RecruitingPhase 2NCT06959082

Efficacy and Safety Evaluation of VS-101 in Combination With Chemoradiotherapy in Patients With Head and Neck Cancer

A Multi-center, Randomized, Open-label, Parallel-group, Phase 2 Study to Evaluate the Efficacy and Safety of VS-101 in Combination With Chemoradiotherapy (CRT) in Patients With Head and Neck Cancer


Sponsor

VSPharmTech Co.,Ltd.

Enrollment

30 participants

Start Date

Mar 1, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This will be a multi-center, randomized, open-label, parallel-group study in adult patients with head and neck cancer.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a new drug called VS-101 added to the standard treatment (chemotherapy plus radiation) for locally advanced head and neck squamous cell carcinoma — cancers of the mouth, throat, voice box, or nearby areas. Researchers want to see if adding this drug makes standard treatment more effective. **You may be eligible if...** - You are 18 or older - You have been diagnosed with head and neck squamous cell carcinoma involving the oral cavity, oropharynx, hypopharynx, or larynx - Your cancer is locally advanced (stage III or IV) but has not spread to distant sites - You have not previously received chemoradiotherapy for this cancer - Your overall health is adequate for chemoradiotherapy **You may NOT be eligible if...** - Your cancer has spread to distant organs (metastatic) - You have had prior radiation to the head and neck region - You have significant kidney, liver, or blood count abnormalities - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGVS-101

VS-101

DRUGCisplatin

Cisplatin

RADIATIONRadiation

Radiation


Locations(3)

Yale Cancer Center

New Haven, Connecticut, United States

Cancer Center of Kansas

Wichita, Kansas, United States

NYU Langone Health

Manhattan, New York, United States

View Full Details on ClinicalTrials.gov

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NCT06959082


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