UK Anemia Drugs Market Analysis

UK Anemia Drugs Market Analysis


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The UK Anemia drugs market was valued at $415 Mn in 2022 and is estimated to expand at a CAGR of 6.9% from 2022-30 and will reach $709 Mn in 2030. One of the main reasons propelling the growth of this market is the introduction of newer technologies, driving demand for anemia drugs. The market is segmented by type, drug, and distribution channel. Some key players in this market are Pfizer, Roche, Amgen, GlaxoSmithKline, Johnson & Johnson, Alcon Laboratories, FibroGen, Vifor Pharma Group, and Akebia Therapeutics among others.

ID: IN10GBPH008 CATEGORY: Pharmaceuticals GEOGRAPHY: UK AUTHOR: Nandini Shah

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UK Anemia Drugs Market Executive Summary

The UK Anemia Drugs market was valued at $415 Mn in 2022 and is estimated to expand at a compound annual growth rate (CAGR) of 6.9% from 2022 to 2030 and will reach $709 Mn in 2030. According to the World Bank, the United Kingdom is a powerful global commercial powerhouse with 67 million residents and a GDP of $3200 billion (2021). Despite its small size, the United Kingdom has the second-largest economy in Europe and will lead the G7 in GDP growth in 2021. (it is roughly the size of Oregon). The contribution of healthcare to GDP increased from 10.2% in 2019 to nearly 12.8% in 2020.

Anaemia is a condition in which the number of red blood cells or the concentration of hemoglobin in them is lower than usual. Haemoglobin is required to carry oxygen, and if you have too few or malformed red blood cells, or not enough hemoglobin, your blood's capacity to carry oxygen to the body's tissues will be reduced. Symptoms include weariness, weakness, dizziness, and shortness of breath, among others. Anaemia is predicted to affect 23% of pregnant women and 14% of non-pregnant women in the UK.

Market Dynamics

Market Growth Drivers

Anemia is a common condition that affects millions of people in the UK, and the prevalence is increasing due to factors such as aging populations, chronic diseases, and poor dietary habits. This trend is expected to continue in the coming years, driving demand for anemia drugs. ESAs are a type of anemia drug that stimulates the production of red blood cells. With the increasing prevalence of anemia, there is a growing demand for ESAs, which are commonly used to treat anemia associated with chronic kidney disease and chemotherapy-induced anemia. The pipeline of anemia drugs in development is robust, with many new drugs undergoing clinical trials. This is expected to lead to new and more effective treatments for anemia, which will drive growth in the market. Advances in technology, such as the development of long-acting ESAs and innovative drug delivery systems, are expected to improve the efficacy and convenience of anemia treatments. This is expected to drive demand for anemia drugs in the UK market. Improved screening and diagnostic techniques are leading to earlier detection and diagnosis of anemia, which will drive demand for anemia drugs as more patients seek treatment.

Market Restraints

Health and care services in the United Kingdom are confronting enormous problems, including persistent staffing shortages and a growing backlog of unmet healthcare needs. These issues have been compounded by the pandemic and are affecting other countries as well. Yet, how much a country spends on health is critical for the sustainability of its health-care system and readiness for future surges in demand (expected and unexpected). Apart from this, the UK government is facing increasing pressure to reduce healthcare costs, and this is leading to efforts to reduce the price of drugs. Anemia drugs are no exception, and manufacturers may find it difficult to maintain profitability if prices continue to be squeezed. Some anemia drugs have been associated with safety concerns, particularly in the case of ESAs, which have been linked to an increased risk of cardiovascular events. This has led to greater caution in prescribing these drugs, which may limit the market size. Despite the prevalence of anemia, there is still a lack of awareness and education about the condition among healthcare professionals and the general public. This may limit the number of patients seeking treatment, particularly in cases where anemia is mild or asymptomatic.

Competitive Landscape

Key Players

  • Pfizer
  • Roche
  • Amgen
  • GlaxoSmithKline
  • Johnson & Johnson
  • Alcon Laboratories
  • FibroGen
  • Vifor Pharma Group
  • Akebia Therapeutics
  • ALK-Abelló

Healthcare Policies and Regulatory Landscape

The National Health Service (NHS) is a government-sponsored universal healthcare system in the United Kingdom. The NHS is a collection of publicly funded healthcare systems in the United Kingdom. It encompasses NHS England, NHS Scotland, NHS Wales, and Health and Social Care in Northern Ireland. Citizens are entitled to healthcare under this system, but they can also purchase private health insurance. The NHS Plan promises people greater control and information, more hospitals and beds, more physicians and nurses, much-reduced appointment wait times, better healthcare for elderly patients, and tougher requirements for NHS organizations.

The NHS commissioning policies play a key role in shaping the provision of anemia treatments. These policies determine which treatments are available to patients and how they are funded. Patient access schemes are agreements between drug manufacturers and the NHS that provide discounts or rebates on the cost of drugs. These schemes are designed to improve patient access to treatments while ensuring value for money for the NHS.

Reimbursement Scenario

The National Institute for Health and Care Excellence (NICE) evaluates the clinical and cost-effectiveness of drugs in the UK. The assessment considers the evidence on the effectiveness of the drug and the cost of the drug compared to other treatments. NICE provides guidance on the use of the drug. This guidance informs the decisions of healthcare professionals and commissioners on the use of the drug and whether it should be funded by the NHS. The NHS commissioning policies determine which treatments are available to patients and how they are funded. Commissioning policies are informed by NICE guidance and consider the clinical and cost-effectiveness of the drug. Drug manufacturers can offer patient access schemes that provide discounts or rebates on the cost of the drug. These schemes are designed to improve patient access to treatments while ensuring value for money for the NHS.

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

Anemia Drugs Market Segmentation

By Type (Revenue, USD Billion):

  • Iron Deficiency
  • CKD (Chronic Kidney Disease)
  • Sickle Cell
  • Aplastic
  • Others

By Drugs

  • Dietary Supplements
  • Medicines

The types of nutritional supplements are further broken down into iron and vitamin supplements, among other categories, whilst the categories of medicines include antibiotics, hormones (erythropoietin), and chelation therapy (lead poisoning), among others.

By Distribution Channel (Revenue, USD Billion):

  • Hospital Pharmacy
  • Store Pharmacy
  • Online
  • Others

The distribution channel for anemia drugs in UK is complex and multifaceted. Pharmaceutical companies must work with a variety of stakeholders, including hospital and retail pharmacies, distributors, and regulatory authorities, to ensure that their products are effectively distributed to patients who need them.

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:

  • Analyzing historical proprietary data collected from multiple projects.
  • Regularly updating our existing data sets with new findings and trends.
  • Ensuring data consistency and accuracy through rigorous validation processes.

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:

  • Searching through academic conferences, published research, citations, and social media platforms
  • Collecting and compiling diverse data to build a comprehensive and detailed database
  • Continuously updating our database with new information to ensure its relevance and accuracy

2. Primary Research

To complement and validate our secondary data, we engage in primary research through local tie-ups and partnerships. This process involves:

  • Collaborating with local healthcare providers, hospitals, and clinics to gather real-time data.
  • Conducting surveys, interviews, and field studies to collect fresh data directly from the source.
  • Continuously refreshing our database to ensure that the information remains current and reliable.
  • Validating secondary data through cross-referencing with primary data to ensure accuracy and relevance.

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:

  • Merging historical data from secondary research with real-time data from primary research.
  • Conducting thorough data validation and cleansing to remove inconsistencies and errors.
  • Organizing data into a structured format that is easily accessible and usable for various applications.
  • Continuously monitoring and updating the database to reflect the latest developments and trends in the healthcare field.

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.

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Last updated on: 12 October 2023
Updated by: Shivam Zalke

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