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Press Release

Dec, 19 2023

開創性突破：透過創新療法改變掌蹠膿皰病患者生活－皮膚病學變革之作的出現

掌蹠膿皰病 (PPP) 具有重要的臨床意義，因為它會影響患者的生活品質。這種慢性皮膚病的特徵是手掌和腳底出現無菌膿皰，會引起疼痛、不適和功能障礙，尤其是在使用手腳的活動中。除了身體症狀之外，PPP 也常帶來社會心理後果，導致情緒困擾和自尊心下降。鑑於其慢性性質，PPP 需要持續管理，有效的治療方案對於緩解症狀和改善患者的整體健康至關重要。

訪問完整報告 @ https://www.databridgemarketresearch.com/reports/japan-palmoplantar-pustulosis-ppp-market

Data Bridge Market Research 分析稱，日本掌蹠膿皰病 (PPP) 市場預計在 2023 年至 2030 年的預測期內以 6.3% 的複合年增長率增長，2022 年市場價值為 1.359 億美元，到 2030 年將增長到 2.216 億美元。掌蹠膿皰病 (PPP) 的治療選擇多種多樣，例如光療、維甲酸以及阿達木單抗、布羅達單抗和賽妥珠單抗等生物製劑，這增加了為個別患者找到有效解決方案的機會。多種治療方式的出現促進了市場需求和潛在成長的增加。

研究的主要發現

日本掌蹠膿皰病（PPP）市場

提高對 PPP 的認識有助於早期診斷，預計將推動市場成長率

患者和醫療保健專業人員對掌蹠膿皰病 (PPP) 的認識不斷提高，這帶來了巨大的市場機會。隨著患者權益團體和教育活動提高了意識，越來越多的病例被診斷出來，對有效 PPP 治療的需求預計會增加。這為製藥公司開發和行銷創新療法以滿足受 PPP 影響的個人日益增長的需求創造了良好的環境。

報告範圍和市場細分

報告指標

細節

預測期

2023年至2030年

基準年

2022

歷史歲月

2021（可訂製為2015年2020年）

定量單位

收入（百萬美元）、銷售（單位）、定價（美元）

涵蓋的領域

疾病類型（A 型和 B 型）、嚴重程度（輕度-中度和中度-重度）、類型（診斷和治療）、人群類型（兒童和成人）、給藥途徑（口服、外用和腸外）、最終用戶（醫院、家庭護理、專科診所、其他）、分銷渠道（醫院藥房、網上藥房、零售藥房）

涵蓋的市場參與者

諾華公司（瑞士）、禮來公司（美國）、羅氏公司（瑞士）、百時美施貴寶公司（美國）、阿斯特捷利康公司（英國）、葛蘭素史克公司（英國）、默克公司（美國）、安進公司。 （美國）、AnGes, Inc.（日本）、強生私人有限公司（美國）、AbbVie Inc.（美國）、Perrigo Company plc（愛爾蘭）、WOCKHARDT（印度）、Bausch Health Companies Inc.（加拿大）、Viatris Inc.（美國）、Amneal Pharmaceuticals LLC。 （美國）、Xiromed（美國）和 Encube Ethicals Private Limited（美國）

報告涵蓋的數據點

除了市場價值、成長率、市場細分、地理覆蓋範圍、市場參與者和市場情景等市場洞察之外，Data Bridge 市場研究團隊策劃的市場報告還包括深入的專家分析、患者流行病學、管道分析、定價分析和監管框架。

細分分析：

日本掌蹠膿皰病 (PPP) 市場根據

疾病類型、嚴重程度、類型、人群類型、給藥途徑、最終用戶和分銷管道進行細分。

  • 根據疾病類型，日本掌蹠膿皰病 (PPP) 市場分為 A 型和 B 型

  • 根據嚴重程度，日本掌蹠膿皰病 (PPP) 市場分為輕度至中度和中度至重度

  • 根據類型，日本掌蹠膿皰病 (PPP) 市場細分為診斷和治療

  • 根據人口類型，日本掌蹠膿皰病 (PPP) 市場分為兒童和成人

  • 根據給藥途徑，日本掌蹠膿皰病 (PPP) 市場分為口服、外用和腸外給藥

  • 根據最終用戶，日本掌蹠膿皰病 (PPP) 市場分為醫院、家庭護理、專科診所和其他

  • 根據分銷管道，日本掌蹠膿皰病 (PPP) 市場分為醫院藥房、網路藥房和零售藥房

主要參與者

Data Bridge Market Research 認為以下公司是日本掌蹠膿皰病 (PPP) 市場的主要參與者，它們是諾華公司 (瑞士)、禮來公司 (美國)、羅氏公司 (瑞士)、百時美施貴寶公司 (美國)、阿斯特捷利康公司 (英國)、葛蘭素史克公司 (英國)、默克公司 (美國)

日本掌蹠膿皰病（PPP）市場

市場發展

  • 2022 年 6 月，專注於嚴重發炎疾病創新藥物開發的臨床階段免疫學公司 Aristea Therapeutics Inc. 宣布，其 RIST4721 治療罕見皮膚病掌蹠膿皰病 (PPP) 的 2b 期臨床試驗的開放標籤擴展 (OLE) 首位受試者給藥

  • 2020 年 7月 ，強生服務公司旗下子公司楊森製藥公司取得了一個重要里程碑，美國食品藥物管理局 (FDA) 批准了 STELARA（烏司奴單抗）。這種單株抗體因其在治療各種發炎方面的功效而獲得批准，並證實了其抑制過度活躍的發炎反應的能力。這項監管批准對楊森製藥來說至關重要，因為它為 STELARA 在治療掌蹠膿皰病方面的商業化打開了大門。這一特定適應症滿足了醫療需求，進一步增強了該藥物的市場潛力。

  • 2020年10月，全球生物製藥公司優時比（UCB）在阿姆斯特丹舉行的歐洲皮膚病和性病學會（EADV）大會上披露了在研IL-17A和IL-17F抑製劑比美珠單抗（bimekizumab）和TNF抑製劑CIMZIA（賽妥珠至單抗）用於治療中度重度斑塊

  • 2020年2月，禮來公司成功收購了著名的皮膚病藥物開發商Dermira Inc.。此次策略性收購標誌著禮來公司的重大擴張，增強了其在皮膚病學領域的產品組合。此舉使禮來公司能夠利用 Dermira 的專業知識和創新的皮膚病治療產品線，進一步增強其在製藥行業的地位和能力

有關日本掌蹠膿皰病 (PPP) 市場報告的更多詳細信息，請點擊此處 –  https://www.databridgemarketresearch.com/reports/japan-palmoplantar-pustulosis-ppp-market

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