Poteligeo (mogamulizumab) vs Lunsumio (mosunetuzumab-axgb)

Poteligeo (mogamulizumab) vs Lunsumio (mosunetuzumab-axgb)

Poteligeo (mogamulizumab) is a monoclonal antibody used for the treatment of certain types of cutaneous T-cell lymphoma (CTCL), specifically for patients who have received at least one prior systemic therapy. It targets the C-C chemokine receptor type 4 (CCR4) on the surface of cancer cells. In contrast, Lunsumio (mosunetuzumab-axgb) is a bispecific T-cell engager antibody indicated for the treatment of relapsed or refractory follicular lymphoma after two or more lines of systemic therapy, and it works by bringing together CD3-positive T-cells and CD20-positive B-cells to induce the killing of lymphoma cells. For someone deciding on which medicine is right for them, it is important to consider the specific type of lymphoma they have, as Poteligeo is approved for CTCL, while Lunsumio is used for follicular lymphoma. Additionally, the individual's prior treatments and their unique medical history should be taken into account when making a treatment decision. It is essential to consult with a healthcare professional to determine the most appropriate treatment based on the patient's specific condition and overall health status.

Difference between Poteligeo and Lunsumio

Metric Poteligeo (mogamulizumab) Lunsumio (mosunetuzumab-axgb)
Generic name mogamulizumab mosunetuzumab-axgb
Indications Relapsed or refractory mycosis fungoides or Sézary syndrome Relapsed or refractory follicular lymphoma
Mechanism of action CCR4-directed monoclonal antibody Bi-specific T-cell engager (BiTE) antibody
Brand names Poteligeo Lunsumio
Administrative route IV infusion IV infusion
Side effects Rash, infusion reactions, fatigue, diarrhea, musculoskeletal pain Cytokine release syndrome, hypotension, fatigue, fever, headache
Contraindications None known None known
Drug class Monoclonal antibody Monoclonal antibody
Manufacturer Kyowa Kirin Genentech

Efficacy

Efficacy of Poteligeo (Mogamulizumab) for Lymphoma

Poteligeo (mogamulizumab-kpkc) is a monoclonal antibody approved by the U.S. Food and Drug Administration (FDA) for the treatment of adult patients with relapsed or refractory mycosis fungoides (MF) or Sézary syndrome (SS), which are types of cutaneous T-cell lymphoma. The drug targets the CC chemokine receptor 4 (CCR4) expressed on the surface of some cancer cells. Clinical trials have demonstrated the efficacy of mogamulizumab in prolonging progression-free survival in patients with MF and SS compared to vorinostat, a previously established treatment. However, it is important to note that while mogamulizumab has shown efficacy in these specific types of lymphoma, its effectiveness in other forms of lymphoma has not been established.

Efficacy of Lunsumio (Mosunetuzumab-axgb) for Lymphoma

Lunsumio (mosunetuzumab-axgb) is an investigational bispecific T-cell engager antibody currently being studied for the treatment of B-cell non-Hodgkin lymphoma (NHL). As an off-label use, its efficacy is not yet fully established and is the subject of ongoing clinical trials. Early clinical trial data suggest that mosunetuzumab-axgb can induce complete remission in a significant proportion of patients with relapsed or refractory B-cell NHL, including those who have failed previous treatments such as CAR T-cell therapy. These promising results indicate that mosunetuzumab-axgb could potentially offer a new treatment option for patients with B-cell NHL, but further research is needed to confirm its efficacy and safety profile.

It is important for patients and healthcare providers to consider the current evidence and regulatory status of new treatments such as Poteligeo and Lunsumio. While Poteligeo has been approved for certain types of cutaneous T-cell lymphoma, Lunsumio is still in the investigational stage for B-cell NHL. The efficacy of these drugs can vary based on the specific type of lymphoma and the patient's individual condition, and treatment decisions should be made in consultation with a healthcare professional who is knowledgeable about the latest research and treatment options for lymphoma.

Both Poteligeo and Lunsumio represent advancements in the targeted treatment of lymphoma, aiming to improve outcomes for patients with these challenging conditions. As the clinical trial landscape evolves and more data become available, the role of these medicines in the treatment of lymphoma may become more clearly defined. For now, their efficacy must be considered within the context of the specific indications for which they have been studied or approved.

Regulatory Agency Approvals

Poteligeo
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Therapeutic Goods Administration (TGA), Australia
Lunsumio
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA

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If Poteligeo or Lunsumio 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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