Complement 3 Glomerulopathy Market Insight, Epidemiology And Market Forecast - 2034

Complement 3 Glomerulopathy Market Insight, Epidemiology And Market Forecast - 2034



Key Highlights

Diamond-Blackfan anemia (DBA) is a rare genetic disorder that primarily affects the bone marrow's ability to produce red blood cells, leading to severe anemia. It is usually diagnosed in infancy or early childhood, with symptoms like pale skin, fatigue, poor growth, and physical abnormalities such as thumb deformities or heart defects in some cases.

In 2023, approximately 7,870 diagnosed cases of Diamond-Blackfan Anemia were reported across the seven major markets (7MM), with the United States representing about 70% of these cases. This prevalence is projected to grow at a compound annual growth rate (CAGR) of XX% during the study period 2020-2034.

In 2023, Germany reported the highest number of Diamond-Blackfan Anemia cases among the EU4 countries and the UK, followed by the UK, which accounted for 20% of the total diagnosed prevalent cases in these regions.

In the United States, a substantial proportion of Diamond-Blackfan Anemia cases reported in 2023, approximately 46%, were associated with mutations in the RPS19 gene. This high prevalence is linked to the gene's significant role in ribosomal protein synthesis.

Several congenital anomalies are commonly associated with Diamond-Blackfan Anemia, with craniofacial and musculoskeletal anomalies being the most prevalent. Notably, craniofacial anomalies were observed in over 30% of DBA patients across the 7MM in the year 2023.

Despite the significant impact of DBA on the patients’ health, no FDA-approved treatments currently exist for the condition. Management primarily involves the use of corticosteroids combinations, chronic blood transfusions, iron chelation, and potentially curative hematopoietic stem cell transplantation (HSCT). In 2023, corticosteroids dominated the therapeutic landscape for DBA, generating USD 1.1 million in revenue, surpassing other treatment options for first line of therapy.

DelveInsight's “Diamond Blackfan Anemia – Market Insights, Epidemiology and Market Forecast – 2034” report delivers an in-depth understanding of the indication Diamond Blackfan Anemia, historical and forecasted epidemiology as well as the Diamond Blackfan Anemia market trends in the United States, EU4 (Germany, Spain, Italy, and France) and the United Kingdom, and Japan.

The Diamond Blackfan Anemia market report provides real-world prescription pattern analysis, approved drugs, market share of individual therapies, and historical and forecasted 7MM Diamond Blackfan Anemia market size from 2020 to 2034. The report also covers current Diamond Blackfan Anemia treatment practices/algorithms and unmet medical needs to curate the best opportunities and assess the market’s underlying potential.

Geography Covered

The United States

EU4 (Germany, France, Italy, and Spain) and the United Kingdom

Japan

Diamond Blackfan Anemia Understanding and Treatment Algorithm

Diamond Blackfan Anemia Overview, Country-Specific Treatment Guidelines and Diagnosis

Diamond-Blackfan anemia (DBA) is a rare inherited bone marrow failure disorder, primarily affecting red blood cell production. It is typically diagnosed in infancy or early childhood, with affected individuals presenting with severe anemia, pale skin, fatigue, and often failure to thrive. In addition to hematologic symptoms, about half of those with DBA also exhibit congenital abnormalities such as thumb malformations, craniofacial deformities, or heart defects. The disorder is linked to mutations in ribosomal protein genes, which are essential for the production of ribosomes, the cell structures responsible for synthesizing proteins. These mutations disrupt red blood cell development, leading to the characteristic anemia. Although the majority of DBA cases are inherited in an autosomal dominant pattern, some occur sporadically without a family history.

Diagnosis of DBA involves a combination of clinical presentation, laboratory tests, and genetic analysis. Blood tests reveal a low red blood cell count (macrocytic anemia), along with normal or slightly elevated white blood cell and platelet counts. A hallmark of DBA is elevated erythrocyte adenosine deaminase (eADA) activity. Bone marrow biopsy usually shows a reduction or absence of red blood cell precursors, while other blood cell lineages remain normal. Genetic testing is used to confirm mutations in genes responsible for DBA, such as RPS19, which is implicated in about quarter of cases. Early and accurate diagnosis is critical to managing the condition effectively and preventing long-term complications.

