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Clinical Trials in China / NCT07138716
Recruiting Not applicable

Research on the Application of 68Ga-DOTA-CCK-FS PET/CT in MTC

NCT07138716 · tracked via the Priya Life Science China tracker
Sponsor
Luo Yaping
Phase
Not applicable
Started
2025-05-10
Last updated
2025-08-24

Condition(s) studied

Medullary Thyroid Carcinoma

Investigational drug(s) / intervention(s)

68Ga-DOTA-CCK-FS PET/CT

68Ga-DOTA-CCK-FS PET/CT: For 68Ga-DOTA-CCK-FS, imaging begins 60±5 minutes post-injection to evaluate cholecystokinin receptor (CCK-R) expression, using a time-of-flight PET/CT system with low-dose CT (120 kVp, 30-50 mAs) for attenuation correction followed by whole-body PET acquisition (2-3 min/bed position). Images are reconstructed using OSEM algorithms.

Study summary

This study explores the clinical application of 68Ga-DOTA-CCK-FS PET/CT in detecting cholecystokinin-2 receptor (CCK-2R)-positive tumors, particularly medullary thyroid cancer (MTC) and other malignancies. Led by Prof. Luo Yaping (PUMCH Nuclear Medicine) and Prof. Liu Zhibo (Peking University, radiochemistry expert), the trial will enroll 30-40 patients to compare 68Ga-DOTA-CCK-FS imaging with standard PET/CT (e.g., 18F-FDG or 68Ga-DOTATATE). The novel tracer shows higher tumor uptake and retention in preclinical studies, potentially improving diagnosis and treatment guidance for aggressive, CCK-2R-expressing cancers. The study leverages PUMCH's Class IV Radioactive Drug License for advanced radiopharmaceutical development. Risks are minimal (diagnostic radiation dose only), and participants receive free imaging assessments. Results aim to refine precision diagnostics for MTC and related tumors.

Eligibility

Sex
ALL
Min age
Max age
Healthy volunteers
Accepted
Inclusion Criteria: 1. Age not limited (male or female). 2. Diagnosis:Confirmed or suspected medullary thyroid carcinoma (MTC) based on: Fine-needle aspiration (FNA) cytology/histopathology, or Elevated serum calcitonin/CEA with thyroid nodule(s), or Clinical/hereditary suspicion (e.g., MEN2 syndrome), or Other histologically confirmed CCK-2R-positive tumors (e.g., neuroendocrine tumors, gastric/ovarian cancers). 3. Performance Status: Life expectancy ≥12 weeks. 4. Contraception: Willingness to use effective birth control (if applicable). 5. Consent: Signed informed consent and compliance with follow-up. Exclusion Criteria: 1. Severe hepatic/renal dysfunction (e.g., ALT/AST \>3×ULN, Cr \>2.0 mg/dL). 2. Pregnancy/lactation or planned pregnancy during the study. 3. Inability to lie still for PET/CT (e.g., severe claustrophobia). 4. Concurrent conditions compromising study safety (investigator's judgment). \*Note: CCK-2R positivity may be confirmed via prior immunohistochemistry (if available) or inferred from tumor type (e.g., MTC).\*

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Peking Union Medical College Hospital Beijing Beijing Municipality Recruiting

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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 NCT07138716 on ClinicalTrials.gov ↗ ← All trials in China