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Study identifier: NCT07327216 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Sapylin Versus Dexamethasone Inhalation for CCRT-Induced Oral Mucositis in Nasopharyngeal Carcinoma

Condition: Nasopharyngeal Carcinoma (NPC)  ·  Sponsor: Affiliated Hospital of Guangdong Medical University

PhasePhase 3
Planned participants180
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

Radiation therapy is the main treatment for nasopharyngeal carcinoma (NPC), and standard care for advanced NPC often includes combination chemotherapy and radiation (CCRT). However, many patients experience serious side effects, such as painful mouth sores (Radiation-Induced Oral Mucositis, RTOM). These side effects can be so severe that they lower a patient's ability to adhere to treatment, potentially making the CCRT less effective. Studies have shown that a significant number of patients stop treatment early due to this toxicity. Current clinical guidelines from organizations like MASCC/ISOO and ESMO agree that preventing RTOM is crucial, but there is currently no specific drug that works for everyone. This study aims to investigate a new approach: using Sapylin, a biological immune regulator, delivered through an atomized inhaler. Preliminary research suggests Sapylin delivered this way may enhance the effectiveness of chemotherapy and boost the body's immunity. The main purpose of this study is to determine the effect of Sapylin inhalation on the incidence and severity of RTOM, and to evaluate its safety and impact on the overall success of CCRT. By participating, you will help researchers find a high-efficiency, low-toxicity method to improve CCRT outcomes and manage RTOM for future NPC patients and specialists.

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

Talk to the study team

Haiqing Luo, PhD  ·  +8613729196345  ·  hqluo@126.com

Always discuss trial participation with your own doctor first.

Locations (1)

Affiliated Hospital of Guangdong Medical UniversityZhanjiang, Guangdong, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07327216