Clinical trial Recruiting at 1 site Early Phase 1 Interventional Ages 18 to 80

Evaluating a new imaging agent for cancer detection

Official title: 18F-FAPIBiotin PET/CT: Dosimetry and Biodistribution Study in Patients With Various Cancers

Run by First Affiliated Hospital of Fujian Medical University · NCT06734572 · Data updated 2026-11-12

This study is testing a new imaging agent for cancer called 18F-FAPI-Biotin to see if it can help doctors find tumors better than current imaging methods.

Quick facts

PhaseEarly Phase 1
Study typeInterventional
Ages18 Years to 80 Years
SexAll
Enrollment5 (estimated)
SponsorFirst Affiliated Hospital of Fujian Medical University
Academic / other
Drugs / interventionsradiation
Locations1 site (Fuzhou, Fujian)
StatusRecruiting
StartedJune 25, 2024
Main results expectedOctober 1, 2025
Study endsDecember 31, 2025
Registry record updatedDecember 16, 2024
Trial IDNCT06734572 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include patients with various solid tumors who have confirmed histopathological findings.

Probably not a fit

Patients who are pregnant, lactating, or have severe hepatic and renal insufficiency may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study investigates the safety, biodistribution, and radiation dosimetry of a novel dual-targeting PET radiotracer called 18F-FAPI-Biotin in patients with various types of cancer. The research aims to compare the imaging efficacy of 18F-FAPI-Biotin with existing PET tracers, 18F-FAPI and 18F-FDG, to assess its potential advantages in detecting tumor lesions. By targeting fibroblast activation protein and biotin, the study seeks to enhance the sensitivity and specificity of cancer imaging. Participants will undergo PET/CT scans to evaluate the pharmacokinetics and dosimetric characteristics of the new tracer.

Why it matters

Potential benefit: If successful, this study could lead to improved cancer imaging techniques, allowing for better diagnosis and treatment planning.

How similar studies have gone: While the approach of using dual-targeting PET tracers is promising, it is relatively novel and has not been extensively tested in prior studies.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Various solid tumors with available histopathological findings • Signed informed consent

Exclusion Criteria:

* pregnant or lactational women • who suffered from severe hepatic and renal insufficiency

Where it's running

  • Department of Nuclear Medicine, First Affiliated Hospital of Fujian Medical University
    Fuzhou, Fujian, China
    Recruiting

Study contacts

  • Principal investigator: Weibing Miao, MD — First Affiliated Hospital of Fujian Medical University
  • Study coordinator: Weibing Miao, MD
  • Email: miaoweibing@126.com
  • Phone: +86-0591-87981618

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 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.