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市場調查報告書
商品編碼
1485292
運甲狀腺素蛋白澱粉樣變性治療市場 - 按類型、疾病類型、藥物類型、給藥途徑、配銷通路- 全球預測 2024 - 2032Transthyretin Amyloidosis Treatment Market - By Type, Disease Type, Drug Type, Route of Administration, Distribution Channel - Global Forecast 2024 - 2032 |
在醫學研究和技術進步的推動下,轉甲狀腺素蛋白澱粉樣變性治療市場規模預計 2024 年至 2032 年間複合年成長率為 7.5%。最近,一些治療創新在阻止疾病進展和改善患者預後方面提供了有希望的結果。轉甲狀腺素蛋白澱粉樣變性的認知和診斷率不斷提高,特別是在人口老化地區,將有助於市場擴張。例如,全球範圍內發生的遺傳性轉甲狀腺素蛋白介導的 (hATTR) 可能會影響約 50,000 人,根據受影響的器官表現出不同的症狀。
此外,製藥公司和研究機構之間也開展了合作,透過利用綜合專業知識和資源來加速發現過程,從而促進新藥和療法的開發。越來越多的監管部門批准新療法以及轉甲狀腺素蛋白澱粉樣變性療法報銷範圍的擴大將進一步提高治療選擇的可及性。
轉甲狀腺素蛋白澱粉樣變性治療產業分為類型、疾病類型、藥物類型、給藥途徑、配銷通路、區域。
就給藥途徑而言,由於將治療劑直接輸送到血流中的功效和便利性,2024年至2032年期間腸胃外細分市場的市場規模預計將達到7.8%的複合年成長率。腸胃外方法確保藥物吸收快速且一致,避免了與口服給藥相關的胃腸道分解和變異性。對於經常出現胃腸道症狀和吸收不良問題的轉甲狀腺素蛋白澱粉樣變性患者來說,腸胃外給藥提供了有效遞送治療藥物的可靠方法。
根據配銷通路,到2032 年,線上藥局領域的轉甲狀腺素蛋白澱粉樣變性治療市場將錄得8% 的成長率。轉甲狀腺素蛋白澱粉樣變性的藥物他們的家。這種便利性對於居住在偏遠地區的患者和行動不便的患者特別有利,他們可能在進入傳統實體藥局時面臨挑戰。
到 2032 年,歐洲轉甲狀腺素蛋白澱粉樣變性治療市場規模將呈現 7.8% 的複合年成長率,這歸因於對醫療基礎設施和專注於罕見疾病的研究計劃的投資不斷增加。歐洲國家正在優先考慮醫療保健的進步,並分配大量資源來支持創新療法和治療方式。此外,監管機構還實施了加速核准途徑和激勵措施,以鼓勵孤兒藥的開發,進一步刺激了區域產業的擴張。
Transthyretin amyloidosis treatment market size is expected to witness 7.5% CAGR between 2024 and 2032, driven by the advancements in medical research and technologies. Lately, several therapeutic innovations are offering promising outcomes in halting disease progression and improving patient outcomes. The increasing awareness and diagnosis rate of transthyretin amyloidosis, particularly in regions with aging population will contribute to the market expansion. For instance, the worldwide occurrence of hereditary transthyretin-mediated (hATTR) is likely to affect roughly 50,000 individuals, showcasing diverse symptoms depending on the organs affected.
Moreover, there have also been collaborations between pharmaceutical companies and research institutions to facilitate the development of new drugs and therapies by leveraging combined expertise and resources to accelerate the discovery process. Growing regulatory approvals for novel treatments and the expansion of reimbursement coverage for transthyretin amyloidosis therapies will further enhance the accessibility of treatment options.
The transthyretin amyloidosis treatment industry is divided into type, disease type, drug type, route of administration, distribution channel, and region.
With respect to route of administration, the market size from the parenteral segment is slated to depict 7.8% CAGR between 2024 to 2032, due to the efficacy and convenience in delivering therapeutic agents directly into the bloodstream. Parenteral method ensures rapid and consistent drug absorption, bypassing gastrointestinal degradation and variability associated with oral administration. For patients with transthyretin amyloidosis, who often experience gastrointestinal symptoms and malabsorption issues, parenteral administration offers a reliable means of delivering therapeutic agents effectively.
Based on distribution channel, the transthyretin amyloidosis treatment market from the online pharmacy segment will record 8% growth rate through 2032. These channels provide a convenient platform for individuals to purchase prescription medications and specialty treatments, including those for transthyretin amyloidosis, from the comfort of their homes. This accessibility is particularly beneficial for patients residing in remote areas and those with mobility limitations, who may face challenges accessing traditional brick-and-mortar pharmacies.
Europe transthyretin amyloidosis treatment market size will exhibit 7.8% CAGR through 2032, attributed to increasing investments in healthcare infrastructure and research initiatives focused on rare diseases. European countries are prioritizing healthcare advancements and allocating substantial resources to support innovative therapies and treatment modalities. Additionally, regulatory agencies have implemented expedited approval pathways and incentives to encourage the development of orphan drugs, further stimulating the regional industry expansion.