The 7 major fibrodysplasia ossificans progressiva markets reached a value of US$ 361.2 Million in 2023. Looking forward, IMARC Group expects the 7MM to reach US$ 503.8 Million by 2034, exhibiting a growth rate (CAGR) of 3.07% during 2024-2034.
Report Attribute
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Key Statistics
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Base Year | 2023 |
Forecast Years | 2024-2034 |
Historical Years |
2018-2023
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Market Size in 2023
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US$ 361.2 Million |
Market Forecast in 2034
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US$ 503.8 Million |
Market Growth Rate 2024-2034
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3.07% |
The fibrodysplasia ossificans progressiva market has been comprehensively analyzed in IMARC's new report titled "Fibrodysplasia Ossificans Progressiva Market: Epidemiology, Industry Trends, Share, Size, Growth, Opportunity, and Forecast 2024-2034". Fibrodysplasia ossificans progressiva (FOP) refers to an extremely rare and debilitating genetic disorder characterized by the abnormal ossification or formation of bone in soft tissues, such as muscles, tendons, and ligaments. It is caused by a mutation in the ACVR1 gene, leading to the inappropriate activation of bone morphogenetic protein (BMP) receptors. The symptoms of this condition usually manifest in early childhood and progressively worsen over time. Initially, patients may develop benign soft tissue swellings, known as flare-ups, which are painful and often lead to immobility. As the disease advances, these flare-ups transform into heterotopic ossification, causing joints to fuse. This results in a severely limited range of motion and significant impairment in daily activities. Diagnosing FOP is primarily based on clinical presentation, medical history, and genetic testing to identify the gene mutation. However, given its rarity and potential for misdiagnosis, it is important for healthcare professionals to be aware of its distinctive features and differentiate it from various other conditions presenting with similar symptoms.
The escalating incidence of somatic mutations in the ACVR1 gene that can lead to the overactivation of a certain receptor in the body, causing the development of abnormal bone in muscles, tendons, and ligaments, is primarily driving the fibrodysplasia ossificans progressiva market. In addition to this, the inflating utilization of effective treatments, such as glucocorticoids and non-steroidal anti-inflammatory drugs (NSAIDs), which aim to control inflammation and mitigate the formation of heterotopic ossification in patients, is also creating a positive outlook for the market. Moreover, the widespread adoption of physical and occupational therapies due to their valuable role in maintaining muscle function, enhancing joint mobility, and managing pain is further bolstering the market growth. Apart from this, the rising usage of surgical interventions and the development of minimally invasive techniques to address disease complications, like joint ankylosis and breathing difficulties, are acting as another significant growth-inducing factor. These surgical procedures, including the excision of ectopic bones, help to restore functional movement and reduce pain in severely affected patients. Additionally, the emerging popularity of gene therapy, since it offers the possibility of correcting the faulty genetic material, thereby halting or even reversing the progression of the illness, is expected to drive the fibrodysplasia ossificans progressiva market during the forecast period.
IMARC Group's new report provides an exhaustive analysis of the fibrodysplasia ossificans progressiva 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 fibrodysplasia ossificans progressiva 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 fibrodysplasia ossificans progressiva 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 fibrodysplasia ossificans progressiva marketed drugs and late-stage pipeline drugs.
In-Market Drugs
Late-Stage Pipeline Drugs
Drugs | Company Name |
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IPN 60130 | Ipsen |
INCB 000928 | Incyte Corporation |
Garetosmab | Regeneron Pharmaceuticals |
Palovarotene | Clementia Pharmaceuticals |
DS 6016a | Daiichi Sankyo |
*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
Fibrodysplasia Ossificans Progressiva: Current Treatment Scenario, Marketed Drugs and Emerging Therapies