Lumoxiti (moxetumomab pasudotox) vs Ezharmia (valemetostat tosilate)

Lumoxiti (moxetumomab pasudotox) vs Ezharmia (valemetostat tosilate)

Lumoxiti (moxetumomab pasudotox) is a CD22-directed cytotoxin indicated for the treatment of adult patients with relapsed or refractory hairy cell leukemia who have received at least two prior systemic therapies, including treatment with a purine nucleoside analog. Valemetostat tosilate (Ezharmia), on the other hand, is an investigational agent and a dual inhibitor of EZH1 and EZH2, which are histone methyltransferases involved in the epigenetic regulation of gene expression, and it is being studied for the treatment of various hematological malignancies and solid tumors. When deciding between these two medications, it is crucial to consider the specific type of cancer being treated, the drug’s approval status, and the patient's previous treatments and overall health profile, as Lumoxiti is approved for a specific leukemia, while Ezharmia is still under investigation and not yet approved for any indication.

Difference between Lumoxiti and Ezharmia

Metric Lumoxiti (moxetumomab pasudotox) Ezharmia (valemetostat tosilate)
Generic name moxetumomab pasudotox valemetostat tosilate
Indications Hairy cell leukemia Adult T-cell leukemia/lymphoma, Peripheral T-cell lymphoma
Mechanism of action CD22-directed cytotoxin EZH2 inhibitor
Brand names Lumoxiti Ezharmia
Administrative route Intravenous Oral
Side effects Infusion reactions, edema, nausea, fatigue, headache, pyrexia, constipation, anemia, diarrhea Thrombocytopenia, neutropenia, anemia, leukopenia, fatigue, febrile neutropenia, diarrhea
Contraindications None known None known
Drug class Immunotoxin Epigenetic modifier
Manufacturer AstraZeneca Daiichi Sankyo

Efficacy

Lumoxiti (moxetumomab pasudotox) for Hairy Cell Leukemia

Lumoxiti, also known by its generic name moxetumomab pasudotox, is an innovative treatment specifically approved for certain adult patients with hairy cell leukemia (HCL) who have already received at least two prior systemic therapies, including treatment with a purine nucleoside analog. HCL is a rare form of leukemia characterized by an overproduction of B cells. Lumoxiti is a CD22-directed cytotoxin and works by binding to the CD22 antigen on B cells and then internalizing into the cell where it releases a toxin that inhibits protein synthesis, leading to cell death.

The efficacy of Lumoxiti was primarily demonstrated in a pivotal, single-arm, open-label clinical trial. In this study, the treatment showed a high rate of durable complete response, which is defined as the absence of disease after treatment. The trial reported that a significant percentage of patients achieved complete remission with the absence of minimal residual disease (MRD), which is a key indicator of depth of response in HCL. The duration of response for these patients was also noteworthy, with many patients maintaining their remission status for extended periods.

Ezharmia (valemetostat tosilate) in Leukemia

Ezharmia, with its active ingredient valemetostat tosilate, is an experimental therapy that is currently being investigated for the treatment of various types of leukemia, including acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL). Valemetostat tosilate is a dual inhibitor of the EZH1 and EZH2 methyltransferases, which are enzymes that can contribute to the development and progression of cancer by altering gene expression. By inhibiting these enzymes, Ezharmia aims to reverse the aberrant gene silencing and thereby exert antitumor effects.

While Ezharmia is still in the clinical trial phase and has not yet been approved for clinical use, early-phase studies have suggested that it may have efficacy in treating leukemia. These studies have evaluated the safety, tolerability, and preliminary efficacy of valemetostat tosilate in patients with relapsed or refractory hematological malignancies. Although the data is still emerging, there have been reports of clinical responses in some patients treated with Ezharmia, indicating its potential as a novel therapeutic option for leukemia. However, further clinical trials are required to fully establish its efficacy and safety profile in this patient population.

Regulatory Agency Approvals

Lumoxiti
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
Ezharmia
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan

Access Lumoxiti or Ezharmia today

If Lumoxiti or Ezharmia 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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