Product Code: GDHC105POA
Human Respiratory Syncytial Virus (RSV) is an enveloped, single-stranded, negative-sense RNA orthopneumovirus belonging to the family of Pneumoviridae. Respiratory Syncytial Virus (RSV) is the leading cause of lower respiratory tract infections (LRTIs) in infants, with a peak age of hospitalization between 2-3 months of age. Severe respiratory disease can manifest as bronchiolitis and pneumonia, which can progress to respiratory failure or death in rare occasions. Respiratory Syncytial Virus (RSV) is also an important cause of hospitalizations and deaths in elderly adults.
The Respiratory Syncytial Virus (RSV) market is expected to grow at a compound annual growth rate (CAGR) of 44.7% from US$36.88m in 2018 to US$1.48bn by 2028 across the five growth markets (*5GM - Australia, India, Japan, South Korea and urban China) in the Asia-Pacific (APAC) region. The main driver of growth will be the launch of new products to prevent medically-significant Respiratory Syncytial Virus (RSV) infections, including the first products to be licensed for Respiratory Syncytial Virus (RSV) in India and urban China.
The level of unmet need in the Respiratory Syncytial Virus (RSV) marketplace is high in India and urban China, where there are currently no prophylactic or therapeutic options. The launch of the first Respiratory Syncytial Virus (RSV) products in 2023 in urban China and 2024 in India is expected to be a strong driver of growth for the 5GM over the forecast period, especially considering the large potential patient populations in these markets.
Research reveals that the current standard of care and only available product for Respiratory Syncytial Virus (RSV), AstraZeneca/AbbVie's Synagis (palivizumab), is likely to be displaced during the forecast period. Synagis is currently the only licensed product in Australia, South Korea and Japan for prevention of Respiratory Syncytial Virus (RSV) infections in young children, but its high price and restrictive label have narrowed its clinical applications to only the highest-risk infants.
In addition, the requirement for five monthly injections of Synagis is a substantial barrier to full patient compliance. Sales of Synagis are expected to drop substantially after the launch of AstraZeneca/Sanofi's pipeline candidate mAb MEDI8897 in 2024, which is projected to reach US$629m in annual revenue by 2028. MEDI8897 will also provide the first prophylactic mAb option for patients in India and urban China.
It is likely that several first-in-class products for the management of Respiratory Syncytial Virus (RSV) will coexist simultaneously by 2028, including both vaccines and antivirals for treatment of severe or breakthrough Respiratory Syncytial Virus (RSV) infections. However, the global impact of new products in reducing the overall Respiratory Syncytial Virus (RSV) burden will depend on the cost-effectiveness of these drugs, as well as how vaccines are eventually integrated into national immunization policies throughout the 5GM - Australia, India, Japan, South Korea and urban China.
The latest research report "Respiratory Syncytial Virus (RSV): Forecast in Asia-Pacific Markets to 2028" helps in answering the following question with regards to Respiratory Syncytial Virus (RSV) and its therapeutic market in Asia Pacific.
- How will the Respiratory Syncytial Virus (RSV) therapeutic market landscape in the 5GM (India, urban China, Australia, South Korea and Japan) change from 2018-2028?
- What are the most promising late-stage pipeline drugs for RSV?
- How do the clinical and commercial attributes of late-stage pipeline therapies compare with one another and against existing treatment options?
- What are the remaining unmet needs in Respiratory Syncytial Virus (RSV) treatment management?
- What drivers and barriers will affect Respiratory Syncytial Virus (RSV) therapeutics sales in the 5GM - Australia, India, Japan, South Korea and urban China over the forecast period?
- Overview of RSV, including epidemiology, etiology, pathophysiology, symptoms, diagnosis, and current management strategies.
- Topline RSV market revenue from 2018-2028. Annual cost of therapy (ACOT) and major pipeline product sales in this forecast period are included.
- Key topics covered include current treatment and prophylactic options, unmet needs and opportunities, and the drivers and barriers affecting RSV therapeutics sales in the 5GM.
