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OncoMatch/Clinical Trials/NCT06693323

Single-Center Eval of Clinical & Radiological Benefit AHCC in Combo W/ SOC Tx for HPV+ Pts W/ HNSCC

Is NCT06693323 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies AHCC®capsules for hnscc.

Phase 2RecruitingUniversity of California, IrvineNCT06693323Data as of May 2026

Treatment: AHCC®capsulesThis is a phase 2, single-arm, open-label clinical trial determining safety and tolerability of AHCC in subjects with HPV-positive patients with Head and Neck Squamous Cell Carcinoma. These are subjects who have undergone surgery or will be undergoing surgery.

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Extracted eligibility criteria

Cancer type

Head and Neck Squamous Cell Carcinoma

Biomarker criteria

Required: HPV positive

diagnosis of pathologically or cytologically proven HPV positive HNSCC

Performance status

ECOG 0–1(Restricted strenuous activity)

Lab requirements

Blood counts

Absolute neutrophil count (ANC) ≥ 1,500/μL; Platelets ≥ 100,000/μL

Kidney function

Creatinine clearance > 30 mL/min using the Cockcroft-Gault formula

Liver function

Total bilirubin ≤ 1.5 × institutional upper limit of normal (ULN); AST or /ALT ≤ 3.0 × institutional ULN

Has adequate organ and marrow function as defined below, based on clinical laboratory assessments obtained ≤ 28 days prior to registration: 1. Absolute neutrophil count (ANC) ≥ 1,500/μL 2. Platelets ≥ 100,000/μL 3. Total bilirubin ≤ 1.5 × institutional upper limit of normal (ULN) 4. AST or /ALT ≤ 3.0 × institutional ULN 5. Creatinine clearance > 30 mL/min using the Cockcroft-Gault formula

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

US trial sites

  • Chao Family Comprehensive Cancer Center, University of California, Irvine · Orange, California

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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