At a glance
ClinicalIndex Comparison RecordPhase 2Recruiting· 25 target
Drug / intervention
Panitumumab-IRDye800drug
Likely dose
Not stated in record
Key inclusion· 5
- ✓Biopsy confirmed diagnosis of squamous cell carcinoma of the head and neck
- ✓Scheduled to undergo surgical resection with curative intent for squamous cell carcinoma
- ✓Any T stage, any subsite within the head and neck, including recurrent disease or new primary
- ✓Age ≥ 18 years
Key exclusion· 9
- ✕Received investigational drug within 30 days prior to first dose
- ✕MI, CVA, or uncontrolled CHF within 6 months prior to enrollment
- ✕History of infusion reactions to any monoclonal antibody therapies
- ✕Pregnant or breast-feeding
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Phase II Open-Label Study Evaluating Panitumumab-IRDye800 as an Optical Imaging Agent to Detect Head and Neck Cancer During Surgical Procedures
In Brief
A Phase 2 clinical trial evaluating Panitumumab-IRDye800 for Head and Neck Cancer. Currently recruiting, targeting 25 participants across 1 site.
Detailed Summary
The purpose of this study is to determine if panitumumab-IRDye800 is effective in identifying cancer, compared to surrounding normal tissue, and the further characterize the safety profile of this drug.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHead and Neck Cancer
CountriesUnited States
Collaborators--
Timeline
Phase 2Recruiting
20212022202320242025202620272028202920302031
First PostedAug 2020
Enrollment StartApr 2021
TodayJul 2026
Primary CompletionDec 2030
First PostedAug 12, 2020
Enrollment StartApr 2, 2021
Primary CompletionDec 31, 2030
TodayJul 2, 2026
Enrollment to primary: 9.7 yearsPosted 5.9 years agoPrimary completion in 4.5 years
Interventions
Panitumumab-IRDye800drug
single dose infusion of panitumumab-IRDye800CW