- Pipeline analysis: comprehensive data split across different phases, emerging novel trends under development, synopses of innovative early-stage projects, and detailed analysis of late-stage pipeline products.
- Analysis of the current and future market competition in the global RSV therapeutics and prophylactics market. Insightful review of the key industry drivers, restraints and challenges. Each trend is independently researched to provide qualitative analysis of its implications.
Reasons to buy
The report will enable you to -
- 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 Asia-Pacific RSV market.
- Drive revenues by understanding the key trends, innovative products and technologies, market segments, and companies likely to impact the RSV therapeutics 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. Table of Contents
- 1.1 List of Tables
- 1.2 List of Figures
2 Respiratory Syncytial Virus: Executive Summary
- 2.1 Strong Growth Projected for the RSV Market from 2018 to 2028
- 2.2 Both Large and Small Developers Are Focused on the Untapped RSV Therapeutics Market
- 2.3 The Market for Cost-Effective Prophylaxis Is Highly Competitive
- 2.4 Despite Projected Entrance of Novel Products, Opportunities Remain for Current and Future Players
- 2.5 Future RSV Management Strategies Will Include Multiple Products
- 2.6 What Do Physicians Think?
- 3.1 Catalyst
- 3.2 Related Reports
- 3.3 Upcoming Related Reports
4 Disease Overview
- 4.1 Etiology and Pathophysiology
- 4.1.1 Etiology
- 4.1.2 Pathophysiology
- 5.1 Disease Background
- 5.2 Risk Factors and Comorbidities
- 5.3 Global and Historical Trends
- 5.4 Forecast Methodology
- 5.4.1 Sources Used and Not Used
- 5.4.2 Forecast Assumptions and Methods
- 5.5 Epidemiological Forecast for RSV Hospitalized Population (2018-2028)
- 5.5.1 Number of Hospitalized Adults with Positive RSV Test
- 5.5.2 Number of Children Hospitalized for Confirmed RSV
- 5.6 Epidemiological Forecast for RSV Prophylactic Population (2018-2028)
- 5.6.1 Number of Preterm Births by Gestational Age
- 5.6.2 Preterm Infants with CLD
- 5.6.3 Number of Live Births with Hemodynamically Significant Heart Disease
- 5.6.4 Diagnosed Prevalent Cases of DMD
- 5.6.5 Number of Diagnosed Prevalent Cases of SMA
- 5.6.6 Number of Third Trimester Pregnant Women
- 5.6.7 Number of Adults Living in Nursing Homes/Long-Term Care Institutions
- 5.7 Discussion
- 5.7.1 Epidemiological Forecast Insight
- 5.7.2 Limitations of Analysis
- 5.7.3 Strengths of Analysis
6 Current Treatment Options
7 Unmet Needs and Opportunity Assessment in Asia-Pacific
- 7.1 Overview
- 7.2 Improved Cost-Effective Passive Prophylaxis
- 7.3 Prophylactic Vaccines
- 7.4 Effective Antivirals
8 R&D Strategies in Asia-Pacific
- 8.1 Overview
- 8.1.1 Leveraging Novel Vaccine Technologies and Strategies
- 8.1.2 Development of Prophylactic Antibodies with Improved Dosing and Efficacy
- 8.1.3 Development of RSV Antiviral Therapeutics with Diverse Mechanisms of Action
- 8.2 Clinical Trials Design
- 8.2.1 Clinical Trials Design of Pipeline Prophylactics for Maternal Immunization
- 8.2.2 Clinical Trials Design of Pipeline Prophylactics for Pediatric Immunization
- 8.2.3 Clinical Trials Design of Pipeline Prophylactics for Adult Immunization
- 8.2.4 Demonstration of Efficacy for Fusion Inhibitor Antivirals
- 8.2.5 Demonstration of Efficacy for Replication Inhibitor Antivirals
9 Pipeline Assessment in Asia-Pacific
- 9.1 Overview
- 9.2 Innovative Early-Stage Approaches
- 9.3 Other Drugs in Development
10 Pipeline Valuation Analysis