Study to Evaluate Immunological Response to PD-1 Inhibition in Squamous Cell Carcinoma of the Head and Neck (SCCHN)

PHASE1CompletedINTERVENTIONAL
Enrollment

15

Participants

Timeline

Start Date

May 1, 2017

Primary Completion Date

December 1, 2022

Study Completion Date

December 1, 2022

Conditions
Squamous Cell Carcinoma of the Head and Neck
Interventions
DRUG

[18F]F-AraG PET Scan, baseline + post anti-PD-1 therapy.

"* Baseline: Blood sampling, tumor biopsy, \[18F\]F-AraG PET/CT scan within two weeks prior to standard of care anti-PD-1 therapeutic dose.~* Anti PD-1 per standard of care~* Blood sampling and tumor biopsy within 2-3 weeks after first anti-PD-1 SOC dose.~* \[18F\]F-AraG PET/CT scan 6 - 12 weeks post first anti-PD-1 dose."

DRUG

[18F]F-AraG PET Scan, baseline + post anti-PD-1 therapy.

"* Baseline: Blood sampling, tumor biopsy, \[18F\]F-AraG PET/CT scan within two weeks prior to treatment.~* Anti PD-1, single dose~* Blood sampling, tumor biopsy and \[18F}F-AraG PET/CT scan within 2-3 weeks after single dose of anti-PD-1 treatment. For patients having surgical resection, biopsy will be immediately prior to resection or from sample of resection."

Trial Locations (1)

94305

Stanford Hospital and Clinics, Stanford

Sponsors
All Listed Sponsors
collaborator

Stanford University

OTHER

lead

CellSight Technologies, Inc.

INDUSTRY

NCT03129061 - Study to Evaluate Immunological Response to PD-1 Inhibition in Squamous Cell Carcinoma of the Head and Neck (SCCHN) | Biotech Hunter | Biotech Hunter