Imaging lung cancer using a novel dual-target agent

A Pilot Study of 68Ga-FAPI-RGD PET/CT Imaging in the Lung Cancer Patients

EARLY_PHASE1 · Peking Union Medical College Hospital · NCT05543954

This study is testing a new imaging agent to see if it can help doctors get a better look at lung cancer compared to standard imaging methods.

Quick facts

PhaseEARLY_PHASE1
Study typeInterventional
Enrollment60 (estimated)
Ages18 Years and up
SexAll
SponsorPeking Union Medical College Hospital (other)
Locations1 site (Beijing)
Trial IDNCT05543954 on ClinicalTrials.gov

What this trial studies

This study evaluates the effectiveness of a new imaging agent, 68Ga-FAPI-RGD, for PET/CT imaging in patients with lung cancer. It aims to improve the visualization of lung cancer lesions by targeting specific receptors that are highly expressed in cancerous tissues and their associated blood vessels. The study compares the dual-target imaging approach with conventional methods like 18F-FDG PET/CT and single-target imaging agents. By utilizing this novel imaging technique, the study seeks to enhance diagnostic accuracy and assist in the management of lung cancer.

Who should consider this trial

Good fit: Ideal candidates for this study are patients with confirmed or suspected lung cancer who can undergo PET/CT imaging.

Not a fit: Patients who are pregnant, breastfeeding, or have medical conditions that may interfere with study compliance will not benefit from this study.

Why it matters

Potential benefit: If successful, this imaging technique could lead to more accurate diagnoses and better treatment planning for lung cancer patients.

How similar studies have performed: While conventional imaging methods have been widely used, this dual-target approach is novel and has not been extensively tested in prior studies.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

* patients with confirmed or suspected lung cancer;
* 68Ga-FAPI-RGD and 18F-FDG(or 68Ga-FAPI or 68Ga-RGD) PET/CT within 2 week;
* signed written consent.

Exclusion Criteria:

* pregnancy;
* breastfeeding;
* any medical condition that in the opinion of the investigator may significantly interfere with study compliance.

Where this trial is running

Beijing

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.

View on ClinicalTrials.gov →

Conditions: Lung Neoplasms

Last reviewed 2026-05-15 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.