
Strategic Intelligence: Orphan Designated Drugs
Description
Strategic Intelligence: Orphan Designated Drugs
Summary
This report consolidates GlobalData’s latest thinking and forecasts around how the healthcare, macroeconomic, technology, and regulatory trends will impact the orphan designated drugs in pharma space, as well as providing insights into the leading players and future challengers across the value chain, and providing insights into key drugs and markets from GlobalData’s Pharma Intelligence Center. Additionally, this report is designed to provide strategic planners, competitive intelligence professionals and key stakeholders in the pharmaceutical industry a clear view of the opportunities and risks over the foreseeable future.
Due to the unmet medical demands of many rare diseases around the world, the number of orphan designated drugs (ODD) by regulatory agencies such as the FDA and EMA has increased in recent years. This has arisen from international recognition of the significant number of people that rare diseases affect daily, paired with limited therapeutic options and low patient populations.
As a result, a wide variety of pharmaceutical companies are expanding their orphan drug portfolio through co-development partnerships and collaborations, innovative means of personalized and precision therapy, as well as receiving financial and legal support from regulatory bodies to meet this unmet medical need.
Scope
Summary
This report consolidates GlobalData’s latest thinking and forecasts around how the healthcare, macroeconomic, technology, and regulatory trends will impact the orphan designated drugs in pharma space, as well as providing insights into the leading players and future challengers across the value chain, and providing insights into key drugs and markets from GlobalData’s Pharma Intelligence Center. Additionally, this report is designed to provide strategic planners, competitive intelligence professionals and key stakeholders in the pharmaceutical industry a clear view of the opportunities and risks over the foreseeable future.
Due to the unmet medical demands of many rare diseases around the world, the number of orphan designated drugs (ODD) by regulatory agencies such as the FDA and EMA has increased in recent years. This has arisen from international recognition of the significant number of people that rare diseases affect daily, paired with limited therapeutic options and low patient populations.
As a result, a wide variety of pharmaceutical companies are expanding their orphan drug portfolio through co-development partnerships and collaborations, innovative means of personalized and precision therapy, as well as receiving financial and legal support from regulatory bodies to meet this unmet medical need.
Scope
- A dedicated report examining the pivotal healthcare, technological, macroeconomic, and regulatory trends shaping the orphan designated drugs field in pharma landscape.
- This report also provides an in-depth analysis of how these trends are poised to either accelerate progress or create obstacles for the growth of the orphan designated drugs market.
- Understand the key trends accelerating or hindering the orphan designated drugs in pharma space.
Table of Contents
50 Pages
- Executive Summary
- Players
- Thematic Briefing
- Trends
- Healthcare trends
- Technology trends
- Macroeconomic trends
- Regulatory trends
- Industry Analysis
- Market size and growth forecasts
- Case studies
- Vyxeos Combination for IV Injection Receives Orphan Drug Designation for the Treatment of High-Risk AML in Japan
- Panavance Therapeutics Awarded ODD for its Pancreatic Cancer Treatment
- PhamAust Limited Reveals Encouraging Results for Monepantel
- Can-Fite Biopharma’s Namodenoson Demonstrating Anti-cancer and Protective Effects in the Liver
- Signals
- M&A trends
- Strategic partnerships
- Funding
- Social media trends
- Value Chain
- Drug discovery and development
- Clinical trials
- Manufacturing
- Patient access
- Companies
- Public companies
- Private companies
- Sector Scorecards
- Clinical trials scorecard
- Who’s who
- Thematic screen
- Valuation screen
- Risk screen
- Abbreviations
- Bibliography
- Further Reading
- GlobalData reports
- Our Thematic Research Methodology
- About GlobalData
- Contact Us
- List of Tables
- Table 1: Healthcare trends
- Table 2: Technology trends
- Table 3: Macroeconomic trends
- Table 4: Regulatory trends
- Table 5: M&A trends
- Table 6: Strategic partnerships
- Table 7: Funding
- Table 8: Public companies
- Table 9: Private companies
- Table 10: Abbreviations
- Table 11: GlobalData reports
- Table 12: Thematic Scores
- List of Figures
- Figure 1: Examples of players in orphan designated drugs and where they sit in the value chain
- Figure 2: Global patient-based forecast for orphan designated drugs, 2018–28
- Figure 3: Global patient-based forecast for orphan designated drugs by highest generating drugs and indications, 2028
- Figure 4: Social media discussions related to orphan designated drugs since 2021
- Figure 5: Word cloud with trends related to orphan designated drugs social media discussions
- Figure 6: Examples of popular posts related to orphan designated drugs
- Figure 7: The orphan designated drugs value chain
- Figure 8: Examples of drug discovery and development providers in orphan designated drugs
- Figure 9: Examples of clinical trial developers in orphan designated drugs
- Figure 10: Examples of manufacturing providers in orphan designated drugs
- Figure 11: Examples of patient access developers in orphan designated drugs
- Figure 12: Who does what in the orphan designated drugs space?
- Figure 13: Thematic screen
- Figure 14: Valuation screen
- Figure 15: Risk screen
- Figure 16: Our five-step approach for generating a sector scorecard
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