Adcetris (brentuximab vedotin) vs Copiktra (duvelisib)

Adcetris (brentuximab vedotin) vs Copiktra (duvelisib)

Adcetris (brentuximab vedotin) is an antibody-drug conjugate specifically targeting CD30, a marker on some lymphoma cells, and is used primarily in the treatment of Hodgkin lymphoma and systemic anaplastic large cell lymphoma. Copiktra (duvelisib) is a small molecule PI3K inhibitor that targets cancer cells by blocking certain cell growth signals, and it is approved for the treatment of chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), and follicular lymphoma. The choice between Adcetris and Copiktra would depend on the specific type of lymphoma a patient has, their overall health, previous treatments, and the presence of specific biomarkers, as each medication has a distinct mechanism of action and is approved for different indications.

Difference between Adcetris and Copiktra

Metric Adcetris (brentuximab vedotin) Copiktra (duvelisib)
Generic name Brentuximab vedotin Duvelisib
Indications Hodgkin lymphoma, systemic anaplastic large cell lymphoma, primary cutaneous anaplastic large cell lymphoma, and certain types of mycosis fungoides Chronic lymphocytic leukemia, small lymphocytic lymphoma, and follicular lymphoma
Mechanism of action Antibody-drug conjugate targeting CD30-expressing cells PI3K inhibitor targeting PI3K-delta and PI3K-gamma
Brand names Adcetris Copiktra
Administrative route Intravenous infusion Oral
Side effects Neutropenia, peripheral neuropathy, anemia, infusion reactions, thrombocytopenia, etc. Diarrhea, neutropenia, rash, fatigue, pyrexia, cough, etc.
Contraindications Hypersensitivity to brentuximab vedotin or any excipients Hypersensitivity to duvelisib or any excipients, history of severe allergic reactions to other PI3K inhibitors
Drug class Antineoplastic agent, monoclonal antibody Antineoplastic agent, kinase inhibitor
Manufacturer Seattle Genetics Verastem Oncology

Efficacy

Efficacy of Adcetris (Brentuximab Vedotin) in Lymphoma Treatment

Adcetris (brentuximab vedotin) is an antibody-drug conjugate specifically indicated for the treatment of several types of lymphoma, including Hodgkin lymphoma and systemic anaplastic large cell lymphoma. Its efficacy in Hodgkin lymphoma was demonstrated in a pivotal clinical trial that showed a significant improvement in overall survival and progression-free survival in patients who received Adcetris as compared to those who received a placebo. In the setting of relapsed or refractory Hodgkin lymphoma, Adcetris has been shown to induce complete remissions in a substantial proportion of patients. Similarly, in systemic anaplastic large cell lymphoma, Adcetris has been effective in achieving objective response rates and durable remissions, making it a valuable treatment option for patients with this type of lymphoma.

Efficacy of Copiktra (Duvelisib) in Lymphoma Treatment

Copiktra (duvelisib) is a small molecule inhibitor of phosphoinositide 3-kinase (PI3K), and it is approved for the treatment of relapsed or refractory chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) and follicular lymphoma. Its efficacy in treating these types of lymphoma has been established through clinical trials that have demonstrated significant improvements in overall response rates. In the case of relapsed or refractory CLL/SLL, Copiktra has shown to be effective in patients who have been heavily pre-treated and have limited treatment options. For follicular lymphoma, Copiktra's efficacy was assessed in a single-arm trial, where it showed a notable proportion of patients achieving partial or complete responses.

While the efficacy of Adcetris and Copiktra in the treatment of lymphoma is well-established, it is important to note that the response to these drugs can vary among patients. Factors such as prior treatments, the specific subtype of lymphoma, and individual patient characteristics can influence the effectiveness of these therapies. Physicians consider these factors when choosing the most appropriate treatment regimen for their patients.

Both Adcetris and Copiktra are important additions to the therapeutic arsenal against lymphoma, offering hope to patients who may have limited options. As with all medications, the use of these drugs should be guided by a thorough understanding of the patient's medical history and the specific characteristics of their disease. Ongoing research and clinical trials continue to refine the understanding of how best to utilize Adcetris and Copiktra to maximize patient outcomes in lymphoma treatment.

Regulatory Agency Approvals

Adcetris
  • 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
  • NMPA (China)
Copiktra
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA

Access Adcetris or Copiktra today

If Adcetris or Copiktra 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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