The UK Cough Hypersensitivity Syndrome Therapeutics Market was valued at $211 Mn in 2022 and is predicted to grow at a CAGR of 3.9% from 2023 to 2030, to $286 Mn by 2030. The key drivers of this industry include the rising prevalence of Cough Hypersensitivity Syndrome, the evolving treatment landscape, and supportive regulatory policies. The industry is primarily dominated by players such as Johnson & Johnson, GSK, Merck, Novartis, AstraZeneca, and Pfizer among others.
The UK Cough Hypersensitivity Syndrome Therapeutics Market is at around $211 Mn in 2022 and is projected to reach $286 Mn in 2030, exhibiting a CAGR of 3.9% during the forecast period.
Cough Hypersensitivity Syndrome (CHS) is characterized by an elevated proclivity to cough in response to minor stimuli, including changes in temperature, mechanical factors, or exposure to specific chemicals. Underlying causes of CHS include conditions such as asthma, upper airway cough syndrome (UACS), gastroesophageal reflux disease (GERD), allergic or nonallergic rhinitis, chronic obstructive pulmonary disease (COPD), and pulmonary fibrosis. Risk factors for CHS involve an increased sensitivity to cough-inducing stimuli like citric acid or capsaicin, as well as sensations in the larynx or chest. Treatment options for CHS encompass various approaches, including antitussive agents, inhaled corticosteroids (ICS), short-acting beta2-agonists (SABA), anticholinergics, antihistamines, P2X3 receptor antagonists, and neurokinin-1 receptor antagonists. Leading pharmaceutical companies involved in the production of CHS treatments include Johnson & Johnson, Bayer AG, Teva Canada Limited, GlaxoSmithKline plc, Pfizer, Novartis, and AstraZeneca. These companies play a pivotal role in developing and marketing therapeutics for CHS, with ongoing research and development focused on innovative pharmacological approaches, such as P2X3 receptor antagonists and neurokinin-1 receptor antagonists.
The estimated prevalence of chronic cough is around 6% of the population in the UK. Key drivers for market growth comprise the growing prevalence of Cough Hypersensitivity Syndrome and subsequently its risk factors like smoking and pollution, the evolving treatment landscape, and supportive regulatory policies. However, conditions such as treatment challenges and off-label therapeutics, limited disease understanding, and market fragmentation impede the growth and potential of the market.
Market Growth Drivers
Rising prevalence of Cough Hypersensitivity Syndrome and contributing conditions: More than 6% of the population in the UK suffers from chronic cough and around 20% of individuals experiencing chronic cough are estimated to be affected by CHS. It often coexists with other long-term respiratory disorders such as asthma, chronic obstructive pulmonary disease (COPD), and allergic rhinitis, which have a high prevalence in the UK. Smoking remains a significant risk factor for both CHS and chronic respiratory illnesses, and a sizable portion of the population continues to smoke, adding to the demand for CHS treatments.
Evolving treatment landscape: The gap in available solutions provides an opportunity for the development of new, effective treatments. Pharmaceutical companies are developing innovative CHS therapies that target a variety of molecular pathways, which have an opportunity to boost market growth.
Supportive regulatory environment: Efficient regulatory processes for innovative CHS treatments help them get to market faster, boosting growth. Supportive National Health Service (NHS) payment policies for successful CHS treatments have the potential to improve patient access while also contributing to the market's long-term development.
Market Restraints
Treatment challenges and Off-label use: No drug is officially licensed for CHS. Physicians often prescribe drugs off-label, which raises concerns about efficacy and safety. The therapy options are limited, with inhaled corticosteroids and antitussives being eligible only for some patients. The diversity in CHS presentations among patients necessitates personalized treatment plans, adding complexity that can impede the establishment of standardized approaches to treatment and hinder market expansion.
Limited disease understanding and underdiagnosis: Diagnosing CHS can be difficult due to symptoms that overlap with other respiratory conditions such as asthma and gastroesophageal reflux disease (GERD). Healthcare professionals' limited awareness of CHS may result in misdiagnosis and delayed treatment. The absence of a specific and universally accepted diagnostic test further adds complexity to achieving accurate diagnoses.
