- Multiple sclerosis (MS) is a chronic disease affecting the central nervous system, which results in symptoms ranging from muscle weakness to vision loss and paralysis.
- It generally strikes in early adulthood, and is more common in women than men.
- Several treatments can slow the progression of the disease, meaning that most people do not experience severe disability.
- Now, a new biosimilar injection of a current drug has been approved by the Food and Drug Administration (FDA) in the United States for use in people with relapsing forms of MS.
- The new drug, Tyruko, may mean more cost-effective treatment is available for many people with the condition.
Multiple sclerosis (MS) — a chronic, inflammatory disease of the nervous system — is thought to affect some
Symptoms range from the mild, such as blurred vision, and tingling and numbness in the limbs, to the more severe, including mobility problems, paralysis, and vision loss, although most people with the condition do not experience severe disability.
There are several types of MS. Relapsing-remitting MS, which is characterized by disease flare-ups and periods of remission when there is partial or total recovery, is the most common.
Treatment can slow the progression of the disease but, as this is a lifelong condition, the cost can mount up, particularly for
One treatment used for people who have not responded well to first-line therapies is natalizumab (Tysabri), a monoclonal antibody.
It can slow the progression of symptoms during an MS flare-up and to decrease the rate of relapse in those with relapsing-remitting MS.
Now, the Food and Drugs Administration (FDA)
The new biosimilar is called Tyruko.
It is highly effective at preventing relapses. Tyruko works in the same way.
However, Tysabri can have side effects, the most serious of which is an increased risk of
Because of this risk, everyone taking Tysabri must be part of the TOUCH program, a national program designed to “minimize the risk of PML, minimize death and disability due to PML, and promote informed risk-benefit decisions regarding Natalizumab use.”
Tyruko will be monitored in the same way, under an FDA risk evaluation and mitigation strategy (REMS).
Dr. Barbara Giesser, neurologist and MS specialist at Pacific Neuroscience Institute at Providence Saint John’s Health Center in Santa Monica, CA, explained to Medical News Today:
“Tyruko is a biosimilar form of a medicine that has been around for almost 2 decades, natalizumab (Tysabri). They have the same mechanism of action, and approval by the FDA means that Tyruko is thought to have very similar efficacy and safety to Tysabri.”
Biosimilars are biologic medications that are highly similar to biologics (or reference products) that have already been approved by the FDA for use.
They have no clinically meaningful differences from the reference product, having the same safety and effectiveness.
- are made from the same types of sources (e.g., living sources)
- provide the same benefits when treating diseases or medical conditions
- are given at the same strength and dosage
- are not expected to cause new or worsening side effects.
In 2010, the annual cost of Tysabri was around
Dr. Giesser explained why approval of the biosimilar is important.
“This agent is not a new class of disease-modifying therapy, and its primary potential advantage is that if it is less expensive than Tysabri, which is often the case with biosimilar medications, more people with MS may be able to access it,” she told us.
According to the National Multiple Sclerosis Society, “comprehensive MS care begins with the diagnosis and lasts a lifetime.”
Most people with MS have short periods of symptoms followed by long stretches of remission, with partial or full recovery. The disease is rarely fatal and most people with MS have a
Medications, such as Tysabri, and now Tyruko are important for dealing with the periods when symptoms are most acute and minimizing these relapses.
Following the FDA approval, Dr. Sarah Yim, director of the Office of Therapeutic Biologics and Biosimilars in the FDA’s Center for Drug Evaluation and Research, said in a
“Today’s approval of the first biosimilar product indicated to treat relapsing forms of multiple sclerosis furthers the FDA’s longstanding commitment to support a competitive marketplace for biological products and ultimately empowers patients by helping to increase access to safe, effective and high-quality medications at potentially lower cost.”
This approval could mark the start of wider access to a more cost-effective treatment for people with relapsing forms of MS.
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