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시장보고서
상품코드
1698062
세계의 폼페병 치료제 시장 : 산업 규모, 점유율, 동향, 기회, 예측, 치료 유형별, 투여 경로별, 최종사용자별, 지역별, 경쟁별(2020-2030년)Pompe Disease Therapeutics Market - Global Industry Size, Share, Trends, Opportunity, & Forecast, Segmented By Treatment Type, By Route of Administration, By End User, By Region, & Competition, 2020-2030F |
폼페병 치료제 세계 시장 규모는 2024년 15억 달러에 달했고, 2030년까지 예측 기간 동안 연평균 4.40%의 꾸준한 성장이 예상됩니다.
세계 폼페병 치료제 시장은 희귀질환 및 희귀질환 치료제 산업에서 빠르게 발전하고 있는 분야로, 과학의 발전과 혁신적인 치료법에 대한 투자 증가에 힘입어 빠르게 성장하고 있습니다. 폼페병(글리코겐 저장병 II형)은 산성 알파-글루코시다아제(GAA)의 결핍으로 인해 근육 조직에 글리코겐이 축적되는 희귀한 라이소좀 질환입니다. 그 결과, 진행성 근력 저하와 심각한 호흡기 합병증을 유발하여 표적화된 치료 개입이 필요합니다.
시장 개요 | |
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예측 기간 | 2026-2030년 |
시장 규모 : 2024년 | 15억 달러 |
시장 규모 : 2030년 | 19억 5,000만 달러 |
CAGR : 2025-2030년 | 4.40% |
급성장 부문 | 효소대체요법(ERT) |
최대 시장 | 북미 |
시장은 주로 글리코겐 청소율과 임상 결과를 개선하는 Myozyme(alglucosidase alfa), Lumizyme, 최근 Nexviazyme(avalglucosidase alfa)과 같은 효소대체요법(ERT)에 의해 형성되고 있습니다. 또한, 2023년 폼비리치(시파글루코시다아제 알파)와 옵디보(미글루스타트)가 승인되면서 특히 기존 ERT에 반응이 불충분한 야간발작형 폼페병(LOPD) 환자들의 치료 옵션이 넓어졌습니다.
이러한 발전에도 불구하고, 높은 치료 비용과 제한된 신생아 선별검사 프로그램으로 인해 진단 지연과 질병 진행이 시장 침투의 제약요인으로 작용하고 있습니다. 그러나 유전자 치료와 차세대 치료제가 획기적인 치료법으로 부상하고 있으며, 현재 진행 중인 임상시험은 보다 내구성 있고 비용 효율적인 치료법을 제공하는 것을 목표로 하고 있습니다.
질병에 대한 인식 및 진단 향상
제한된 질병 인식 및 진단 지연
개인맞춤의료와 정밀치료
Global Pompe Disease Therapeutics Market was valued at USD 1.50 Billion in 2024 and is anticipated to project steady growth in the forecast period with a CAGR of 4.40% through 2030. The Global Pompe Disease Therapeutics Market is a rapidly evolving segment within the rare disease and orphan drug industry, driven by scientific advancements and increasing investment in innovative therapies. Pompe disease, or glycogen storage disease type II, is a rare lysosomal disorder caused by the deficiency of acid alpha-glucosidase (GAA), leading to glycogen accumulation in muscle tissues. This results in progressive muscle weakness and severe respiratory complications, necessitating targeted therapeutic interventions.
Market Overview | |
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Forecast Period | 2026-2030 |
Market Size 2024 | USD 1.50 Billion |
Market Size 2030 | USD 1.95 Billion |
CAGR 2025-2030 | 4.40% |
Fastest Growing Segment | Enzyme Replacement Therapy (ERT) |
Largest Market | North America |
The market is primarily shaped by enzyme replacement therapies (ERTs) such as Myozyme (alglucosidase alfa), Lumizyme, and the more recent Nexviazyme (avalglucosidase alfa), which offer improved glycogen clearance and clinical outcomes. Additionally, the approval of Pombiliti (cipaglucosidase alfa) and Opfolda (miglustat) in 2023 has expanded treatment options for patients, particularly those with late-onset Pompe disease (LOPD) who exhibit suboptimal responses to conventional ERTs.
