+353-1-416-8900REST OF WORLD
+44-20-3973-8888REST OF WORLD
1-917-300-0470EAST COAST U.S
1-800-526-8630U.S. (TOLL FREE)

Aicardi-Goutieres Syndrome Marketed and Pipeline Drugs Assessment, Clinical Trials and Competitive Landscape

  • PDF Icon

    Report

  • 52 Pages
  • June 2022
  • Region: Global
  • GlobalData
  • ID: 5625095
This reports provides a data-driven overview of the current and future competitive landscape in Aicardi-Goutieres Syndrome therapeutics.

Synopsis

  • There will be more than 4,000 prevalent cases of AGS each in 2022 across the 16 countries covered in the publisher's epidemiology forecast.
  • No FDA-approved marketed drugs are available for AGS, only symptomatic treatment is indicated for disease management.
  • The drug currently in late-stage clinical development targets tyrosine kinase.
  • Non-commercial sponsors dominate clinical trial development in AGS.
  • No deals involving companies developing AGS assets were seen over the past 10 years.
  • No regulator filing or commercial launch is expected for AGS in the next 18 months.

Scope


The publisher's Aicardi-Goutieres Syndrome Marketed and Pipeline Drugs Assessment, Clinical Trials, Social Media and Competitive Landscape, 2022 Update combines data from the Pharma Intelligence Center with in-house analyst expertise to provide a competitive assessment of the disease marketplace.

Components of the report include:
  • Disease Landscape
  • Disease Overview
  • Epidemiology Overview
  • Treatment Overview
  • Marketed Products Assessment
  • Pipeline Assessment
  • Breakdown by Development Stage, Mechanism of Action, Molecule Type, Route of Administration
  • Late-stage Pipeline Drugs
  • Phase Transition Success Rate and Likelihood of Approval
  • Clinical Trials Assessment
  • Breakdown of Trials by Phase, Status, Sponsors and Geography
  • Enrolment Analytics, Site Analytics, Feasibility Analysis
  • Deals Landscape
  • Commercial Assessment
  • Key Market Players
  • Future Market Catalysts

Reasons to Buy

  • Develop and design your in-licensing and out-licensing strategies through a review of pipeline products and technologies, and by identifying the companies with the most robust pipeline.
  • Develop business strategies by understanding the trends shaping and driving the Aicardi-Goutieres Syndrome market.
  • Drive revenues by understanding the key trends, innovative products and technologies, market segments, and companies likely to impact the global Aicardi-Goutieres Syndrome market in the future.
  • Formulate effective sales and marketing strategies by understanding the competitive landscape and by analyzing the performance of various competitors.
  • Identify emerging players with potentially strong product portfolios and create effective counter-strategies to gain a competitive advantage.
  • Organize your sales and marketing efforts by identifying the market categories and segments that present maximum opportunities for consolidations, investments, and strategic partnerships.

Table of Contents

1 Preface
1.1 Contents
1.2 Report Scope
1.3 List of Tables and Figures
1.4 Abbreviations
2 Key Findings
3 Disease Landscape
3.1 Disease Overview
3.2 Epidemiology Overview
3.3 Treatment Overview
4 Marketed Drugs Assessment
5 Pipeline Drugs Assessment
5.1 Late-stage Pipeline Drugs
5.2 Overview by Development Stage
5.3 Overview by Molecule Type
5.4 Overview by Mechanism of Action
5.5 Overview by Route of Administration
5.6 Therapy Area and Indication-specific PTSR and LoA
6 Clinical Trials Assessment
6.1 Historical Overview
6.2 Overview by Phase
6.3 Overview by Status
6.4 Geographic Overview
6.5 Top 20 Sponsors with Breakdown by Phase
6.6 Top 20 Sponsors with Breakdown by Status
6.7 Enrollment Data
6.8 Top 20 countries for Trial Sites
6.9 Top 20 Sites Globally
6.10 Feasibility Analysis - Geographic Overview
6.11 Feasibility Analysis - Benchmark Models
7 Deals Landscape
8 Commercial Assessment
8.1 Key Market Players
9 Future Market Catalysts
10 Appendix
10.1 Methodology
10.2 Methodology - PTSR and LoA Analysis
10.3 About the Authors
10.4 Contact the Publisher
10.5 Disclaimer