Further details related to country-based variations in diagnosis are provided in the report

Diamond Blackfan Anemia Treatment

Treatment for DBA focuses on managing anemia and maintaining normal red blood cell levels. The first line of treatment often includes corticosteroids, such as prednisone, which can stimulate the production of red blood cells in about 80% of patients. However, long-term use of steroids can lead to significant side effects, including stunted growth, bone thinning, and immune suppression. For patients who do not respond to steroids or cannot tolerate them, regular blood transfusions are necessary to maintain adequate hemoglobin levels. Over time, repeated transfusions can lead to iron overload, which is managed with iron chelation therapy. For severe cases, bone marrow or stem cell transplantation may be considered, offering the only potential cure for DBA. However, this procedure carries risks and is generally reserved for patients with life-threatening anemia or severe complications. Lifelong monitoring is essential to manage treatment-related complications and the increased risk of leukemia or other cancers associated with DBA.

Diamond Blackfan Anemia Epidemiology

The Diamond Blackfan Anemia epidemiology chapter in the report provides historical as well as forecasted incidence in the 7MM covering the United States, EU4 countries (Germany, France, Italy, and Spain), the United Kingdom, and Japan from 2024 to 2034. The Diamond Blackfan Anemia epidemiology is segmented with detailed insights into:

Total Diagnosed Prevalent Cases of Diamond Blackfan Anemia in the 7MM [2020-2034]

Cases of DBA by Mutated Gene in the 7MM [2020-2034].

Cases of DBA by Congenital Anomaly in the 7MM [2020-2034]

Total Treated Cases of DBA in the 7MM [2020-2034]

Key Epidemiological Highlights

In 2023, approximately 7,870 diagnosed cases of Diamond-Blackfan Anemia were reported across the seven major markets (7MM), with the United States representing about 70% of these cases. This prevalence is projected to grow at a compound annual growth rate (CAGR) of XX% through 2034.

In 2023, Germany reported the highest number of Diamond-Blackfan Anemia cases among the EU4 countries and the UK, followed by the UK, which accounted for 20% of the total diagnosed prevalent cases in these regions.

In the United States, a substantial proportion of Diamond-Blackfan Anemia cases reported in 2023, approximately 46%, were associated with mutations in the RPS19 gene. This high prevalence is linked to the gene's significant role in ribosomal protein synthesis.

Several congenital anomalies are commonly associated with Diamond-Blackfan Anemia, with craniofacial and musculoskeletal anomalies being the most prevalent. Notably, craniofacial anomalies are observed in over 30% of DBA patients across the seven major markets (7MM).

In 2023, 50% of Diamond-Blackfan Anemia patients in the United States advanced to second-line treatments after initially receiving first-line therapy indicating corticosteroids may become less effective over time.

Diamond Blackfan Anemia Market Outlook

Diamond-Blackfan Anemia (DBA) current treatment landscape includes glucocorticosteroids, blood transfusions, and hematopoietic stem cell transplantation (HSCT). However, each of these therapies faces limitations: steroid resistance, iron overload, and transplantation risks. The United States leads the 7MM (United States, Europe, and Japan) market for Diamond-Blackfan Anemia, driven by its large patient population and opportunities for innovation. In 2023, the total market size for Diamond-Blackfan Anemia was USD 1.56 million in the 7MM and is projected to increase with a CAGR of XX% by 2034.

The United States represents the largest share of the Diamond Blackfan Anemia market, accounting for a significant proportion compared to the EU4 (Germany, Spain, Italy, France), the United Kingdom, and Japan.

Among EU4 and the UK, the Germany had the largest market size accounting for approximately USD 0.06 million, followed by the United Kingdom, with XX having the smallest market size in 2023.

As no FDA-approved therapies currently exist and no emerging players are addressing this gap, there is a substantial opportunity for new, effective treatments, such as gene therapy, to make a significant impact and meet the needs of DBA patients.

In 2023, corticosteroids dominated the therapeutic landscape for DBA, generating USD 1.1 million in revenue, surpassing other treatment options such as red blood cell transfusions and hematopoietic stem cell transplantation.

Drug Uptake

This section focuses on the uptake rate of potential drugs expected to be launched in the market during 2024–2034, which depends on the competitive landscape, safety, and efficacy data along with order of entry. It is important to understand that the key players evaluating their novel therapies in the pivotal and confirmatory trials should remain vigilant when selecting appropriate comparators to stand the greatest chance of a positive opinion from regulatory bodies, leading to approval, smooth launch, and rapid uptake.

Pipeline Development Activities

This section covers information on collaborations, acquisitions and mergers, licensing, and patent details for emerging therapies.

KOL Views

To keep up with the real-world scenario in current market trends, we take opinions from Key Industry leaders working in the domain through primary research to fill the data gaps and validate our secondary research. Industry Experts were contacted for insights on the evolving treatment landscape, patient reliance on conventional therapies, patient therapy switching acceptability, and drug uptake along with challenges related to accessibility.

DelveInsight’s analysts connected with 10+ KOLs to gather insights; however, interviews were conducted with 5+ KOLs in the 7MM. Their opinion helps understand and validate current treatment patterns of Diamond Blackfan Anemia. This will support the clients in potential upcoming novel treatments by identifying the overall scenario of the market and the unmet needs.

Qualitative Analysis

We perform Qualitative and market Intelligence analysis using various approaches, such as SWOT analysis and Conjoint Analysis. In the SWOT analysis, strengths, weaknesses, opportunities, and threats in terms of gaps in disease diagnosis, patient awareness, physician acceptability, competitive landscape, cost-effectiveness, and geographical accessibility of therapies are provided.

Conjoint Analysis analyzes multiple approved therapies based on relevant attributes such as safety, efficacy, frequency of administration, route of administration, and order of entry. Scoring is given based on these parameters to analyze the effectiveness of therapy.

In efficacy, the trial’s primary and secondary outcome measures are evaluated; for instance, in event-free survival, one of the most important primary outcome measures is event-free survival and overall survival.

Further, the therapies’ safety is evaluated wherein the acceptability, tolerability, and adverse events are majorly observed, and it sets a clear understanding of the side effects posed by the drug in the trials. In addition, the scoring is also based on the probability of success, and the addressable patient pool for each therapy.

Market Access and Reimbursement

The section provides detailed insights on the country-wise accessibility and reimbursement scenarios, cost-effectiveness scenario of currently used therapies, programs making accessibility easier and out-of-pocket costs more affordable, insights on patients insured under federal or state government prescription drug programs, etc.

Scope of the Report

The report covers a segment of key events, an executive summary, descriptive overview of Diamond Blackfan Anemia, explaining its causes, signs and symptoms, pathogenesis, and currently available therapies.

Comprehensive insight has been provided into the epidemiology segments and forecasts, the future growth potential of diagnosis rate, and disease progression along with country specific treatment guidelines.

Additionally, an all-inclusive account of the current therapies, along with the elaborative profiles of prominent therapies and how will they have an impact on the current treatment landscape.

A detailed review of the Diamond Blackfan Anemia market, historical and forecasted market size, market share by therapies, detailed assumptions, and rationale behind our approach is included in the report, covering the 7MM drug outreach.

The report provides an edge while developing business strategies, by understanding trends, through SWOT analysis and expert insights/KOL views, patient journey, and treatment preferences that help in shaping and driving the 7MM Diamond Blackfan Anemia.

Diamond Blackfan Anemia Report Insights

Patient Population

Therapeutic Approaches

Diamond Blackfan Anemia Market Size and Trends

Existing and future Market Opportunity

Diamond Blackfan Anemia Report Key Strengths

Eleven Years Forecast

7MM Coverage

Diamond Blackfan Anemia Epidemiology Segmentation

Inclusion of Country specific treatment guidelines

KOL’s feedback on approved therapies

Conjoint analysis

Drugs Uptake and Key Market Forecast Assumptions

Diamond Blackfan Anemia Report Assessment

Current Treatment Practices

Unmet Needs

Pipeline Product Profiles

Market Attractiveness

Qualitative Analysis (SWOT and Conjoint Analysis)

FAQs

What is the growth rate of the 7MM Diamond Blackfan Anemia treatment market?

What was the Diamond Blackfan Anemia total market size, the market size by therapies, market share (%) distribution in 2020, and what would it look like in 2034? What are the contributing factors/key catalysts for this growth?

Is there any unexplored patient setting that can open the window for growth in the future?

What are the pricing variations among different geographies for approved and off-label therapies?

How would the market drivers, barriers, and future opportunities affect the market dynamics and subsequent analysis of the associated trends?

What are the current options for the treatment of Diamond Blackfan Anemia?

What are the recent novel therapies, targets, mechanisms of action, and technologies developed to overcome the limitations of existing therapies?

Patient acceptability in terms of preferred treatment options as per real-world scenarios?

What are the country-specific accessibility issues of expensive, recently approved therapies?

Reasons to buy

The report will help in developing business strategies by understanding the latest trends and changing treatment dynamics driving the Diamond Blackfan Anemia Market.

Insights on patient burden/disease incidence, evolution in diagnosis, and factors contributing to the change in the epidemiology of the disease during the forecast years

Understand the existing market opportunities in varying geographies and the growth potential over the coming years.

Distribution of historical and current patient share based on real-world prescription data along with reported sales of approved products in the US, EU4 (Germany, France, Italy, and Spain), the United Kingdom, and Japan.

Highlights of access and reimbursement policies of therapies, barriers to accessibility of expensive off-label therapies, and patient assistance programs.

To understand Key Opinion Leaders’ perspectives around the accessibility, acceptability, and compliance-related challenges of existing treatment to overcome barriers in the future.

