France Gaucher Disease Therapeutics Market Report 2023 to 2030

France Gaucher Disease Therapeutics Market Analysis

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France Gaucher Disease Therapeutics Market is projected to grow from $xx Mn in 2023 to $xx Mn by 2030, registering a CAGR of xx% during the forecast period of 2023 - 2030. The market for gaucher disease drugs is growing rapidly as a result of rising incidence and prevalence of gaucher disease, increasing infrastructure spending for healthcare, rising acceptance rate of early diagnosis, increasing number of government initiatives to raise awareness and an increasing number of approved therapies for the treatment of Gaucher disease. Aptalis Pharma, Abbott Laboratories, Genzyme Corporation, Pfizer Inc., GlaxoSmithKline (GSK), Eli Lilly and Company, AVROBIO, Shire Human Genetic Therapies, Inc., Anthera Pharmaceuticals, Inc., Enobia Pharma Inc., BioMarin Pharmaceutical Inc., Merck Serono, Zymenex A/S, and MedPro Rx are the top key players of Gaucher Disease Therapeutics Market .

ID: IN10FRRD027 CATEGORY: Rare Diseases GEOGRAPHY: France AUTHOR: Sakshi Mantri

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France Gaucher Disease Therapeutics Market Analysis Summary

France Gaucher Disease Therapeutics Market is valued at around $0.041 Mn in 2022 and is projected to reach $0.06 Mn by 2030, exhibiting a CAGR of 2.6% during the forecast period 2023-2030.

Gaucher disease is a rare type of liposomal disease which occurs due to a deficiency of the enzyme glucocerebrosidase, which breaks down the fatty compound glucocerebroside and causes Gaucher cells to accumulate in the spleen, liver, and bone marrow. One in 50,000 to one in 100,000 individuals are thought to be affected by Gaucher's disease globally. The condition affects about 1 in 800 Ashkenazi Jews, who are more likely than other ethnic groups to have it (prevalence varies among different ethnic groups). For Gaucher's disease patients, a better prognosis and quality of life are absolutely necessary, as well as access to the right kind of treatment. Major symptoms of this disease include an enlarged liver or spleen, weariness, anaemia, bone discomfort and fractures and easy bleeding while brushing. The Gaucher disease has three different types Type I, Type II, and Type III. The most prevalent form of Gaucher illness, Type I, does not impact the nervous system of the patient. Type 1, Type 2, and Type 3 drugs are available on the market for Gaucher disease. The Type I Gaucher disease category is anticipated to occupy a sizable part of the Gaucher disorder market due to the increase in incidences across the globe. The short-term treatment objectives for Type I include symptoms related to anaemia, bleeding propensity, visceral issues, and general health. Another long-term therapy goal for Type I disease is to address respiratory issues. The effective treatment of Type I Gaucher disorder will be aided by factors such as the correct patient and family education on the condition and available treatments. The enzyme replacement therapy segment is expected to dominate the global gauche disease market in terms of revenue contribution during the forecast period due to its higher adoption rate as compared to other therapies available for treating gaucher disease. Regular oral or intravenous administration of a synthetic or recombinant version of glucocerebrosidase is done in ERT. ERT thus seeks to replace the lacking enzyme and lessen the buildup of glucocerebroside. The segment would expand because there are more approved drugs in the ERT. Aptalis Pharma, Abbott Laboratories, Genzyme Corporation, Pfizer Inc., GlaxoSmithKline (GSK), Eli Lilly and Company, AVROBIO, Shire Human Genetic Therapies, Inc., Anthera Pharmaceuticals, Inc., Enobia Pharma Inc., BioMarin Pharmaceutical Inc., are the key global market players.

Market Dynamics

Market Drivers

The market for treating Gaucher disease is primarily driven by the increasing number of medicinal approvals, which encourages leading market players to adopt a new strategy when developing new drugs. Collaboration between various biopharmaceutical companies and research institutes will also help the market flourish. Additionally, there are government programmes to raise awareness about Gaucher's illness. Increase incidence and prevalence of disease, orphan drug designations, patient advocacy programmes and emerging therapies all act as market growth drivers.

Market Development

Prevail Therapeutics is working in Phase II of the clinical development of R-001 for Gaucher Disease Type I. The phase transition success rate (PTSR) indication benchmark for Phase II medicines for Gaucher Disease Type I is 60% in order to advance into Phase III.

The drug FLT-201 is being developed to treat type 1 Gaucher disease. An intravenous method is used to give the medication candidate. The GBA1 gene is encoded by an adeno-associated virus (AAV) vector. The next-generation proprietary AAV vector technology is the foundation on which the therapeutic candidate is created.

Restraints of France Gaucher Disease Therapeutics Market

The high cost associated with the treatment of Gaucher's disease may restrain the growth of this market during the forecast period.

Key players

Sanofi Pfizer Genzyme Shire Amicus Therapeutics Protalix BioTherapeutics Sarepta Therapeutics Spark Therapeutics uniQure Bluebird Bio

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

Market Segmentations For France Gaucher Disease Therapeutics Market

By Type

Type 1
Type 2
Type 3

By Therapy

Enzyme replacement therapy
Substrate replacement therapy

By Diagnosis

Physical Examination
Blood tests
Imaging Tests
Preconception Screening
Prenatal Testing
Others

By end users

Hospitals
Speciality clinics
Homecare
Others

By Route of Administration

Oral
Parenteral
Others

By Distribution Channels

Hospital pharmacies
Retail pharmacies
Online pharmacies
Others

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.

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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.