OncoMatch

OncoMatch/Clinical Trials/NCT06455410

GP Plus Adebrelimab Versus GP Neoadjuvant Chemotherapy for Nasopharyngeal Carcinoma

Is NCT06455410 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies multiple treatments including GP and Adebrelimab for nasopharyngeal carcinoma.

Phase 2RecruitingSun Yat-sen UniversityNCT06455410Data as of Jun 2026Location: China

Treatment: GP · Adebrelimab · concurrent chemoradiotherapy (CCRT)The purpose of this study is to explore the efficacy and safety of neoadjuvant GP chemotherapy plus adebrelimab versus neoadjuvant GP chemotherapy in treating high-risk locoregionally advanced nasopharyngeal carcinoma patients.

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Extracted eligibility criteria

Treatments studied

Immunotherapy

Adebrelimab

Other

GPconcurrent chemoradiotherapy (CCRT)

Cancer type

Head and Neck Squamous Cell Carcinoma

Disease stage

Required: Stage T4N0-1M0, T1-4N2-3M0 (AJCC 8th)

Tumor staged as T4N0-1M0 or T1-4N2-3M0 (AJCC 8th)

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≤ 65

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Cannot have received: radiation therapy

Prior therapy with radiation or systemic chemotherapy

Cannot have received: cytotoxic chemotherapy

Prior therapy with radiation or systemic chemotherapy

Cannot have received: immune checkpoint inhibitor (anti-PD-1, anti-PD-L1, anti-CTLA-4)

Prior exposure to immune checkpoint inhibitors,including anti-PD-1, anti- PD-L1, anti-CTLA-4 antibodies

Lab requirements

Blood counts

WBC ≥4.0×10^9 /L, Hemoglobin ≥ 90g/L, Platelet count ≥100×10^9/L

Kidney function

creatinine clearance rate ≥ 60 ml/min or Creatinine ≤ 1.5× upper limit of normal value

Liver function

ALT, AST, TBIL ≤2×upper limit of normal (ULN)

Adequate marrow function: White blood cell count (WBC)≥4.0×109 /L, Hemoglobin ≥ 90g/L, Platelet count ≥100×109/L. Alanine aminotransferase (ALT), aspartate aminotransferase (AST), serum total bilirubin (TBIL) ≤2×upper limit of normal (ULN). Adequate renal function: creatinine clearance rate ≥ 60 ml/min or Creatinine ≤ 1.5× upper limit of normal value.

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

Frequently asked questions

Is NCT06455410 currently recruiting?

Yes, this trial is currently recruiting patients.

Can patients have received prior systemic therapy?

No. This trial requires treatment-naive patients — prior systemic therapy is an exclusion criterion.

What disease stage is eligible?

Stage T4N0-1M0 or T1-4N2-3M0 is required.

Is there an age limit?

Yes. Patients must be 65 years or younger.

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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