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Clinical Application of FL-261 Radionuclide Imaging in the Diagnosis and Staging of Malignant Tumors

Clinical Application of FL-261 Radionuclide Imaging in the Diagnosis and Staging of Malignant Tumors

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500113891
Enrollment
Unknown
Registered
2025-12-04
Start date
2025-12-04
Completion date
Unknown
Last updated
2025-12-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Advanced malignant tumors, including non-small cell lung cancer, colorectal cancer, and head-and-neck cancers

Interventions

Gold Standard:Histopathological diagnosis or clinical follow-up findings will serve as the reference standard.
Index test:[68Ga]Ga-FL-261[111ln]In-FL-261 radionuclide imaging

Sponsors

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.The subject, or his/her legally authorized representative, is able to sign the informed consent form. 2. The subject agrees to comply with study procedures and to participate in the entire research process. 3. Adult patients (>=18 years of age), of any sex. 4. Patients with clinically suspected or confirmed tumors such as non-small cell lung cancer, colorectal cancer, or head-and-neck cancers, supported by evidence including, but not limited to, serum tumor markers, ultrasound, CT, MRI, or histopathological examination. 5. Patients with generally good overall physical condition. 6. Willingness to permit the use of existing tissue specimens.

Exclusion criteria

Exclusion criteria: 1. Patients or their legally authorized representatives who are unable or unwilling to sign the informed consent form. 2. Inability to comply with or complete the full study procedures. 3. Presence of acute systemic illness or significant electrolyte imbalance. 4. Pregnant or breastfeeding women. 5. Any other condition that, in the opinion of the investigator, makes the subject unsuitable for participation, such as patients with a known intolerance or hypersensitivity to c-MET–targeting agents.

Design outcomes

Primary

MeasureTime frame
SUVmax;

Countries

China

Contacts

Public ContactXiaoli Lan

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

hzslxl@163.com+86 27 85726685

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026