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市場調査レポート
商品コード
1462305
オクトレオチド市場:市場規模、予測、市場洞察-2032年Octreotide Market Size, Forecast, and Market Insight - 2032 |
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カスタマイズ可能
適宜更新あり
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オクトレオチド市場:市場規模、予測、市場洞察-2032年 |
出版日: 2024年04月01日
発行: DelveInsight
ページ情報: 英文 30 Pages
納期: 2~10営業日
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オクトレオチドは、合成ソマトスタチン類似体であり、血管作動性腸管ペプチド(VIP)などの多くのホルモンの分泌低下、腸管通過時間の延長、水分および電解質の分泌低下と吸収増加など、いくつかのメカニズムを介して作用します。米国食品医薬品局(FDA)により、VIP分泌腫瘍に関連した下痢およびカルチノイド症候群による症状の治療薬として承認されています。オクトレオチドはフルオロピリミジン、イリノテカン、および5-FUベースの化学放射線療法によるCIDの患者に有益です。5-FU治療患者41人を対象とした1件のランダム化試験で、オクトレオチドは標準用量のロペラミドよりも有効であることが示されましたが(3日目までの下痢の消失率は90%対15%)、オクトレオチドはコストが高いため、一般に、ロペラミドの増量にもかかわらず48時間後に不応となった患者に対する第2選択治療として留保されています。重度の下痢、吐き気、嘔吐、食欲不振、腹部けいれんなどの消化器症候群を発症した患者には、点滴とオクトレオチドの前投与による積極的な管理が必要です。
今後数年間で、化学療法誘発性下痢(CID)の市場シナリオは、世界中の広範な調査と医療支出の増加により変化します。各社は、病状を治療/改善するための新たなアプローチに焦点を当てた治療法を開発し、課題を評価し、オクトレオチドの優位性に影響を与える可能性のある機会を模索しています。CIDに対する他の新興製品がオクトレオチドに厳しい市場競争を与えることが予想され、近い将来、後発の新興治療薬の発売が市場に大きな影響を与えるとみられています。
当レポートでは、主要7ヶ国における化学療法誘発性下痢(CID)治療薬のオクトレオチド市場について調査し、市場の概要とともに、競合情勢、2032年までの市場規模予測、および国別市場分析などを提供しています。
"Octreotide Market Size, Forecast, and Market Insight - 2032" report provides comprehensive insights about octreotide for Chemotherapy-induced Diarrhea (CID) in the seven major markets. A detailed picture of the octreotide for CID in the 7MM, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan for the study period 2019 -2032 is provided in this report along with a detailed description of the octreotide for CID. The report provides insights about mechanism of action, dosage and administration, as well as research and development including regulatory milestones, along with other developmental activities. Further, it also consists of future market assessments inclusive of the octreotide market forecast analysis for CID in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in CID.
Octreotide, a synthetic somatostatin analog, acts via several mechanisms: decreased secretion of a number of hormones, such as vasoactive intestinal peptide (VIP); prolongation of intestinal transit time and reduced secretion and increased absorption of fluid and electrolytes. It is approved by the US Food and Drug Administration for the treatment of diarrhea related to VIP-secreting tumors and symptoms due to carcinoid syndrome. Octreotide is beneficial in patients with CID from fluoropyrimidines, irinotecan, and 5-FU-based chemoradiotherapy. Although one randomized trial in 41 5-FU-treated patients showed that octreotide was more effective than standard-dose loperamide (90 versus 15% resolution of diarrhea by day 3), octreotide is generally reserved as a second-line treatment for patients who are refractory after 48 hours, despite a loperamide escalation, because of its high cost. Patients developing a gastrointestinal syndrome including severe diarrhea, nausea, vomiting, anorexia, and abdominal cramping should receive an aggressive management with intravenous fluids and upfront octreotide.
The report provides insights into:
The report is built using data and information sourced primarily from internal databases, primary and secondary research and in-house analysis by DelveInsight's team of industry experts. Information and data from the secondary sources have been obtained from various printable and nonprintable sources like search engines, news websites, global regulatory authorities websites, trade journals, white papers, magazines, books, trade associations, industry associations, industry portals and access to available databases.
Octreotide Analytical Perspective by DelveInsight
This report provides a detailed market assessment of octreotide for Chemotherapy-induced Diarrhea (CID) in the seven major markets, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan. This segment of the report provides forecasted sales data from 2024 to 2032.
The report provides the clinical trials information of octreotide for CID covering trial interventions, trial conditions, trial status, start and completion dates.