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Alphamannosidosis Market was valued at USD 210 million in 2024 and is projected to reach USD 420 million by 2034

12-09-2025 07:50 AM CET | Business, Economy, Finances, Banking & Insurance

Press release from: Exactitude Consultancy

Alphamannosidosis Market

Alphamannosidosis Market

Market Overview
The Alphamannosidosis Market was valued at USD 210 million in 2024 and is projected to reach USD 420 million by 2034, registering a CAGR of 7.2% during the forecast period.
Alphamannosidosis is an ultra-rare lysosomal storage disorder caused by deficient α-mannosidase enzyme activity, leading to progressive multi-systemic complications including skeletal abnormalities, hearing impairment, immunodeficiency, and neurological decline.

Market growth is driven by increasing newborn screening programs, advancements in enzyme replacement therapy (ERT), rising awareness of rare genetic disorders, and expanded access to specialized treatment centers. Growing clinical focus on early diagnosis and intervention is strengthening long-term therapeutic outcomes, thereby positively impacting market demand.

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Market Dynamics
Drivers
• Increasing use of enzyme replacement therapy (ERT), particularly velmanase alfa, which significantly improves immune function and motor capabilities.
• Rising newborn screening and genetic testing adoption enabling earlier detection.
• Strong regulatory support for orphan drugs, including priority reviews, market exclusivity, and financial incentives.
• Growing prevalence of rare disease awareness campaigns and patient advocacy initiatives.
• Expanding access to specialized metabolic and pediatric neurology centers, especially in Europe and North America.

Restraints
• Extremely high cost of ERT and ongoing infusion therapy requirements.
• Limited number of approved treatment options; ERT remains the primary modality.
• Challenges in diagnosing mild or late-onset forms, leading to underreporting.
• Limited healthcare infrastructure in emerging regions to support long-term therapy.

Opportunities
• Development of next-generation therapies, including gene therapy and substrate reduction therapy.
• Increasing research activity focused on improving blood-brain barrier penetration to address neurological symptoms.
• Expansion of newborn screening programs in Asia Pacific, Latin America, and the Middle East.
• Potential for combination treatment strategies to enhance ERT effectiveness.

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Market Growth Outlook (2024-2034)
The Alphamannosidosis Market is expected to grow from USD 210 million in 2024 to USD 420 million by 2034, driven by wider ERT adoption, improved diagnostic capabilities, and significant investment in rare disease drug development. Long-term market expansion will also be supported by the increasing availability of genetic counseling services and continued regulatory backing for orphan drug innovation.

Segmentation Analysis
By Treatment Type
Enzyme replacement therapy (ERT) is the dominant segment and accounts for the majority of global revenue. Velmanase alfa remains the primary therapeutic option, offering improved endurance, reduced infections, and enhanced quality of life for patients.

Hematopoietic stem cell transplantation (HSCT) is used in select early-stage cases but carries higher risks and is typically considered only when neurological deterioration progresses rapidly.
Supportive treatment-such as physiotherapy, hearing aids, orthopedic management, and speech therapy-plays a vital role in improving functional outcomes.

By Diagnosis
Diagnosis relies heavily on enzyme activity assays, genetic sequencing, and clinical assessment of characteristic symptoms such as developmental delays and immune dysfunction.
MRI imaging is commonly used to monitor neurological progression, while audiological testing remains essential due to the high prevalence of hearing impairment.

Newborn screening adoption is gradually increasing and is expected to significantly enhance early diagnosis over the next decade.

By End User
Hospitals and specialized metabolic disease centers are the primary providers of ERT infusions and long-term management.
Research institutes play an essential role in advancing therapeutic innovation and conducting clinical trials.
Home-based infusion care services are emerging as a convenient option for eligible patients in developed regions.

Regional Insights
North America
North America holds a significant share of the global market due to strong orphan drug frameworks, advanced diagnostic infrastructure, and widespread availability of ERT. Rising participation in clinical trials and patient registries also supports long-term growth.

Europe
Europe is one of the most active regions in alphamannosidosis research, supported by national newborn screening initiatives, early adoption of ERT, and well-established rare disease centers. Strong government support and patient advocacy groups further accelerate market development.

Asia Pacific
Asia Pacific is projected to record the fastest CAGR, driven by increasing investments in healthcare infrastructure, improving genetic diagnosis capabilities, and growing awareness of lysosomal storage disorders. China, Japan, Australia, and South Korea are key contributors to emerging market expansion.

Latin America & Middle East/Africa
These regions show gradual growth as healthcare systems strengthen and rare disease awareness increases. Access remains limited, but improving pathways for orphan drug approvals and imports are creating new opportunities over the forecast period.

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Competitive Landscape
The market is dominated by companies developing ERT solutions and exploring gene therapy platforms to target the disease at its root cause.

Key Companies Include:
• Chiesi Farmaceutici
• Zymenex (now part of Chiesi Group)
• Takeda
• Sanofi
• Orchard Therapeutics
• Pfizer
• Novartis
• BioMarin Pharmaceutical
• Amicus Therapeutics
• Ultragenyx Pharmaceutical
These companies are actively investing in gene therapy research, neurological outcome improvement, and strategies that enhance cross-tissue enzyme delivery.

Recent Developments
• Expanded clinical adoption of velmanase alfa as the first approved ERT for alphamannosidosis.
• Increasing global participation in long-term natural history studies to refine treatment guidelines.
• Advancements in gene therapy platforms showing early promise in preclinical trials.
• Strengthening partnerships between pharmaceutical companies and patient advocacy groups for expanded access to treatment.

This report is also available in the following languages : Japanese (アルファマンノシドーシス市場), Korean (알파만노시도시스 시장), Chinese (α-甘露糖苷酶缺乏症市场), French (Marché de l'alphamannosidose), German (Markt für Alphamannosidose), and Italian (Mercato dell'alfamannosidosi), etc.

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About Us
Exactitude Consultancy is a market research & consulting services firm which helps its client to address their most pressing strategic and business challenges. Our market research helps clients to address critical business challenges and also helps make optimized business decisions with our fact-based research insights, market intelligence, and accurate data.
https://bulletin.exactitudeconsultancy.com/

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https://exactitudeconsultancy.com/

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Irfan Tamboli
PHONE NUMBER +1 (704) 266-3234
EMAIL ADDRESS: sales@exactitudeconsultancy.com

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