(function(){ var content_array=["

關于<\/b>PPF<\/b><\/p> \n

進展性肺纖維化(PPF)影響著全球多達560萬人。[8]<\/sup>這是一種進展性疾病,最終會導致患者死亡,其特征是肺部出現不可逆的瘢痕,并且隨著時間的推移而加重。[8]<\/sup>肺部瘢痕可能與類風濕性關節炎或系統性硬化癥等基礎疾病有關,也可能由吸入性物質引起。[1]<\/sup>,[8]<\/sup>,[9]<\/sup>在這些疾病中,肺組織的慢性瘢痕往往是導致早期死亡的主要原因。大約半數的PPF患者在確診后五年內死亡。[2]<\/sup>平均而言,確診延遲長達兩年,而且多達一半的確診患者未接受治療。[13],[14]<\/sup><\/p> \n

關于那米司特<\/b><\/p> \n

那米司特是一款口服、選擇性磷酸二酯酶4B(PDE4B)抑制劑,已在中國獲批用于治療成人IPF和PPF。該藥已獲得美國食品藥品監督管理局(FDA)授予的優先審評資格和突破性療法認定,并獲批用于治療IPF;目前,FDA正在優先審評該藥用于治療成人PPF。<\/p> \n

那米司特用于治療IPF和PPF的上市申請也正在歐盟、英國、日本和其他國家\/地區進行注冊審查,2026年預計將有更多國家\/地區獲批該產品。<\/p> \n

關于勃林格殷格翰<\/b><\/p> \n

勃林格殷格翰是全球領先的生物制藥企業,布局人用藥品、動物保健兩大業務領域。公司研發投入位居行業前列,致力于研究突破性療法,解決巨大未滿足的醫療需求,從而幫助改善或延長生命。自1885年成立以來,勃林格殷格翰一直是獨立的家族企業,始終著眼長遠發展,將可持續發展理念貫穿全價值鏈。公司在全球有超過5.45萬名員工,服務逾130個市場,致力于打造一個更健康、更可持續、更公平的未來。更多詳情,請訪問:www.boehringer-ingelheim.cn<\/a>, www.boehringer-ingelheim.com<\/a><\/p> \n

References<\/b><\/p> \n

[1] Kondoh Y, Inoue Y. Progressive Pulmonary Fibrosis: Current Status in Terminology and Future Directions. Adv Ther<\/span><\/i>. 2025;42(7):2988–3001
[2] Cen Z, et al.<\/i> Outcomes and predictors of progression in progressive pulmonary fibrosis. Ann Med<\/i>. 2024;56(1):2406439.
[3] Siegel RL, et al.<\/i> Cancer statistics, 2024. CA: A Cancer Journal for Clinicians. 2024;74(1):12–49.
[4] JASCAYD®<\/sup> (nerandomilast). Package Insert of Nerandomilast Tablets. China<\/span>. (Last updated: Dec 2025<\/span>)
[5] JASCAYD®<\/sup> (nerandomilast). Prescribing Information. Ridgefield, CT<\/span>: Boehringer Ingelheim Pharmaceuticals, Inc; 202. (Last updated: Oct 2025<\/span>).
[6] Ofev SmPC — Boehringer?Ingelheim, 2025.
[7] Maher T, et al. <\/i>Nerandomilast in Patients with Progressive Pulmonary Fibrosis. N Engl J Med<\/i>. 2025 Jun 12;392(22):2193-2202.
[8] Cottin V, et al. The Burden of Progressive-Fibrosing Interstitial Lung Diseases. Front Med<\/i> (Lausanne). 2022;9:799912.
[9] Wang J, et al.<\/i> Pathogenesis and therapeutic targets in pulmonary fibrosis. MedComm. 2024;5:e744.
[10] Nasser M, Larrieu S, Boussel L, et al.<\/i> Estimates of epidemiology, mortality and disease burden associated with progressive fibrosing interstitial lung disease in France<\/span> (the PROGRESS study). Respir Res<\/i> 2021. 22 :162
[11] Torrisi S, et al.<\/i> HRCT and histology in the evaluation of fibrotic lung diseases: A correlation study. Eur Respir Rev<\/i>. 2017;26(145).
[12] Levra S et al<\/i>. Long-term safety of antifibrotic drugs in IPF: a real-world experience. Biomedicine<\/i>s. 2022;10(12):3229.
[13] Chaudhuri et al. Respiratory Research<\/i> 2024; 25:364
[14] Wijsenbeek M et al. Current Medical Research and Opinion <\/i>2019; 35 (11): 2015-2024<\/p>"]; $("#dvExtra").html(content_array[0]);})();

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