Aliqopa (copanlisib) vs Copiktra (duvelisib)

Aliqopa (copanlisib) vs Copiktra (duvelisib)

Aliqopa (copanlisib) is a pan-class I phosphatidylinositol 3-kinase (PI3K) inhibitor, specifically used for the treatment of adult patients with relapsed follicular lymphoma who have received at least two prior systemic therapies. Copiktra (duvelisib), on the other hand, is a dual inhibitor of PI3K-delta and PI3K-gamma, indicated for the treatment of adult patients with relapsed or refractory chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) and follicular lymphoma after at least two prior systemic therapies. The choice between the two medications would depend on the specific type of lymphoma, the patient's prior treatment history, and their overall health profile, which should be carefully evaluated by a healthcare professional.

Difference between Aliqopa and Copiktra

Metric Aliqopa (copanlisib) Copiktra (duvelisib)
Generic name copanlisib duvelisib
Indications Relapsed follicular lymphoma Chronic lymphocytic leukemia (CLL), Small lymphocytic lymphoma (SLL), Follicular lymphoma
Mechanism of action PI3K inhibitor, predominantly of the PI3K-alpha and PI3K-delta isoforms PI3K inhibitor, predominantly of the PI3K-delta and PI3K-gamma isoforms
Brand names Aliqopa Copiktra
Administrative route Intravenous Oral
Side effects Hyperglycemia, hypertension, neutropenia, diarrhea, decreased general strength and energy, etc. Diarrhea, neutropenia, rash, fatigue, pyrexia, cough, anemia, etc.
Contraindications None known None known
Drug class Antineoplastic agent, PI3K inhibitor Antineoplastic agent, PI3K inhibitor
Manufacturer Bayer Verastem Oncology

Efficacy

Aliqopa (Copanlisib) Efficacy in Lymphoma

Aliqopa (copanlisib) is an intravenous phosphatidylinositol 3-kinase (PI3K) inhibitor approved by the U.S. Food and Drug Administration (FDA) for the treatment of adult patients with relapsed follicular lymphoma who have received at least two prior systemic therapies. The efficacy of Aliqopa in lymphoma was demonstrated in a single-arm clinical trial, which included 104 patients with follicular lymphoma. The overall response rate (ORR) was the primary endpoint, and results showed an ORR of 59%, with a complete response rate of 14% and a partial response rate of 45%. The median duration of response (DOR) was 12.2 months, indicating that the responses were durable for a significant period.

Copiktra (Duvelisib) Efficacy in Lymphoma

Copiktra (duvelisib) is an oral PI3K inhibitor that is FDA-approved for the treatment of adult patients with relapsed or refractory chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) after at least two prior therapies and for relapsed or refractory follicular lymphoma after at least two prior systemic therapies. The approval for CLL/SLL was based on a randomized, multicenter, open-label clinical trial comparing duvelisib to ofatumumab. Duvelisib demonstrated a median progression-free survival (PFS) of 13.3 months compared to 9.9 months for ofatumumab. For follicular lymphoma, the efficacy was evaluated in a single-arm trial with an ORR of 42% and a median DOR of 10 months, showing its potential as a treatment option for patients who have exhausted other therapies.

Comparative Efficacy in Lymphoma

When comparing Aliqopa and Copiktra, it is important to note that both drugs target the PI3K pathway, which is critical in the proliferation and survival of malignant B-cells in lymphoma. However, Aliqopa is more selective for the PI3K-alpha and PI3K-delta isoforms, while Copiktra inhibits both PI3K-delta and PI3K-gamma. This difference may influence their efficacy and safety profiles. Both medications have shown efficacy in relapsed follicular lymphoma, with Aliqopa demonstrating a slightly higher ORR. Nevertheless, direct comparison is difficult without head-to-head clinical trials.

Conclusion on Efficacy

In conclusion, both Aliqopa and Copiktra have shown efficacy in the treatment of relapsed lymphoma, specifically follicular lymphoma and CLL/SLL for Copiktra. These treatments offer additional options for patients who have relapsed or are refractory to prior therapies. The choice of therapy should be individualized based on the patient's specific disease characteristics, prior treatments, and overall health status, as well as the distinct safety profiles of each medication. Ongoing research and clinical trials continue to refine the understanding of the efficacy and optimal use of these targeted therapies in lymphoma.

Regulatory Agency Approvals

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

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