Braftovi (encorafenib) vs Libtayo (cemiplimab)

Braftovi (encorafenib) vs Libtayo (cemiplimab)

Braftovi (encorafenib) is a targeted therapy known as a BRAF inhibitor, specifically used for the treatment of melanoma with a BRAF V600E or V600K mutation, often in combination with other medications such as MEK inhibitors. Libtayo (cemiplimab), on the other hand, is an immune checkpoint inhibitor that works by enhancing the immune system's ability to fight cancer, and it is used for the treatment of advanced cutaneous squamous cell carcinoma, basal cell carcinoma, and non-small cell lung cancer. The choice between Braftovi and Libtayo would depend on the specific type of cancer a patient has, its genetic makeup, and the overall treatment goals, and should be made in consultation with an oncologist who can consider the individual's unique medical circumstances.

Difference between Braftovi and Libtayo

Metric Braftovi (encorafenib) Libtayo (cemiplimab)
Generic name Encorafenib Cemiplimab
Indications Unresectable or metastatic melanoma with a BRAF V600E or V600K mutation, as detected by an FDA-approved test Cutaneous squamous cell carcinoma (CSCC) that is metastatic or locally advanced and cannot be cured by surgery or radiation; Basal cell carcinoma (BCC) that is locally advanced or metastatic and has received prior hedgehog inhibitor therapy; Non-small cell lung cancer (NSCLC) with ≥50% PD-L1 expression, as determined by an FDA-approved test, with no EGFR, ALK, or ROS1 aberrations
Mechanism of action BRAF inhibitor Programmed death receptor-1 (PD-1) blocking antibody
Brand names Braftovi Libtayo
Administrative route Oral Intravenous
Side effects Fatigue, nausea, vomiting, abdominal pain, arthralgia, rash, anemia, increased AST/ALT Fatigue, rash, diarrhea, musculoskeletal pain, pruritus
Contraindications None known None known
Drug class Kinase inhibitor Monoclonal antibody
Manufacturer Pfizer Regeneron Pharmaceuticals in collaboration with Sanofi

Efficacy

Efficacy of Braftovi (Encorafenib) in Treating Skin Cancer

Braftovi, known generically as encorafenib, is a medication specifically indicated for the treatment of certain types of skin cancer. It is most commonly used for unresectable or metastatic melanoma with a BRAF V600E or V600K mutation, as detected by an FDA-approved test. Encorafenib is part of a class of drugs known as BRAF inhibitors, which work by targeting and inhibiting the activity of the mutated BRAF protein that can lead to cancer cell growth.

Clinical trials have demonstrated the efficacy of encorafenib in treating melanoma with BRAF mutations. When used in combination with another medication called binimetinib, a MEK inhibitor, encorafenib has been shown to significantly improve progression-free survival compared to treatment with BRAF inhibitor vemurafenib alone. This combination therapy has also been associated with a higher overall response rate, meaning that more patients experienced a reduction in tumor size.

Efficacy of Libtayo (Cemiplimab) in Treating Skin Cancer

Libtayo, with the generic name cemiplimab, is a relatively new medication approved for the treatment of patients with metastatic or locally advanced cutaneous squamous cell carcinoma (CSCC) who are not candidates for curative surgery or curative radiation. Cemiplimab is a type of immunotherapy known as a PD-1 blocker. It works by enhancing the body's immune response against cancer cells.

In clinical studies, Libtayo has shown significant efficacy in treating advanced CSCC. The results have indicated a robust response rate, with a considerable proportion of patients experiencing a reduction in tumor size. Some patients achieved complete remission. Additionally, cemiplimab has been associated with durable responses, meaning that the effects of the treatment are long-lasting for many patients. The drug's approval marked a significant advancement in the treatment options available for CSCC, which is the second most common form of skin cancer.

Regulatory Agency Approvals

Braftovi
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan
Libtayo
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada

Access Braftovi or Libtayo today

If Braftovi or Libtayo 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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