Clinical Trials in China / NCT06688188
Recruiting
Early Phase 1
68Ga-JH12 PET/CT: Dosimetry and Biodistribution Study
NCT06688188 · tracked via the Priya Life Science China tracker
Condition(s) studied
Malignant Neoplasm
Investigational drug(s) / intervention(s)
68Ga-JH12
68Ga-JH12: The dose will be 148-222 MBq given intravenously.
Study summary
68Ga-JH12 is a novel radiotracer targeting C-X-C motif chemokine receptor 4 (CXCR4). In this study, we observed the safety, biodistribution, and radiation dosimetry of 68Ga-JH12 in patients with different types of cancer.
Eligibility
Inclusion Criteria:
* Various solid tumors with available histopathological findings
* Signed informed consent
Exclusion Criteria:
* pregnant or lactational women
* who suffered from severe hepatic and renal insufficiency
Primary outcome measure(s)
- safety and tolerability — up to 1 week
Hematologic status, liver function, renal function and General vital signs were recorded before and 1 week after administration of radiopharmaceutical. Adverse events were categorized using the Common Toxicity Criteria for Adverse Events 5.0.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Department of Nuclear Medicine, First Affiliated Hospital of Fujian Medical University | Fuzhou | Fujian | Recruiting |
More First Affiliated Hospital of Fujian Medical University trials in China
Other trials for the same condition
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06688188 on ClinicalTrials.gov ↗ ← All trials in China