市場調査レポート
商品コード
1226535
キャンディン新薬の考察と市場予測(2032年)CANDIN Emerging Drug Insight and Market Forecast - 2032 |
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キャンディン新薬の考察と市場予測(2032年) |
出版日: 受注後更新
発行: DelveInsight
ページ情報: 英文 30 Pages
納期: 2~10営業日
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当レポートでは、キャンディン新薬の主要7市場(米国・ドイツ・フランス・イタリア・スペイン・英国・日本)について調査分析し、作用機序、用法と用量、研究開発活動についての考察、市場予測などを提供しています。
"CANDIN Emerging Drug Insight and Market Forecast - 2032" report provides comprehensive insights about CANDIN for Common Warts in the seven major markets. A detailed picture of the CANDIN for Common Warts 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 CANDIN for Common Warts. The report provides insight about mechanism of action, dosage and administration, as well as research and development activity including regulatory milestones, along with other developmental activities. Further, it also consists of future market assessments inclusive of the CANDIN market forecast, analysis for Common Warts in the 7MM descriptive analysis such as SWOT, analyst views, comprehensive overview of market competitors, and brief about other emerging therapies in Common Warts.
CANDIN is a clear, colorless, sterile solution with a pH of 8.0-8.5. It is made from the culture filtrate and cells of two strains of Candida albicans. The fungi are propagated in a chemically defined medium consisting of inorganic salts, biotin, and sucrose.
Cellular hypersensitivity, or delayed-type hypersensitivity (DTH), can be assessed by intracutaneous testing with bacterial, viral, and fungal antigens to which most healthy persons are sensitized.
The active ingredient in CANDIN, currently approved as a skin test antigen for the assessment of cellular hypersensitivity to Candida albicans, is currently under investigation for the treatment of verruca vulgaris or common warts. The antigen in CANDIN is not currently approved for the treatment of common warts or any other indications.
Results in Phase II research involving common and non-common warts among adults were highly encouraging and are now advancing clinical research into the use of the antigen in common and non-common warts. Though not treated, plantar, periungual, flat, facial, and genital warts were evaluated in the Phase II subjects. Nielsen BioSciences has completed a Phase II clinical trial and is currently planning for a pivotal Phase III study for this indication.
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.
CANDIN Analytical Perspective by DelveInsight
This report provides a detailed market assessment of CANDIN in Common Warts 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 2025 to 2032.
The report provides the clinical trials information of CANDIN in Common Warts covering trial interventions, trial conditions, trial status, start and completion dates.
Key Questions
Which are the late-stage emerging therapies under development for the treatment of Common Warts?