表紙:SAGE-217の新興薬剤に関する洞察と市場予測:2032年
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1381103

SAGE-217の新興薬剤に関する洞察と市場予測:2032年

SAGE-217 Emerging Drug Insight and Market Forecast - 2032

出版日: | 発行: DelveInsight | ページ情報: 英文 30 Pages | 納期: 1~3営業日

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SAGE-217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
  • 全表示
  • 概要
  • 図表
  • 目次
概要

ズラノロン(SAGE-217)は、産後うつ病(PPD)治療薬として開発中の経口新薬です。1日1回、2週間投与の神経活性ステロイド(NAS)GABAA受容体陽性アロステリックモジュレーター(PAM)で、PPD、大うつ病性障害(MDD)、治療抵抗性うつ病を含むいくつかのうつ病性障害を緩和するために特別にデザインされています。GABAシステムは脳の主要な抑制性シグナル伝達経路であり、中枢神経系(CNS)はCNS機能を著しく制御しています。SAGE-217は、シナプスおよびシナプス外のA型γ-アミノ酪酸(GABAA)受容体に対する選択性と、1日1回の経口投与に適した薬物動態プロファイルに最適化されています。

今後数年間で、産後うつ病(PPD)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、SAGE-217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。PPDの他の新興製品がSAGE-217と厳しい市場競争を繰り広げることが予想され、近い将来、後発の新興治療薬が上市されれば、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、米国におけるSAGE-217市場について調査し、産後うつ病(PPD)治療薬であるSAGE-217市場の概要とともに、2023年~2032年の売上予測データ、競合情勢などを提供しています。

目次

第1章 レポートのイントロダクション

第2章 産後うつ病(PPD)に対するSAGE-217の概要

  • 製品の詳細
  • 臨床開発
    • 臨床研究
    • 臨床試験情報
    • 安全性と有効性
  • その他の開発活動
  • 製品概要

第3章 競合情勢(上市済み治療法)

第4章 競合情勢(後期段階の新興治療法)

第5章 SAGE-217市場評価

  • PPDに対するSAGE-217の市場展望
  • 米国の分析
    • 米国におけるPPDに対するSAGE-217の市場規模

第6章 SWOT分析

第7章 アナリストの見解

第8章 付録

第9章 DelveInsightのサービス内容

第10章 免責事項

第11章 DelveInsightについて

第12章 レポート購入オプション

図表

List of Tables

  • Table 1: SAGE-217, Clinical Trial Description, 2023
  • Table 2: SAGE-217, General Description
  • Table 3: Competitive Landscape (Marketed Therapies)
  • Table 4: Competitive Landscape (Emerging Therapies)
  • Table 5: SAGE-217 Market Size in the US, in USD million (2019-2032)

List of Figures

  • Figure 1: SAGE-217 Market Size in the United States, USD million (2019-2032)
目次
Product Code: DIDM1027

“"SAGE-217 Emerging Drug Insight and Market Forecast - 2032" report provides comprehensive insights about SAGE-217 for Postpartum depression (PPD) in the United States. A detailed picture of the SAGE-217 for PPD in the United States for the study period 2019 -2032 is provided in this report along with a detailed description of the SAGE-217 for PPD. 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 SAGE-217 market forecast analysis for PPD in the US, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in PPD.

Drug Summary:

Zuranolone (SAGE-217) is an investigational, oral, novel medicine in development for postpartum depression (PPD). It is given once daily, a 2-week therapy neuroactive steroid (NAS) GABAA receptor positive allosteric modulator (PAM) specifically designed to relieve several depression disorders, including PPD, major depressive disorder (MDD), and treatment-resistant depression. The GABA system is the major inhibitory signaling pathway of the brain, and the central nervous system (CNS) significantly regulates CNS function. SAGE-217 has been optimized for selectivity to synaptic and extrasynaptic type A γ-aminobutyric acid (GABAA) receptors and a pharmacokinetic profile for daily oral dosing.

Scope of the Report:

The report provides insights into:

  • A comprehensive product overview including the SAGE-217 description, mechanism of action, dosage and administration, research and development activities in postpartum depression (PPD).
  • Elaborated details on SAGE-217 regulatory milestones and other development activities have been provided in this report.
  • The report also highlights the SAGE-217 research and development activities in PPD across the United States.
  • The report also covers the patents information with expiry timeline around SAGE-217.
  • The report contains forecasted sales of SAGE-217 for PPD till 2032.
  • Comprehensive coverage of the late-stage emerging therapies for PPD.
  • The report also features the SWOT analysis with analyst views for SAGE-217 in PPD.

Methodology:

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.

SAGE-217 Analytical Perspective by DelveInsight

In-depth SAGE-217 Market Assessment

This report provides a detailed market assessment of SAGE-217 for postpartum depression (PPD) in the United States. This segment of the report provides forecasted sales data from 2023 to 2032.

SAGE-217 Clinical Assessment

The report provides the clinical trials information of SAGE-217 for PPD covering trial interventions, trial conditions, trial status, start and completion dates.

Report Highlights:

  • In the coming years, the market scenario for postpartum depression (PPD) is set to change due to the extensive research and incremental healthcare spending across the world; which would expand the size of the market to enable the drug manufacturers to penetrate more into the market.
  • The companies are developing therapies that focus on novel approaches to treat/improve the disease condition, assess challenges, and seek opportunities that could influence SAGE-217 dominance.
  • Other emerging products for PPD are expected to give tough market competition to SAGE-217 and launch of late-stage emerging therapies in the near future will significantly impact the market.
  • A detailed description of regulatory milestones, and developmental activities, provide the current development scenario of SAGE-217 in PPD.
  • Our in-depth analysis of the forecasted sales data of SAGE-217 from 2023 to 2032 will support the clients in the decision-making process regarding their therapeutic portfolio by identifying the overall scenario of the SAGE-217 in PPD.

Key Questions:

  • What is the product type, route of administration and mechanism of action of SAGE-217?
  • What is the clinical trial status of the study related to SAGE-217 in postpartum depression (PPD) and study completion date?
  • What are the key collaborations, mergers and acquisitions, licensing and other activities related to the SAGE-217 development?
  • What are the key designations that have been granted to SAGE-217 for PPD?
  • What is the forecasted market scenario of SAGE-217 for PPD?
  • What are the forecasted sales of SAGE-217 in the United States?
  • What are the other emerging products available and how are these giving competition to SAGE-217 for PPD?
  • Which are the late-stage emerging therapies under development for the treatment of PPD?

Table of Contents

1. Report Introduction

2. SAGE-217 Overview in PPD

  • 2.1. Product Detail
  • 2.2. Clinical Development
    • 2.2.1. Clinical studies
    • 2.2.2. Clinical trials information
    • 2.2.3. Safety and efficacy
  • 2.3. Other Developmental Activities
  • 2.4. Product Profile

3. Competitive Landscape (Marketed Therapies)

4. Competitive Landscape (Late-stage Emerging Therapies)

5. SAGE-217 Market Assessment

  • 5.1. Market Outlook of SAGE-217 in PPD
  • 5.2. The United States Analysis
    • 5.2.1. Market Size of SAGE-217 in the United States for PPD

6. SWOT Analysis

7. Analysts' Views

8. Appendix

  • 8.1. Bibliography
  • 8.2. Report Methodology

9. DelveInsight Capabilities

10. Disclaimer

11. About DelveInsight

12. Report Purchase Options