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PUBLISHER: GlobalData | PRODUCT CODE: 1663766

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PUBLISHER: GlobalData | PRODUCT CODE: 1663766

Progressive Supranuclear Palsy: Competitive Landscape

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PAGES: 62 Pages
DELIVERY TIME: 1-2 business days
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This reports provides a data-driven overview of the current and future competitive landscape in Progressive Supranuclear Palsy therapeutics.

GlobalData epidemiologists estimate that there will be 263,657 diagnosed prevalent cases of PSP in 2024, which is expected to increase to 268,041 diagnosed prevalent cases by 2029.

Currently, there are no approved treatments in the PSP market.

The PSP pipeline holds 28 molecules, with no assets in the pre-registration stage, one asset in Phase III development, and seven assets in Phase II development.

Over the past decade, 52 clinical trials have been conducted in PSP. The years with the most studies initiated were 2018 and 2024 with eight trials each, followed by 2019, 2021, and 2023 with seven trials each.

During the past decade, partnerships were the most common deal type in North America. Licensing agreements were dominant in the APAC region. In Europe, licensing agreements and partnerships contributed equally to completed deals. In South and Central America as well as in Africa, licensing agreements accounted for all transactions.

Scope

GlobalData's Progressive Supranuclear Palsy: Competitive Landscape 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
  • Breakdown by Mechanism of Action, Route of Administration
  • Product Profiles with Sales Forecast
  • Pricing and Reimbursement Assessment
  • Annual Therapy Cost
  • Time to Pricing and Time to Reimbursement
  • Pipeline Assessment
  • Breakdown by Development Stage, Mechanism of Action, Molecule Type, Route of Administration
  • Product Profiles with Sales Forecast
  • Late-to-mid-stage Pipeline Drugs
  • Phase Transition Success Rate and Likelihood of Approval
  • Clinical Trials Assessment
  • Breakdown of Trials by Phase, Status, Virtual Components, Sponsors, Geography, and Endpoint Status
  • Enrolment Analytics, Site Analytics, Feasibility Analysis
  • Deals Landscape
  • Mergers, Acquisitions, and Strategic Alliances by Region
  • Overview of Recent Deals
  • 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 Progressive Supranuclear Palsy market.
  • Drive revenues by understanding the key trends, innovative products and technologies, and companies likely to impact the global Progressive Supranuclear Palsy market in the future.
  • Formulate effective sales and marketing strategies by understanding the competitive landscape and 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 that present the maximum opportunities for consolidations, investments, and strategic partnerships.
Product Code: GDHC188CL

Table of Contents

1 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

  • 4.1 Leading Marketed Drugs
  • 4.2 Overview by Mechanism of Action
  • 4.3 Overview by Molecule Type
  • 4.4 Product Profiles and Sales Forecast

5 Pricing and Reimbursement Assessment

  • 5.1 Annual Cost of Therapy
  • 5.2 Time to Pricing and Reimbursement

6 Pipeline Drugs Assessment

  • 6.1 Mid-to-late-stage Pipeline Drugs
  • 6.2 Overview by Development Stage
  • 6.3 Overview by Mechanism of Action
  • 6.4 Overview by Molecule Type
  • 6.5 Drug Specific Phase Transition Success Rate (PTSR) and Likelihood of Approval (LoA)
  • 6.6 Therapy Area and Indication-specific PTSR and LoA

7 Clinical Trials Assessment

  • 7.1 Historical Overview
  • 7.2 Overview by Phase
  • 7.3 Overview by Status
  • 7.4 Overview by Phase for Ongoing and Planned Trials
  • 7.5 Trials with Virtual Components
  • 7.6 Overview of Trials by Geography
  • 7.7 Single-Country and Multinational Trials by Region
  • 7.8 Top 20 Sponsors with Breakdown by Phase
  • 7.9 Top 20 Sponsors with Breakdown by Status
  • 7.10 Overview by Endpoint Status
  • 7.11 Overview by Race and Ethnicity
  • 7.12 Enrollment Data
  • 7.13 Top 20 countries for Trial Sites
  • 7.14 Top 20 Sites Globally
  • 7.15 Feasibility Analysis - Geographic Overview
  • 7.16 Feasibility Analysis - Benchmark Models

8 Deals Landscape

  • 8.1 Mergers, Acquisitions, and Strategic Alliances by Region
  • 8.2 Recent Mergers, Acquisitions, and Strategic Alliances

9 Commercial Assessment

  • 9.1 Key Market Players

10 Future Market Catalysts

11 Appendix

  • 11.1 Methodology
  • 11.2 Methodology - Sales Forecast
  • 11.3 Methodology - Pricing and Reimbursement
  • 11.4 Methodology - PTSR and LoA Analysis
  • 11.5 About the Authors
  • 11.6 Contact Us
  • 11.7 Disclaimer
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Jeroen Van Heghe

Manager - EMEA

+32-2-535-7543

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Christine Sirois

Manager - Americas

+1-860-674-8796

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