Rydapt (midostaurin) vs Venclyxto/Venclexta (venetoclax)

Rydapt (midostaurin) vs Venclyxto/Venclexta (venetoclax)

Rydapt (midostaurin) is a kinase inhibitor specifically approved for the treatment of acute myeloid leukemia (AML) with a certain mutation (FLT3) and for adults with advanced systemic mastocytosis, whereas Venclexta (venetoclax) is a BCL-2 inhibitor indicated for use in chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), and AML in combination with other agents, but not as a single agent in AML. The choice between Rydapt and Venclexta would depend on the specific type and genetic characteristics of the leukemia, as well as the patient's overall health and treatment goals. It is important for patients to discuss with their healthcare provider to determine the most appropriate medication based on their individual diagnosis and the molecular profile of their cancer.

Difference between Rydapt and Venclyxto/Venclexta

Metric Rydapt (midostaurin) Venclyxto/Venclexta (venetoclax)
Generic name Midostaurin Venetoclax
Indications Acute Myeloid Leukemia (AML), Mastocytosis Chronic Lymphocytic Leukemia (CLL), Small Lymphocytic Lymphoma (SLL), Acute Myeloid Leukemia (AML)
Mechanism of action Protein kinase inhibitor BCL-2 inhibitor
Brand names Rydapt Venclyxto, Venclexta
Administrative route Oral Oral
Side effects Febrile neutropenia, nausea, mucositis, vomiting, headache Neutropenia, diarrhea, nausea, anemia, upper respiratory tract infection
Contraindications Hypersensitivity to midostaurin or excipients Hypersensitivity to venetoclax or excipients
Drug class Multi-kinase inhibitor BCL-2 inhibitor
Manufacturer Novartis AbbVie and Genentech (Roche)

Efficacy

Efficacy of Rydapt (Midostaurin) in Leukemia

Rydapt, known generically as midostaurin, is a kinase inhibitor approved by the FDA for the treatment of adult patients with newly diagnosed acute myeloid leukemia (AML) that is FLT3 mutation-positive, as detected by an FDA-approved test. This medication is used in combination with standard cytarabine and daunorubicin induction and cytarabine consolidation. Clinical trials have demonstrated that Rydapt, when added to standard chemotherapy, has led to significant improvements in overall survival rates compared to chemotherapy alone. The efficacy of Rydapt in this setting highlights its role as a targeted therapy that can potentially alter the course of AML in patients with the FLT3 mutation.

Efficacy of Venclyxto/Venclexta (Venetoclax) in Leukemia

Venclyxto/Venclexta, with the generic name venetoclax, is a BCL-2 inhibitor indicated for the treatment of patients with chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL), with or without 17p deletion, who have received at least one prior therapy. In clinical trials, venetoclax has shown a high rate of response in patients with CLL, including those with difficult-to-treat forms of the disease, such as those with 17p deletion. This medication has been associated with deep and durable responses, which can be measured by the number of patients achieving complete remission and the duration of response.

Furthermore, venetoclax is also approved in combination with azacitidine, decitabine, or low-dose cytarabine for the treatment of newly diagnosed AML in adults who are age 75 years or older, or who have comorbidities that preclude the use of intensive induction chemotherapy. In this population, venetoclax has been shown to improve overall survival when compared to conventional care regimens. The combination of venetoclax with hypomethylating agents or low-dose cytarabine represents a new standard of care for older AML patients who are not candidates for intensive chemotherapy.

It is important to note that while both Rydapt and Venclyxto/Venclexta have shown efficacy in the treatment of different types of leukemia, they are used in different patient populations and are not interchangeable. The choice of treatment depends on various factors, including the specific type of leukemia, the presence of genetic mutations, patient age, and overall health. As with all medications, the efficacy of Rydapt and Venclyxto/Venclexta must be weighed against potential side effects, and their use should be guided by a healthcare professional experienced in the treatment of leukemia.

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)
Venclyxto/Venclexta
  • 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
  • Medsafe (NZ)

Access Rydapt or Venclyxto/Venclexta today

If Rydapt or Venclyxto/Venclexta 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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