USD 5.30 billion
Report ID:
SQMIG35I2224 |
Region:
Global |
Published Date: March, 2024
Pages:
219
|Tables:
62
|Figures:
75
Global Cystic Fibrosis Therapeutics Market size was valued at around USD 5.30 billion in 2022 and is expected to rise from USD 6.02 billion in 2023 to reach a value of USD 16.57 Billion by 2031, at a CAGR of 13.50% over the forecast period (2024-2031).
One of the important factors boosting the demand for cystic fibrosis treatments during the forecast period is the rising prevalence of cystic fibrosis (CF) combined with the rising treatment rate. Furthermore, an increase in R&D financing by both private and governmental organizations, an increase in the number of projects performed by nonprofit organizations, and the availability of favorable reimbursement policies represent a few of the critical aspects projected to drive the marketplace in years to come.
Increased year-on-year patient growth results in increased demand for effective and efficient CF therapies. Cystic fibrosis Transmembrane Conductivity Regulator (CFTR) modulators, bronchodilators, mucolytic medications, anti-infective, antibiotics (oral, breathed in, or parents feeding formulae), anti-inflammatory medications, and pancreatic enzyme supplements are just a few of the readily accessible approved drug classes.
One of the critical aspects projected to drive market expansion is the increasing number of medication compositions in the pipelines of the leading players. Furthermore, a growing number of studies conducted to extend its target client base with its existing therapeutic portfolio is one of the market's drivers. Increasing R&D activities are projected to drive market expansion.
The presence of various charitable organizations such as CF Worldwide, Cystic Fibrosis Organization, Cystic Fibrosis Canada as well, South African Cystic Fibrosis confidence, and South African Cystic Fibrosis Organization, that are consistently involved in CF-related activities, is another important factor that can account for promoting growth of the cystic fibrosis therapeutics market. These organizations are investing large sums of money to find various therapies for CF and to assist major actors' research and development operations.
Global Market Size
USD 5.30 billion
Largest Segment
Oral drugs
Fastest Growth
Oral drugs
Growth Rate
13.50% CAGR
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The global cystic fibrosis therapeutics market is segmented based on drug class, route of administration, and region. In terms of drug class, the market is segmented into CFTR modulators, mucolytics, pancreatic enzyme supplements, and bronchodilators. With respect to route of administration, the market is segmented into oral drugs, and inhaled drugs. Based on region, the global cystic fibrosis therapeutics market is segmented into North America, Europe, Asia-Pacific, South America, and MEA.
Global Cystic Fibrosis Therapeutics Market Analysis by Route of Administration
The oral category dominated the market's expansion in 2022 and is predicted to be the fastest-growing industry during the forecast period, 2023-2030, due to the ease and convenience of eating medications. If novel formulations of drugs that may be conveniently administered without the risk of invasive techniques become available, oral medication forms may lose market share to alternative form types, such as inhaled medications.
Global Cystic Fibrosis Therapeutics Market Analysis by Drug Class
The cystic fibrosis (CF) market revenue was driven by CFTR modulators in 2022 and is predicted to grow at the quickest rate during the forecast period, 2022-2030.This is explained by a rise in the treatment of CF using these medicines. These drugs are currently widely employed to treat CF, and more CFTR treatments are now being studied in clinical trials. The primary purpose of these drugs is to help people live longer lives.
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Asia Pacific had the largest cystic fibrosis market share in 2022 and is further expected to continue the same during the forecast period. The number of patients within the area is increasing and the urban lifestyle becomes more popular. This, together with increased healthcare spending, will most likely drive the APAC market. Furthermore, China's cystic fibrosis market had the highest market share, while India's cystic fibrosis market is the fastest expanding in the area.
Europe is expected to grow at the fastest CAGR from 2022 to 2030, owing to a rise in cystic fibrosis prevalence. Rising government backing for creativity, as well as increased funding for programs to research and develop innovative CF therapies, are driving market expansion in this sector. The United Kingdom provides the most money because of the significant incidence of the illness in this part of the world. In addition, the UK cystic fibrosis market has the largest share of the market, while the nation of Germany's cystic fibrosis industry was also the region's fastest growing.
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Global Cystic Fibrosis Therapeutics Market Drivers
Increasing Prevalence of Cystic Fibrosis
Growing Demand for Personalized Medicine
Global Cystic Fibrosis Therapeutics Market Restraints
High Cost of Cystic Fibrosis Therapies
Limited Patient Pool
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The cystic fibrosis therapeutics market competition consists of respiratory device manufacturers as well as standalone cystic fibrosis therapeutics producers. New technical advancements, such as the use of artificial intelligence, will generate growth prospects for new market entrants. For example, NuvoAir, a Swedish health care firm, created a digital platform that allows customers to perform at-home lung function tests. Companies are battling for market share, particularly in nations with advanced technology such as the United Kingdom, Germany, and the United States. Acquisitions and cooperation amongst market participants to strengthen their position have occurred. This is projected to increase market competition over the projection period.
