectiveness of the designed GPC-3 targeted fluorophore for clinical application.
Eligibility criteria
Qualifiers
Patients who have been diagnosed with hepatocellular carcinoma.
Planned to receive hepatectomy.
Liver function Child-Pugh A/B.
GPC-3 was validated highly expressed preoperatively.
Disqualifiers
Allergic to IRDye800.
Enrolled in other trials in the past 3 months.
Another malignant tumor was found.
Undesirable function of heart, lung, kidney, or any other organs.
Trial design
Treatments tested in this trial
- Anti-GPC3-IRDye800CW