Detailed insights on the unmet needs of the existing market so that the upcoming players can strengthen their development and launch strategy.


1. Key Insights
2. Report Introduction
3. Executive Summary Of Complement 3 Glomerulopathy
4. Complement 3 Glomerulopathy Market Overview At A Glance
4.1. Market Share By Therapies (%) Distribution Of C3g In 2020 In The 7mm
4.2. Market Share By Therapies (%) Distribution Of C3g In 2034 In The 7mm
5. Key Events
6. Epidemiology And Market Forecast Methodology
7. Disease Background And Overview
7.1. Introduction
7.2. Familiar Forms Of C3g
7.2.1. Cfhr5 Nephropathy
7.2.2. Other Familiar Forms Of C3g
7.2.3. Dense Deposit Disease (Ddd)
7.2.4. Complement 3 Glomerulonephritis (C3gn)
7.3. Causes And Risk Factors
7.3.1. Genetic Or Hereditary Risk Factors
7.3.2. Acquired Risk Factors
7.4. Clinical Presentation
7.5. Histological Patterns
7.6. Symptoms
7.7. Pathophysiology
7.8. Pathogenesis
7.9. Diagnosis
7.10. Challenges In Diagnosis
7.10.1. Immune Complex Glomerulonephritis
7.10.2. Post-infectious Glomerulonephritis
7.10.3. Predictors Of Progression
7.11. Differential Diagnosis
7.12. Prognosis
8. Treatment
8.1. Algorithm For Diagnosis And Management Of C3g
9. Clinical Practice Guideline For The Management Of Glomerular Diseases: Kdigo 2021
9.1. Complement 3 Glomerulopathy
10. Epidemiology And Patient Population
10.1. Key Findings
10.2. Assumptions And Rationales
10.3. Total Diagnosed Prevalent Population Of C3g In The 7mm
10.4. The United States
10.4.1. Total Diagnosed Prevalent Population Of C3g In The United States
10.4.2. Type-specific Diagnosed Prevalent Population Of C3g In The United States
10.4.3. Age-specific Diagnosed Prevalent Population Of C3g In The United States
10.5. Eu4 And The Uk
10.5.1. Total Diagnosed Prevalent Population Of C3g In Eu4 And The Uk
10.5.2. Type-specific Diagnosed Prevalent Population Of C3g In Eu4 And The Uk
10.5.3. Age-specific Diagnosed Prevalent Population Of C3g In Eu4 And The Uk
10.6. Japan
10.6.1. Total Diagnosed Prevalent Population Of C3g In Japan
10.6.2. Type-specific Diagnosed Prevalent Population Of C3g In Japan
10.6.3. Age-specific Diagnosed Prevalent Population Of C3g In Japan
11. Patient Journey
12. Emerging Therapies
12.1. Key Cross
12.2. Iptacopan (Lnp023): Novartis Pharmaceuticals
12.2.1. Product Description
12.2.2. Other Developmental Activities
12.2.3. Clinical Development
12.2.4. Safety And Efficacy
12.3. Pegcetacoplan (Apl-2): Apellis Pharmaceuticals
12.3.1. Product Description
12.3.2. Other Developmental Activities
12.3.3. Clinical Development
12.3.4. Safety And Efficacy
13. Complement 3 Glomerulopathy (C3g): Seven Major Market Analysis
13.1. Key Findings
13.2. Total Market Size Of C3g In The 7mm
13.3. Market Outlook
13.4. Conjoint Analysis
13.5. Key Market Forecast Assumptions
13.6. The United States Market Size
13.6.1. Total Market Size Of C3g In The United States
13.6.2. Market Size Of C3g By Therapies In The United States
13.7. Eu4 And The Uk Market Size
13.7.1. Total Market Size Of C3g In Eu4 And The Uk
13.7.2. Market Size Of C3g By Therapies In Eu4 And The Uk
13.8. Japan Market Size
13.8.1. Total Market Size Of C3g In Japan
13.8.2. Market Size Of C3g By Therapies In Japan
14. Unmet Needs
15. Swot Analysis
16. Kol Views
17. Market Access And Reimbursement
17.1. United States
17.1.1. Centre For Medicare And Medicaid Services (Cms)
17.2. Eu4 And The Uk
17.2.1. Germany
17.2.2. France
17.2.3. Italy
17.2.4. Spain
17.2.5. United Kingdom
17.3. Japan
17.3.1. Mhlw
17.4. Complement 3 Glomerulopathy (C3g): Market Access And Reimbursement
17.4.1. Patient Access Programs
17.4.2. Hta Decisions
18. Appendix
18.1. Bibliography
18.2. Report Methodology
19. Delveinsight Capabilities
20. Disclaimer
21. About Delveinsight

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