Radiolabelled Nectin-4 Targeted LMW Probe PET/CT in Patients With Lung Lesions
Run by Peking University Cancer Hospital & Institute · NCT06648317 · Data updated 2026-11-12
This study is testing a new imaging method using a special probe to see if it can help doctors better identify lung lesions in patients.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 75 Years |
| Sex | All |
| Enrollment | 20 (estimated) |
| Sponsor | Peking University Cancer Hospital & Institute Academic / other |
| Locations | 1 site (Beijing, Beijing Municipality) |
| Status | Recruiting |
| Started | November 21, 2024 |
| Main results expected | March 1, 2025 |
| Study ends | December 1, 2025 |
| Registry record updated | November 25, 2024 |
| Trial ID | NCT06648317 on ClinicalTrials.gov |
Is this trial a fit for you?
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✕Probably not a fit
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A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
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Why it matters
Potential benefit: Unknown
How similar studies have gone: Unknown
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. 18-75 years old, male or female; 2. Heart function is normal; 3. Normal heart function; 4. Estimated survival ≥12 weeks; 5. Good follow-up compliance; 6. presence of at least one measurable target lesion according to RECIST1.1 criteria; 7. Women of childbearing age (15-49 years) must have a negative pregnancy test within 7 days before starting the test; Fertile men and women must agree to use effective contraception to prevent pregnancy during the study period and for 3 months after the test; 8. Patients recommended by clinicians to undergo PET/CT examination for tumor diagnostic staging; 9. The subject patients could fully understand and voluntarily participate in the experiment, and signed the informed consent. Exclusion Criteria: 1. Serious abnormality of liver, kidney and blood; 2. Pregnant patients; 3. Pregnant and lactation women; 3\) unable to lie flat for half an hour; 4) Refuse to join the clinical investigator; 5) Suffering from claustrophobia or other mental diseases; 6) Other conditions that researchers deem unsuitable for participating in the experiment.
Where it's running
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Peking University Cancer Hospital & Institute
Beijing, Beijing Municipality, China Recruiting
Study contacts
- Principal investigator: Nan Li, MD — Peking University Cnacer Hospital & Institute
- Study coordinator: Nan Li
- Email: rainbow6283@sina.com
- Phone: +86-13693090647
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.