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How has the exondys 51 market size evolved in recent years?

In recent times, the market size for Exondys 51 has witnessed a XX (HCAGR). The prediction stands that it will escalate from $XX million, as recorded in 2024, to an impressive estimate of $XX million in 2025, showing a compound annual growth rate (CAGR) of XX%. This significant increase in the previous period can be associated with factors such as the surge in DMD’s awareness and diagnosis, favourable governmental policies, rising prevalence of rare diseases, and an increase in Duchenne muscular dystrophy’s frequency.

What are the predictions for the exondys 51 market size in the coming years?

In the upcoming years, the market size for exondys 51 is projected to witness an XX (FCAGR). By 2029, it is forecasted to expand to $XX million, demonstrating a compound annual growth rate (CAGR) of XX%. This projected growth during the forecast period can be attributed to factors such as the escalating incidence of Duchenne muscular dystrophy (DMD), the surge in new drug introductions, the amplifying focus on research and development activities, and the growing DMD disease burden. The forecast period is set to see significant trends like advancements in diagnostic technology, progress in mutation-targeted therapies, evolution in mutation suppressing therapies, increased R&D activities aimed at creating novel drug therapies, and headway in gene therapies.

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What key factors are fueling the growth of the exondys 51 market?

The increasing prevalence of genetic disorders is projected to drive the expansion of the exondys 51 market. Genetic disorders are conditions caused by abnormalities or mutations in a person’s DNA or genetic makeup. The growing incidence of these disorders can be linked to advancements in medical technology, demographic shifts, and improved diagnostic procedures and awareness. Exondys 51 (eteplirsen) confronts genetic disorders by initiating exon 51 skipping in the dystrophin gene, which promotes the production of a viable, albeit truncated, dystrophin protein to hinder muscle degeneration. For instance, data from the National Health Service, a government department in the UK, showed that in July 2024, around 70,000 people were dealing with muscular dystrophy (MD) or a similar condition in the UK. Duchenne MD was the most common type. Every year, about 100 boys are diagnosed with Duchenne MD, and an estimated 2,500 people in the UK are living with the disease at any given moment. For these reasons, the escalating prevalence of genetic disorders is fueling the growth of the exondys 51 market.

How is the global exondys 51 market divided into key segments?

The exondys 51 market covered in this report is segmented –

1) By Clinical Indication: Relapsing-Remitting Multiple Sclerosis (RRMS), Secondary Progressive Multiple Sclerosis (SPMS), Other Multiple Sclerosis Forms

2) By Distribution Channel: Hospital Pharmacies, Specialty Pharmacies, Online Pharmacies

3) By Application: Subcutaneous Injection, Long-Term Disease Management, Prophylactic Use

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Who are the key firms paving the way for growth in the exondys 51 market?

Major companies operating in the exondys 51 market include Sarepta Therapeutics

Which trends are expected to transform the exondys 51 market?

The primary trend surfacing in the exondys 51 market involves gaining regulatory endorsements with the aim to broaden its application amongst an extensive scope of Duchenne muscular dystrophy (DMD) patients, including those with variant genetic mutations, and the intention to escalate accessibility in international markets. Regulatory endorsements are essentially the formal permissions granted by health bodies such as the FDA or EMA, permitting a drug or medication to be commercialized and utilized due to its validated safety and efficacy. An example of this, the American biotech company Sarepta Therapeutics achieved FDA approval for a couple of substantial gene therapies for Duchenne muscular dystrophy (DMD). The escalated sanctioning of Elevidys offers its use for ambulatory and non-ambulatory patients who are at least four years old with confirmed DMD gene mutations, thereby making it the first gene therapy given approval for this situation. Moreover, Amondys 45 earned approval for patients with specific alterations in the dystrophin gene, aiming at around 8% of DMD instances. Said approvals underscore Sarepta’s dedication to progress treatment alternatives for individuals impacted by this incapacitating illness.

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What regions are contributing significantly to the growth of the exondys 51 market?

North America was the largest region in the exondys 51 market in 2024. Europe is expected to be the fastest-growing region in the forecast period. The regions covered in the exondys 51 market report are Asia-Pacific, Western Europe, Eastern Europe, North America, South America, Middle East and Africa.

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