The 7 major AL amyloidosis markets reached a value of US$ 3,374.5 Million in 2023. Looking forward, IMARC Group expects the 7MM to reach US$ 13,300.4 Million by 2034, exhibiting a growth rate (CAGR) of 13.1% during 2024-2034.
Report Attribute
|
Key Statistics
|
---|---|
Base Year | 2023 |
Forecast Years | 2024-2034 |
Historical Years |
2018-2023
|
Market Size in 2023
|
US$ 3,374.5 Million
|
Market Forecast in 2034
|
US$ 13,300.4 Million
|
Market Growth Rate (2024-2034)
|
13.1%
|
The AL amyloidosis market has been comprehensively analyzed in IMARC's new report titled "AL Amyloidosis Market: Epidemiology, Industry Trends, Share, Size, Growth, Opportunity, and Forecast 2024-2034". AL amyloidosis, also referred to as primary amyloidosis, is a rare ailment characterized by the abnormal accumulation of amyloid proteins. It can cause a wide range of symptoms depending on the organs and tissues affected by the amyloid deposits. The most commonly impacted organs are the heart, kidneys, liver, and nervous system, and indications may include fatigue, shortness of breath, swelling in the legs and ankles, irregular heartbeat, chest pain, difficulty swallowing, nausea, vomiting, diarrhea, weight loss, etc. As the disease progresses, it can lead to organ failure, which can be life-threatening. The diagnosis of AL amyloidosis can be challenging, as its symptoms are often non-specific and can mimic other common conditions. Physicians typically start with a thorough medical history and physical exam, followed by blood and urine tests to look for abnormal protein levels and evidence of organ damage. A biopsy of affected tissue is usually necessary to confirm the presence of amyloid fibrils and to determine the specific type of amyloidosis. Several imaging tests, such as echocardiograms and CT scans, may also be used to evaluate the extent of organ involvement.
The increasing cases of mutations in the DNA of plasma cells and the rising incidence of underlying plasma cell disorders, such as multiple myeloma and monoclonal gammopathy of undetermined significance, are primarily driving the AL amyloidosis market. In addition to this, the widespread adoption of amyloid stabilizers, which stabilize the amyloid protein and prevent it from accumulating in tissues and organs, for treating the ailment is further bolstering the market growth. Moreover, the escalating utilization of novel agents, including proteasome inhibitors, immunomodulatory drugs, monoclonal antibodies, etc., which target the underlying mechanisms of AL amyloidosis, has significantly improved response rates and prolonged progression-free survival in patients. This, in turn, is acting as another significant growth-inducing factor. Additionally, the emerging popularity of high-dose chemotherapy, followed by autologous stem cell transplantation, as a treatment option for eligible patients with AL amyloidosis is also propelling the market growth. This procedure aims to eliminate abnormal cells that produce the amyloid protein and improve organ function. Furthermore, the ongoing advancements in diagnostic techniques, such as the introduction of serum-free light chain assays and mass spectrometry, have facilitated earlier diagnosis, allowing for prompt initiation of treatment and better management of disease-related complications. This, in turn, is expected to drive the AL amyloidosis market during the forecast period.
IMARC Group's new report provides an exhaustive analysis of the AL amyloidosis market in the United States, EU5 (Germany, Spain, Italy, France, and United Kingdom) and Japan. This includes treatment practices, in-market, and pipeline drugs, share of individual therapies, market performance across the seven major markets, market performance of key companies and their drugs, etc. The report also provides the current and future patient pool across the seven major markets. According to the report the United States has the largest patient pool for AL amyloidosis and also represents the largest market for its treatment. Furthermore, the current treatment practice/algorithm, market drivers, challenges, opportunities, reimbursement scenario and unmet medical needs, etc. have also been provided in the report. This report is a must-read for manufacturers, investors, business strategists, researchers, consultants, and all those who have any kind of stake or are planning to foray into the AL amyloidosis market in any manner.
Time Period of the Study
Countries Covered
Analysis Covered Across Each Country
This report also provides a detailed analysis of the current AL amyloidosis marketed drugs and late-stage pipeline drugs.
In-Market Drugs
Late-Stage Pipeline Drugs
Drugs | Company Name |
---|---|
Darzalex Faspro (Daratumumab/hyaluronidase) | Janssen Biotech |
CAEL-101 | Caelum Biosciences |
NEOD 001 | Prothena |
ZN d5 | Zentera Therapeutics |
STI-6129 | Sorrento Therapeutics |
*Kindly note that the drugs in the above table only represent a partial list of marketed/pipeline drugs, and the complete list has been provided in the report.
Market Insights
Epidemiology Insights
AL Amyloidosis: Current Treatment Scenario, Marketed Drugs and Emerging Therapies