The Congenital Ichthyosis market reached a value of US$ 5.0 Million across the top 7 markets (US, EU4, UK, and Japan) in 2023. Looking forward, IMARC Group expects the 7MM to reach US$ 8.0 Million by 2034, exhibiting a growth rate (CAGR) of 4.22% during 2024-2034.
Report Attribute
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Key Statistics
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Base Year |
2023
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Forecast Years | 2024-2034 |
Historical Years |
2018-2023
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Market Size in 2023
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US$ 5.0 Million |
Market Forecast in 2034
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US$ 8.0 Million |
Market Growth Rate 2024-2034 | 4.22% |
The Congenital Ichthyosis market has been comprehensively analyzed in IMARC's new report titled "Congenital Ichthyosis Market: Epidemiology, Industry Trends, Share, Size, Growth, Opportunity, and Forecast 2024-2034". Congenital Ichthyosis is a rare genetic disorder characterized by the abnormal development of the skin's outermost layer, known as the epidermis. Individuals suffering from this condition have dry, thickened, and scaly skin resembling fish scales. This hereditary disease is typically present at birth and remains a lifelong challenge for those affected. The symptoms of the ailment can vary in severity, with some patients experiencing mild scaling and others facing more pronounced and widespread skin involvement. The skin's appearance can range from fine scales to larger, plate-like formations, leading to discomfort, itching, and potential skin infections.
Additionally, dry and tight skin can limit mobility and cause physical discomfort. The diagnosis of Congenital Ichthyosis is primarily based on a clinical examination and a thorough medical history. Dermatologists and pediatricians often collaborate to identify characteristic skin features and rule out various other skin disorders with similar symptoms. Additionally, genetic testing is recommended to confirm the diagnosis and determine the specific subtype of the ailment. The escalating cases of genetic mutations in certain genes, particularly those responsible for skin barrier function, leading to the manifestation of chronic skin disorders, are primarily driving the Congenital Ichthyosis market. In addition to this, the inflating utilization of effective treatment modalities, such as emollients, topical retinoids, keratolytics, etc., to alleviate symptoms of the disease and improve skin barrier function is also creating a positive outlook for the market. These medications aim to moisturize and exfoliate the affected skin, reducing scaling and promoting a smoother skin texture. Moreover, the widespread adoption of supportive therapies, including regular bathing and moisturizing routines, which can manage the condition and prevent exacerbations in patients, is also bolstering market growth. Apart from this, the rising usage of physical and occupational therapies, since they aid in enhancing motor skills, mobility, and overall quality of life for individuals suffering from congenital ichthyosis, is acting as another significant growth-inducing factor. Additionally, the emerging popularity of gene therapy, which involves introducing functional genetic material into the skin cells to correct the mutated genes responsible for the disorder, thereby providing a long-term and targeted solution for patients, is expected to drive the Congenital Ichthyosis market during the forecast period.
IMARC Group's new report provides an exhaustive analysis of the Congenital Ichthyosis 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 Congenital Ichthyosis and 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 stake or are planning to foray into the Congenital Ichthyosis market in any manner.
Inetagugene Geperpavec, previously known as KB105, is an HSV-1 viral vector that cannot replicate and integrate into the host genome. It functions by expressing human transglutaminase 1 (TGM1). Currently, it is undergoing Phase I/II clinical trials for the treatment of ichthyosis disease. Additionally, it has received orphan drug designation from the FDA.
Isotretinoin, an oral medication designed mainly to affect sebaceous glands, is frequently recommended for treating severe acne. Presently, it's in phase 3 clinical trials as a potential treatment for Congenital Ichthyosiform Erythroderma. This drug is classified as a small molecule and is manufactured by Timber Pharmaceuticals.
Time Period of the Study
Countries Covered
Analysis Covered Across Each Country
This report also provides a detailed analysis of the current congenital ichthyosis marketed drugs and late-stage pipeline drugs.
In-Market Drugs
Late-Stage Pipeline Drugs
Drugs | Company Name |
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KB 105 | Krystal Biotech |
Isotretinoin | Timber Pharmaceuticals |
*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
Congenital Ichthyosis: Current Treatment Scenario, Marketed Drugs and Emerging Therapies