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OncoMatch/Clinical Trials/NCT05183048

Comparison of 89Zr Panitumumab and (18)F-Fluorodeoxyglucose to Identify Head and Neck Squamous Cell Carcinoma

Is NCT05183048 recruiting? Yes, currently enrolling (Jun 2026). This Early Phase 1 trial studies [89Zr]Panitumumab Tracer for head and neck squamous cell carcinoma.

Early Phase 1RecruitingUniversity of Alabama at BirminghamNCT05183048Data as of Jun 2026

Treatment: [89Zr]Panitumumab TracerThis pilot clinical study will investigate if Zirconium-89 (89Zr) panitumumab- Positron Emission Tomography/ Magnetic Resonance Imaging (PET/MRI) imaging can more accurately determine size and location of primary tumors compared to standard of care Fludeoxyglucose (18F-FDG) -PET/MRI in newly diagnosed patients with head and neck squamous cell carcinoma (HNSCC) who are undergoing surgical resection. This study is for imaging purposes only and is not a treatment study. The results of this study will not change the clinical treatment plan.

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Extracted eligibility criteria

Treatments studied

Other

[89Zr]Panitumumab Tracer

Cancer type

Head and Neck Squamous Cell Carcinoma

Prior therapy

Cannot have received: investigational drug

Received an investigational drug within 30 days prior to the first dose of [89Zr]panitumumab.

Cannot have received: surgical resection

Previous HNSCC resection.

Lab requirements

Blood counts

Hemoglobin ≥ 9 gm/dL; White blood cell count ≥ 3000/mm3; Platelet count ≥ 100,000/mm3

Kidney function

Serum creatinine ≤ 1.5 times upper reference range; Creatinine within normal institutional limits OR Creatinine clearance ≥60 mL/min/1.73 m2 for patients with creatinine levels; Severe renal disease or anuria [excluded]

Liver function

ALT (SGPT) 7-56 units/liter, AST (SGOT) 5-40 units/liter

Have acceptable hematologic status, coagulation status (11 to 13.5 seconds. international normalized ratio (INR) of 0.8 to 1.1), kidney function, and liver function including the following clinical results: Hemoglobin ≥ 9 gm/dL; White blood cell count ≥ 3000/mm3; Platelet count ≥ 100,000/mm3; Serum creatinine ≤ 1.5 times upper reference range; ALT (SGPT) 7-56 units/liter, AST (SGOT) 5-40 units/liter. Severe renal disease or anuria [excluded].

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • UAB · Birmingham, Alabama

Showing up to 5 US sites.

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Frequently asked questions

Is NCT05183048 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior investigational drug, surgical resection disqualifies patients from enrollment.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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