Suspended

Toripalimab with Concurrent Chemoradiotherapy for High-risk Nasopharyngeal Carcinoma

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What is being tested

Cisplatin+Toripalimab

+ Cisplatin+placebo

Drug
Who is being recruted

Nasopharyngeal Carcinoma+11

+ Carcinoma

+ Head and Neck Neoplasms

From 18 to 65 Years
+26 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Placebo-ControlledPhase 2
Interventional
Study Start: December 2019
See protocol details

Summary

Principal SponsorSun Yat-sen University
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: December 8, 2019

Actual date on which the first participant was enrolled.

Nasopharyngeal carcinoma (NPC) is a type of cancer common in Southern China and Southeast Asia. For advanced NPC, particularly high-risk cases with plasma EBV DNA levels at 1500 copies/ml or higher, treatment failure rates remain high. Current treatments like concurrent chemoradiotherapy (CCRT) aim to improve patient outcomes, but around 25% of advanced NPC patients still experience relapse or metastasis. Therefore, there's an urgent need for new treatments to enhance survival and decrease side effects. Research suggests that PD-1 antibody therapy, such as Toripalimab, could be beneficial for patients with recurrent or metastatic NPC. This Phase II clinical trial investigates the effectiveness and safety of Toripalimab combined with CCRT, compared to CCRT with a placebo, for high-risk NPC patients (Stage III-IVa, AJCC 8th, and EBV DNA ≥ 1500 copies/ml). In this study, participants are randomly assigned to receive either Toripalimab in combination with CCRT or CCRT with a placebo. The primary goal is to evaluate progression-free survival (PFS), which is the time from randomization to the first instance of disease progression or death from any cause. This trial aims to determine whether adding Toripalimab to the current standard treatment can improve patient outcomes and reduce the risk of relapse or metastasis.

Official TitleRandomized, Placebo-controlled, Double-blind Phase II Clinical Trial of Neoadjuvant and Adjuvant Anti-PD-1 Antibody Toripalimab Immunotherapy Combined With Concurrent Chemoradiotherapy for High-risk Nasopharyngeal Carcinoma
NCT03925090
Principal SponsorSun Yat-sen University
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

150 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 65 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Nasopharyngeal CarcinomaCarcinomaHead and Neck NeoplasmsStomatognathic DiseasesNasopharyngeal DiseasesNasopharyngeal NeoplasmsNeoplasmsNeoplasms by Histologic TypeNeoplasms by SiteNeoplasms, Glandular and EpithelialOtorhinolaryngologic DiseasesOtorhinolaryngologic NeoplasmsPharyngeal DiseasesPharyngeal Neoplasms

Criteria

8 inclusion criteria required to participate
Patients with newly histologically confirmed non-keratinizing nasopharyngeal carcinoma, including WHO II or III Original clinical staged as III-IVa (according to the 8th AJCC edition)

No evidence of distant metastasis (M0)

Plasm EB Virus DNA≥1500copies/ml

Male and no pregnant female

Show More Criteria

18 exclusion criteria prevent from participating
Patients have evidence of relapse or distant metastasis

Histologically confirmed keratinizing squamous cell carcinoma (WHO I)

Receiving radiotherapy or chemotherapy previously

The presence of uncontrolled life-threatening illness

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

50% chance of being blinded to the placebo group

Treatment Groups

Group I

Experimental
Drug: Cisplatin cisplatin 100mg/m2(every three weeks),D1,D22,D43 of intensity modulated radiotherapy Other Names: DDP Drug: Toripalimab Toripalimab 240mg every 2 weeks with a total of 2 cycles as neoadjuvant anti-PD-1 immunotherapy; Toripalimab240mg every 3 weeks with a total of 8 cycles as adjuvant anti-PD-1 immunotherapy 2 weeks after CCRT Other Names:anti-PD-1 antibody, JS001

Group II

Placebo
Drug: Cisplatin cisplatin 100mg/m2(every three weeks),D1,D22,D43 of intensity modulated radiotherapy Other Names: DDP Drug: placebo placebo 240mg every 2 weeks with a total of 2 cycles as neoadjuvant treatment; placebo 240mg every 3 weeks with a total of 8 cycles as adjuvant treatment 2 weeks after CCRT.

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Sun Yat-sen Universitty Cancer Center

Guangzhou, ChinaOpen Sun Yat-sen Universitty Cancer Center in Google Maps
SuspendedOne Study Center
Toripalimab with Concurrent Chemoradiotherapy for High-risk Nasopharyngeal Carcinoma | PatLynk