Active Ingredient: Cemiplimab
Cemiplimab as monotherapy is indicated for the treatment of adult patients with metastatic or locally advanced cutaneous squamous cell carcinoma who are not candidates for curative surgery or curative radiation.
For this indication, competent medicine agencies globally authorize below treatments:
Intravenous
350 - 350 mg
From 350 To 350 mg once every day
The recommended dose is 350 mg cemiplimab, every 3 weeks, administered as an intravenous infusion over 30 minutes.
Treatment may be continued until disease progression or unacceptable toxicity.
No dose reductions are recommended. Dosing delay or discontinuation may be required based on individual safety and tolerability. Recommended modifications to manage adverse reactions are provided in the folllowing table.
Detailed guidelines for the management of immune-related adverse reactions are described in the folllowing table.
Recommended treatment modifications:
Intravenous infusion over 30 minutes.
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