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Study identifier: NCT05772208 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Intensified Treatments for Patients With Locally Advanced Nasopharyngeal Carcinoma With Detectable EBV DNA After One Cycle GP Regime Neoadjuvant Chemotherapy

Condition: Nasopharyngeal Carcinoma  ·  Sponsor: Fudan University

PhasePhase 3
Planned participants459
Who can joinAll sexes, 18 Years to 70 Years
Healthy volunteersNo

About this study

The goal of this multicenter randomized non-inferior study is to compare the additon of camrelizumab or nimotuzumab to neoadjuvant chemotherapy followed by concurrent chemoradiotherapy in locally advanced nasopharyngeal carcinoma patients whose EBV DNA remained detectable after one cycle neoadjuvant chemotherapy using GP regimen. The main question it aims to answer is: whether the addition of carrilizumab or nituzumab improve the treatment outcomes in the relatively poor prognostic patients identified by the response of EBV DNA. Participants will be randomized to the combination of carrilizumab and standard treatment , the combination of nituzumab and standard treatment or the standard treatment alone if their EBV DNA didn't decrease to undetectable level post first cycle of neoadjuvant chemotherapy.

This description comes directly from the study's public registry record.

Talk to the study team

Chengrun Du  ·  +86-15001733593  ·  duchengrun@qq.com

Always discuss trial participation with your own doctor first.

Locations (1)

Fudan Universtiy Shanghai Cancer CentreShanghai, Shanghai Municipality, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT05772208