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IC Plus Low-dose Radiation Plus Cadonilimab in LANPC

StatusRecruiting
PhasePhase 3
Started2024-01-10
View on ClinicalTrials.gov ↗

Amendment history

2026-05-06
critical
Study Status, Sponsor/Collaborators v6
Primary completion pushed: 2026-12 → 2027-12
2026-03-16
notable
Active, Not Recruiting→Recruiting Study Status, Sponsor/Collaborators, Oversight, Contacts/Locations v5
Trial statusActive, Not Recruiting→Recruiting
Lead sponsorSun Yat-Sen University Cancer Center→Sun Yat-sen University
Study sitesdetails revised at 3 of 3 sites
2025-05-13
notable
Recruiting→Active, Not Recruiting Study Status, Sponsor/Collaborators, Oversight, Contacts/Locations v4
Trial statusRecruiting→Active, Not Recruiting
Lead sponsorSun Yat-sen University→Sun Yat-Sen University Cancer Center
Study sitesdetails revised at 3 of 3 sites
2024-03-14
minor
Study Status v3
Start dateestimated 2024-01→confirmed 2024-01-10
2024-01-02
notable
Not Yet Recruiting→Recruiting Study Status, Contacts/Locations v2
Trial statusNot Yet Recruiting→Recruiting
Start date2023-12→2024-01
Study sites0→3
2023-11-26
minor
Study Status v1
Primary completion date2026-09→2026-12
Completion date2029-09→2029-12
Start date2023-09→2023-12
2023-07-11
minor
Original filing
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.
Trial Details
NCT Number NCT05941741
Lead Sponsor Sun Yat-sen University
Conditions Nasopharyngeal Carcinoma, Immune Checkpoint Inhibitor, Radiotherapy, Chemotherapy
Enrollment 380 participants
Start Date 2024-01-10
Primary Completion 2027-12 (estimated)
Study Completion 2029-12 (estimated)
Updated on ClinicalTrials.gov 2026-05-11