Efficacy and Safety Evaluation of VS-101 in Combination With Chemoradiotherapy in Patients With Head and Neck Cancer
NCT06959082 · Status: RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 30
Last updated 2026-03-11
Summary
This will be a multi-center, randomized, open-label, parallel-group study in adult patients with head and neck cancer.
Conditions
- Head and Neck Cancer Squamous Cell Carcinoma
Interventions
- DRUG
-
VS-101
VS-101
- DRUG
-
Cisplatin
- RADIATION
-
Radiation
Radiation
Sponsors & Collaborators
-
VSPharmTech Co.,Ltd.
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-03-31
- Primary Completion
- 2027-06-30
- Completion
- 2027-06-30
- FDA Drug
- Yes
Countries
- United States
Study Locations
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