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Clinical Trial Summary

The goal of this prospective, randomized, single-blind controlled clinical study is to explore the efficacy of maintenance therapy with Sintilimab after chemoradiotherapy in locally advanced head and neck squamous cell carcinoma. The main questions it aims to answer are: How works well the Sintilimab was in the treatment group? How safe the Sintilimab is? Participants will intravenous Sintilimab or placebo (a look-alike substance that contains no active drug) within 1 month after the end of chemoradiotherapy, and 21 days is a cycle. Blood tests, electrocardiogram are rechecked every 2 cycles, and CT was rechecked every 4 cycles to evaluate toxicity and side effects and recurrence. Researchers will compare invention group to control group to see if the Sintilimab works well.


Clinical Trial Description

The experimental group and the control group start treatment within 1 month after the end of chemoradiotherapy, and Sintilimab was given intravenously on the first day of each cycle in the experimental group while placebo was given in the control group, and a cycle of 21 days, and a total of 18 cycles were expected to be administered, or until disease progression. ;


Study Design


Related Conditions & MeSH terms

  • Head and Neck Neoplasms
  • Locally Advanced Head and Neck Squamous Cell Carcinoma
  • Squamous Cell Carcinoma of Head and Neck

NCT number NCT06240689
Study type Interventional
Source Second Affiliated Hospital, School of Medicine, Zhejiang University
Contact Ting Zhang, prof.
Phone +8615157125533
Email zezht@zju.edu.cn
Status Recruiting
Phase Phase 2
Start date January 25, 2024
Completion date January 5, 2027

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