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市場調査レポート
商品コード
1614784
MAXIGESIC IV市場:市場規模、予測、新たな洞察-2032年MAXIGESIC IV 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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MAXIGESIC IV市場:市場規模、予測、新たな洞察-2032年 |
出版日: 2024年12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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MAXIGESIC IVは、新規特許取得済みのデュアルモード非オピオイド鎮痛治療薬で、パラセタモール(米国ではアセトアミノフェン)1,000mgとイブプロフェン300mgを配合した独自の輸液製剤です。
MAXIGESICは、頭痛、片頭痛、緊張型頭痛、副鼻腔痛、歯痛、歯科処置、背部痛、咽頭痛、関節炎、テニス肘、生理痛、筋肉痛、リウマチ痛、風邪やインフルエンザに伴う痛みを、発熱を抑え、一時的に緩和します。この医薬品は、パラセタモールとイブプロフェンのユニークな組み合わせで特許を取得しており、幅広い痛みの症状を迅速かつ効果的に緩和することが証明されています。欧州17カ国で販売許可を取得し、オーストラリア、ニュージーランド、アラブ首長国連邦で発売され、欧州と香港での展開と商業化を加速するために複数のライセンス契約と販売契約を締結しました。米国での承認申請をサポートするため、2回目の第III相試験が終了しました。
当レポートでは、主要7ヶ国におけるMAXIGESIC IV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。
"MAXIGESIC IV Market Size, Forecast, and Market Insight - 2032" report provides comprehensive insights about MAXIGESIC IV for Postoperative pain in the seven major markets. A detailed picture of the MAXIGESIC IV for Postoperative pain 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 MAXIGESIC IV for Postoperative pain. 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 MAXIGESIC IV market forecast analysis for Postoperative pain in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in Postoperative pain.
MAXIGESIC IV, a novel, patented, dual mode-of-action nonopioid pain treatment, is a unique combination of paracetamol (known as acetaminophen in the US) 1,000 mg + Ibuprofen 300 mg solution for infusion for use postoperatively in hospitals for patients for whom the use of oral analgesics is limited.
MAXIGESIC reduces fever and temporarily relieves pain associated with headaches, migraines, tension headaches, sinus pain, toothache, dental procedures, backache, sore throat, arthritis, tennis elbow, period pain, muscular pain, rheumatic pain, aches and pains associated with colds and flu. The drug is a unique patented combination of paracetamol and ibuprofen, proven to provide fast and effective relief from a wide range of pain symptoms (This information is for New Zealand only) (Maxigesic, n.d.). The product has obtained marketing authorizations in 17 European countries, launched in Australia, New Zealand, and the United Arab Emirates, and multiple license and distribution agreements signed to accelerate roll-out and commercialization in Europe and Hong Kong. The second Phase III study was completed to support regulatory submission in the US.
Dosage and administration
Adults and children over 12 years: The usual dosage is one to two tablets taken every 6 h, as required, up to a maximum of eight tablets in 24 h.
Children under 12 years: It is not recommended for children under 12.
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.
MAXIGESIC IV Analytical Perspective by DelveInsight
This report provides a detailed market assessment of MAXIGESIC IV for Postoperative pain 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 MAXIGESIC IV for Postoperative pain covering trial interventions, trial conditions, trial status, start and completion dates.