Top Player’s Company Profiles in Global Cystic Fibrosis Therapeutics Market
Recent Developments
In May 2023, the Cystic Fibrosis Foundation announced the success of their $1 billion fund raise with the purpose of new treatment research for cystic fibrosis. The funding will support research into gene editing, gene therapy, and other promising new technologies.
In April 2023, Vertex Pharmaceuticals announced that it has entered into a collaboration with CRISPR Therapeutics to develop gene editing therapies for cystic fibrosis. The collaboration will focus on developing CRISPR-based therapies that target the underlying genetic defects that cause cystic fibrosis.
In March 2023, AbbVie announced that the FDA granted fast track designation to its investigational drug ABBV-555 for the treatment of cystic fibrosis. ABBV-555 is a small molecule corrector that is designed to target the G551D mutation, the second most common mutation that causes cystic fibrosis.
In February 2023, Shionogi announced that the FDA granted orphan drug designation to its investigational drug SHP616 for the treatment of cystic fibrosis. SHP616 is a small molecule corrector that is designed to target the F508del mutation, the most common mutation that causes cystic fibrosis.
In January 2023, Vertex Pharmaceuticals announced that the FDA approved Trikafta (elexacaftor/ivacaftor/tezacaftor), a triple combination therapy for the treatment of cystic fibrosis in patients 12 years of age and older. Trikafta is the first and only triple combination therapy for cystic fibrosis and has been shown to significantly improve lung function and quality of life in patients.
In October 2021, Vertex Pharmaceuticals announced that the European Medicines Agency (EMA) had accepted the Marketing Authorization Application (MAA) for their investigational triple combination therapy for cystic fibrosis, VX-121/tezacaftor/ivacaftor.
In August 2021, Vertex Pharmaceuticals received approval from the U.S. Food and Drug Administration (FDA) for their triple combination therapy, Trikafta, for patients with cystic fibrosis ages 6 through 11 who have at least one F508del mutation.
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According to our global cystic fibrosis therapeutics market analysis, one of the important factors expected to drive demand for these treatments is the rising prevalence of cystic fibrosis (CF) combined with the rising treatment rate. Furthermore, an increase in R&D financing by both private and governmental organizations, an increase in the number of projects performed by nonprofit organizations, and the availability of favorable reimbursement policies represent a few of the critical aspects projected to drive the marketplace in years to come.
Report Metric | Details |
---|---|
Market size value in 2022 | USD 5.30 billion |
Market size value in 2031 | USD 16.57 Billion |
Growth Rate | 13.50% |
Base year | 2023 |
Forecast period | 2024-2031 |
Forecast Unit (Value) | USD Billion |
Segments covered |
|
Regions covered | North America (US, Canada), Europe (Germany, France, United Kingdom, Italy, Spain, Rest of Europe), Asia Pacific (China, India, Japan, Rest of Asia-Pacific), Latin America (Brazil, Rest of Latin America), Middle East & Africa (South Africa, GCC Countries, Rest of MEA) |
Companies covered |
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Customization scope | Free report customization with purchase. Customization includes:-
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Executive Summary
Market overview
Parent Market Analysis
Market overview
Market size
KEY MARKET INSIGHTS
COVID IMPACT
MARKET DYNAMICS & OUTLOOK
Market Size by Region
KEY COMPANY PROFILES
For the Cystic Fibrosis Therapeutics Market, our research methodology involved a mixture of primary and secondary data sources. Key steps involved in the research process are listed below:
1. Information Procurement: This stage involved the procurement of Market data or related information via primary and secondary sources. The various secondary sources used included various company websites, annual reports, trade databases, and paid databases such as Hoover's, Bloomberg Business, Factiva, and Avention. Our team did 45 primary interactions Globally which included several stakeholders such as manufacturers, customers, key opinion leaders, etc. Overall, information procurement was one of the most extensive stages in our research process.
2. Information Analysis: This step involved triangulation of data through bottom-up and top-down approaches to estimate and validate the total size and future estimate of the Cystic Fibrosis Therapeutics Market.
3. Report Formulation: The final step entailed the placement of data points in appropriate Market spaces in an attempt to deduce viable conclusions.
4. Validation & Publishing: Validation is the most important step in the process. Validation & re-validation via an intricately designed process helped us finalize data points to be used for final calculations. The final Market estimates and forecasts were then aligned and sent to our panel of industry experts for validation of data. Once the validation was done the report was sent to our Quality Assurance team to ensure adherence to style guides, consistency & design.
Customization Options
With the given market data, our dedicated team of analysts can offer you the following customization options are available for the Cystic Fibrosis Therapeutics Market:
Product Analysis: Product matrix, which offers a detailed comparison of the product portfolio of companies.
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Competitive Analysis: Detailed analysis and profiling of additional Market players & comparative analysis of competitive products.
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Innovation Mapping: Identify racial solutions and innovation, connected to deep ecosystems of innovators, start-ups, academics, and strategic partners.
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Report ID: SQMIG35I2224
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