Beleodaq (belinostat) vs Rylaze (asparaginase erwinia chrysanthemi (recombinant)-rywn)

Beleodaq (belinostat) vs Rylaze (asparaginase erwinia chrysanthemi (recombinant)-rywn)

Beleodaq (belinostat) is a histone deacetylase inhibitor used for the treatment of patients with relapsed or refractory peripheral T-cell lymphoma, a type of non-Hodgkin lymphoma. Rylaze (asparaginase erwinia chrysanthemi (recombinant)-rywn) is an asparagine-specific enzyme indicated as a component of a multi-agent chemotherapeutic regimen for acute lymphoblastic leukemia (ALL) in pediatric and adult patients who have developed hypersensitivity to E. coli-derived asparaginase. The choice between Beleodaq and Rylaze would depend on the specific type of blood cancer a patient has, as they are used to treat different conditions and have distinct mechanisms of action.

Difference between Beleodaq and Rylaze

Metric Beleodaq (belinostat) Rylaze (asparaginase erwinia chrysanthemi (recombinant)-rywn)
Generic name Belinostat Asparaginase erwinia chrysanthemi (recombinant)-rywn
Indications Relapsed or refractory peripheral T-cell lymphoma Acute lymphoblastic leukemia (ALL) or lymphoblastic lymphoma
Mechanism of action HDAC inhibitor Enzyme that depletes the amino acid asparagine
Brand names Beleodaq Rylaze
Administrative route Intravenous Intramuscular
Side effects Nausea, vomiting, fatigue, fever, etc. Allergic reactions, pancreatitis, glucose intolerance, etc.
Contraindications Hypersensitivity to belinostat or any component of the formulation Hypersensitivity to asparaginase or any component of the formulation
Drug class Antineoplastic agent, histone deacetylase inhibitor Antineoplastic agent, asparagine specific enzyme
Manufacturer Spectrum Pharmaceuticals, Inc. Jazz Pharmaceuticals, Inc.

Efficacy

Beleodaq (Belinostat) for the Treatment of Lymphoma

Beleodaq (belinostat) is a histone deacetylase inhibitor approved by the U.S. Food and Drug Administration (FDA) for the treatment of patients with relapsed or refractory peripheral T-cell lymphoma (PTCL). This is a type of non-Hodgkin lymphoma that affects the T-cells of the immune system. The efficacy of Beleodaq was evaluated in a multicenter, single-arm trial that involved patients with refractory or relapsed PTCL. In this study, Beleodaq demonstrated a 25.8% overall response rate with a median duration of response of 8.4 months, which provided evidence for its clinical benefit in this patient population.

While Beleodaq has shown efficacy in PTCL, its effectiveness in other types of lymphoma has not been established. It is important for patients to understand that the use of Beleodaq for conditions other than PTCL is considered off-label, and its efficacy for such uses has not been confirmed by the FDA. The safety and effectiveness of Beleodaq continue to be monitored in post-marketing surveillance and ongoing clinical trials.

Rylaze (Asparaginase Erwinia Chrysanthemi (Recombinant)-rywn) for the Treatment of Lymphoma

Rylaze, also known as asparaginase erwinia chrysanthemi (recombinant)-rywn, is an asparagine-specific enzyme approved by the FDA as a component of a multi-agent chemotherapeutic regimen for acute lymphoblastic leukemia (ALL) and lymphoblastic lymphoma (LBL). The drug is indicated for patients who have developed hypersensitivity to E. coli-derived asparaginase. Rylaze works by depleting the amino acid asparagine, which is essential for the growth of ALL and LBL cells, leading to cell death. The efficacy of Rylaze was supported by a clinical trial where the drug maintained nadir serum asparaginase activity above the threshold believed to be therapeutic in 94% of patients, indicating its effectiveness in this patient population.

It is important to note that while Rylaze is used in the treatment of LBL, a type of non-Hodgkin lymphoma, its use is specifically for the lymphoblastic form. The efficacy of Rylaze in other types of lymphoma or for off-label uses has not been established. As with all medications, the use of Rylaze should be guided by a healthcare professional with consideration of the individual patient's diagnosis and treatment plan.

Regulatory Agency Approvals

Beleodaq
  • Food and Drug Administration (FDA), USA
Rylaze
  • Food and Drug Administration (FDA), USA

Access Beleodaq or Rylaze today

If Beleodaq or Rylaze 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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