Copiktra (duvelisib) vs Polivy (polatuzumab vedotin-piiq)

Copiktra (duvelisib) vs Polivy (polatuzumab vedotin-piiq)

Copiktra (duvelisib) is a small molecule inhibitor that targets the PI3K-delta and gamma pathways, which are often active in certain types of blood cancers; it is primarily used in the treatment of chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), and follicular lymphoma. Polivy (polatuzumab vedotin-piiq), on the other hand, is an antibody-drug conjugate that targets CD79b, a protein expressed on the surface of B-cells, and is used in combination with other drugs for the treatment of relapsed or refractory diffuse large B-cell lymphoma (DLBCL). The choice between Copiktra and Polivy would largely depend on the specific type of blood cancer a patient has, its stage, previous treatments, and the patient's overall health status, as each medication is tailored for different indications and has its own side effect profile.

Difference between Copiktra and Polivy

Metric Copiktra (duvelisib) Polivy (polatuzumab vedotin-piiq)
Generic name Duvelisib Polatuzumab vedotin-piiq
Indications Chronic lymphocytic leukemia (CLL), Small lymphocytic lymphoma (SLL), Follicular lymphoma (FL) Relapsed or refractory diffuse large B-cell lymphoma (DLBCL)
Mechanism of action PI3K inhibitor Antibody-drug conjugate targeting CD79b
Brand names Copiktra Polivy
Administrative route Oral Intravenous
Side effects Diarrhea, neutropenia, rash, fatigue, pyrexia, cough, nausea, anemia, upper respiratory infection Neutropenia, thrombocytopenia, anemia, peripheral neuropathy, fatigue, diarrhea, fever
Contraindications History of severe allergic reactions to duvelisib or any of its components History of severe allergic reactions to polatuzumab vedotin-piiq or any of its components
Drug class Antineoplastic agent, PI3K inhibitor Antineoplastic agent, monoclonal antibody
Manufacturer Secura Bio, Inc. Genentech, Inc.

Efficacy

Efficacy of Copiktra (duvelisib) for Lymphoma

Copiktra (duvelisib) is a small molecule inhibitor of phosphoinositide 3-kinase (PI3K) that has been approved for the treatment of certain types of lymphoma. Specifically, it is indicated for adult patients with relapsed or refractory chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) after at least two prior therapies. Duvelisib has also been approved for adult patients with relapsed or refractory follicular lymphoma (FL) after at least two prior systemic therapies. The efficacy of Copiktra was established in a clinical trial where it demonstrated a significant improvement in progression-free survival compared to the control group in patients with CLL/SLL and FL. However, it is important to note that the treatment is associated with a risk of serious toxicities, which may limit its use in certain patient populations.

Efficacy of Polivy (polatuzumab vedotin-piiq) for Lymphoma

Polivy (polatuzumab vedotin-piiq) is an antibody-drug conjugate targeting CD79b, a protein expressed on the surface of most B-cells. It is approved in combination with bendamustine and a rituximab product for the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL), not otherwise specified, after at least two prior therapies. This combination has shown a significant improvement in overall survival and progression-free survival in a pivotal clinical trial compared to bendamustine with rituximab alone. The efficacy of Polivy, as part of this combination regimen, has provided a new therapeutic option for patients with relapsed or refractory DLBCL, a population that historically has had limited treatment options and poor prognosis.

Comparative Efficacy in Lymphoma Treatment

When comparing the efficacy of Copiktra and Polivy for the treatment of lymphoma, it is important to recognize that they are approved for different types of the disease and are not directly comparable. Copiktra is used for CLL/SLL and FL, while Polivy is indicated for DLBCL. Both drugs have shown efficacy in improving patient outcomes in their respective indications and represent important advancements in the treatment of relapsed or refractory lymphomas. The choice of therapy would depend on the specific type of lymphoma, the patient's prior treatment history, and their overall health status.

Considerations for Treatment Selection

When considering the use of Copiktra or Polivy for lymphoma, healthcare providers must weigh the benefits of treatment against potential risks. Both medications have been associated with serious side effects, and their use is generally reserved for patients who have not responded to or have relapsed after other treatments. The decision to use these drugs should involve a thorough discussion of the potential risks and benefits, as well as consideration of the patient's preferences and quality of life. Additionally, ongoing monitoring and supportive care are crucial to manage any adverse effects that may arise during treatment.

Regulatory Agency Approvals

Copiktra
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
Polivy
  • Food and Drug Administration (FDA), USA
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan
  • Therapeutic Goods Administration (TGA), Australia

Access Copiktra or Polivy today

If Copiktra or Polivy 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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