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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05047510
Other study ID # Chinese Academy of Sciences
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 10, 2021
Est. completion date December 31, 2026

Study information

Verified date August 2023
Source Chinese Academy of Sciences
Contact Zeyu Zhang, Ph.D.
Phone 86-18201082715
Email zhangzeyu@fingerpass.net.cn
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date December 31, 2026
Est. primary completion date December 31, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: 1. Patients who have been diagnosed with hepatocellular carcinoma. 2. Planned to receive hepatectomy. 3. Liver function Child-Pugh A/B. 4. GPC-3 was validated highly expressed preoperatively. 5. Aged 18 to 75, and the expected lifetime is longer than 6 months. 6. Approved to sign the informed consent. Exclusion Criteria: 1. Allergic to IRDye800. 2. Enrolled in other trials in the past 3 months. 3. Another malignant tumor was found. 4. Undesirable function of heart, lung, kidney, or any other organs. 5. Unable to tolerate a hepatectomy. 6. The researchers considered inappropriate to be included.

Study Design


Intervention

Drug:
Anti-GPC3-IRDye800CW
Drug Injection: Anti-GPC3-IRDye800CW

Locations

Country Name City State
China The Affiliated Hospital of Southwest Medical University Luzhou Sichuan
China Zhuhai People's Hospital Zhuhai Guangdong

Sponsors (1)

Lead Sponsor Collaborator
Chinese Academy of Sciences

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary HCC lesions Numbers of intraoperatively detected hepatocellular carcinoma lesions. During hepatocellular resection surgery.
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