[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.
Quick facts
| Phase | Phase 2 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 20 (estimated) |
| Sponsor | University of Lausanne Hospitals Academic / other |
| Locations | 1 site (Lausanne, Canton of Vaud) |
| Status | Recruiting |
| Started | June 23, 2025 |
| Main results expected | October 2026 |
| Study ends | December 2026 |
| Registry record updated | May 6, 2026 |
| Trial ID | NCT06794372 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Unknown
✕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
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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
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.