A Study to Evaluate Immune Biomarker Modulation in Response to VTX-2337 in Combination With an Anti- PD-1 Inhibitor in Head and Neck Cancer
Purpose
This is an open label, Phase 1b pre-operative window of opportunity biomarker trial to analyze the combination of intravenous (IV) anti-PD-1 inhibitor, nivolumab, given along with toll-like receptor 8 (TLR 8) agonist motolimod delivered either subcutaneously (SC) or by intratumoral injection (IT) in subjects with squamous cell carcinoma of the head and neck (SCCHN). Subjects with previously untreated, resectable SCCHN, will be recruited onto this trial and will initially undergo pre-treatment diagnostic imaging and biological sample collection. These subjects will undergo pre-operative study treatment for a 3 to 4-week period prior to a scheduled surgical resection.
Condition
- Carcinoma, Squamous Cell
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Genders
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Subject is ≥ 18 years of age at the time of signing the informed consent form (ICF). - Subject has Eastern Cooperative Oncology Group (ECOG) PS of 0 or 1. - Subject has a new clinical or pathologic diagnosis of resectable HPV+ or HPV- SCCHN of the oral cavity, pharynx, or larynx - Macroscopic complete resection of the primary tumor must be planned and subjects should have no medical contraindication to surgery. - Subject consents to and has tumor accessible for tumor biopsy pre-treatment. - Subjects must have acceptable hematopoietic, liver, renal, and coagulation function as assessed by laboratory tests.
Exclusion Criteria
- Subject has any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from participating in the study - Subject has unresectable or inoperable tumors - Subject has primary tumors of the sinuses, paranasal sinuses, or nasopharynx, or unknown primary tumors - Subject has evidence of distant metastasis - Subject is a pregnant or nursing female. - Subject has active or uncontrolled infection including known HIV infection or known chronic hepatitis B or C. - Subject has active autoimmune disease. - Subject has clinically significant ophthalmologic disease.
Study Design
- Phase
- Phase 1
- Study Type
- Interventional
- Allocation
- Non-Randomized
- Intervention Model
- Parallel Assignment
- Primary Purpose
- Treatment
- Masking
- None (Open Label)
Arm Groups
Arm | Description | Assigned Intervention |
---|---|---|
Experimental Monotherapy Arm 1: Nivolumab |
Nivolumab IV every 2 weeks |
|
Experimental Monotherapy Arm 2: Motolimod |
Motolimod IT injection weekly |
|
Experimental Combination Arm 3: Nivolumab and Motolimod |
Nivolumab IV every 2 weeks and Motolimod IT injection weekly |
|
Experimental Combination Arm 4: Nivolumab and Motolimod |
Nivolumab IV every 2 weeks and Motolimod SC injection weekly |
|
More Details
- Status
- Terminated
- Sponsor
- Celgene