Beleodaq (belinostat) vs Ukoniq (umbralisib)

Beleodaq (belinostat) vs Ukoniq (umbralisib)

Beleodaq (belinostat) is a histone deacetylase inhibitor approved for the treatment of relapsed or refractory peripheral T-cell lymphoma, working by interfering with the function of enzymes needed for cell division and survival of cancer cells. Ukoniq (umbralisib), on the other hand, is a dual inhibitor of PI3K-delta and casein kinase-1 epsilon, indicated for the treatment of marginal zone lymphoma and follicular lymphoma, targeting specific signaling pathways that are critical for the survival and proliferation of certain cancer cells. The choice between Beleodaq and Ukoniq would depend on the specific type of lymphoma a patient has, their overall health, previous treatments, and the specific recommendation of their healthcare provider based on the latest clinical guidelines and individual patient factors.

Difference between Beleodaq and Ukoniq

Metric Beleodaq (belinostat) Ukoniq (umbralisib)
Generic name Belinostat Umbralisib
Indications Relapsed or refractory peripheral T-cell lymphoma Marginal zone lymphoma, Follicular lymphoma
Mechanism of action HDAC inhibitor PI3K delta and CK1 epsilon inhibitor
Brand names Beleodaq Ukoniq
Administrative route Intravenous Oral
Side effects Nausea, vomiting, fatigue, fever, anemia Increased liver enzymes, diarrhea, fatigue, musculoskeletal pain
Contraindications Known hypersensitivity to belinostat or any of its components None known
Drug class Antineoplastic agent Antineoplastic agent
Manufacturer Spectrum Pharmaceuticals, Inc. TG Therapeutics, Inc.

Efficacy

Beleodaq (Belinostat) for the Treatment of Lymphoma

Beleodaq, also known by its generic name belinostat, is a histone deacetylase inhibitor approved by the Food and Drug Administration (FDA) for the treatment of peripheral T-cell lymphoma (PTCL). PTCL is a diverse group of aggressive lymphomas that originate from T-lymphocytes. The efficacy of Beleodaq was evaluated in a multicenter, single-arm clinical trial that involved patients with relapsed or refractory PTCL. In this study, Beleodaq demonstrated an overall response rate (ORR), which is the proportion of patients with a reduction in tumor burden, of 25.8%. The median duration of response for patients who achieved partial or complete response was 13.6 months, indicating a potential for long-term benefit in a subset of patients.

Ukoniq (Umbralisib) for the Treatment of Lymphoma

Ukoniq, with the generic name umbralisib, is a kinase inhibitor that targets both PI3K-delta and CK1-epsilon. It is FDA-approved for the treatment of marginal zone lymphoma (MZL) and follicular lymphoma (FL) after at least one prior anti-CD20-based therapy. In clinical trials, Ukoniq has shown efficacy in patients with MZL and FL. For MZL, the ORR was 49%, with 16% of patients achieving a complete response. For FL, the ORR was 43%, with a complete response rate of 1%. These results indicate that Ukoniq can induce tumor shrinkage in a significant proportion of patients with these types of lymphoma.

Comparative Efficacy in Lymphoma Treatment

When comparing the efficacy of Beleodaq and Ukoniq, it is important to consider the specific subtypes of lymphoma they are approved to treat. Beleodaq is specifically indicated for PTCL, while Ukoniq is used for MZL and FL. Both medications have shown the ability to induce responses in their respective patient populations, although the response rates and complete response rates vary. The choice of medication would depend on the lymphoma subtype, previous treatments, and the individual patient's response to therapy.

Conclusion

In conclusion, Beleodaq and Ukoniq have demonstrated efficacy in the treatment of different subtypes of lymphoma. Beleodaq offers a treatment option for patients with PTCL, showing a meaningful duration of response in some patients. Ukoniq, on the other hand, benefits patients with MZL and FL, providing another therapeutic option after failure of prior therapies. The efficacy data from clinical trials support their use in their respective indications, contributing to the expanding arsenal of targeted therapies for lymphoma.

Regulatory Agency Approvals

Beleodaq
  • Food and Drug Administration (FDA), USA
Ukoniq
  • Food and Drug Administration (FDA), USA

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