Squamous Cell Carcinoma of Head and Neck Clinical Trial
Official title:
Randomized Pre-surgical Window-of-Opportunity Trial of TTI-101 in Patients With Stage II-IV Resectable HPV-negative Squamous Cell Carcinoma of the Head and Neck
To learn if TTI-101 can reduce the growth of HPV-negative squamous cell carcinomas of the head and neck when given before standard of care surgery.
Objectives: Primary: • To determine the change in pY-STAT3 H-score in tumor tissue in post-treatment resection specimens versus pre-treatment biopsy specimens. Secondary: - To determine the safety and tolerability of pre-surgery TTI-101 in patients with Stage II-IV HPV-negative HNSCC who are planned for definitive local surgery with or without radiation. - To determine the individual pre/post treatment changes in pY-STAT3 H-scores in epithelial and stromal tumor cells. - To determine the pathologic response rate to pre-surgery TTI-101. - To determine the overall response rate (ORR) to pre-surgery TTI-101 using RECIST v1.1 criteria. - To determine the disease free, disease specific and overall survival (DFS, DSS, OS) after pre-surgery TTI-101 treatment and SOC surgery. Exploratory: - To evaluate the effects of pre-surgery TTI-101 on circulating and tumor-infiltrating immunocytes, and on the intratumoral expression of PD-1 along with other immune related molecules. - To compare outcome measures (response rate and survival) in control versus TTI-101-treated patients. - To determine the association of immunologic changes with treatment response. - To determine the association of pharmacokinetic (PK) measures with treatment response. ;
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