Opdivo (Nivolumab) vs Darvias (darinaparsin) ()

Opdivo (Nivolumab) vs Darvias (darinaparsin) ()

Opdivo (nivolumab) is an immunotherapy drug that works by blocking the PD-1 pathway, which cancer cells can use to hide from the immune system, and is primarily used to treat various types of cancers including melanoma, lung cancer, and kidney cancer. Darzalex (daratumumab), not Darvias (darinaparsin), is a monoclonal antibody that targets CD38, a protein highly expressed on the surface of multiple myeloma cells, leading to their destruction, and is used in the treatment of multiple myeloma. When deciding between these two medications, it is essential to consider the type of cancer being treated, as Opdivo is not indicated for multiple myeloma, while Darzalex is specifically approved for this condition and would not be appropriate for the cancers Opdivo targets.

Difference between Opdivo and Darvias (darinaparsin)

Metric Opdivo (Nivolumab) Darvias (darinaparsin)
Generic name Nivolumab Darinaparsin
Indications Various types of cancers including melanoma, non-small cell lung cancer, renal cell carcinoma, Hodgkin lymphoma, and others Currently being investigated for the treatment of various cancers, including hematologic malignancies and solid tumors
Mechanism of action PD-1 immune checkpoint inhibitor that enables the immune system to better detect and attack cancer cells Organic arsenic compound that induces apoptosis and disrupts mitochondrial function in cancer cells
Brand names Opdivo Darvias
Administrative route Intravenous injection Investigational, primarily studied as an intravenous formulation
Side effects Fatigue, rash, musculoskeletal pain, pruritus, diarrhea, nausea, and others Not fully characterized due to investigational status, but may include gastrointestinal disturbances, fatigue, and hematologic abnormalities
Contraindications Known hypersensitivity to nivolumab or any of its excipients Not fully established due to investigational status
Drug class Immune checkpoint inhibitor Organic arsenical
Manufacturer Bristol Myers Squibb ZIOPHARM Oncology

Efficacy

Overview of Opdivo (Nivolumab) in Lymphoma Treatment

Opdivo (Nivolumab) is a programmed death-1 (PD-1) immune checkpoint inhibitor that has shown efficacy in the treatment of several types of cancer, including lymphoma. Specifically, Nivolumab has been evaluated in patients with classical Hodgkin Lymphoma (cHL) after failure of autologous stem cell transplant (ASCT) or after at least two prior therapies in patients who are not ASCT candidates. The drug works by blocking the PD-1 pathway, thereby enhancing T-cell function against cancer cells. Clinical trials have demonstrated that Nivolumab can induce durable responses with an acceptable safety profile in relapsed or refractory cHL.

Efficacy of Opdivo in Clinical Trials

Clinical trials such as the CheckMate 205 and CheckMate 039 have investigated the efficacy of Nivolumab in lymphoma patients. Results have shown significant response rates, with a portion of patients achieving complete remission. The median duration of response has also been noteworthy, suggesting sustained benefits for those who respond to treatment. However, the efficacy can vary based on prior treatments and the specific characteristics of the lymphoma subtype.

Darzalex (Daratumumab) in Lymphoma Treatment

Darzalex (Daratumumab) is a CD38-directed cytolytic antibody indicated for the treatment of multiple myeloma, which is a type of cancer that originates in plasma cells, a kind of white blood cell that can be related to lymphoma. While Darzalex is not specifically approved for the treatment of lymphoma, its mechanism of action, targeting CD38, suggests potential utility in certain lymphoma subtypes where CD38 is expressed. Off-label use in lymphoma may be considered based on the specific case and scientific rationale, but it is important to note that the majority of the efficacy data for Daratumumab pertains to multiple myeloma.

Considerations for Off-Label Use

While the use of Darzalex in lymphoma may be contemplated on an off-label basis, it is crucial to consider the lack of extensive clinical trial data supporting its use in this context. Physicians may consider this option in cases where standard treatments have failed, and the lymphoma cells express CD38. However, such use should be approached with caution, and it is advised to be conducted within the framework of a clinical trial or a comprehensive treatment plan that includes close monitoring for efficacy and safety.

Regulatory Agency Approvals

Opdivo
  • 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)
Darvias (darinaparsin)
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan

Access Opdivo or Darvias (darinaparsin) today

If Opdivo 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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