Mektovi (binimetinib) vs Zynyz (retifanlimab-dlwr)

Mektovi (binimetinib) vs Zynyz (retifanlimab-dlwr)

Mektovi (binimetinib) is a kinase inhibitor specifically designed for the treatment of patients with certain types of melanoma, the most serious form of skin cancer, that cannot be removed by surgery or has metastasized, and it targets mutations in the BRAF gene. On the other hand, Zynyz (retifanlimab-dlwr) is an immune checkpoint inhibitor indicated for the treatment of adult patients with locally advanced or metastatic squamous cell carcinoma of the anal canal (SCAC) who have progressed on, or who are intolerant of, platinum-based chemotherapy. When deciding between these two medications, it is crucial to consider the specific type of cancer diagnosed, the genetic makeup of the tumor, and the overall health and treatment history of the individual, as each medication is tailored for different indications and mechanisms of action.

Difference between Mektovi and Zynyz

Metric Mektovi (binimetinib) Zynyz (retifanlimab-dlwr)
Generic name Binimetinib Retifanlimab-dlwr
Indications Unresectable or metastatic melanoma with a BRAF V600E or V600K mutation, as detected by an FDA-approved test, in combination with encorafenib Advanced or metastatic solid tumors with disease progression following prior treatment and who have no satisfactory alternative treatment options
Mechanism of action MEK inhibitor that works by interfering with the MEK1 and MEK2 enzymes, which may prevent the growth of cancer cells Programmed death receptor-1 (PD-1) blocking antibody, which may help the immune system in detecting and fighting cancer cells
Brand names Mektovi Zynyz
Administrative route Oral Intravenous
Side effects Fatigue, nausea, diarrhea, vomiting, abdominal pain, and rash Infusion-related reactions, fatigue, musculoskeletal pain, diarrhea, and rash
Contraindications None known None known
Drug class Antineoplastic agent, MEK inhibitor Immune checkpoint inhibitor, PD-1 inhibitor
Manufacturer Array BioPharma Inc. (a subsidiary of Pfizer) Inc. (a subsidiary of Gilead Sciences)

Efficacy

Mektovi (binimetinib) for Skin Cancer

Mektovi (binimetinib) is a medication that is specifically indicated for the treatment of patients with unresectable or metastatic melanoma with a BRAF V600E or V600K mutation, as detected by an FDA-approved test. In the context of skin cancer, melanoma is one of the most aggressive forms and can be life-threatening if it spreads to other parts of the body. Mektovi, as part of a combination therapy with encorafenib, has shown efficacy in improving progression-free survival (PFS) in patients with this type of melanoma. Clinical trials have demonstrated that this combination results in a significant delay in the progression of the disease when compared to treatments with BRAF inhibitors alone.

The approval of Mektovi for use in melanoma was largely based on the results from the COLUMBUS trial, a phase 3 clinical study. In this trial, patients treated with the combination of binimetinib and encorafenib exhibited a median progression-free survival of 14.9 months, compared to 7.3 months for patients treated with vemurafenib, a BRAF inhibitor. Overall response rates and duration of response were also improved in the combination therapy arm, highlighting the efficacy of Mektovi in this patient population.

Zynyz (retifanlimab-dlwr) for Skin Cancer

Zynyz (retifanlimab-dlwr) is an investigational monoclonal antibody designed to target the programmed death receptor-1 (PD-1) on the surface of immune cells. While it is not specifically approved for skin cancer, PD-1 inhibitors like retifanlimab have shown promise in the treatment of various types of cancer, including melanoma, by enhancing the body's immune response against tumor cells. The efficacy of PD-1 inhibitors in melanoma is based on their ability to block the interaction between PD-1 and its ligands, PD-L1 and PD-L2, which can otherwise lead to the inhibition of the immune response to cancer cells.

While clinical data specifically for Zynyz (retifanlimab-dlwr) in skin cancer are not widely available, the efficacy of PD-1 inhibitors as a class has been well-documented in melanoma. These drugs have been associated with improved overall survival and progression-free survival in patients with advanced melanoma. The use of PD-1 inhibitors has become a standard of care in the treatment of advanced melanoma, particularly for patients who have not responded to other therapies. As an investigational drug, retifanlimab may offer similar benefits, but its efficacy and safety profile will need to be confirmed through clinical trials before it can be considered for approval in skin cancer or any other indication.

Regulatory Agency Approvals

Mektovi
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan
Zynyz
  • Food and Drug Administration (FDA), USA

Access Mektovi or Zynyz today

If Mektovi or Zynyz 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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