Odomzo (sonidegib phosphate)

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Last reviewed · Source: First Databank (FDB) drug data

Overview

Sonidegib, a hedgehog signaling pathway inhibitor, is an antineoplastic agent.

Sonidegib is an antineoplastic agent that inhibits the hedgehog pathway by binding to and selectively inhibiting Smoothened, a transmembrane protein involved in hedgehog signal transduction. The hedgehog signaling pathway plays an important role during embryonic organ and tissue development and is a key regulator of bone development and maintenance of tissues and stem cells in adults and during postnatal development. However, genetic mutations that allow for aberrant activation of the hedgehog pathway have been implicated in the development of several malignancies such as basal cell carcinoma.

Inhibition of Smoothened by sonidegib results in inhibition of the hedgehog pathway.

Following oral administration, less than 10% of sonidegib is absorbed. Area under the serum concentration-time curve (AUC) and peak plasma concentrations of sonidegib are dose proportional over a dosage range of 100-400 mg. Peak plasma concentrations of sonidegib are achieved 2-4 hours following oral administration of a single dose of sonidegib (100 mg to 3 g) under fasting conditions in cancer patients.

Following administration of sonidegib, steady-state concentrations of the drug are achieved in approximately 4 months and the estimated accumulation is 19-fold. Administration of sonidegib with a high-fat meal (approximately 1000 calories with 50% of calories from fat) increased systemic exposure (AUC and peak plasma concentrations) of sonidegib by 7.4- to 7.8-fold. In a population pharmacokinetic analysis, administration of sonidegib with a high-fat meal increased bioavailability of the drug fivefold.

Sonidegib is metabolized in the liver principally by cytochrome P-450 (CYP) isoenzyme 3A. In vitro, sonidegib is more than 97% bound to plasma proteins. Following oral administration of sonidegib, approximately 70% of the absorbed dose is recovered in feces and 30% is recovered in urine; unchanged drug is not excreted in urine.

The estimated plasma elimination half-life of the drug is 28-29.6 days.

Population pharmacokinetic analyses indicate that age, sex, body weight, and ethnicity generally do not have clinically important effects on the exposure of sonidegib. A cross-study comparison indicates that systemic exposure following administration of sonidegib (single 200-mg dose) is increased by 1.7-fold in healthy Japanese individuals compared with individuals from Western countries.

USES: This medication is used to treat a certain type of skin cancer (basal cell carcinoma).

Generic name: sonidegib phosphate
Pronunciation: (SOE-ni-DEG-ib)

Reference product & biosimilars

No reference, biosimilar or interchangeable associated with this drug.

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Indications

The following indications are listed for Odomzo:

  • Basal Cell Carcinoma Of Skin

Also known as: Basal Cell Epithelioma, Basalioma.

Dosing

No dosing information is available for this tab.

Drug interactions

Sonidegib is metabolized principally by cytochrome P-450 (CYP) isoenzyme 3A. In vitro studies indicate that sonidegib inhibits CYP isoenzymes 2B6 and 2C9, but does not induce CYP 1A2, 2B6, or 3A.

In vitro studies indicate that sonidegib inhibits breast cancer resistance protein (BCRP, ABCG2), but does not inhibit P-glycoprotein (P-gp, ABCB1), multidrug resistance protein 2 (MRP2, ABCC2), organic cation transporter (OCT) 1, OCT2, organic anion transporter (OAT) 1, OAT3, organic anion transport protein (OATP) 1B1, and OATP1B3. In vitro studies also indicate that the drug is not a substrate of P-gp, MRP2, or BCRP.

Contraindications

The manufacturer states that there are no known contraindications to the use of sonidegib.

Adverse reactions

Adverse effects reported in 10% or more of patients with advanced basal cell carcinoma receiving sonidegib in the principal efficacy study include muscle spasms, alopecia, dysgeusia, fatigue, nausea, diarrhea, musculoskeletal pain, weight loss, decreased appetite, myalgia, abdominal pain, headache, pain, vomiting, pruritus, and arthralgia.

Laboratory abnormalities reported in more than 15% of patients receiving sonidegib include elevated concentrations of serum creatinine, elevated concentrations of serum CK, hyperglycemia, elevated concentrations of lipase, anemia, lymphopenia, elevated concentrations of aminotransferases (i.e., AST, ALT), and elevated concentrations of amylase.

Amenorrhea lasting at least 18 months also has been reported in 2 of 14 premenopausal women receiving sonidegib (200 or 800 mg once daily).

Precautions

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ICD codes

No ICD codes are available for this drug.

Formulary status

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Last reviewed · Source: First Databank (FDB) drug data