OncoMatch

OncoMatch/Clinical Trials/NCT06851247

GAPP Induction and Concurrent Chemoradiotherapy Followed by Toripalimab Maintenance for Nasopharyngeal Carcinoma.

Is NCT06851247 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies multiple treatments including Toripalimab and Anlotinib for nasopharyngeal carcinoma.

Phase 2RecruitingSun Yat-sen UniversityNCT06851247Data as of Jun 2026Location: China

Treatment: Toripalimab · Anlotinib · Gemcitabine · CisplatinIn order to explore the efficacy and safety of targeted therapy and immunotherapy combined with GP chemotherapy in the treatment of high risk advanced nasopharyngeal carcinoma, the investigators design a single-arm, Phase II clinical trial targeted high-risk patients with local stage nasopharyngeal carcinoma (stage IVa: TanyN3M0/T4N0-2M0,8th AJCC/UICC staging) for Toripalimab Plus Anlotinib Combined With GP Induction Chemotherapy and Concurrent Chemoradiotherapy Followed by Toripalimab Maintenance Therapy.

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Extracted eligibility criteria

Treatments studied

Immunotherapy

Toripalimab

Targeted therapy

Anlotinib

Chemotherapy

GemcitabineCisplatin

Cancer type

Head and Neck Squamous Cell Carcinoma

Disease stage

Required: Stage IVA

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: anti-PD-1 therapy

Prior use of anti-PD-1 antibodies

Cannot have received: anti-PD-L1 therapy

Prior use of anti-PD-L1 antibodies

Cannot have received: anti-PD-L2 therapy

Prior use of anti-PD-L2 antibodies

Cannot have received: anti-CTLA-4 therapy

Prior use of anti-CTLA-4 antibodies (or any other antibody that acts on the T-cell co-stimulation or checkpoint pathway)

Lab requirements

Blood counts

Hemoglobin (HGB) ≥90 g/L, white blood cells (WBC) ≥4.0×10^9 /L, platelets (PLT) ≥100×10^9 /L

Kidney function

serum creatinine <1.5×ULN

Liver function

ALT and AST < 2.5 times the upper limit of normal (ULN), total bilirubin <2.0×ULN

Cardiac function

no serious dysfunction of heart

Hemoglobin (HGB) ≥90 g/L, white blood cells (WBC) ≥4.0×10^9 /L, platelets (PLT) ≥100×10^9 /L. Liver function: ALT and AST< 2.5 times the upper limit of normal (ULN), total bilirubin <2.0×ULN. Renal function: serum creatinine <1.5×ULN. no serious dysfunction of heart, lung, liver, kidney and other vital organs.

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

Frequently asked questions

Is NCT06851247 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 IVA 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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