Rilutek (riluzole) vs Relyvrio (sodium phenylbutyrate and taurursodiol)

Rilutek (riluzole) vs Relyvrio (sodium phenylbutyrate and taurursodiol)

Rilutek (riluzole) is a medication approved for the treatment of amyotrophic lateral sclerosis (ALS) that works by reducing the release of glutamate, which is thought to be involved in the damage of motor neurons. Relyvrio (sodium phenylbutyrate and taurursodiol), also approved for ALS, works through a different mechanism, combining two compounds that are believed to protect nerve cells by reducing stress in the endoplasmic reticulum and improving mitochondrial function. When deciding between the two, it is important to consult with a healthcare provider to consider the specific aspects of one's medical condition, potential side effects, drug interactions, and the mechanism of action of each medication to determine the most appropriate treatment option.

Difference between Rilutek and Relyvrio

Metric Rilutek (riluzole) Relyvrio (sodium phenylbutyrate and taurursodiol)
Generic name Riluzole Sodium phenylbutyrate and taurursodiol
Indications Amyotrophic lateral sclerosis (ALS) Amyotrophic lateral sclerosis (ALS)
Mechanism of action Glutamate antagonist Not fully understood, proposed mechanisms include neurometabolic modulation and reduction of neuronal cell death
Brand names Rilutek, Tiglutik Relyvrio
Administrative route Oral Oral
Side effects Dizziness, gastrointestinal disturbances, elevated liver enzymes, decreased lung function Nausea, diarrhea, abdominal pain, vomiting
Contraindications Liver disease, caution with renal impairment None known
Drug class Riluzole: Benzothiazole Combination drug: Sodium phenylbutyrate is a prodrug of phenylacetate, taurursodiol is a bile acid
Manufacturer Sanofi-Aventis Amylyx Pharmaceuticals

Efficacy

Efficacy of Rilutek (Riluzole) for ALS

Rilutek, the brand name for riluzole, is a medication that has been approved for the treatment of Amyotrophic Lateral Sclerosis (ALS), a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. Clinical trials have shown that riluzole can modestly prolong survival in individuals with ALS. The efficacy of Rilutek is generally measured by its ability to extend survival time. Studies have indicated that riluzole may prolong the life of a person with ALS by a few months, particularly by delaying the time to tracheostomy or the need for ventilatory support.

While Rilutek does not reverse the damage already caused by ALS, nor does it stop the progression of the disease, its neuroprotective properties are thought to slow down the deterioration of motor neurons. This slowing of disease progression can lead to an improvement in quality of life for some patients. However, the degree of benefit varies among individuals, and not all patients may experience a significant extension in survival or delay in disease progression.

Efficacy of Relyvrio (Sodium Phenylbutyrate and Taurursodiol) for ALS

Relyvrio, a combination of sodium phenylbutyrate and taurursodiol, is another medication approved for the treatment of ALS. The efficacy of Relyvrio in ALS was demonstrated in a randomized, double-blind, placebo-controlled clinical trial. In this trial, patients treated with Relyvrio experienced a slower decline in the ALS Functional Rating Scale-Revised (ALSFRS-R) score, which is a measure of the patient's functional status in performing daily activities, compared to those who received a placebo.

Furthermore, Relyvrio has been shown to have a statistically significant impact on the survival of ALS patients. The combination of sodium phenylbutyrate and taurursodiol is believed to exert its effects by mitigating cellular stress and improving mitochondrial function in neurons, potentially protecting against the loss of motor neurons that characterizes ALS. This can translate into a more prolonged functional state for patients and may extend their survival. However, as with Rilutek, individual responses to Relyvrio can vary, and not all patients may experience the same level of benefit from the treatment.

Regulatory Agency Approvals

Rilutek
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia
  • Medicines & Healthcare products Regulatory Agency (MHRA), United Kingdom
  • Medsafe (NZ)
Relyvrio
  • Food and Drug Administration (FDA), USA

Access Rilutek or Relyvrio today

If Rilutek or Relyvrio 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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