EGFR Antibody Combined With PD-1 Inhibitor and Chemotherapy in R/M Nasopharyngeal Carcinoma

NCT06802835 · Status: RECRUITING · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 148

Last updated 2026-05-11

No results posted yet for this study

Summary

This is a prospective, single-arm, phase II clinical trial. The purpose of this study is to evaluate the efficacy and adverse effect of EGFR antibody combined with programmed death 1 (PD-1) antibody and chemotherapy in recurrent/metastatic nasopharyngeal carcinoma patients.

Conditions

  • Nasopharyngeal Cancinoma (NPC)
  • Recurrent Nasopharynx Carcinoma
  • Metastatic Nasopharyngeal Carcinoma

Interventions

DRUG

PD-1 antibody

6 cycles for combined therapy. Maintenance for 1 year.

DRUG

Gemcitabine, Cisplatin

6 cycles for combined therapy.

RADIATION

IMRT

IMRT for primary lesion

DRUG

EGFR Antibody

6 cycles for combined therapy. Maintenance for 1 year.

Sponsors & Collaborators

  • Zhejiang Cancer Hospital

    collaborator OTHER
  • Wuhan TongJi Hospital

    collaborator OTHER
  • Xijing hospital of The fourth military medical university

    collaborator UNKNOWN
  • Dongguan People's Hospital

    collaborator OTHER_GOV
  • Liuzhou Workers' Hospital

    collaborator OTHER_GOV
  • Chongqing University Cancer Hospital

    collaborator OTHER
  • Second Affiliated Hospital, School of Medicine, Zhejiang University

    collaborator OTHER
  • Jiangxi Provincial Cancer Hospital

    collaborator OTHER
  • Fujian Province Tumor Hospital

    collaborator OTHER
  • The First Affiliate Hospital of Guangxi Medical College

    collaborator UNKNOWN
  • Sun Yat-sen University

    lead OTHER

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-07-09
Primary Completion
2027-06-30
Completion
2029-06-30

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06802835 on ClinicalTrials.gov