Ninlaro (ixazomib) vs Sarclisa (isatuximab)

Ninlaro (ixazomib) vs Sarclisa (isatuximab)

Ninlaro (ixazomib) is an oral proteasome inhibitor used in combination with other medications to treat multiple myeloma, specifically in patients who have received at least one prior therapy. Sarclisa (isatuximab) is an intravenous monoclonal antibody that targets a specific protein on myeloma cells and is also used in combination with other drugs for the treatment of multiple myeloma in patients who have received at least two prior therapies, including lenalidomide and a proteasome inhibitor. When deciding between Ninlaro and Sarclisa, it is important to consider factors such as the patient's previous treatments, potential side effects, mode of administration (oral for Ninlaro, intravenous for Sarclisa), and the specific recommendations of the healthcare provider based on the patient's individual health status and treatment history.

Difference between Ninlaro and Sarclisa

Metric Ninlaro (ixazomib) Sarclisa (isatuximab)
Generic name Ixazomib Isatuximab
Indications Multiple myeloma Multiple myeloma
Mechanism of action Proteasome inhibitor CD38-directed cytolytic antibody
Brand names Ninlaro Sarclisa
Administrative route Oral Intravenous
Side effects Diarrhea, constipation, thrombocytopenia, peripheral neuropathy, nausea, peripheral edema, vomiting, back pain Neutropenia, infusion-related reactions, pneumonia, upper respiratory tract infection, diarrhea
Contraindications Hypersensitivity to ixazomib or any of its excipients Hypersensitivity to isatuximab or any of its components
Drug class Proteasome inhibitor Monoclonal antibody
Manufacturer Takeda Pharmaceuticals Sanofi

Efficacy

Ninlaro (Ixazomib) Efficacy in Multiple Myeloma

Ninlaro (ixazomib) is an oral proteasome inhibitor approved by the U.S. Food and Drug Administration (FDA) for the treatment of multiple myeloma. It is specifically indicated for use in combination with lenalidomide and dexamethasone for patients who have received at least one prior therapy. Clinical trials have demonstrated that ixazomib, when added to lenalidomide and dexamethasone, can significantly improve progression-free survival (PFS) in patients with relapsed or refractory multiple myeloma. The efficacy of ixazomib was established in a pivotal phase 3 trial known as TOURMALINE-MM1, which showed a median PFS of 20.6 months for patients receiving the ixazomib regimen compared to 14.7 months for patients receiving lenalidomide and dexamethasone alone.

Sarclisa (Isatuximab) Efficacy in Multiple Myeloma

Sarclisa (isatuximab) is a monoclonal antibody that targets the CD38 molecule on the surface of multiple myeloma cells. It is approved by the FDA for use in combination with pomalidomide and dexamethasone for the treatment of adults with multiple myeloma who have received at least two prior therapies including lenalidomide and a proteasome inhibitor. Isatuximab works by helping the immune system attack the cancer cells and also directly induces cancer cell death. The approval of Sarclisa was based on the results of the ICARIA-MM clinical trial, which demonstrated that the addition of isatuximab to pomalidomide and dexamethasone resulted in a significant improvement in PFS. The median PFS for patients treated with the isatuximab combination was 11.53 months compared to 6.47 months for those receiving pomalidomide and dexamethasone alone.

Comparative Efficacy and Considerations

While both Ninlaro and Sarclisa have shown efficacy in the treatment of multiple myeloma, they are used in different combinations and lines of therapy. The choice of treatment regimen depends on various factors, including the patient's prior treatment history, tolerance to previous therapies, and specific disease characteristics. Both treatments represent important options in the relapsed or refractory multiple myeloma setting, offering patients the potential for improved outcomes. It is important for healthcare providers to assess the individual needs of each patient and consider the most appropriate therapy based on the clinical evidence available.

Conclusion

In conclusion, Ninlaro and Sarclisa have each shown to be effective in improving progression-free survival in patients with multiple myeloma when used in combination with other therapies. The efficacy of these drugs highlights the advancement in multiple myeloma treatment and provides additional therapeutic options for patients with this challenging disease. Continuous research and clinical trials are essential to further understand the full potential and optimal use of these treatments in the multiple myeloma treatment landscape.

Regulatory Agency Approvals

Ninlaro
  • 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
Sarclisa
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada

Access Ninlaro or Sarclisa today

If Ninlaro or Sarclisa 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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