![]() |
市場調査レポート
商品コード
1377997
Invossaの新興薬剤に関する洞察と市場予測:2032年Invossa Emerging Drug Insight and Market Forecast - 2032 |
||||||
カスタマイズ可能
|
Invossaの新興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
|
Invossa(TG-C)は、初代ヒト軟骨細胞(軟骨細胞)と治療用成長因子TGF-B1を発現するように形質転換されたヒト細胞を含む同種(ドナー)細胞・遺伝子治療薬です。Invossa(TG-C)はこの2つの組み合わせです。膝関節OAを治療するために開発され、膝関節内に1回注射することで投与されます。
クラス初の細胞介在型遺伝子治療薬であるTG-C LDは、1回の関節内注射で膝関節OAを治療します。米国におけるTG-C(TG-C LDではない)のライセンス保有者であるKolon TissueGeneは、米国における第II相臨床試験を完了し、初期データとして、膝関節に1回注射するだけで、最大2年間、持続的な疼痛緩和と運動機能改善を実証しました。現在、米国においてTG-Cの安全性と有効性を確認するため、1,020人の患者を対象とした第III相臨床試験が進行中です。さらに、米国第II相臨床試験で観察された統計学的に有意な疼痛軽減と機能改善を確認するため、DMOAD(変形性関節症治療薬)指定に向けた疾患進行の遅延を示す試験が計画されています。
当レポートでは、主要6ヶ国およびカナダにおけるInvossa市場について調査し、市場の概要とともに、2024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。
“"Invossa Emerging Drug Insight and Market Forecast - 2032" report provides comprehensive insights about invossa for osteoarthritis in the six major markets. A detailed picture of the invossa for osteoarthritis in the 6MM, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, along with Canada for the study period 2019 -2032 is provided in this report along with a detailed description of the invossa for osteoarthritis. 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 invossa market forecast analysis for osteoarthritis in the 6MM, along with Canada, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in osteoarthritis.
Invossa (TG-C) is an allogeneic (donor) cell and gene therapy involving primary human chondrocytes (cartilage cells) and human cells transduced to express the therapeutic growth factor TGF-B1. Invossa (TG-C) is a combination of the two. It has been developed to treat knee OA and is delivered via one intra-articular injection into the knee.
A first-in-class cell-mediated gene therapy, TG-C LD targets knee OA through a single intra-articular injection. Kolon TissueGene, the license holder for TG-C in the United States (not TG-C LD), has completed a Phase II clinical trial in the United States, with initial data demonstrating sustained pain relief and mobility improvement following a single injection in the knee joint, for possibly up to 2 years. Phase III clinical trials in the United States comprising 1,020 patients are currently ongoing to confirm the safety and efficacy of TG-C. In addition, to confirm the statistically significant pain reduction and function improvements observed from the US Phase II clinical trial, the trials are designed to show the delay of disease progression to achieve a DMOAD (Disease Modifying Osteoarthritis Drug) designation.
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.
Invossa Analytical Perspective by DelveInsight
This report provides a detailed market assessment of invossa for osteoarthritis in the six major markets, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, along with Canada. This segment of the report provides forecasted sales data from 2024 to 2032.
The report provides the clinical trials information of invossa for osteoarthritis covering trial interventions, trial conditions, trial status, start and completion dates.
Key Questions