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市場調査レポート
商品コード
1378359
エヌプレート薬剤に関する洞察と市場予測:2032年NPLATE Drug Insight and Market Forecast - 2032 |
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カスタマイズ可能
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エヌプレート薬剤に関する洞察と市場予測:2032年 |
出版日: 2023年11月01日
発行: DelveInsight
ページ情報: 英文 30 Pages
納期: 1~3営業日
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エヌプレート(ロミプロスチム)は、コルチコステロイド、免疫グロブリン、脾臓摘出術で十分な効果が得られない成人の慢性ITP患者において、血小板数の減少を治療するために、他の特定の薬剤や脾臓摘出術が十分に奏効しない場合に使用される合成蛋白製剤です。
エヌプレートは、出血のリスクを下げるために血小板数を約50,000/μLに保ちます。エヌプレートは血小板数の正常化には使用されないです。18歳未満の患者におけるエヌプレートの安全性と有効性は不明です。エヌプレートはTPO受容体に結合して活性化することにより血小板産生を増加させるが、その機序は内因性TPOに類似しています。日本では、本剤は重症再生不良性貧血患者の治療薬としても承認されています。
免疫性血小板減少症(ITP)患者には、週1回1mcg/kgを皮下注射します。血小板反応に基づいて投与量を調節します。エヌプレートは、内因性TPOに類似したメカニズムであるTPO受容体に結合し活性化することにより、血小板産生を増加させます。
当レポートでは、主要7ヶ国におけるエヌプレート市場について調査し、市場の概要とともに、2023年~2032年の売上予測データ、競合情勢、および国別動向などを提供しています。
“"NPLATE Drug Insight and Market Forecast - 2032" ” report provides comprehensive insights about NPLATE for immune thrombocytopenic purpura (ITP) in the seven major markets. A detailed picture of the NPLATE for ITP 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 NPLATE for ITP. 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 NPLATE market forecast analysis for ITP in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in ITP.
NPLATE (romiplostim) is a synthetic protein medicine used when certain other medicines, or surgery to remove the spleen, have not worked well enough to treat low blood platelet counts in adults with chronic ITP who have had an insufficient response to corticosteroids, immunoglobulins, or splenectomy.
NPLATE keeps the platelet count at about 50,000/µL to lower the risk of bleeding. NPLATE is not used to normalize the platelet count. The safety and efficacy of NPLATE are not known in people under the age of 18. NPLATE increases platelet production by binding and activating the TPO receptor, whose mechanism is analogous to endogenous TPO. In Japan, this drug is also approved for the treatment of patients with severe aplastic anemia.
For patients with ITP ¬ the recommended initial dose is 1 mcg/kg once weekly as a subcutaneous injection. Adjust dose based on platelet response.
NPLATE increases platelet production by binding and activating the TPO receptor, a mechanism analogous to endogenous TPO.
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.
This report provides a detailed market assessment of NPLATE for immune thrombocytopenic purpura (ITP) 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 2023 to 2032.
The report provides the clinical trials information of NPLATE for ITP covering trial interventions, trial conditions, trial status, start and completion dates.