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Side Effects of Odomzo (sonidegib)
Odomzo (sonidegib) is a cancer medication used to treat adults with basal cell carcinoma that has recurred following surgery or radiation treatment or that cannot be treated with surgery or radiation.
Odomzo is an inhibitor of the hedgehog biological signaling pathway, a pathway that promotes the growth of normal and cancer cells. Odomzo binds to and inhibits smoothened, a protein involved in hedgehog signaling. Inhibiting smoothened disrupts cell signaling and growth of cancer cells.
Common side effects of Odomzo include:
Women taking Odomzo may experience amenorrhea. It is unknown if amenorrhea is permanent. Women who wish to get pregnant in the future should talk to their doctor.
Drug interactions of Odomzo may result in high blood levels of Odomzo, leading to increased side effects. These drug interactions include ketoconazole, itraconazole, voriconazole, certain HIV medications, and telithromycin.
The following drugs may decrease blood levels of Odomzo, causing treatment failure:
- carbamazepine,
- efavirenz,
- modafinil,
- phenobarbital,
- phenytoin,
- rifampin, and
- St. John’s wort.
Use of Odomzo during pregnancy is not recommended because it may cause death and severe birth defects. Female patients who have been exposed to Odomzo during pregnancy should report their pregnancy to Novartis Pharmaceuticals Corporation by calling 1-888-669-6682.
It is unknown if Odomzo is excreted in breast milk. Breastfeeding is not recommended while using Odomzo and for at least 20 months after the last dose because there is a potential for serious side effects in the breastfed baby.
What are the side effects of Odomzo (sonidegib)?
The most common side effects of sonidegib include:
- hair loss,
- weakness,
- nausea,
- decreased appetite,
- vomiting,
- taste changes,
- diarrhea,
- weight loss,
- stomach pain,
- headache,
- pain,
- muscle pain and spasms, and
- itching.
Women taking sonidegib may experience amenorrhea. It is not known if amenorrhea is permanent. Women who wish to get pregnant in the future should talk to their doctor for advice.
Odomzo (sonidegib) side effects list for healthcare professionals
The following clinically significant adverse reactions are described elsewhere in the labeling:
- Musculoskeletal Adverse Reactions.
Clinical Trials Experience
Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice.
The safety of Odomzo was evaluated in BOLT, a randomized, double-blind, multiple cohort trial in which 229 patients received Odomzo at either 200 mg or 800 mg daily.
The frequency of common adverse reactions was greater in patients treated with Odomzo 800 mg as compared to 200 mg, including:
- muscle spasms,
- alopecia,
- dysgeusia,
- fatigue,
- nausea,
- decreased weight,
- decreased appetite,
- myalgia,
- pain, and
- vomiting.
The data described reflect exposure to Odomzo 200 mg daily in 79 patients with locally advanced BCC or metastatic BCC enrolled in Study 1. Patients were followed for at least 18 months unless discontinued earlier. The median duration of treatment with Odomzo was 11.0 months.
The study population characteristics were:
- median age of 67 years (59% were ≥65 years),
- 61% male, and
- 90% white.
The majority of patients had:
- prior surgery (75%),
- radiotherapy (24%),
- systemic chemotherapy (4%), or
- topical or photodynamic therapies (18%) for treatment of BCC.
No patient had prior exposure to a Hh pathway inhibitor.
Odomzo was permanently discontinued in 34% of patients or temporarily interrupted in 20% of patients for adverse reactions. Adverse reactions reported in at least two patients that led to discontinuation of the drug were:
- muscle spasms, and dysgeusia (each 5%),
- asthenia, increased lipase, and nausea (each 4%),
- fatigue, decreased appetite, alopecia, and decreased weight (each 3%).
Serious adverse reactions occurred in 18% of patients.
The most common adverse reactions occurring in ≥10% of patients treated with Odomzo 200 mg were:
- muscle spasms,
- alopecia,
- dysgeusia,
- fatigue,
- nausea,
- musculoskeletal pain,
- diarrhea,
- decreased weight,
- decreased appetite,
- myalgia,
- abdominal pain,
- headache,
- pain,
- vomiting, and
- pruritus.
The key laboratory abnormalities are described in Table 2.
Table 1: Adverse Reactions Occurring in ≥10% of Patients in BOLT
Adverse Reaction | Odomzo 200 mg (N=79) |
|
All Grades a % |
Grade 3 % |
|
Musculoskeletal and connective tissue | ||
Muscle spasms | 54 | 3 |
Musculoskeletal pain | 32 | 1 |
Myalgia | 19 | 0 |
Skin and subcutaneous tissue | ||
Alopecia | 53 | 0 |
Pruritus | 10 | 0 |
Nervous system | ||
Dysgeusia | 46 | 0 |
Headache | 15 | 1 |
General | ||
Fatigue | 41 | 4 |
Pain | 14 | 1 |
Gastrointestinal | ||
Nausea | 39 | 1 |
Diarrhea | 32 | 1 |
Abdominal pain | 18 | 0 |
Vomiting | 11 | 1 |
Investigations | ||
Decreased weight | 30 | 3 |
Metabolism and nutrition | ||
Decreased appetite | 23 | 1 |
a No Grade 4 adverse reactions were reported. |
Table 2: Key Laboratory Abnormalities a in BOLT
Laboratory Test | Odomzo 200 mg (N=79) |
|
All Grades % |
Grades 3-4 % |
|
Chemistry | ||
Increased serum creatinine | 92 b | 0 |
Increased serum creatine kinase (CK) | 61 | 8 |
Hyperglycemia | 51 | 4 |
Increased lipase | 43 | 13 |
Increased alanine aminotransferase | 19 | 4 |
Increased aspartate aminotransferase | 19 | 4 |
Increased amylase | 16 | 1 |
Hematology | ||
Anemia | 32 | 0 |
Lymphopenia | 28 | 3 |
a Based on worst post-treatment laboratory value regardless of baseline; grading by CTCAE v4.03. b The serum creatinine level remained within normal range in 76% (60/79) of patients. |
Amenorrhea
Amenorrhea lasting for at least 18 months occurred in two of 14 pre-menopausal women treated with Odomzo 200 mg or 800 mg once daily.
What drugs interact with Odomzo (sonidegib)?
Effects Of Other Drugs On Odomzo
Strong And Moderate CYP3A Inhibitors
Avoid concomitant administration of Odomzo with strong CYP3A inhibitors.
Avoid concomitant administration of Odomzo with moderate CYP3A inhibitors. If a moderate CYP3A inhibitor must be used, administer the moderate CYP3A inhibitor for less than 14 days and monitor closely for adverse reactions particularly musculoskeletal adverse reactions.
Strong And Moderate CYP3A Inducers
Avoid concomitant administration of Odomzo with strong and moderate CYP3A inducers.
Summary
Odomzo (sonidegib) is a cancer medication used to treat adults with basal cell carcinoma that has recurred following surgery or radiation treatment or that cannot be treated with surgery or radiation. Common side effects of Odomzo include hair loss, weakness, nausea, decreased appetite, vomiting, taste changes, diarrhea, weight loss, stomach pain, headache, pain, muscle pain and spasms, and itching. Women taking Odomzo may experience amenorrhea. Use of Odomzo during pregnancy is not recommended because it may cause death and severe birth defects. It is unknown if Odomzo is excreted in breast milk.