Mayzent (Siponimod) vs Tecfidera (dimethyl fumarate)

Mayzent (Siponimod) vs Tecfidera (dimethyl fumarate)

Mayzent (Siponimod) and Tecfidera (dimethyl fumarate) are both oral medications approved for the treatment of relapsing forms of multiple sclerosis (MS), but they work through different mechanisms. Mayzent is a sphingosine 1-phosphate receptor modulator that traps immune cells in lymph nodes, reducing their ability to cause damage in the central nervous system, and is also specifically approved for secondary progressive MS with active disease. Tecfidera is thought to modulate the immune response and provide neuroprotective effects by activating the Nrf2 pathway, but it is not specifically indicated for secondary progressive MS. Patients should consult their healthcare provider to determine which medication is more appropriate for their specific condition, taking into account factors such as disease progression, side effect profiles, and individual health considerations.

Difference between Mayzent and Tecfidera

Metric Mayzent (Siponimod) Tecfidera (dimethyl fumarate)
Generic name Siponimod Dimethyl fumarate
Indications Multiple sclerosis (specifically for secondary progressive multiple sclerosis with active disease) Multiple sclerosis (relapsing forms, including clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease)
Mechanism of action Sphingosine 1-phosphate receptor modulator Nrf2 pathway activator
Brand names Mayzent Tecfidera
Administrative route Oral Oral
Side effects Headache, high blood pressure, liver function abnormalities Flushing, abdominal pain, diarrhea, nausea
Contraindications CYP2C9*3/*3 genotype, recent myocardial infarction, stroke, certain types of heart block without a pacemaker, severe untreated sleep apnea, active infections Known hypersensitivity to dimethyl fumarate or any of its excipients
Drug class Sphingosine 1-phosphate receptor modulator Fumaric acid ester
Manufacturer Novartis Biogen

Efficacy

Mayzent (Siponimod) Efficacy in Multiple Sclerosis

Mayzent (Siponimod) is a medication approved for the treatment of relapsing forms of multiple sclerosis (MS), including clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease. Clinical trials have demonstrated the efficacy of Siponimod in reducing the frequency of relapses and delaying the progression of disability associated with MS. The EXPAND study, a pivotal phase III clinical trial, showed that Siponimod significantly reduced the risk of three-month confirmed disability progression compared to placebo. Additionally, Siponimod was associated with a lower annualized relapse rate, indicating its effectiveness in controlling disease activity.

Tecfidera (Dimethyl Fumarate) Efficacy in Multiple Sclerosis

Tecfidera (dimethyl fumarate) is another oral medication approved for the treatment of relapsing forms of MS. It has been shown to reduce the rate of MS relapses and to slow the progression of physical disability. The efficacy of Tecfidera was established in two key phase III clinical trials, DEFINE and CONFIRM, which demonstrated that dimethyl fumarate significantly reduced the annualized relapse rate compared to placebo. Furthermore, the drug also showed a reduction in the number of new or enlarging T2-hyperintense lesions and gadolinium-enhancing lesions on MRI scans, which are indicative of disease activity in MS.

Comparative Efficacy

When comparing Mayzent to Tecfidera, both drugs have shown efficacy in the management of relapsing forms of MS, although they work through different mechanisms of action. Direct comparative studies between the two drugs are limited, and healthcare providers often make treatment decisions based on the individual patient's disease characteristics, tolerance to medication, and preference. Both medications have been instrumental in expanding the therapeutic options available to patients with MS, offering different modes of administration and safety profiles.

Conclusion

In conclusion, both Mayzent (Siponimod) and Tecfidera (dimethyl fumarate) have been proven to be effective in reducing relapse rates and slowing the progression of disability in patients with relapsing forms of MS. Their inclusion in the treatment landscape for MS provides valuable options for patients and healthcare professionals to tailor treatment plans according to individual needs and preferences. Ongoing research and post-marketing surveillance continue to refine the understanding of the long-term efficacy and safety of these medications in diverse patient populations.

Regulatory Agency Approvals

Mayzent
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Therapeutic Goods Administration (TGA), Australia
Tecfidera
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia
  • Medsafe (NZ)

Access Mayzent or Tecfidera today

If Mayzent or Tecfidera 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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