Libtayo Generic Name & Formulations
Legal Class
General Description
Pharmacological Class
How Supplied
Manufacturer
Generic Availability
Mechanism of Action
Libtayo Indications
Indications
Treatment of metastatic cutaneous squamous cell carcinoma (mCSCC) or locally advanced CSCC in patients who are not candidates for curative surgery or curative radiation. Treatment of locally advanced or metastatic basal cell carcinoma (laBCC or mBCC) in patients previously treated with a hedgehog pathway inhibitor or for whom a hedgehog pathway inhibitor is not appropriate.
Libtayo Dosage and Administration
Adult
Give by IV infusion over 30mins. 350mg every 3 weeks until disease progression, unacceptable toxicity, or up to 24 months. Dose modifications for adverse reactions: see full labeling.
Children
Libtayo Contraindications
Not Applicable
Libtayo Boxed Warnings
Not Applicable
Libtayo Warnings/Precautions
Warnings/Precautions
Libtayo Pharmacokinetics
Absorption
Steady-exposure is achieved after 4 months.
Distribution
Volume of distribution: 5.9 L.
Elimination
Half-life: 22 days. Steady-state clearance: 0.22 L/day.
Libtayo Interactions
Not Applicable
Libtayo Adverse Reactions
Adverse Reactions
Musculoskeletal pain, fatigue, rash, diarrhea; in combination with platinum-based chemotherapy: also, alopecia, nausea, peripheral neuropathy, decreased appetite; Grade 3–4 lab abnormalities (lymphopenia, hyponatremia, hypophosphatemia, increased AST, anemia, hyperkalemia); other immune-mediated adverse reactions (eg, ocular, gastrointestinal, musculoskeletal/connective tissue, hematologic/immune), infusion-related reactions.
Libtayo Clinical Trials
See Literature
Libtayo Note
Not Applicable
Libtayo Patient Counseling
See Literature
Libtayo Generic Name & Formulations
Legal Class
General Description
Pharmacological Class
How Supplied
Manufacturer
Generic Availability
Mechanism of Action
Libtayo Indications
Indications
In combination with platinum-based chemotherapy for the first-line treatment of locally advanced or metastatic non-small cell lung cancer (NSCLC) in adults who are not candidates for surgical resection or definitive chemoradiation, with no EGFR, ALK or ROS1 aberrations. As a single agent for the first-line treatment of locally advanced or metastatic NSCLC in adults who are not candidates for surgical resection or definitive chemoradiation, and whose tumors have high-PD-L1 expression [Tumor Proportion Score (TPS) ≥50%] as determined by an FDA-approved test, with no EGFR, ALK or ROS1 aberrations.
Libtayo Dosage and Administration
Adult
Give by IV infusion over 30mins. 350mg every 3 weeks until disease progression or unacceptable toxicity. Dose modifications for adverse reactions: see full labeling.
Children
Libtayo Contraindications
Not Applicable
Libtayo Boxed Warnings
Not Applicable
Libtayo Warnings/Precautions
Warnings/Precautions
Libtayo Pharmacokinetics
Absorption
Steady-exposure is achieved after 4 months.
Distribution
Volume of distribution: 5.9 L.
Elimination
Half-life: 22 days. Steady-state clearance: 0.22 L/day.
Libtayo Interactions
Not Applicable
Libtayo Adverse Reactions
Adverse Reactions
Musculoskeletal pain, fatigue, rash, diarrhea; in combination with platinum-based chemotherapy: also, alopecia, nausea, peripheral neuropathy, decreased appetite; Grade 3–4 lab abnormalities (lymphopenia, hyponatremia, hypophosphatemia, increased AST, anemia, hyperkalemia); other immune-mediated adverse reactions (eg, ocular, gastrointestinal, musculoskeletal/connective tissue, hematologic/immune), infusion-related reactions.
Libtayo Clinical Trials
See Literature
Libtayo Note
Not Applicable
Libtayo Patient Counseling
See Literature
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