Xpovio (selinexor) vs Aphexda (motixafortide)

Xpovio (selinexor) vs Aphexda (motixafortide)

Xpovio (selinexor) is an oral selective inhibitor of nuclear export, approved for use in combination with other agents for the treatment of multiple myeloma and certain types of diffuse large B-cell lymphoma, working by blocking the export of tumor suppressor proteins. Aphexda (motixafortide), on the other hand, is a novel peptide antagonist of the CXCR4 receptor, which is being investigated for its potential to enhance stem cell mobilization and improve outcomes in oncology and hematological treatments. When deciding between the two, it is essential to consider the specific type of cancer, the stage of disease, the patient's overall health, and the treatment regimen recommended by the healthcare provider, as each medication has distinct mechanisms of action and approved indications.

Difference between Xpovio and Aphexda

Metric Xpovio (selinexor) Aphexda (motixafortide)
Generic name Selinexor Motixafortide
Indications Multiple myeloma, diffuse large B-cell lymphoma Currently investigated for hematological malignancies and solid tumors
Mechanism of action Selective inhibitor of nuclear export (SINE) compounds that inhibits exportin 1 (XPO1) CXCR4 antagonist that inhibits the CXCR4 chemokine receptor
Brand names Xpovio Aphexda
Administrative route Oral Investigational, primarily intravenous (IV) in clinical trials
Side effects Nausea, vomiting, fatigue, anorexia, weight loss, diarrhea, pyrexia, constipation, thrombocytopenia Not fully characterized, but may include gastrointestinal symptoms, hematological abnormalities, and injection site reactions
Contraindications Known hypersensitivity to selinexor or any of its components Not yet fully established
Drug class Antineoplastic agent Investigational chemokine receptor antagonist
Manufacturer Karyopharm Therapeutics BioLineRx

Efficacy

Xpovio (Selinexor) Efficacy in Treating Multiple Myeloma

Xpovio (selinexor) is a prescription medicine specifically approved by the U.S. Food and Drug Administration (FDA) for the treatment of multiple myeloma in certain adult patients. It is an oral selective inhibitor of nuclear export (SINE) compound that works by blocking the exportin 1 (XPO1) protein, leading to the accumulation of tumor suppressor proteins in the cell nucleus and enhancing their anti-cancer activity. Xpovio is typically used in combination with dexamethasone, a corticosteroid, for patients who have received at least four prior therapies and whose disease is resistant to several other forms of treatment, including at least two proteasome inhibitors, two immunomodulatory agents, and an anti-CD38 monoclonal antibody.

The efficacy of Xpovio in treating multiple myeloma was demonstrated in a clinical trial that led to its accelerated approval. In this study, patients treated with Xpovio in combination with dexamethasone showed a significant response rate, with a certain percentage of patients achieving partial or complete response to the treatment. The duration of response varied among patients, but some experienced a prolonged response, indicating the potential of Xpovio to provide clinical benefits in a heavily pre-treated population.

Aphexda (Motixafortide) Efficacy in Treating Multiple Myeloma

Aphexda (motixafortide) is an investigational drug and has not been approved by the FDA for the treatment of multiple myeloma or any other indication. Motixafortide is a CXCR4 antagonist designed to sensitize cancer cells to other therapies and mobilize stem cells. While preclinical studies and early clinical trials have suggested that motixafortide may enhance the efficacy of other treatments in multiple myeloma, its definitive efficacy and safety profile are still being determined through ongoing clinical trials.

As of the knowledge cutoff date, any efficacy data for Aphexda (motixafortide) in treating multiple myeloma would be preliminary and derived from ongoing clinical trials. Therefore, it is important to wait for the results of these trials to be published and peer-reviewed to fully understand the potential benefits and risks associated with motixafortide in the context of multiple myeloma. Until then, the drug remains experimental and is not available for general clinical use outside of clinical trial settings.

Regulatory Agency Approvals

Xpovio
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
Aphexda
  • Food and Drug Administration (FDA), USA

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If Xpovio or Aphexda 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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