Bavencio (avelumab) vs Libtayo (cemiplimab)

Bavencio (avelumab) vs Libtayo (cemiplimab)

When comparing Bavencio (avelumab) with Libtayo (cemiplimab), it is important to note that both are types of immunotherapy drugs known as checkpoint inhibitors, but they target different proteins. Bavencio is a PD-L1 inhibitor approved for the treatment of Merkel cell carcinoma, urothelial carcinoma, and renal cell carcinoma, among other indications. In contrast, Libtayo is a PD-1 inhibitor primarily approved for the treatment of cutaneous squamous cell carcinoma, basal cell carcinoma, and non-small cell lung cancer. The choice between these medications should be based on the specific type of cancer, the patient's overall health, and the treatment plan determined by an oncologist.

Difference between Bavencio and Libtayo

Metric Bavencio (avelumab) Libtayo (cemiplimab)
Generic name Avelumab Cemiplimab
Indications Metastatic Merkel cell carcinoma, urothelial carcinoma, renal cell carcinoma Cutaneous squamous cell carcinoma, basal cell carcinoma, non-small cell lung cancer
Mechanism of action PD-L1 blocking antibody PD-1 blocking antibody
Brand names Bavencio Libtayo
Administrative route Intravenous infusion Intravenous infusion
Side effects Fatigue, musculoskeletal pain, diarrhea, nausea, infusion-related reactions, rash, decreased appetite Fatigue, rash, diarrhea, musculoskeletal pain, pruritus
Contraindications Severe hypersensitivity to avelumab or its excipients Severe hypersensitivity to cemiplimab or its excipients
Drug class Monoclonal antibody, Immune checkpoint inhibitor Monoclonal antibody, Immune checkpoint inhibitor
Manufacturer Merck KGaA and Pfizer Regeneron Pharmaceuticals, Inc. and Sanofi

Efficacy

Bavencio (Avelumab) and Its Efficacy in Treating Skin Cancer

Bavencio, known generically as avelumab, is a type of immunotherapy drug classified as a PD-L1 inhibitor. It has been approved for the treatment of Merkel cell carcinoma, a rare and aggressive form of skin cancer. The efficacy of Bavencio for this indication was demonstrated in a multicenter, single-arm, open-label clinical trial. In this study, avelumab showed a meaningful response rate in patients with metastatic Merkel cell carcinoma who had previously undergone chemotherapy. These responses were not only high in rate but also durable, with many patients experiencing prolonged periods of disease control.

Libtayo (Cemiplimab) and Its Role in Skin Cancer Treatment

Libtayo, or cemiplimab, is another immunotherapy agent, specifically an anti-PD-1 antibody, that has been 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. The approval of Libtayo was based on data from a combined analysis of two open-label clinical trials. These trials demonstrated a significant response rate in patients treated with cemiplimab, with many patients achieving partial or complete tumor shrinkage. The responses observed were durable, and some patients experienced a stabilization of their disease.

Comparative Efficacy in Skin Cancer Treatment

While both Bavencio and Libtayo are effective in treating different types of skin cancer, their efficacy must be considered in the context of the specific condition they are approved to treat. Bavencio's efficacy is established in the context of Merkel cell carcinoma, whereas Libtayo's efficacy is demonstrated in cutaneous squamous cell carcinoma. Both drugs work by targeting and inhibiting pathways that cancer cells use to evade the immune system, but their use and efficacy are specific to the type of skin cancer being treated.

Conclusion on the Efficacy of Bavencio and Libtayo in Skin Cancer

In conclusion, Bavencio and Libtayo have shown significant efficacy in the treatment of different types of skin cancer. Their approval and use in clinical practice have provided valuable options for patients with Merkel cell carcinoma and cutaneous squamous cell carcinoma, respectively. It is important for healthcare providers to consider the individual characteristics of each drug and the specific skin cancer type when recommending these treatments to ensure the best possible patient outcomes.

Regulatory Agency Approvals

Bavencio
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan
  • Therapeutic Goods Administration (TGA), Australia
Libtayo
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada

Access Bavencio or Libtayo today

If Bavencio 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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