Beleodaq (belinostat) vs Darvias (darinaparsin) ()

Beleodaq (belinostat) vs Darvias (darinaparsin) ()

Beleodaq (belinostat) and Darinaparsin (marketed as Darvias) are both used to treat cancer, but they have different mechanisms of action and are approved for different indications. Beleodaq is a histone deacetylase (HDAC) inhibitor approved by the FDA for the treatment of relapsed or refractory peripheral T-cell lymphoma, a type of non-Hodgkin lymphoma. Darinaparsin, a mitochondrial-targeted agent, is being investigated for the treatment of various hematologic and solid tumors, but as of my knowledge cutoff date, it has not received FDA approval and should be considered experimental. When deciding which medicine is right for an individual, it is crucial to consult with a healthcare professional to consider the specific type of cancer, the drug's approval status, potential side effects, and the individual's overall health condition.

Difference between Beleodaq and Darvias (darinaparsin)

Metric Beleodaq (belinostat) Darvias (darinaparsin)
Generic name Belinostat Darinaparsin
Indications Peripheral T-cell lymphoma Currently in clinical trials for various types of cancer, including lymphoma and solid tumors
Mechanism of action HDAC inhibitor Induces apoptosis and disrupts mitochondrial function
Brand names Beleodaq Darvias (not yet commercially available)
Administrative route Intravenous Intravenous (in clinical trials)
Side effects Nausea, vomiting, fatigue, fever, anemia Not fully characterized, but may include gastrointestinal symptoms, fatigue, hematological abnormalities
Contraindications Hypersensitivity to belinostat or any component of the formulation Not yet established
Drug class Antineoplastic agent, HDAC inhibitor Antineoplastic agent (organic arsenic)
Manufacturer Spectrum Pharmaceuticals, Inc. ZIOPHARM Oncology

Efficacy

Beleodaq (Belinostat) for the Treatment of Lymphoma

Beleodaq, with the active ingredient belinostat, is a histone deacetylase inhibitor approved by the U.S. Food and Drug Administration (FDA) for the treatment of relapsed or refractory peripheral T-cell lymphoma (PTCL). This is a rare 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 clinical trial that involved patients with refractory or relapsed PTCL. Results from this study showed that Beleodaq achieved an overall response rate, which includes complete and partial responses, indicating a reduction in tumor burden in a proportion of patients treated with this medication.

While the response rates provide an indication of Beleodaq's efficacy, the duration of response is also a critical aspect of its effectiveness. In the clinical trial, some patients experienced a prolonged duration of response, which suggests that Beleodaq can offer meaningful clinical benefits for certain individuals with PTCL. However, it is important to note that responses to treatment can vary among patients, and not all patients will experience the same level of benefit from Beleodaq.

Darvias (Darinaparsin) for the Treatment of Lymphoma

Darvias, known by its investigational name darinaparsin, is a novel organic arsenic compound that has been studied for its potential use in treating various types of cancer, including lymphoma. Although darinaparsin has not been approved by the FDA for the treatment of lymphoma, it has been investigated in clinical trials for its efficacy against this disease. In these studies, darinaparsin has demonstrated some anti-tumor activity in patients with lymphoma, particularly in those with Hodgkin's lymphoma and certain subtypes of non-Hodgkin lymphoma.

The clinical trials of darinaparsin have focused on evaluating its efficacy as a single agent and in combination with other chemotherapeutic drugs. The results have shown that darinaparsin can induce responses in a subset of patients with lymphoma. However, as an investigational drug, further research is needed to fully understand the efficacy and safety profile of darinaparsin for the treatment of lymphoma. Until such time as it receives FDA approval, darinaparsin remains an experimental therapy and is not widely available for the treatment of lymphoma outside of clinical trials.

Regulatory Agency Approvals

Beleodaq
  • Food and Drug Administration (FDA), USA
Darvias (darinaparsin)
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan

Access Beleodaq or Darvias (darinaparsin) today

If Beleodaq or Darvias (darinaparsin) 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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