Rydapt (midostaurin) vs Besponsa (inotuzumab ozogamicin)

Rydapt (midostaurin) vs Besponsa (inotuzumab ozogamicin)

Rydapt (midostaurin) is a kinase inhibitor used for the treatment of acute myeloid leukemia (AML) with a specific genetic mutation, as well as advanced systemic mastocytosis. Besponsa (inotuzumab ozogamicin) is an antibody-drug conjugate indicated for the treatment of adults with relapsed or refractory B-cell precursor acute lymphoblastic leukemia (ALL). The choice between Rydapt and Besponsa would depend on the specific type and characteristics of the leukemia a patient has, as they target different forms of the disease and are not interchangeable.

Difference between Rydapt and Besponsa

Metric Rydapt (midostaurin) Besponsa (inotuzumab ozogamicin)
Generic name Midostaurin Inotuzumab ozogamicin
Indications Acute myeloid leukemia (AML), Mastocytosis Acute lymphoblastic leukemia (ALL)
Mechanism of action Protein kinase inhibitor Antibody-drug conjugate, CD22-directed
Brand names Rydapt Besponsa
Administrative route Oral Intravenous
Side effects Febrile neutropenia, nausea, mucositis, vomiting, headache Fever, nausea, headache, hemorrhage, increased liver enzymes
Contraindications Hypersensitivity to midostaurin or excipients Hypersensitivity to inotuzumab ozogamicin or excipients
Drug class Protein kinase inhibitor Antibody-drug conjugate
Manufacturer Novartis Pharmaceuticals Corporation Pfizer Inc.

Efficacy

Efficacy of Rydapt (Midostaurin) in Leukemia

Rydapt, known generically as midostaurin, is a medication approved for the treatment of certain types of leukemia. Specifically, it is indicated for adults with newly diagnosed acute myeloid leukemia (AML) that is FLT3 mutation-positive, as detected by an FDA-approved test, in combination with standard cytarabine and daunorubicin induction and cytarabine consolidation. Midostaurin is a multitargeted kinase inhibitor that works by blocking multiple enzymes that promote cell growth, which can be beneficial in the treatment of cancerous cells in leukemia. Clinical trials have demonstrated that midostaurin, when added to standard chemotherapy, improves overall survival rates compared to chemotherapy alone, thus representing a significant advancement in the treatment of FLT3-mutated AML.

Efficacy of Besponsa (Inotuzumab Ozogamicin) in Leukemia

Besponsa, with the generic name inotuzumab ozogamicin, is an antibody-drug conjugate indicated for the treatment of adults with relapsed or refractory B-cell precursor acute lymphoblastic leukemia (ALL). Inotuzumab ozogamicin targets the CD22 antigen on B cells and releases a cytotoxic agent once inside the cells, leading to cell death. Clinical trials have shown that Besponsa significantly improves complete remission rates and has a measurable effect on overall survival when compared to standard therapy. This medication offers a targeted approach to treatment, which can be particularly effective for patients who have not responded to or have relapsed after standard chemotherapy treatments.

Both Rydapt and Besponsa represent important options in the management of different types of leukemia, addressing the needs of specific patient populations with their targeted mechanisms of action. Their efficacy in improving patient outcomes highlights the importance of personalized medicine in the field of oncology. As with any medication, the use of Rydapt and Besponsa should be carefully considered by healthcare professionals, taking into account the individual patient's health status, the presence of specific biomarkers, and the potential benefits and risks of treatment.

It is crucial for patients and healthcare providers to engage in thorough discussions regarding treatment options for leukemia, including the efficacy and potential side effects of medications like Rydapt and Besponsa. Ongoing research and clinical trials continue to provide valuable information on the effectiveness of these drugs, contributing to the evolving landscape of leukemia treatment and offering hope for improved patient outcomes.

Regulatory Agency Approvals

Rydapt
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia
  • Medsafe (NZ)
Besponsa
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA

Access Rydapt or Besponsa today

If Rydapt or Besponsa 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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