Despite these advancements, market penetration is constrained by high treatment costs and limited newborn screening programs, leading to delayed diagnoses and disease progression. However, gene therapy and next-generation therapeutics are emerging as potential breakthroughs, with ongoing clinical trials aiming to provide more durable and cost-effective treatment alternatives.
Key Market Drivers
Increased Disease Awareness and Diagnosis
Pompe disease, often considered a rare or orphan disease, historically suffered from a lack of recognition and understanding. Pompe disease is a complex, multisystem genetic disorder with a prevalence of approximately 1 in 40,000 individuals in the United States. Increasing awareness of this rare condition is crucial, as early diagnosis and timely intervention can significantly improve patient outcomes and quality of life. Efforts to enhance disease recognition are being driven by medical institutions, patient advocacy groups, and biotech companies focused on expanding access to diagnostics and treatment. Newborn screening programs, physician education initiatives, and targeted awareness campaigns are playing a pivotal role in identifying patients earlier and facilitating access to advanced therapies. Patients faced delayed or misdiagnoses, leading to prolonged suffering and a dearth of effective treatments. Advocacy groups dedicated to Pompe disease have played a pivotal role in driving disease awareness. These organizations tirelessly work to raise public awareness, educate healthcare professionals, and provide support to affected individuals and their families. By leveraging social media, organizing awareness campaigns, and collaborating with healthcare institutions, these groups have succeeded in putting Pompe disease on the radar. The evolution of diagnostic technologies is another catalyst for increased disease awareness. Cutting-edge tools such as genetic testing and biomarker identification have revolutionized the diagnostic process. Physicians can now identify Pompe disease more accurately and swiftly, enabling timely intervention and treatment initiation. This, in turn, has elevated the importance of early diagnosis in improving patient outcomes.
Key Market Challenges
Limited Disease Awareness and Late Diagnosis
One of the foremost challenges in the Pompe Disease Therapeutics Market is the limited awareness of the disease itself, leading to delayed or missed diagnoses. Pompe disease is considered a rare condition, making it less well-known among healthcare professionals and the general public. This lack of awareness often results in late-stage diagnoses, which can significantly impact treatment outcomes.
Pompe disease's rarity, with an estimated incidence of 1 in 40,000 to 1 in 300,000 births, contributes to its obscurity. As healthcare professionals encounter rare diseases less frequently, the likelihood of prompt recognition and diagnosis diminishes. Pompe disease presents with symptoms that can overlap with those of other more common conditions, such as muscle weakness and respiratory problems. This lack of distinctiveness can lead to misdiagnoses or a failure to consider Pompe disease as a potential cause.
Key Market Trends
Personalized Medicine and Precision Therapies
One of the most significant trends in the Pompe Disease Therapeutics Market is the shift towards personalized medicine and precision therapies. Traditional treatment approaches often took a one-size-fits-all approach, but advancements in genetics and diagnostics have paved the way for tailored treatments that address the specific genetic mutations of individual patients. Advances in genetic research have provided insights into the precise genetic mutations that cause Pompe disease. This knowledge allows for the development of therapies that target the specific genetic defects in individual patients, maximizing treatment efficacy. Pharmaceutical companies are investing in innovative approaches, such as gene therapy and RNA-based therapies, that can be customized to target specific genetic mutations. These therapies hold the potential to correct the underlying genetic causes of Pompe disease. Advanced diagnostic tools, including genetic testing and biomarker identification, enable healthcare providers to identify the specific genetic mutations in Pompe disease patients. This information guides treatment decisions, ensuring that therapies are tailored to each patient's unique genetic profile.
In this report, the Global Pompe Disease Therapeutics Market has been segmented into the following categories, in addition to the industry trends which have also been detailed below:
Company Profiles: Detailed analysis of the major companies present in the Global Pompe Disease Therapeutics Market.
Global Pompe Disease Therapeutics market report with the given market data, TechSci Research offers customizations according to a company's specific needs. The following customization options are available for the report: