Product Code: RA100387
INTRODUCTION
The term rare kidney diseases represents around 150 different indications. It is worth highlighting that the prevalence rate of rare kidney disorders (RKD) is estimated to be 60-80 per 100,000 cases / individuals in the US and Europe. Despite their relatively low prevalence, these set of indications are believed to be one of the leading causes of renal diseases, along with diabetes and other rare genetic kidney disorders. The low disease incidence rate of such disorders, coupled to the lack of awareness among the general population, often leads to late or erroneous diagnosis. This, in turn, enables suboptimal therapeutic management, as well as compromised long-term outcomes. The aforementioned factors are some of the key reasons that are believed to be responsible for high mortality rates and severe compromise on chance of survival of a patient suffering with rare kidney disorders. It is worth mentioning that, post the onset of the COVID-19 pandemic, the treatment of patients affected with rare kidney disorders became even more challenging. This can be primarily attributed to the fact that the current treatment options for such indications are heavily reliant on regular patient visits to the hospitals or medical centers. Consequently, during the pandemic, a 30% increase in mortality rate was observed in affected patients. This increase in mortality has compelled players engaged in the pharmaceutical domain to undertake necessary research initiatives in order to identify novel drugs that can efficiently treat rare kidney disorders.
Given the complexity associated with conventional treatment options, such as dialysis, kidney transplant and biopsy, drug developers engaged in this domain have shifted their focus towards the development of drugs that can target a myriad of rare kidney disorders. It is worth highlighting that, since 2020, over seven drugs have received marketing approval for the treatment of rare kidney disorders; these are (in reverse chronological order of approval) Galafold® (Fabry disease, European Medicines Agency (EMA), 2021), Lupkynis™ (Lupus Nephritis (LN), United States Food and Drug Administration (USFDA), 2021), Sibnayal™ (distal Renal Tubular Acidosis (dRTA), EMA, 2021), Tarpeyo® (Immunoglobulin A Nephropathy (IgAN), USFDA, 2021), Benlysta® (LN, USFDA, 2020), Cystadrops® (Cystinosis, USFDA, 2020), and Ultomiris® (Atypical Hemolytic Uremic Syndrome (aHUS), Japan, 2020). Further, more than 90 candidates targeting rare kidney disorders are currently under clinical investigation, while several novel leads are being evaluated in early stages of development. Given the lucrative opportunity associated with these targets, this domain has gained attention of both private and public investors in the past few years. In fact, over USD 4.5 billion has been invested in this domain since 2020. As more candidates are likely to progress towards advanced stages of development, we expect the market to witness aggressive growth in the foreseen future.
SCOPE OF THE REPORT
The Rare Kidney Disorders Market - Distribution by Target Indications (IgA Nephropathy, Lupus Nephritis, Focal Segmental Glomerular Sclerosis, Membranous Nephropathy, C3 Glomerulopathy and Others), Type of Molecule (Small Molecules and Biologics (Monoclonal Antibody, Hormone, Recombinant Protein, and Others)), Route of Administration (Oral, Intravenous, Subcutaneous, and Others) and Key Geographies (North America, Europe, Asia Pacific and Rest of the World): Industry Trends and Global Forecast, 2022-2035 report features an extensive study of the current market landscape and the likely future potential associated with the rare kidney disorders market, over the next decade. The study also features an in-depth analysis, highlighting the capabilities of various industry stakeholders engaged in this field. Amongst other elements, the report features:
- A detailed executive summary of key insights captured during our research. It offers a high-level view on the current state of rare kidney disorders market and its likely evolution in the mid to long term.
- A brief introduction to various aspects of rare kidney disorders. It includes a detailed discussion on the historical evolution and factors contributing to the treatment of rare kidney disorders. Further, it highlights various prominent target indications associated with rare kidney disorders, application of omics technology and its future perspectives.
- A detailed overview of the current market landscape of more than 127 drug candidates that are either approved or currently under development for the treatment of various rare kidney disorders, based on several relevant parameters, such as phase of development (approved, registration, phase III, phase II, phase I, pre-clinical and discovery), target molecule (complement component 5 (C5), complement component 3 (C3), a proliferation-inducing ligand (APRIL), B lymphocyte stimulator (BLyS), Complement Factor B, and others), route of administration (oral, intravenous, subcutaneous, and others), and target indication (complement 3 glomerulopathy (C3G), focal segmental glomerular sclerosis (FSGS), IgA nephropathy (IgAN), lupus nephritis (LN), membranous nephropathy (MN)), type of molecule (biologics and small molecules), and type of biologic (monoclonal antibody (mAb), hormone, recombinant protein, enzyme replacement therapy (ERT), gene therapy, small interfering ribonucleic acid (siRNA) molecule and others). In addition, it presents details of the companies engaged in the development of drugs targeting rare kidney disorders, based on several relevant parameters, such as year of establishment, company size (in terms of number of employees), location of headquarters, and most active players.
- Elaborate profiles of approved and clinical stage drugs indicated for rare kidney disorders (phase II / III or above). Each profile features an overview of the drug developer, clinical trial information related to the drug, clinical trial results, and estimated sales revenues (if available).
- A detailed competitiveness analysis of companies engaged in the development of rare kidney disorders targeting drugs, based on their developer strength (in terms of years of experience), portfolio strength (in terms of number of drugs developed), and portfolio diversity (in terms of phase of development, target indication, and drug designation).
- An in-depth analysis of the various collaborations and partnerships that have been inked by players engaged in the development of drugs targeting various rare kidney disorders since 2017, based on several relevant parameters, such as year of partnership, type of partnership, focus area, type of partner and regional distribution of partnerships.
- An analysis of the funding and investments made within the domain, during the period 2016-2022, based on several relevant parameters, such as year of funding, type of funding (seed financing, venture capital financing, debt financing, grants, IPOs and other offerings), leading players (in terms of amount invested) and key investors (in terms of number of funding instances).
- A detailed clinical trial analysis of ongoing clinical studies for the evaluation of various drug candidates targeting rare kidney disorders, based on several relevant parameters, such as trial registration year, current trial status, phase of development, key target indications, patient age, study design and key geographical regions.
- A detailed analysis of the clinical and commercial attractiveness for drugs targeting rare kidney disorders, based on several relevant parameters, such as target patient population, dosing frequency and dose strength.
- A case study highlighting the companies engaged in offering kidney care services, along with information on their year of establishment, company size (in terms of number of employees), location of headquarters and target indication.
One of the key objectives of this report was to evaluate the current market size and the future potential associated with rare kidney disorders market, over the coming years. We have developed an informed estimate on the likely evolution of the market in the short to mid-term and long term, for the period 2022-2035. Additionally, the report features the likely distribution of the current and forecasted opportunity across relevant parameters, such as [A] target indications (complement 3 glomerulopathy (C3G), FSGS, IgAN, LN, membranous nephropathy (MN)), [B] type of molecule (small molecules and biologics (monoclonal antibody, hormone, recombinant protein, and others)),[C] route of administration (oral, intravenous, subcutaneous, and others) [D] key geographical regions (North America, Europe, Asia-Pacific, and Rest of the World (RoW)). In order to account for future uncertainties and to add robustness to our model, we have provided three market forecast scenarios, namely conservative, base and optimistic scenarios, representing different tracks of the industry's growth.
All actual figures have been sourced and analyzed from publicly available information forums and primary research discussions. Financial figures mentioned in this report are in USD, unless otherwise specified.
RESEARCH METHODOLOGY
The data presented in this report has been gathered via secondary research. For all our projects, we have conducted interviews / surveys with various experts in this domain (academia, industry, medical practice and other associations) in order to solicit their opinions on emerging trends in the market. This is primarily useful for us to draw out our own opinion on how the market will evolve across different regions and technology segments. Wherever possible, the available data has been checked for accuracy from multiple sources of information.
The secondary sources of information include:
- Annual reports
- Investor presentations
- SEC filings
- Industry databases
- News releases from company websites
- Government policy documents
- Industry analysts' views
While the focus has been on forecasting the market till 2035, the report also provides our independent view on various technological and non-commercial trends emerging in the industry. This opinion is solely based on our knowledge, research and understanding of the relevant market gathered from various secondary and primary sources of information.
KEY QUESTIONS ANSWERED
- Who are the leading players engaged in the development of drugs targeting rare kidney disorders?
- Which are the key drugs being developed across early and late stages of development?
- Who are the key players providing services related to kidney care?
- Which are the key indications targeted by drugs indicated for rare kidney disorders?
- What type of partnership models are commonly adopted by stakeholders engaged in this domain?
- Who are the key investors in the domain?
- Which regions have emerged as the key hubs for conducting clinical studies focused on rare kidney disorders?
- How is the current and future market opportunity likely to be distributed across key market segments?
CHAPTER OUTLINES
Chapter 2 is an executive summary of key insights captured during our research. It offers a high-level view on the current state of rare kidney disorders market and its likely evolution in the mid to long term.
Chapter 3 provides a brief introduction to various aspects of rare kidney disorders. It includes a detailed discussion on the historical evolution and factors contributing to the treatment of rare kidney disorders. Further, it highlights various prominent target indications associated with rare kidney disorders, application of omics technology and its future perspectives.
Chapter 4 provides a detailed overview of the current market landscape of more than 127 drug candidates that are either approved or currently under development for the treatment of various rare kidney disorders, based on several relevant parameters, such as phase of development ( approved, registration, phase III, phase II, phase I, pre-clinical and discovery), target molecule (complement component 5 ( C5), complement component 3 (C3), a proliferation-inducing ligand (APRIL), B lymphocyte stimulator (BLyS), Complement Factor B, and others), route of administration (oral, intravenous, subcutaneous, and others), and target indication (complement 3 glomerulopathy (C3G), FSGS, IgAN, LN, membranous nephropathy (MN)), type of molecule (biologics and small molecules), and type of biologic (monoclonal antibody (mAb), hormone, recombinant protein, enzyme replacement therapy (ERT), gene therapy, small interfering ribonucleic acid (siRNA) molecule and others). In addition, it presents details of the companies engaged in the development of drugs targeting rare kidney disorders, based on several relevant parameters, such as year of establishment, company size (in terms of number of employees), location of headquarters, and most active players.
Chapter 5 provides detailed profiles of approved and clinical stage drugs indicated for rare kidney disorders (phase II / III or above). Each profile features an overview of the drug developer, clinical trial information related to the drug, clinical trial results, and estimated sales revenues (if available).
Chapter 6 features a detailed competitiveness analysis of companies engaged in the development of rare kidney disorders targeting drugs, based on their developer strength (in terms of years of experience), portfolio strength (in terms of number of drugs developed), and portfolio diversity (in terms of phase of development, target indication, and drug designation).
Chapter 7 features an elaborate analysis of the various collaborations and partnerships that have been inked by players engaged in the development of drugs targeting various rare kidney disorders since 2017. It includes details of deals that were / are focused on the rare kidney disorders, which were analyzed on the basis of year of partnership, type of partnership, focus area, type of partner and regional distribution of partnerships. It also consists of a schematic representation showcasing the players that have established the maximum number of alliances related to the rare kidney disorders. Furthermore, we have provided a world map representation of all the deals inked in this field, highlighting those that have been established within and across different continents.
Chapter 8 presents detailed analysis of the funding and investments made within the domain, during the period 2016-2022, based on several relevant parameters, such as year of funding, type of funding (seed financing, venture capital financing, debt financing, grants, IPOs and other offerings), leading players (in terms of amount invested) and key investors (in terms of number of funding instances).
Chapter 9 presents a detailed clinical trial analysis of ongoing clinical studies for the evaluation of various drug candidates targeting rare kidney disorders, based on several relevant parameters, such as trial registration year, current trial status, phase of development, key target indications, patient age, study design and key geographical regions.
Chapter 10 features an analysis of the clinical and commercial attractiveness for drugs targeting rare kidney disorders, based on several relevant parameters, such as target patient population, dosing frequency and dose strength
Chapter 11 presents an elaborate market forecast analysis, highlighting the future potential of the market till the year 2035. It also includes future sales projections of rare kidney disorders that are either marketed or in advanced stages of clinical development (phase II/III and above). Additionally, the report features the likely distribution of the current and forecasted opportunity across relevant parameters, such as [A] target indications (complement 3 glomerulopathy (C3G), FSGS, IgAN, LN, membranous nephropathy (MN)), [B] type of molecule (small molecules and biologics (monoclonal antibody, hormone, recombinant protein, and others)),[C] route of administration (oral, intravenous, subcutaneous, and others) [D] key geographical regions (North America, Europe, Asia-Pacific, and Rest of the World (RoW)). In order to account for future uncertainties and to add robustness to our model, we have provided three market forecast scenarios, namely conservative, base and optimistic scenarios, representing different tracks of the industry's growth.
Chapter 12 presents case study highlighting the companies engaged in offering kidney care services, along with information on their year of establishment, company size (in terms of number of employees), location of headquarters and target indication.
Chapter 13 is an appendix, which provides tabulated data and numbers for all the figures included in the report.
Chapter 14 is an appendix, which contains a list of companies and organizations mentioned in the report.
TABLE OF CONTENTS
1. PREFACE
- 1.1. Scope of the Report
- 1.2. Market Segmentation
- 1.3. Research Methodology
- 1.4. Key Questions Answered
- 1.5. Chapter Outlines
2. EXECUTIVE SUMMARY
3. INTRODUCTION
- 3.1. An Overview of Rare Kidney Disorders
- 3.2. Key Historical Events
- 3.3. Factors Contributing to Rare Kidney Disorders
- 3.4. Rare Kidney Disorders: Target Indications
- 3.5. Rare Kidney Disorders: Applications of Omics Technology
- 3.6. Rare Kidney Disorders: Future Outlook
4. MARKET LANDSCAPE
- 4.1. Rare Kidney Disorders: List of Drugs
- 4.1.1. Analysis by Stage of Development
- 4.1.2. Analysis by Target Molecule
- 4.1.3. Analysis by Target Molecule and Route of Administration
- 4.1.4. Analysis by Target Indication
- 4.1.5. Analysis by Stage of Development and Target Indication
- 4.1.6. Analysis by Type of Target Molecule
- 4.1.7. Analysis by Stage of Development and Type of Target Molecule
- 4.2. Rare Kidney Disorders: List of Drug Developers
- 4.2.1. Analysis by Year of Establishment
- 4.2.2. Analysis by Company Size
- 4.2.3. Analysis by Region
- 4.2.4. Most Active Players: Analysis by Number of Drugs
5. DRUG PROFILES
- 5.1. Benlysta
- 5.1.1. Company Overview
- 5.1.2. Drug Overview
- 5.1.3. Clinical Trial Information
- 5.1.4. Clinical Trial Results
- 5.1.5. Estimated Sales Revenue
- 5.2. Cystadrops®
- 5.2.1. Company Overview
- 5.2.2. Drug Overview
- 5.2.3. Clinical Trial Information
- 5.2.4. Clinical Trial Results
- 5.2.5. Estimated Sales Revenue
- 5.3. Galafold®
- 5.3.1. Company Overview
- 5.3.2. Drug Overview
- 5.3.3. Clinical Trial Information
- 5.3.4. Clinical Trial Results
- 5.3.5. Estimated Sales Revenue
- 5.4. Tarpeyo®
- 5.4.1. Company Overview
- 5.4.2. Drug Overview
- 5.4.3. Clinical Trial Information
- 5.4.4. Clinical Trial Results
- 5.4.5. Estimated Sales Revenue
- 5.5. Ultomiris®
- 5.5.1. Company Overview
- 5.5.2. Drug Overview
- 5.5.3. Clinical Trial Information
- 5.5.4. Clinical Trial Results
- 5.5.5. Estimated Sales Revenue
- 5.6. Thiola®
- 5.6.1. Company Overview
- 5.6.2. Drug Overview
- 5.6.3. Clinical Trial Information
- 5.6.4. Clinical Trial Results
- 5.6.5. Estimated Sales Revenue
- 5.7. Lupkynis™
- 5.7.1. Company Overview
- 5.7.2. Drug Overview
- 5.7.3. Clinical Trial Information
- 5.7.4. Clinical Trial Results
- 5.7.5. Estimated Sales Revenue
- 5.8. Sibnayal™
- 5.8.1. Company Overview
- 5.8.2. Drug Overview
- 5.8.3. Clinical Trial Information
- 5.8.4. Clinical Trial Results
- 5.8.5. Estimated Sales Revenue
- 5.9. Pegunigalsidase Alfa
- 5.9.1. Company Overview
- 5.9.2. Drug Overview
- 5.9.3. Clinical Trial Information
- 5.9.4. Clinical Trial Results
- 5.9.5. Estimated Sales Revenue
- 5.10. Saphnelo™
- 5.10.1. Company Overview
- 5.10.2. Drug Overview
- 5.10.3. Clinical Trial Information
- 5.10.4. Clinical Trial Results
- 5.10.5. Estimated Sales Revenue
- 5.11. Atrasentan
- 5.11.1. Company Overview
- 5.11.2. Drug Overview
- 5.11.3. Clinical Trial Information
- 5.11.4. Clinical Trial Results
- 5.11.5. Estimated Sales Revenue
- 5.12. Bardoxolone Methyl
- 5.12.1. Company Overview
- 5.12.2. Drug Overview
- 5.12.3. Clinical Trial Information
- 5.12.4. Clinical Trial Results
- 5.12.5. Estimated Sales Revenue
- 5.13. Crovalimab
- 5.13.1. Company Overview
- 5.13.2. Drug Overview
- 5.13.3. Clinical Trial Information
- 5.13.4. Clinical Trial Results
- 5.13.5. Estimated Sales Revenue
- 5.14. Ianalumab
- 5.14.1. Company Overview
- 5.14.2. Drug Overview
- 5.14.3. Clinical Trial Information
- 5.14.4. Estimated Sales Revenue
- 5.15. Cozaar®
- 5.15.1. Company Overview
- 5.15.2. Drug Overview
- 5.15.3. Clinical Trial Information
- 5.15.4. Clinical Trial Results
- 5.15.5. Estimated Sales Revenue
- 5.16. Cosentyx®
- 5.16.1. Company Overview
- 5.16.2. Drug Overview
- 5.16.3. Clinical Trial Information
- 5.16.4. Estimated Sales Revenue
- 5.17. Empaveli®
- 5.17.1. Company Overview
- 5.17.2. Drug Overview
- 5.17.3. Clinical Trial Information
- 5.17.4. Clinical Trial Results
- 5.17.5. Estimated Sales Revenue
- 5.18. Rituxan®
- 5.18.1. Company Overview
- 5.18.2. Drug Overview
- 5.18.3. Clinical Trial Information
- 5.18.4. Clinical Trial Results
- 5.18.5. Estimated Sales Revenue
- 5.19. Sparsentan
- 5.19.1. Company Overview
- 5.19.2. Drug Overview
- 5.19.3. Clinical Trial Information
- 5.19.4. Clinical Trial Results
- 5.19.5. Estimated Sales Revenue
- 5.20. Iptacopan
- 5.20.1. Company Overview
- 5.20.2. Drug Overview
- 5.20.3. Clinical Trial Information
- 5.20.4. Clinical Trial Results
- 5.20.5. Estimated Sales Revenue
- 5.21. Narsoplimab
- 5.21.1. Company Overview
- 5.21.2. Drug Overview
- 5.21.3. Clinical Trial Information
- 5.21.4. Clinical Trial Results
- 5.21.5. Estimated Sales Revenue
6. COMPANY COMPETITIVENESS ANALYSIS
- 6.1. Key Methodology and Parameters
- 6.2. Company Competitiveness Analysis: Biologic Developers (Peer Group 1)
- 6.3. Company Competitiveness Analysis: Small Molecule Developers (Peer Group 2)
7. PARTNERSHIPS AND COLLABORATIONS
- 7.1. Rare Kidney Disorders: List of Partnerships
- 7.2. Analysis by Year of Partnership
- 7.3. Analysis by Type of Partnership
- 7.4. Analysis by Year and Type of Partnership
- 7.5. Analysis by Type of Partnership and Company Size
- 7.6. Analysis by Target Indication
- 7.7. Most Active Players: Analysis by Number of Partnerships
- 7.8. Analysis by Region
- 7.9. Analysis by Country
- 7.10. Intercontinental and Intracontinental Agreements
8. FUNDING AND INVESTMENTS
- 8.1. Rare Kidney Disorders: List of Funding and Investments
- 8.2. Cumulative Year-wise Trend of Funding, 2016 - 2022
- 8.3. Analysis of Instances by Type of Funding
- 8.4. Analysis of Instances by Type of Venture Funding
- 8.5. Analysis of Instances by Year of Funding and Type of Funding
- 8.6. Analysis by Type of Funding and Amount Invested
- 8.7. Analysis of Instances by Type of Investor
- 8.8. Analysis by Focus Area
- 8.9. Analysis by Region
- 8.11. Most Active Investors: Analysis by Number of Instances
- 8.12. Most Active Players: Analysis by Number of Instances
- 8.13. Most Active Players: Analysis by Amount Raised (USD Million)
9. CLINICAL TRIAL ANALYSIS
- 9.1. Methodology and Parameters
- 9.2. Cumulative Trend by Trial Registration Year, 2016 - 2022
- 9.3. Analysis by Target Indication
- 9.4. Analysis by Study Design
- 9.5. Analysis by Region
- 9.6. Analysis by Number of Trials, Phase of Development and Region
- 9.7. Analysis by Patient Age
- 9.8. Analysis by Trial Registration Year, Number of Trials and Region
- 9.9. Analysis by Trial Status and Phase of Development
- 9.10. Analysis of Patients Enrolled by Trial Registration Year
