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Recruiting NCT06648317

NCT06648317 Radiolabelled Nectin-4 Targeted LMW Probe PET/CT in Patients With Lung Lesions

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Clinical Trial Summary
NCT ID NCT06648317
Status Recruiting
Phase
Sponsor Peking University Cancer Hospital & Institute
Condition Lung Cancer, Non-Small Cell
Study Type OBSERVATIONAL
Enrollment 20 participants
Start Date 2024-11-21
Primary Completion 2025-03-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 75 Years
Study Type OBSERVATIONAL
Interventions
FDG-PET

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 20 participants in total. It began in 2024-11-21 with a primary completion date of 2025-03-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

To evaluate the ability of \[68Ga\]N188 to detect nectin-4 overexpression in patients with lung lesions.

Eligibility 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.

Contact & Investigator

Central Contact

Nan Li

✉ rainbow6283@sina.com

📞 +86-13693090647

Principal Investigator

Nan Li, MD

PRINCIPAL INVESTIGATOR

Peking University Cnacer Hospital & Institute

Frequently Asked Questions

Who can join the NCT06648317 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 75 Years, studying Lung Cancer, Non-Small Cell. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06648317 currently recruiting?

Yes, NCT06648317 is actively recruiting participants. Contact the research team at rainbow6283@sina.com for enrollment information.

Where is the NCT06648317 trial being conducted?

This trial is being conducted at Beijing, China.

Who is sponsoring the NCT06648317 clinical trial?

NCT06648317 is sponsored by Peking University Cancer Hospital & Institute. The principal investigator is Nan Li, MD at Peking University Cnacer Hospital & Institute. The trial plans to enroll 20 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology