Clinical trial Recruiting at 1 site Phase 2 Interventional Ages 18 and up

[68Ga]Ga-FAPI-46 in Staging of Head and Neck Carcinomas

Official title: [68Ga]Ga-FAPI-46 PET/CT in Early Detection of Lymph Node Metastasis in Head and Neck Squamous Cell Carcinomas

Run by University of Lausanne Hospitals · NCT06794372 · Data updated 2026-11-12

This study is testing if a new imaging method can help doctors better stage head and neck cancers.

More Head and Neck Squamous Cell Carcinoma (HNSCC) trials

Quick facts

PhasePhase 2
Study typeInterventional
Ages18 Years and up
SexAll
Enrollment20 (estimated)
SponsorUniversity of Lausanne Hospitals
Academic / other
Locations1 site (Lausanne, Canton of Vaud)
StatusRecruiting
StartedJune 23, 2025
Main results expectedOctober 2026
Study endsDecember 2026
Registry record updatedMay 6, 2026
Trial IDNCT06794372 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

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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:

* Age ≥18 years old
* Karnofsky index ≥80%
* Patients with operable head and neck cancer presenting histologically proven HNSCC (including Oral Cavity Cancer, Pharyngeal Cancer, Laryngeal Cancer)
* Patients with at least one nodal metastasis
* Patients scheduled for neck dissection
* SOC imaging (MRI, ceCT and 18F-FDG-PET/CT) performed as pre-surgery exams
* Written informed consent obtained

Exclusion Criteria:

* Known pregnancy or ongoing breast feeding
* Claustrophobia
* Severe renal insufficiency (GFR\<30 mL/min/1,73 m2)
* Liver enzymes (ALAT, ASAT)\>5 times the standard upper limit
* Bilirubin\>3 times the standard upper limit
* Hemoglobin\<8 g/dL
* Absolute neutrophil count\<1000/mm3
* Platelets\<75000/µL
* insufficient knowledge of project language, inability to give consent or to follow trial-associated procedures
* the patient makes use of his/her "right not to know" and refuses to be informed about incidental findings

Where it's running

  • Centre hospitalier universitaire vaudois
    Lausanne, Canton of Vaud, Switzerland
    Recruiting

Study contacts

  • Principal investigator: Niklaus Schaefer, MD — Centre Hospitalier Universitaire Vaudois
  • Study coordinator: John O Prior, MD, PhD
  • Email: john.prior@chuv.ch
  • Phone: +41 21 314 4348

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.