Velexbru (tirabrutinib hydrochloride) vs Monjuvi (tafasitamab-cxix)

Velexbru (tirabrutinib hydrochloride) vs Monjuvi (tafasitamab-cxix)

Velexbru (tirabrutinib hydrochloride) is a Bruton's tyrosine kinase (BTK) inhibitor used primarily in the treatment of B-cell malignancies, such as mantle cell lymphoma, and is designed to block B-cell receptor signaling that promotes cancer cell survival and proliferation. Monjuvi (tafasitamab-cxix), on the other hand, is a CD19-directed cytolytic antibody indicated for the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL), and it works by engaging the immune system to target and kill the cancer cells. When deciding between these medications, a patient should consider the specific type of lymphoma they have, the mechanism of action of each drug, and discuss with their healthcare provider the potential benefits, side effects, and the overall treatment plan tailored to their individual condition.

Difference between Velexbru and Monjuvi

Metric Velexbru (tirabrutinib hydrochloride) Monjuvi (tafasitamab-cxix)
Generic name Tirabrutinib hydrochloride Tafasitamab-cxix
Indications Treatment of various types of B-cell malignancies Treatment of relapsed or refractory diffuse large B-cell lymphoma
Mechanism of action Bruton's tyrosine kinase (BTK) inhibitor CD19-directed cytolytic antibody
Brand names Velexbru Monjuvi
Administrative route Oral Intravenous
Side effects Neutropenia, thrombocytopenia, diarrhea, cough, musculoskeletal pain Infusion-related reactions, fatigue, neutropenia, anemia, diarrhea, thrombocytopenia
Contraindications Hypersensitivity to tirabrutinib or any component of the formulation Hypersensitivity to tafasitamab or any component of the formulation
Drug class BTK inhibitor Monoclonal antibody
Manufacturer Asahi Kasei Pharma MorphoSys and Incyte

Efficacy

Velexbru (Tirabrutinib Hydrochloride) in Lymphoma Treatment

Velexbru, known by its generic name tirabrutinib hydrochloride, is a Bruton's tyrosine kinase (BTK) inhibitor used in the treatment of certain types of lymphoma. It has shown efficacy in treating relapsed or refractory mantle cell lymphoma (MCL), which is a subtype of non-Hodgkin lymphoma. Tirabrutinib has been studied in clinical trials where it demonstrated significant antitumor activity in patients with MCL who had previously received other treatments. The drug works by blocking BTK, which is an enzyme crucial for the growth and survival of malignant B cells. By inhibiting this pathway, tirabrutinib can induce apoptosis and inhibit proliferation of these cancerous cells.

In clinical trials, tirabrutinib has shown a favorable response rate in patients with MCL, with many achieving partial or complete remission. The efficacy of Velexbru in these trials is measured by the overall response rate (ORR), duration of response (DOR), and progression-free survival (PFS). The data indicates that tirabrutinib has the potential to provide a significant clinical benefit for patients with MCL, especially for those who have limited treatment options due to the refractory nature of their disease.

Monjuvi (Tafasitamab-cxix) in Lymphoma Treatment

Monjuvi, or tafasitamab-cxix, is a monoclonal antibody that has been approved for use in combination with lenalidomide for the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) who are not eligible for autologous stem cell transplant (ASCT). Tafasitamab-cxix targets CD19, a protein expressed on the surface of pre-B and mature B lymphocytes and on many B-cell malignancies. By binding to CD19, Monjuvi recruits the body's immune system to attack and kill the malignant B cells.

The efficacy of Monjuvi in combination with lenalidomide was demonstrated in a pivotal phase II trial, which showed a significant improvement in ORR and complete response rates compared to historical controls. The combination therapy has been associated with a meaningful improvement in PFS and overall survival (OS) in some patient populations. The use of Monjuvi with lenalidomide represents an important advancement in the treatment of DLBCL, particularly for patients who have few therapeutic options due to the aggressive nature of their disease or their inability to undergo ASCT.

Regulatory Agency Approvals

Velexbru
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan
Monjuvi
  • Food and Drug Administration (FDA), USA

Access Velexbru or Monjuvi today

If Velexbru or Monjuvi 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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