CI

At a glance

ClinicalIndex Comparison Record
Phase 3Recruiting· 380 target
Drug / intervention
Chemotherapy +3 moredrug
Likely dose
Immune checkpoint inhibitor 10mg/kgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05941741
NCT05941741Phase 3RecruitingOn Track

Induction Chemotherapy Combined With Low-dose Radiation Plus Cadonilimab in Loco-regionally Advanced Nasopharyngeal Carcinoma: a Multi-center, Open-label, Randomized Controlled Phase III Clinical Trial

Sun Yat-sen University·interventional·Posted Jul 12, 2023·Updated May 11, 2026

In Brief

A Phase 3 clinical trial evaluating Intensity Modulated Radiation Therapy, Chemotherapy, and 2 other interventions for Nasopharyngeal Carcinoma and 3 related conditions. Currently recruiting, targeting 380 participants across 3 sites.

Detailed Summary

This is a multi-center, open-label, randomized controlled phase III clinical trial in primary diagnosed loco-regionally advanced nasopharyngeal carcinoma (NPC) patients. The purpose of this study is to evaluate the efficacy of induction chemotherapy (IC) combined with low-dose radiation and immune checkpoint inhibitor (ICI) followed by concurrent chemoradiotherapy (CCRT) versus IC+CCRT, and compare the treatment-related adverse events and quality of life in two groups.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina
Collaborators--

Timeline

Phase 3Recruiting
2024202520262027202820292030
First PostedJul 12, 2023
Enrollment StartJan 10, 2024
Primary CompletionDec 1, 2027
Study CompletionDec 1, 2029
TodayJul 1, 2026
Enrollment to primary: 3.9 yearsPosted 3.0 years agoPrimary completion in 1.4 years

Interventions

Intensity Modulated Radiation Therapyradiation

All target volumes will be outlined slice by slice on the axial contrast-enhanced CT with MR fusion images in the treatment planning system. The target volumes are defined in accordance with the International Commission on Radiation Units and Measurements Reports 83. The prescribed dose is 70-72 Gy to PTVp (Planning target volume of the primary tumor), 64-70 Gy to PTVn (Planning target volume of the lymph node), 60- 64Gy to PTV1 (High-risk planning target volume), and 54-58 Gy to PTV2 (Low-risk planning target volume) in 30-32 fractions.

Chemotherapydrug

Induction chemotherapy: gemcitabine and cisplatin, Q3W, 3 cycles Concurrent chemotherapy: cisplatin, Q3W, 2-3 cycles

Immune checkpoint inhibitorbiological

Cadonilimab: 10mg/kg, Q3W, 3 cycles

Low-dose radiotherapyradiation

Low-dose radiotherapy will be performed to study group, with the use of IMRT.