Clinical Trial · NCT05048810

Clinical Application of 68Ga-DOTA-NT-20.3 in the Early Diagnosis of Pancreatic Ductal Adenocarcinoma

Overview

The purpose of this study is to determine the pharmacokinetics, dosimetry, tolerance, tumor detection rate of 68Ga-DOTA-NT-20.3 in patient with pancreatic ductal adenocarcinoma (PDAC).

Sponsor

Nanjing First Hospital, Nanjing Medical University

Phase

N/A

Contacts

Feng Wang, Ph.D (STUDY_DIRECTOR)

ClinicalTrials.gov

NCT05048810

Drug / Compound

DOTA-NT-20.3

Isotope(s):
Target(s):
  • NTSR-1
Ligand Class: Peptides
Chelator: DOTA

Eligibility

Inclusion

  • patient with complete clinical data.
  • patient with pathohistologically proven localized or metastatic PDAC;

Exclusion

  • patient who cannot stay on PET/CT camera for app. 90 minutes;
  • patient who cannot stand MRI;
  • patient with other active cancer;
  • patient with serious mental, neurological, cardiovascular, respiratory and other system diseases;
  • patient with PDAC under the treatment blocking NT receptors;
  • patient simultaneously participating in another clinical trial;
  • pregnant or lactating women;
  • patient with severe severe refractory mental disorder.
  • patient with HIV, HCV, HVB infection or other serious chronic infection
  • patient with liver and kidney function (GFR less than 50 ml/min) disease;