The U.S. transthyretin amyloidosis treatment market is estimated to be valued at USD 65.4 Mn in 2025 and is expected to exhibit a CAGR of 9.6% during the forecast period (2025-2032). Transthyretin amyloidosis is a rare, progressive, and fatal disorder caused by mutations in the transthyretin (TTR) gene. These mutations lead to deposition of abnormal TTR protein fibers known as amyloid in vital organs like heart, nerves, and gastrointestinal tract. The accumulation of amyloid fibrils in these organs progressively damages their structure and function. With no approved disease-modifying therapies available so far, ATTR amyloidosis was considered untreatable and fatal. However, recent advancements in understanding the disease pathogenesis along with approvals of novel therapies have provided new hope to patients. The U.S. transthyretin amyloidosis treatment market has witnessed significant growth due to these approval milestones.
Market Dynamics:
The U.S. transthyretin amyloidosis treatment market growth is driven by increasing disease awareness, approvals of novel disease-modifying therapies, and expansion of treatment landscape beyond symptom management. Factors such as longer life expectancy and improved diagnosis are also contributing to market growth. Despite the positive momentum, high treatment costs remain a key restraint. Infrastructure challenges in effective diagnosis also hamper market potential. However, ongoing clinical trials evaluating new treatment options and expansion of approval to different subtypes present lucrative opportunities. Partnerships between players to enhance access further boost the market outlook.
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