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市場調査レポート
商品コード
1692372
ウィルソン病治療薬市場- 世界の産業規模、シェア、動向、機会、予測、製品別、流通チャネル別、地域別、競合別、2020~2030年Wilson's Disease Drugs Market - Global Industry Size, Share, Trends, Opportunity, and Forecast, Segmented By Product, By Distribution Channel, By Region & Competition, 2020-2030F |
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ウィルソン病治療薬市場- 世界の産業規模、シェア、動向、機会、予測、製品別、流通チャネル別、地域別、競合別、2020~2030年 |
出版日: 2025年03月24日
発行: TechSci Research
ページ情報: 英文 182 Pages
納期: 2~3営業日
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ウィルソン病治療薬の世界市場規模は、2024年には6億1,050万米ドルと評価され、2030年までのCAGRは5.50%で、予測期間中に目覚しい成長を遂げると予測されています。
ウィルソン病は別名肝レンズ核変性症とも呼ばれ、銅を代謝する体の能力に影響を及ぼす稀な遺伝病です。この疾患は常染色体劣性遺伝します。つまり、罹患した個人は、両親からそれぞれ1つずつ、変異した遺伝子のコピーを受け継いでいます。ウィルソン病は様々な臓器、主に肝臓と脳、そして体内の他の組織に過剰な銅の蓄積を引き起こします。ウィルソン病は様々な症状を示すため、診断が難しい場合があります。一般的な症状および合併症には、肝疾患(肝炎、肝硬変)、神経学的問題(振戦、協調運動障害)、精神医学的症状(性格変化、抑うつ、不安)、および眼の異常(角膜の周囲に緑色または茶色がかった輪ができるカイザー・フライシャー輪)があります。ウィルソン病の診断には通常、銅の濃度を測定する血液検査、肝機能検査、ATP7B遺伝子の変異を特定する遺伝子検査が行われます。肝臓に蓄積した銅を評価するために、肝臓超音波検査やMRIのような画像検査が行われることもあります。
市場概要 | |
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予測期間 | 2026~2030年 |
市場規模:2024年 | 6億1,050万米ドル |
市場規模:2030年 | 8億3,494万米ドル |
CAGR:2025~2030年 | 5.50% |
急成長セグメント | オンライン薬局 |
最大市場 | 北米 |
診断の進歩
薬剤耐性
患者支援プログラム
Global Wilson's Disease Drugs Market was valued at USD 610.50 million in 2024 and is anticipated to witness an impressive growth in the forecast period with a CAGR of 5.50% through 2030. Wilson's Disease, also known as hepatolenticular degeneration, is a rare genetic disorder that affects the body's ability to metabolize copper. This condition is inherited in an autosomal recessive manner, meaning that an affected individual inherits two copies of the mutated gene, one from each parent. Wilson's Disease leads to the accumulation of excess copper in various organs, primarily the liver and brain, as well as other tissues in the body. Wilson's Disease can manifest with a wide range of symptoms, which can make diagnosis challenging. Common symptoms and complications include liver disease (hepatitis, cirrhosis), neurological problems (tremors, difficulty with coordination and movement), psychiatric symptoms (personality changes, depression, anxiety), and eye abnormalities (Kayser-Fleischer rings, which are green or brownish rings around the cornea). Diagnosis of Wilson's Disease typically involves blood tests to measure copper levels, liver function tests, and genetic testing to identify mutations in the ATP7B gene. Imaging studies like liver ultrasound or MRI may also be used to assess copper buildup in the liver.
Market Overview | |
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Forecast Period | 2026-2030 |
Market Size 2024 | USD 610.50 Million |
Market Size 2030 | USD 834.94 Million |
CAGR 2025-2030 | 5.50% |
Fastest Growing Segment | Online Pharmacies |
Largest Market | North America |
Key Market Drivers
Advancements in Diagnosis
Genetic testing has become a cornerstone in the diagnosis of Wilson's Disease. Identifying mutations in the ATP7B gene, responsible for copper transport in the body, is a highly specific and reliable method for confirming the disease. For instance, according to the Wilson Disease Association, in May 2022, the FDA approved CUVRIOR (trientine tetrahydrochloride), marking the first new treatment for Wilson's disease in three decades. Advances in genetic testing techniques have made it more accessible and affordable. Non-invasive imaging techniques such as liver ultrasound and magnetic resonance imaging (MRI) have become valuable tools in assessing copper overload in the liver and other organs. These methods are less invasive than traditional liver biopsies and provide important diagnostic information. Laboratory tests measuring various markers related to copper metabolism in the blood and urine have become more sophisticated and informative. These markers include serum ceruloplasmin levels, 24-hour urinary copper excretion, and non-caeruloplasmin bound copper (NCC) measurements.
Key Market Challenges
Drug Resistance
Wilson's Disease requires lifelong treatment to maintain copper levels within a normal range. Patients often need to take medications, such as chelators like penicillamine or trientine, consistently over many years. Over time, some patients may develop resistance to the drugs they are taking. Drug resistance in Wilson's Disease means that the medications that were initially effective in lowering copper levels may become less so. This can result in a failure to adequately control copper accumulation in the body. In some cases, healthcare providers may need to increase the dosage of medications to overcome resistance. This can lead to higher doses and potentially an increased risk of side effects or adverse reactions. Maintaining consistent adherence to a lifelong treatment regimen can be challenging for patients, especially if they experience side effects or do not perceive a direct benefit from the medications. Poor adherence can contribute to treatment resistance. Detecting drug resistance requires close monitoring of copper levels in the body and the patient's response to treatment. Managing resistance often involves adjustments to the treatment plan, which can be complex and may require consultation with specialists. In cases of drug resistance, healthcare providers may explore alternative therapies or medications to manage Wilson's Disease. The availability and effectiveness of these alternatives can impact the market dynamics for Wilson's Disease drugs. Genetic factors can influence how a patient responds to treatment. Variations in genes related to copper metabolism can affect the effectiveness of certain medications and may contribute to resistance in some cases.
Key Market Trends
Patient Assistance Programs
APs aim to improve access to costly medications by providing financial assistance to patients who may otherwise have difficulty affording them. This is especially important for individuals with Wilson's Disease, as treatment can be expensive and lifelong. Patients with Wilson's Disease often require ongoing treatment, and the cost of medications and medical care can add up. PAPs can help alleviate the financial burden on patients and their families, making treatment more manageable. PAPs are particularly beneficial for individuals who are uninsured or underinsured, as they may face higher out-of-pocket costs for medications. These programs bridge the gap in coverage, ensuring that all eligible patients can access the drugs they need. Some PAPs offer co-pay assistance, covering a portion of the patient's out-of-pocket costs, including deductibles and co-pays. This can make it more affordable for patients to continue their treatment. Many PAPs provide educational resources and support to patients, helping them better understand their condition, treatment options, and how to navigate the healthcare system. PAPs often work to simplify the application process, making it easier for patients to enroll and receive assistance. Pharmaceutical companies that manufacture Wilson's Disease drugs may establish PAPs as part of their corporate social responsibility efforts or to support patients using their medications. Some PAPs collaborate with patient advocacy organizations focused on Wilson's Disease. These partnerships can help identify and reach eligible patients in need of assistance.
In this report, the Global Wilson's Disease Drugs Market has been segmented into the following categories, in addition to the industry trends which have also been detailed below:
Company Profiles: Detailed analysis of the major companies present in the Global Wilson's Disease Drugs Market.
Global Wilson's Disease Drugs Market report with the given market data, TechSci Research offers customizations according to a company's specific needs. The following customization options are available for the report: