France Blood Disorder Therapeutics Market

France Blood Disorder Therapeutics Market


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France Blood Disorder Therapeutics Market valued at $369 Mn in 2022, projected to reach $610 Mn by 2030 with a 6.5% CAGR. The key drivers of the market include greater disposable income among the French population, leading to an increased ability to afford expensive prescription drugs and specialized treatments for blood problems, and changes in the Western lifestyle causing a higher prevalence of the disease in the country. The France Market encompasses various players across different segments, including Takeda, Roche, Sanofi, Novartis, Novo Nordisk, CSL Ltd, Pfizer, LFB Biomedicaments, Walvax Biotech, Janssen-Cilag etc, among various others.

ID: IN10FRPH437 CATEGORY: Pharmaceuticals GEOGRAPHY: France AUTHOR: Dr. Netal Patel

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France Blood Disorder Therapeutics Market Executive Summary

France Blood Disorder Therapeutics Market valued at $369 Mn in 2022, projected to reach $610 Mn by 2030 with a 6.5% CAGR.

Blood diseases are illnesses that impact the red, white, platelets, plasma, and white blood cells that make up blood. These conditions can be inherited or acquired, and they can be malignant or non-malignant. Many symptoms, such as bleeding, clotting, anemia, and weariness, can be brought on by blood problems. There are several different causes; some are hereditary, while others result from underlying medical issues or outside influences. The degree and kind of the ailment determine the available treatment choices for blood diseases. While some may not need therapy, others would need constant monitoring and medication. Bone marrow transplants, stem cell transplants, infusion therapy, drugs, blood transfusions, and chemotherapy are among the available treatment options. Blood-component therapy, such as platelet transfusions or clotting factors, may be necessary for bleeding disorders like hemophilia, whereas medications that prevent the development of clots may be used to treat clotting-related illnesses. Treatments for blood disorders have recently advanced thanks to developments in gene treatments, blood component therapies, bone marrow transplants, immune therapy, and other areas.

Sickle Cell Disease (SCD) is one of the most prevalent blood illnesses in France. An estimated 19,800–32,400 people in France are expected to have SCD. 1.51 cases of aplastic anemia per Mn people live in France every year. Additionally, hereditary bleeding disorders such as hemophilia, von Willebrand disease, and other bleeding disorders are prevalent, with a significant number of new patients diagnosed each month.

The key drivers of the market include greater disposable income among the French population, leading to an increased ability to afford expensive prescription drugs and specialized treatments for blood problems, and changes in the Western lifestyle causing a higher prevalence of the disease in the country.

Takeda is a major player in the hemophilia business, especially with medications like Advate and Iclusig. Because of its wider portfolio, Sanofi has the greatest total revenue in the French blood disease medicines market. Other regional companies are offering a large selection of generic products.

France blood disorder therapeutics market

Market Dynamics

Market Growth Drivers

Greater Disposable Income: As a result of their higher incomes, French people can now afford more costly prescription drugs and specialist treatment related to blood problems. Even while sophisticated treatment choices come with a larger price tag, patients and their families may be encouraged to investigate them due to the increased financial freedom. Pharma firms may profit from this desire to spend money on better health outcomes by creating and releasing high-end treatments.

Demand for Cutting-Edge Solutions: Patients and medical professionals are increasingly favoring sophisticated medicines like gene therapy and customized medicine. The promise of more long-lasting benefits, higher effectiveness, and fewer side effects in comparison to conventional therapies is what is causing this transition. Pharma companies can leverage this trend by focusing R&D on innovative solutions and effectively conveying their value proposition to patients and physicians.

Rising Prevalence of Blood Disorders: Increased awareness and improved diagnostics lead to more accurate diagnoses of blood disorders, like hemophilia and sickle cell disease. France has a particular focus on hemophilia, with national programs contributing to a higher prevalence compared to other countries. An aging population can be more susceptible to certain blood disorders, adding to the overall patient pool.

Market Restraints

High Cost of Advanced Therapies: Patients and healthcare systems may find it difficult to pay the high costs associated with novel therapies like gene therapy and customized medicine. In particular, for treatments aimed at smaller patient groups, this may result in restricted access and slower market uptake. To guarantee a larger patient base and long-term market viability, pharmaceutical companies need to figure out how to strike a compromise between innovation and affordability.

Lack of Education and Awareness: There may be a lack of public knowledge of certain blood illnesses and the alternatives for treating them, which can delay diagnosis and result in the underuse of existing treatments. To optimize market potential, more education initiatives for patients, medical professionals, and the general public are necessary. To increase awareness and enhance access to care, patient advocacy groups and healthcare organizations can be extremely important.

Competition and Market Saturation: There are already several well-established businesses and a wide variety of treatment alternatives available in the market for some blood diseases, such as hemophilia. In congested markets, new entrants may encounter difficulties distinguishing their offerings and gaining market share. To differentiate themselves in a crowded market, businesses must concentrate on specialized markets, individualized medical strategies, or distinctive value offerings.

Healthcare Policies and Regulatory Landscape

The management of the French healthcare system falls under national jurisdiction, with the Ministry of Social Affairs, Health, and Women’s Rights tasked with formulating the national health strategy and executing government policies related to public health. This includes the arrangement and financial aspects of healthcare services. Hospital, physician, long-term care, and prescription drug expenses are predominantly covered by the French healthcare system, with patients having responsibilities for coinsurance, copayments, and any balance bills resulting from physician charges surpassing covered fees. The National Agency for the Safety of Medicines and Health Products (ANSM) serves as the regulatory authority for drugs in France, ensuring the safety, effectiveness, accessibility, and appropriate usage of health products in the country. ANSM plays a crucial role in authorizing the approval of new medicines and biologics, monitoring health products throughout their life cycle, examining the impacts of their usage, gathering and analyzing reports on side effects, conducting quality control at its laboratories, and inspecting manufacturing and distribution facilities. The authorization for marketing drugs can be acquired either at the national or European level, with ANSM previously recognized as the French Agency for the Medical Safety of Health.

Competitive Landscape

Key Players:

  • Takeda
  • Roche
  • Sanofi
  • Novartis
  • Novo Nordisk
  • CSL Ltd
  • Pfizer
  • LFB Biomedicaments
  • Walvax Biotech
  • Janssen-Cilag

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

France Blood Disorder Therapeutics Market Segmentation

By Disorder:

  • Anemia
  • Hemophilia
  • Leukemia
  • Myeloma
  • Lymphoma
  • Rare blood disorders

By Product Type

  • Plasma-derived therapeutics
  • Recombinant therapeutics
  • Gene therapy
  • Other therapies

By End User

  • Hospitals
  • Specialty clinics
  • Ambulatory care
  • Home healthcare

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: 18 April 2024
Updated by: Ritu Baliya

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