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NCT07914764Recruiting

68Ga-labeled Cholecystokinin Receptor (CCK2R) Targeted Molecular Probes in Early Tumor Diagnosis

Clinical Application Research of 68Ga-labeled Cholecystokinin Receptor (CCK2R) Targeted Molecular Probes in Early Tumor Diagnosis

Source: ClinicalTrials.gov · Last updated 4 Nov 2026

Brief summary (registry, in English)

Evaluate the safety of the novel radioactive nuclide-labeled cholecystokinin receptor (CCK2R) targeted molecular probe, 68Ga-YQ-CC05, in clinical application, and verify its effectiveness in tumor diagnosis.

Status (registry)
Recruiting
Study type
Observational
Enrollment
20 (estimated)
First submitted
29 Oct 2026
Start date
1 Aug 2026
Primary completion date
31 Oct 2026
Lead sponsor
Nanjing First Hospital, Nanjing Medical University
NCT number
NCT07914764

What you commit to

  • Study type: Observational
  • Planned participants: 20
  • From 1 Aug 2026 to the primary completion date, 31 Oct 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study design.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Those who are currently participating in other clinical drug studies, or have previously participated in any clinical drug studies (excluding vitamins and minerals);
  • Expected survival duration less than half a year; chemotherapy within 6 months;
  • Having severe acute concomitant diseases or severe treatment-resistant mental disorders;

Other illness

  • Individuals with a history of allergy to similar drugs (drugs with similar chemical or biological components to CCK2R), allergic constitution, or current allergic diseases;
  • Other uncontrollable clinical issues (such as HIV, hepatitis C virus infection, active hepatitis B, or other severe chronic infections, as well as severe mental, neurological, cardiovascular, respiratory, and other systemic diseases);

Lab values

  • Red blood cells (RBC) count less than 4×10\^12, white blood cells (WBC) count less than 3×10\^9, hemoglobin level less than 110g/L, and platelet count (PLT) less than 75,000×10\^9;
  • Obvious abnormalities in liver and kidney function, with GFR less than 50 ml/min;

Other

  • Tumor burden greater than 50%, or significant spinal cord compression;
  • Pregnant and lactating women (where pregnancy is defined as a positive urine pregnancy test result);
  • Patients who are physically unfit for radiological examinations;
  • Other situations where the researcher deems it inappropriate for the participant to participate in the trial.

Who the study is looking for

  • Volunteer to participate in the trial, with the patient or their legal guardian signing the informed consent form;
  • Volunteers are not limited by gender, and the age range is from 18 to 75 years old, inclusive;
  • Other imaging examination methods (CT, MRI, etc.) reveal tumor occupying lesions;
  • Tumor patients who can obtain the final pathological results.
  • Kidney: GFR \> 50 ml/min, ERPF \> 280 ml/min, platelet count (PLT) \> 75,000/μL, white blood cell (WBC) \> 3,000/μL, alanine aminotransferase (ALT) and aspartate aminotransferase (AST) less than 3 times the normal value.

Age in the registry: 18 years to 75 years · Sex: All

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Nanjing First Hospital
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NanjingChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.