Actively Recruiting
Clinical Application of FL-091 Radionuclide Imaging in Diagnosis and Staging of Malignant Tumors
Led by Union Hospital, Tongji Medical College, Huazhong University of Science and Technology · Updated on 2026-01-13
100
Participants Needed
1
Research Sites
100 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Malignant tumors pose a serious threat to human health, and early diagnosis and early treatment are crucial to improving the patient's prognosis. Nuclear medicine imaging technology injects radioisotope labeled molecules (such as monoclonal antibodies and peptides) into the body to identify and bind specific targets of different tumor cells, thereby achieving accurate early diagnosis of different tumors. Neurotensin receptor 1 (NTSR1) is overexpressed in many malignant tumors such as colon cancer, pancreatic cancer, gastric cancer, head and neck cancer, and is closely related to tumor occurrence, development and prognosis. At the same time, NTSR1 is low expressed in surrounding normal tissues, so NTSR1 is an excellent target for the diagnosis and diagnosis of the above-mentioned series of malignant tumors. Probes targeting NTSR1 have been gradually explored. FL-091 is a new NTSR1-targeted radionuclide conjugated drug (RDC) that has high affinity and specificity for NTSR1 in previous preclinical studies. Compared with conventional NTSR1 inhibitors, FL-091 has the following potential advantages: ① Potential for radiotherapy: FL-091 can combine with radioactive isotopes such as 177Lu or 225Ac to directly deliver radioactive energy to tumor cells. This radiation therapy can produce cytotoxicity in a local area, killing tumor cells while causing less damage to surrounding healthy tissues;② Selectivity and specificity: Since FL-091 is designed based on the high affinity of NTSR1, it can more selectively target tumor cells that express NTSR1. This high degree of specificity can reduce the impact on normal cells and increase the accuracy of imaging and treatment.③ Biodistribution and rapid clearance: FL-091 demonstrated optimized biodistribution characteristics, such as higher tumor uptake rates and faster clearance of normal tissues. This means it can effectively deliver radioactive material to tumor tissue while reducing radiation exposure to healthy tissue. Based on the above advantages, FL-091 labeled with imaging nuclide or therapeutic nuclide is expected to be used for precise imaging and treatment of targeted NTSR1, bringing new diagnosis and treatment methods to patients. In this project, it is planned to use 68Ga and 111In to label FL-091 respectively for PET or SPECT imaging to initially evaluate the biodistribution of the probe in the human body, and diagnose and stage various malignant tumors including head and neck cancer, colorectal cancer and pancreatic adenocarcinoma. We will discuss the detection performance of 68Ga-FL-091 and 111In-FL-091 on malignant tumors, and lay the foundation for future use of therapeutic nuclide labeled FL-091 for nuclide targeted internal irradiation treatment of malignant tumors.
CONDITIONS
Official Title
Clinical Application of FL-091 Radionuclide Imaging in Diagnosis and Staging of Malignant Tumors
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Able to sign informed consent personally or via legal representative
- Willing to follow study procedures fully
- Adult patients or healthy volunteers aged 18 or older, any sex
- Clinically suspected or confirmed malignant tumors such as head and neck cancer, colorectal cancer, or pancreatic cancer with supporting evidence and good general condition
- Meet specific laboratory test requirements
- Females of childbearing potential must have used contraception for at least one month before screening and agree to continue during and after the study
- Other entry criteria as set by the study
You will not qualify if you...
- Unable to complete PET/MR or PET/CT imaging due to physical or psychological conditions
- Presence of other serious medical conditions
- Known allergy to FL-091 components or related substances
- Fasting blood glucose higher than 11.0 mmol/L before 18F-FDG injection
- History of using certain drugs affecting the study
- Poor compliance as judged by the investigator
- Pregnant or breastfeeding women
- Other factors making participation unsuitable
AI-Screening
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Trial Site Locations
Total: 1 location
1
Wuhan Union Hospital,China
Wuhan, Hubei, China, 430030
Actively Recruiting
Research Team
X
Xiaoli Lan, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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