- 9.11. Analysis of Patients Enrolled by Phase of Development
- 9.12. Analysis by Number of Trials, Trial Status and Region
- 9.13. Analysis of Patients Enrolled by Region
- 9.14. Analysis of Patients Enrolled by Trial Status and Region
10. MARKET FORECAST
- 10.1. Scope and Limitations
- 10.2. Key Assumptions and Forecast Methodology
- 10.3. Global Rare Kidney Disorders Market, 2022-2035
- 10.4. Rare Kidney Disorders Market: Analysis by Type of Molecule, 2022-2035
- 10.4.1. Rare Kidney Disorders Market for Biologics, 2022-2035
- 10.4.2. Rare Kidney Disorders Market for Small Molecules, 2022-2035
- 10.5. Rare Kidney Disorders Market: Analysis by Route of Administration, 2022-2035
- 10.5.1. Rare Kidney Disorders Market for Oral Delivery, 2022-2035
- 10.5.2. Rare Kidney Disorders Market for Intravenous Delivery, 2022-2035
- 10.5.3. Rare Kidney Disorders Market for Subcutaneous Delivery, 2022-2035
- 10.5.4. Rare Kidney Disorders Market for Other Delivery Routes, 2022-2035
- 10.6. Rare Kidney Disorders Market: Analysis by Target Indication, 2022-2035
- 10.6.1. Rare Kidney Disorders Market for Alport Syndrome, 2022-2035
- 10.6.2. Rare Kidney Disorders Market for Atypical Hemolytic Uremic Syndrome, 2022-2035
- 10.6.3. Rare Kidney Disorders Market for C3 Glomerulopathy, 2022-2035
- 10.6.4. Rare Kidney Disorders Market for Cystinosis, 2022-2035
- 10.6.5. Rare Kidney Disorders Market for Cystinuria, 2022-2035
- 10.6.6. Rare Kidney Disorders Market for Dense Deposit Disease, 2022-2035
- 10.6.7. Rare Kidney Disorders Market for Distal Renal Tubular Acidosis, 2022-2035
- 10.6.8. Rare Kidney Disorders Market for Fabry Disease, 2022-2035
- 10.6.9. Rare Kidney Disorders Market for IgA Nephropathy, 2022-2035
- 10.6.10. Rare Kidney Disorders Market for Lupus Nephritis, 2022-2035
- 10.6.11. Rare Kidney Disorders Market for Refractory Gout, 2022-2035
- 10.7. Rare Kidney Disorders Market, 2022-2035: Analysis by Geography
- 10.7.1. Rare Kidney Disorders Market in North America, 2022-2035
- 10.7.2. Rare Kidney Disorders Market in Europe, 2022-2035
- 10.7.3. Rare Kidney Disorders Market in Asia-Pacific, 2022-2035
- 10.7.4. Rare Kidney Disorders Market in Rest of the World, 2022-2035
11. CLINICAL COMMERCIAL ATTRACTIVENESS
- 11.1. Scope and Limitations
- 11.2. Key Assumptions and Methodology
- 11.3.1. Clinical and Commercial Attractiveness Analysis: Atypical Hemolytic Uremic Syndrome
- 11.3.2. Clinical and Commercial Attractiveness Analysis: C3 Glomerulopathy
- 11.3.3. Clinical and Commercial Attractiveness Analysis: Cystinuria
- 11.3.4. Clinical and Commercial Attractiveness Analysis: Dense Deposit Disease
- 11.3.5. Clinical and Commercial Attractiveness Analysis: Fabry Disease
- 11.3.6. Clinical and Commercial Attractiveness Analysis: IgA Nephropathy
- 11.3.7. Clinical and Commercial Attractiveness Analysis: Lupus Nephritis
- 11.3.8. Clinical and Commercial Attractiveness Analysis: Refractory Gout
- 11.3.9. Clinical and Commercial Attractiveness Analysis: Other Target Indications
12. CASE STUDY
- 12.1. Scope and Key Parameters
- 12.2. Rare Kidney Disorders: List of Kidney Care Providers
- 12.3. Rare Kidney Disorders: Advantages of Kidney Care
- 12.4. Rare Kidney Disorders: Future Perspectives
- 12.5. Rare Kidney Disorders: Approach for Recent Initiatives
13. APPENDIX I: TABULATED DATA
14. APPENDIX II: LIST OF COMPANIES AND ORGANIZATIONS