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HIPAA Compliant
ISO 27001 Certified

Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
ID07760012

Evaluation of 68Ga-SorB PETCT Imaging for Diagnosing Sortilin-Expressing Solid Tumors in Adults with Melanoma, Liver, Lung, Pancreatic, Breast, or Ovarian Cancer

Led by Peking University Third Hospital · Updated on 2026-08-12

50

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the safety, feasibility, and diagnostic accuracy of a new PET tracer called 68Ga-SorB targeting Sortilin, a receptor highly expressed in several solid tumors including melanoma, liver, lung, pancreatic, breast, and ovarian cancers. This exploratory diagnostic study compares 68Ga-SorB PETCT imaging to the standard 18F-FDG PETCT, aiming to improve tumor detection and characterization by using a more tumor-specific tracer with fewer false positives. Participants will receive a single intravenous dose of 68Ga-SorB followed by whole-body PETCT imaging about 60 minutes after injection. The study compares these imaging results with clinically indicated 18F-FDG PETCT scans done within a set timeframe. No therapeutic treatments are given as part of this study. Approximately 40 to 50 adults with confirmed or suspected tumors will be enrolled for imaging and follow-up. During the study, participants are monitored for adverse events from tracer administration until about 24 hours post-imaging. Tumor uptake is measured using quantitative PET parameters such as SUVmax and tumor-to-background ratio. Follow-up includes pathology review and clinical assessments up to 3 months after imaging to evaluate lesion detection, diagnostic sensitivity, specificity, and overall accuracy. This research will provide initial clinical evidence to support further development of Sortilin-targeted imaging and potential future therapeutic applications.

CONDITIONS

Brief Title

68Ga-SorB PET/CT Imaging in Patients With Solid Tumors

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 75 years
  • Histologically confirmed or clinically suspected melanoma, hepatocellular carcinoma, lung cancer, breast cancer, pancreatic cancer, or ovarian cancer
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
  • Adequate blood counts and organ function as defined by specified laboratory thresholds
  • Normal cardiac function
  • Estimated life expectancy of at least 12 weeks
  • Willing and able to comply with study procedures and follow-up
  • At least one measurable target lesion according to RECIST version 1.1
  • Use of effective contraception during the study and for 3 months after imaging for participants of childbearing potential
  • Clinically indicated to undergo 18F-FDG PET/CT for tumor evaluation
  • Able to understand the study procedures and provide written informed consent
Not Eligible

You will not qualify if you...

  • Pregnant or breastfeeding women
  • Severe dysfunction of major organs including heart, liver, or kidney judged as unsuitable by investigator
  • Inability to tolerate PET/CT imaging or complete study follow-up
  • Any other condition judged by the investigator to make the participant unsuitable for the study

Research Team

M

Meixin Zhao

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