The 7 major pachyonychia congenita markets reached a value of USD 813.1 Million in 2024. Looking forward, IMARC Group expects the 7MM to reach USD 955.5 Million by 2035, exhibiting a growth rate (CAGR) of 1.48% during 2025-2035.
Report Attribute
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Key Statistics
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Base Year |
2024
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Forecast Years | 2025-2035 |
Historical Years |
2019-2024
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Market Size in 2024
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USD 813.1 Million |
Market Forecast in 2035
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USD 955.5 Million |
Market Growth Rate 2025-2035
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1.48% |
The pachyonychia congenita market has been comprehensively analyzed in IMARC's new report titled "Pachyonychia Congenita Market: Epidemiology, Industry Trends, Share, Size, Growth, Opportunity, and Forecast 2025-2035". Pachyonychia congenita refers to a rare genetic disorder that affects the skin, nails, and mucous membranes. This disease is primarily characterized by abnormally thick nails and painful blisters or calluses on the soles of the feet. Individuals suffering from the condition might also experience hair abnormalities, such as coarse hair or hair that is absent or grows slowly. Numerous other symptoms associated with this ailment include white, thick patches on the tongue and inside of the cheeks, cysts in the skin, excessive sweating, discomfort, trouble walking, redness in various areas of the body, oral lesions, hoarse voice, etc. The diagnosis of pachyonychia congenita is typically based on a combination of family history, clinical findings, and a physical examination. A skin biopsy may also be conducted to assess the structural changes in the affected sites. Furthermore, genetic testing is recommended to identify the specific gene mutation responsible for the condition. In some cases, the healthcare provider may perform a microscopic examination of nail clippings that might reveal characteristic nail changes indicative of the underlying disease.
The increasing incidences of genetic mutations that disrupt the normal functioning of certain proteins, leading to abnormal nail and skin development, are primarily driving the pachyonychia congenita market. In addition to this, the inflating utilization of non-steroidal anti-inflammatory drugs (NSAIDs), since they work by inhibiting the production of prostaglandins to alleviate pain and discomfort in patients, is also creating a positive outlook for the market. Moreover, the widespread adoption of retinoid therapy, which can reduce the buildup of keratin, thereby leading to a softening and thinning of the affected skin, is further bolstering the market growth. Apart from this, the rising application of orthopedic devices, such as insoles or padding, on account of their various advantages, like providing better support, slowing down the progression of foot deformities, enabling mobility and independence, etc., is acting as another significant growth-inducing factor. Additionally, the emerging demand for intralesional corticosteroid injections to decrease the size and severity of the skin lesions by precisely delivering medication directly into the affected areas is expected to drive the pachyonychia congenita market during the forecast period.
IMARC Group's new report provides an exhaustive analysis of the pachyonychia congenita market in the United States, EU4 (Germany, Spain, Italy, and France), 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 pachyonychia congenita and also represents the largest market for its treatment. Furthermore, the current treatment practice/algorithm, market drivers, challenges, opportunities, reimbursement scenario, 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 pachyonychia congenita market in any manner.
PTX-022 is a topical formulation of rapamycin, under development by Palvella Therapeutics to treat pachyonychia congenita. PTX-022 inhibits the creation of mTOR, a kinase responsible for the development of certain keratin proteins. In disorders such as pachyonychia congenita that are associated with the overproduction of aberrant keratin proteins, the inhibition of mTOR may decrease the translation of mutant keratin-expressing genes and potentially block signaling pathways linked to skin fragility, keratoderma, pain, and ambulatory impairment.
Time Period of the Study
Countries Covered
Analysis Covered Across Each Country
This report also provides a detailed analysis of the current pachyonychia congenita marketed drugs and late-stage pipeline drugs.
In-Market Drugs
Late-Stage Pipeline Drugs
Drugs | Company Name |
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PTX-022 | Palvella 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
Pachyonychia Congenita: Current Treatment Scenario, Marketed Drugs and Emerging Therapies