Monjuvi (tafasitamab-cxix) vs Jaypirca (pirtobrutinib)

Monjuvi (tafasitamab-cxix) vs Jaypirca (pirtobrutinib)

Monjuvi (tafasitamab-cxix) is a CD19-directed cytolytic antibody indicated for the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL), to be used in combination with lenalidomide, followed by Monjuvi monotherapy for patients who are not eligible for autologous stem cell transplant (ASCT). Jaypirca (pirtobrutinib) is a Bruton's tyrosine kinase (BTK) inhibitor designed for the treatment of adult patients with mantle cell lymphoma (MCL) who have received at least one prior therapy. When deciding between these two medications, it is crucial to consider the specific type of lymphoma being treated, as Monjuvi is approved for DLBCL, while Jaypirca is intended for MCL, and the choice of treatment should be based on the individual patient's diagnosis, prior treatments, and overall health status, in consultation with their healthcare provider.

Difference between Monjuvi and Jaypirca

Metric Monjuvi (tafasitamab-cxix) Jaypirca (pirtobrutinib)
Generic name Tafasitamab-cxix Pirtobrutinib
Indications Relapsed or refractory diffuse large B-cell lymphoma Relapsed or refractory B-cell malignancies
Mechanism of action CD19-directed cytolytic antibody Bruton's tyrosine kinase (BTK) inhibitor
Brand names Monjuvi Jaypirca
Administrative route Intravenous infusion Oral
Side effects Fatigue, neutropenia, diarrhea, cough, fever, etc. Fatigue, diarrhea, muscle and bone pain, rash, etc.
Contraindications Hypersensitivity to tafasitamab or any of its excipients Hypersensitivity to pirtobrutinib or any of its excipients
Drug class Monoclonal antibody Tyrosine kinase inhibitor
Manufacturer MorphoSys Loxo Oncology at Lilly

Efficacy

Efficacy of Monjuvi (tafasitamab-cxix) in Lymphoma Treatment

Monjuvi (tafasitamab-cxix) is a CD19-directed cytolytic antibody indicated for the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL), not otherwise specified, including DLBCL arising from low-grade lymphoma, and who are not eligible for autologous stem cell transplant (ASCT). The efficacy of Monjuvi, in combination with lenalidomide, was evaluated in a multicenter, single-arm, open-label trial known as L-MIND. In this study, the combination treatment demonstrated a meaningful improvement in overall response rates (ORR), with a significant percentage of patients achieving a complete response (CR). The median duration of response (DOR) was also notable, suggesting that Monjuvi can provide a durable response for patients with this challenging condition.

It is important to consider that the efficacy of Monjuvi may vary based on the patient's prior treatment history and the specific characteristics of their lymphoma. However, the approval of Monjuvi was based on substantial evidence of its efficacy in a difficult-to-treat population, offering a new therapeutic option for patients with limited alternatives. The clinical benefit of Monjuvi, particularly in combination with lenalidomide, has been recognized by various health authorities, leading to its approval for use in specific lymphoma settings.

Efficacy of Jaypirca (pirtobrutinib) in Lymphoma Treatment

Jaypirca (pirtobrutinib) is a Bruton's tyrosine kinase (BTK) inhibitor under investigation for the treatment of B-cell malignancies, including certain types of lymphoma. Although Jaypirca is not yet approved for clinical use, it has shown promising results in early clinical trials. In particular, studies have demonstrated that Jaypirca can inhibit BTK with high selectivity and potency, potentially leading to reduced tumor growth and improved patient outcomes in lymphoma cases where BTK is a key driver of disease progression.

Current clinical trials are evaluating the efficacy of Jaypirca in various lymphoma subtypes, including mantle cell lymphoma (MCL), chronic lymphocytic leukemia (CLL), and Waldenström's macroglobulinemia (WM). Preliminary data suggests that Jaypirca has a favorable efficacy profile, with a number of patients achieving partial or complete responses to the treatment. As research continues, Jaypirca may become an important addition to the lymphoma treatment landscape, particularly for patients who have exhausted other therapeutic options or who have developed resistance to existing BTK inhibitors.

Regulatory Agency Approvals

Monjuvi
  • Food and Drug Administration (FDA), USA
Jaypirca
  • Food and Drug Administration (FDA), USA

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If Monjuvi or Jaypirca 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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