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

Study acronym: SORB-PET
StatusRecruiting
PhaseNot applicable
Started

Free. We email you which fields changed when ClinicalTrials.gov updates this record.

Track this trial
View on ClinicalTrials.gov ↗

Record History

See every version on ClinicalTrials.gov ↗

  1. Notable Primary endpoints: details revised at 2 of 3 entries Show 5 more changesShow less
    • Start date changed from estimate of Jul 24, 2026 to Aug 13, 2026
    • Interventions: 68Ga-SorB PET/CT (Diagnostic Test) to 68Ga-SorB PET/CT (Diagnostic Test)
    • Eligibility criteria expanded, about 22 words
    • Secondary endpoints: details revised at 10 of 10 entries
    • Study description revised
  2. Minor Study First Submitted
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
5,455 trials monitored
See 306 trials at risk
4,798 trials monitored
See 270 trials at risk
1,740 trials monitored
See 105 trials at risk
and 4 more diseases
This prospective, single-center, open-label exploratory diagnostic study aims to evaluate the safety, feasibility, and diagnostic performance of the novel Sortilin-targeted PET tracer 68Ga-SorB in patients with solid tumors. Eligible participants with confirmed or suspected melanoma, hepatocellular carcinoma, lung cancer, pancreatic cancer, breast cancer, ovarian cancer, or cholangiocarcinoma will undergo 68Ga-SorB PET/CT imaging. The imaging findings will be compared with standard-of-care 18F-FDG PET/CT, using pathology results and/or clinical follow-up as the reference standard. The primary objectives are to evaluate the safety and tolerability of 68Ga-SorB, assess imaging feasibility, and characterize tumor uptake using quantitative PET parameters, including SUVmax and tumor-to-background ratio (TBR). Secondary exploratory objectives include comparing lesion detection between 68Ga-SorB PET/CT and 18F-FDG PET/CT, assessing diagnostic sensitivity and specificity, evaluating imaging characteristics across different tumor types, and exploring the correlation between Sortilin expression and tracer uptake. This study will provide preliminary clinical evidence supporting the development of Sortilin-targeted molecular imaging and future theranostic applications.
Trial Details
NCT Number NCT07760012
Lead Sponsor Peking University Third Hospital
Conditions
(from sponsor)
Melanoma (Skin Cancer), Hepatocellular Carcinoma, Lung Cancer, Breast Cancer, Pancreatic Cancer, Ovarian Cancer, Cholangiocarcinoma
Related terms Breast Neoplasms, Carcinoma, Hepatocellular, Cholangiocarcinoma, Lung Neoplasms, Melanoma, Neoplasms, Ovarian Neoplasms, Pancreatic Neoplasms
Enrollment 50 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov