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Hereditary Transthyretin Amyloidosis Market Report 2025-2034: Industry Overview, Trends, And Forecast Analysis
The Hereditary Transthyretin Amyloidosis Market Report by The Business Research Company delivers a detailed market assessment, covering size projections from 2025 to 2034. This report explores crucial market trends, major drivers and market segmentation by [key segment categories].What Is the Current Hereditary Transthyretin Amyloidosis Market Size and Its Estimated Growth Rate?
The market for hereditary transthyretin amyloidosis has experienced a robust growth in the recent past. It is forecasted to expand from $1.36 billion in 2024 to $1.50 billion in 2025, demonstrating a compound annual growth rate (CAGR) of 9.7%. The growth observed during the historic period can be attributed to factors such as the increasing prevalence of the disease, escalating research and development initiatives, a rise in the number of cardiac amyloidosis instances, heightened disease awareness, and an expanded healthcare infrastructure.
In the coming years, the hereditary transthyretin amyloidosis market is projected to experience significant growth, reaching $2.14 billion in 2029 with a compound annual growth rate (CAGR) of 9.4%. This surge during the predicted period can be credited to several factors such as an increasing elderly population, higher disposable income levels, a rise in cases of hereditary transthyretin amyloidosis, advancements in new drug development, and an increase in genetic testing. The forecast period also indicates major trends like cutting-edge therapeutic products, improvement in diagnostic methods, progress in medication development, the need for efficacious therapies, and medical technology advancements.
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How Are Emerging Segments Shaping the Hereditary Transthyretin Amyloidosis Market Landscape?
The hereditary transthyretin amyloidosis market covered in this report is segmented -
1) By Type: Oral, Subcutaneous Injection, Other Types
2) By Drug Class: RNAi Agents (Patisiran), Small Interfering RNAs (siRNAs) (Vutrisiran)
3) By Distribution Channel: Hospital Pharmacies, Retail Pharmacies
4) By Application: Hospital, Clinic, Other Applications
Subsegments:
1) By Oral: Tafamidis, Diflunisal, Experimental Oral Therapies
2) By Subcutaneous Injection: Patisiran, Inotersen, Vutrisiran
3) By Other Types: Intravenous Therapies, Gene Silencing Therapies, CRISPR-Based Therapies
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Which Growth Factors Are Influencing Hereditary Transthyretin Amyloidosis Market Expansion?
The hereditary transthyretin amyloidosis market is set to expand due to the anticipated increase in the number of older adults. The term elderly population refers to those over the age of 65, who typically need specialised medical care and assistance as a result of ageing. This segment of the population is on the rise, thanks to improved healthcare and living conditions that have extended life expectancy. Older adults are significantly affected by hereditary transthyretin amyloidosis (hATTR), which results in progressive neuropathy and cardiomyopathy, adding to the health complications of the elderly. The Population Reference Bureau, a non-profit organization in the US, forecasted in January 2024 that the population of Americans aged 65 and over is likely to surge from 58 million in 2022 to 82 million by 2050, indicating a 47% growth. Thus, the increasing elderly population is contributing to the expanding demand in the hereditary transthyretin amyloidosis market.
Who Are the Dominant Players Across Different Hereditary Transthyretin Amyloidosis Market Segments?
Major companies operating in the hereditary transthyretin amyloidosis market are Pfizer Inc., AbbVie Inc., Sanofi S.A., AstraZeneca plc, Novo Nordisk, Regeneron Pharmaceuticals Inc., Alexion Pharmaceuticals Inc., Alnylam Pharmaceuticals Inc., PTC Therapeutics Inc., Ionis Pharmaceuticals Inc., BridgeBio Pharma Inc., Akcea Therapeutics, Prothena Corporation plc, Intellia Therapeutics Inc., YoITech Therapeutics, Corino Therapeutics Inc., Attralus Inc., BSIM Therapeutics SA, Eidos Therapeutics, Autotac Bio Inc.
What Are the Latest Developing Trends in the Hereditary Transthyretin Amyloidosis Market?
Leading businesses in the hereditary transthyretin amyloidosis marketplace are creating novel therapeutic solutions, such as RNAi therapeutics, to identify and decrease transthyretin (TTR) protein levels. RNAi therapeutics belong to a drug category that leverages RNA interference tech to suppress specific genes and subsequently decrease the generation of proteins causing diseases. For example, in October 2024, Alnylam Pharmaceuticals, Inc., a biopharmaceutical firm based in the US, put forward a supplemental new drug application (sNDA) to the US FDA for Vutrisiran (AMVUTTRA) to be utilized as a therapy for transthyretin amyloidosis with cardiomyopathy. This submission emphasizes their groundbreaking RNAi therapeutic method, aimed at identifying and reducing transthyretin (TTR) protein, a major contributor to the progression of the disease. As opposed to traditional intravenous treatments, Vutrisiran's subcutaneous administration provides a more accessible and patient-centric dosage scheme, highlighting it as a potential game-changing option for patients with this severe ailment.
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Which Geographic Regions Are Expected to Dominate the Hereditary Transthyretin Amyloidosis Market in the Coming Years?
North America was the largest region in the hereditary transthyretin amyloidosis market in 2024. Asia-Pacific is expected to be the fastest-growing region in the forecast period. The regions covered in the hereditary transthyretin amyloidosis market report are Asia-Pacific, Western Europe, Eastern Europe, North America, South America, Middle East, Africa.
Frequently Asked Questions:
1. What Is the Market Size and Growth Rate of the Hereditary Transthyretin Amyloidosis Market?
2. What is the CAGR expected in the Hereditary Transthyretin Amyloidosis Market?
3. What Are the Key Innovations Transforming the Hereditary Transthyretin Amyloidosis Industry?
4. Which Region Is Leading the Hereditary Transthyretin Amyloidosis Market?
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