Odomzo (sonidegib) vs Braftovi (encorafenib)

Odomzo (sonidegib) vs Braftovi (encorafenib)

Odomzo (sonidegib) and Braftovi (encorafenib) are both oral medications used to treat different types of cancer, but they work through distinct mechanisms and are approved for different indications. Odomzo is a hedgehog pathway inhibitor indicated for the treatment of adults with locally advanced basal cell carcinoma (BCC) that has recurred following surgery or radiation therapy, or those who are not candidates for surgery or radiation therapy. Braftovi, on the other hand, is a BRAF inhibitor used in combination with other medications to treat adults with metastatic or unresectable melanoma that has a BRAF V600E or V600K mutation, as detected by an FDA-approved test. It is important for patients to consult with their healthcare provider to determine which medication is appropriate for their specific type of cancer and genetic profile.

Difference between Odomzo and Braftovi

Metric Odomzo (sonidegib) Braftovi (encorafenib)
Generic name Sonidegib Encorafenib
Indications Treatment of adults with locally advanced basal cell carcinoma (BCC) that has recurred following surgery or radiation therapy, or those who are not candidates for surgery or radiation therapy. Treatment of unresectable or metastatic melanoma with a BRAF V600E or V600K mutation, in combination with binimetinib.
Mechanism of action Hedgehog pathway inhibitor BRAF inhibitor
Brand names Odomzo Braftovi
Administrative route Oral Oral
Side effects Muscle spasms, alopecia, dysgeusia, fatigue, nausea, musculoskeletal pain, diarrhea, decreased weight, decreased appetite, myalgia, abdominal pain, headache, vomiting, and pruritus. Fatigue, nausea, vomiting, abdominal pain, arthralgia, rash, anemia, increased aspartate aminotransferase, increased alanine aminotransferase, decreased appetite, and edema.
Contraindications Pregnancy, severe hepatic impairment Pregnancy, concurrent administration with strong CYP3A4 inducers
Drug class Smoothened (SMO) antagonist BRAF kinase inhibitor
Manufacturer Sun Pharmaceutical Industries Pfizer Inc.

Efficacy

Odomzo (Sonidegib) Efficacy in Treating Skin Cancer

Odomzo (sonidegib) is a medication approved for the treatment of adults with locally advanced basal cell carcinoma (BCC) that has recurred following surgery or radiation therapy, or for those who are not candidates for surgery or radiation therapy. Sonidegib is a hedgehog pathway inhibitor that works by targeting the molecular pathways involved in the growth of cancerous cells in BCC, which is the most common form of skin cancer. Clinical trials have demonstrated the efficacy of Odomzo in shrinking or eliminating tumors in a significant proportion of patients. The BOLT study, which was pivotal in the approval of Odomzo, showed that the drug led to an objective response rate (ORR) in 58% of patients with locally advanced BCC and 44% of patients with metastatic BCC.

While Odomzo has shown promise in treating BCC, it is important to note that its efficacy can vary among individuals. Factors such as the size and location of the tumor, previous treatments, and individual patient health can influence the effectiveness of the drug. Additionally, the long-term efficacy and safety of Odomzo are still under investigation, as ongoing studies continue to monitor patients for recurrence of the disease and any long-term adverse effects.

Braftovi (Encorafenib) Efficacy in Treating Skin Cancer

Braftovi (encorafenib), in combination with binimetinib, is approved for the treatment of patients with unresectable or metastatic melanoma with a BRAF V600E or V600K mutation, as detected by an FDA-approved test. Melanoma is a more dangerous form of skin cancer and can be aggressive and challenging to treat. Encorafenib is a BRAF inhibitor that directly targets the BRAF mutation, which is a driver of cancer cell growth in a subset of melanoma patients. Clinical trials have shown that the combination of encorafenib and binimetinib significantly improves progression-free survival (PFS) and overall survival (OS) compared to BRAF inhibitor monotherapy.

The COLUMBUS trial, which was a phase 3 study, demonstrated that patients treated with the combination of encorafenib and binimetinib had a median PFS of 14.9 months compared to 7.3 months for patients treated with vemurafenib, a BRAF inhibitor monotherapy. Furthermore, the combination therapy also showed an improvement in overall survival, with a median OS of 33.6 months compared to 16.9 months for vemurafenib alone. These results highlight the efficacy of Braftovi in combination with binimetinib in extending the lives of patients with BRAF-mutant metastatic melanoma.

Regulatory Agency Approvals

Odomzo
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Therapeutic Goods Administration (TGA), Australia
Braftovi
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan

Access Odomzo or Braftovi today

If Odomzo or Braftovi are not approved or available in your country (e.g. due to supply issues), you can access them via Everyone.org.

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