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Cemiplimab(Libtayo)

Names
西米普利单抗、C药
Indicatons
PD-1 inhibitor for advanced cutaneous squamous cell carcinoma, basal cell carcinoma, and non-small cell lung cancer...
Price:
Manufacturer:
Regeneron
Dosage form:
INJECTION
Validity period:
24 months

Reminder: The outer packaging is for reference only, please purchase and use under the guidance of a pharmacist. For read by medical and pharmaceutical professionals only.

Vesanoid(Cemiplimab) Instructions:Uses,Dosage, Side Effects

This section summarizes the key characteristics of VESANOID.VESANOID (tretinoin) is an orally administered retinoid capsule indicated for the treatment of a specific form of leukemia. 

Its active component, all-trans retinoic acid, functions by inducing cellular differentiation in malignant promyelocytes. It is specifically targeted for patients with confirmed genetic markers and requires careful clinical management due to its significant side effect profile and specific handling requirements.

Generic name
Cemiplimab(Libtayo)
English name
Cemiplimab
Alternative Names
西米普利单抗、C药
Drug prices
Indications

1.Cutaneous Squamous Cell Carcinoma (CSCC): For metastatic or locally advanced disease not amenable to curative surgery or radiation.

2.Basal Cell Carcinoma (BCC): For locally advanced or metastatic disease after hedgehog pathway inhibitor therapy or when such therapy is not appropriate.

3.Non-Small Cell Lung Cancer (NSCLC):

In combination with platinum-based chemotherapy for first-line treatment in patients without EGFR, ALK, or ROS1 aberrations.

As monotherapy for first-line treatment in patients with high PD-L1 expression (TPS ≥50%) without EGFR, ALK, or ROS1 aberrations.

Therapeutic Target
Programmed Death Receptor-1 (PD-1)
Active Ingredients
Cemiplimab
Dosage Form
INJECTION
Specifications
350mg/7mL/bottle/box
Dosage and Administration

Administer as an intravenous infusion over 30 minutes.

CSCC and BCC: 350 mg every 3 weeks until disease progression, unacceptable toxicity, or up to 24 months.

NSCLC: 350 mg every 3 weeks until disease progression or unacceptable toxicity.

Dose modifications or discontinuation may be required based on severity of immune-mediated adverse reactions.

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