Highlight
- First-in-human phase 1 study evaluating low-dose intralesional cemiplimab for early-stage cutaneous squamous cell carcinoma (CSCC).
- Intralesional administration demonstrated acceptable safety with no grade 3 or higher adverse events.
- High visual and pathologic complete response rates observed at week 13, especially with weekly 5 mg dosing.
- Findings suggest a promising non-surgical therapeutic option warranting further clinical trials.
Study Background
Specialty calculators
For clinical reference; use professional judgment.