Market fragmentation: The market for CHS therapeutics is compact and controlled, with a handful of key companies holding a significant market share. This restricted competition has the potential to impede innovation and could result in elevated treatment expenses. Pharmaceutical firms might prioritize research and development initiatives for more widespread respiratory conditions, resulting in fewer specialized treatment options for CHS.
In the UK, the main regulatory body overseeing the approval and licensure of drugs and pharmaceuticals is the Medicines and Healthcare Products Regulatory Agency (MHRA). The MHRA operates independently as an executive agency of the Department of Health and Social Care. Its primary responsibility is to ensure the safety, quality, and efficacy of medicines and medical devices. The regulatory process involves a thorough evaluation of scientific and clinical data submitted by manufacturers to determine whether a product meets the necessary standards for approval.
The process of obtaining licensure for drugs and pharmaceuticals in the UK typically involves several stages. First, manufacturers submit a comprehensive application to the MHRA. The MHRA then conducts a rigorous assessment to ensure that the product is safe, effective, and of high quality. If the evaluation is successful, the MHRA grants marketing authorization, allowing the product to be legally marketed and sold in the UK. Throughout the product lifecycle, the MHRA continues to monitor safety and may take regulatory action if new risks emerge.
The regulatory environment for new entrants is stringent, requiring compliance with strict standards and thorough documentation to ensure the safety and efficacy of pharmaceutical products entering the market.
Key Players
1. Executive Summary
1.1 Disease Overview
1.2 Global Scenario
1.3 Country Overview
1.4 Healthcare Scenario in Country
1.5 Patient Journey
1.6 Health Insurance Coverage in Country
1.7 Active Pharmaceutical Ingredient (API)
1.8 Recent Developments in the Country
2. Market Size and Forecasting
2.1 Epidemiology of Disease
2.2 Market Size (With Excel & Methodology)
2.3 Market Segmentation (Check all Segments in Segmentation Section)
3. Market Dynamics
3.1 Market Drivers
3.2 Market Restraints
4. Competitive Landscape
4.1 Major Market Share
4.2 Key Company Profile (Check all Companies in the Summary Section)
4.2.1 Company
4.2.1.1 Overview
4.2.1.2 Product Applications and Services
4.2.1.3 Recent Developments
4.2.1.4 Partnerships Ecosystem
4.2.1.5 Financials (Based on Availability)
5. Reimbursement Scenario
5.1 Reimbursement Regulation
5.2 Reimbursement Process for Diagnosis
5.3 Reimbursement Process for Treatment
6. Methodology and Scope
By Drug Class
By Route of Administration
By End Users
By Distribution Channel
Methodology for Database Creation
Our database offers a comprehensive list of healthcare centers, meticulously curated to provide detailed information on a wide range of specialties and services. It includes top-tier hospitals, clinics, and diagnostic facilities across 30 countries and 24 specialties, ensuring users can find the healthcare services they need.
Additionally, we provide a comprehensive list of Key Opinion Leaders (KOLs) based on your requirements. Our curated list captures various crucial aspects of the KOLs, offering more than just general information. Whether you're looking to boost brand awareness, drive engagement, or launch a new product, our extensive list of KOLs ensures you have the right experts by your side. Covering 30 countries and 36 specialties, our database guarantees access to the best KOLs in the healthcare industry, supporting strategic decisions and enhancing your initiatives.
How Do We Get It?
Our database is created and maintained through a combination of secondary and primary research methodologies.
1. Secondary Research
With many years of experience in the healthcare field, we have our own rich proprietary data from various past projects. This historical data serves as the foundation for our database. Our continuous process of gathering data involves:
With extensive experience in the field, we have developed a proprietary GenAI-based technology that is uniquely tailored to our organization. This advanced technology enables us to scan a wide array of relevant information sources across the internet. Our data-gathering process includes:
2. Primary Research
To complement and validate our secondary data, we engage in primary research through local tie-ups and partnerships. This process involves:
Combining Secondary and Primary Research
By integrating both secondary and primary research methodologies, we ensure that our database is comprehensive, accurate, and up-to-date. The combined process involves:
Through this meticulous process, we create a final database tailored to each region and domain within the healthcare industry. This approach ensures that our clients receive reliable and relevant data, empowering them to make informed decisions and drive innovation in their respective fields.
We value your inquiry and offer free customization with every report to fulfil your exact research needs.