Clinical trial Recruiting at 1 site Early Phase 1 Interventional Ages 18 to 90

Imaging with a new PET tracer in cancer patients

Official title: 68Ga-FAPI-Biotin PET/CT in Patients With Various Types of Cancer

Run by First Affiliated Hospital of Fujian Medical University · NCT06740240 · Data updated 2026-11-12

This study is testing a new imaging tool for cancer patients to see if it can find tumors better than current methods.

More Solid Tumor trials

Quick facts

PhaseEarly Phase 1
Study typeInterventional
Ages18 Years to 90 Years
SexAll
Enrollment30 (estimated)
SponsorFirst Affiliated Hospital of Fujian Medical University
Academic / other
Drugs / interventionsradiation
Locations1 site (Fuzhou)
StatusRecruiting
StartedMarch 1, 2024
Main results expectedJune 1, 2026
Study endsDecember 31, 2026
Registry record updatedDecember 18, 2024
Trial IDNCT06740240 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 evaluates the safety and effectiveness of a novel dual-targeting PET radiotracer, 68Ga-FAPI-Biotin, in patients with various types of cancer. It aims to assess the biodistribution, pharmacokinetics, and dosimetry of the tracer while comparing its diagnostic efficacy against existing imaging agents like 68Ga-FAPI and 18F-FDG. By targeting fibroblast activation protein and biotin, the study seeks to enhance tumor detection sensitivity and specificity. The findings could provide insights into the potential of this new imaging agent in clinical practice.

Why it matters

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

How similar studies have gone: While some studies have shown promise with similar imaging approaches, this specific dual-targeting method is relatively novel and untested.

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

  • First Affiliated Hospital of Fujian Medical University
    Fuzhou, 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

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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.