Brazil Fabry Disease Therapeutics Market Report 2023 to 2030

Brazil Fabry Disease Therapeutics Market Analysis

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Brazil Fabry 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. A lack of lysosomal hydrolase -galactosidase causes Fabry disease (FD), an X-linked inborn error of lysosomal storage disorder. A activity brought on by harmful variations in the GLA gene. The market for fabry disease drugs is growing rapidly as a result of increase in incidence and prevalence of fabry disease globally, increase in awareness about the disease globally, better diagnosis rates, improved access to treatment, development of new emerging therapies, orphan drug designations provided by regulatory bodies, increase in stratergic collaborations, rise in research and development activities and approval of promising pipeline products. Chiesi Farmaceutici SpA, Sanofi, Shire, Takeda Pharmaceutical Company Limited, Amicus Therapeutics, Inc., JCR Pharmaceuticals, Moderna are the key market players operating in global fabry disease Therapeutics Market.

ID: IN10BRRD022 CATEGORY: Rare Diseases GEOGRAPHY: Brazil AUTHOR: Nipun Arora

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Brazil Fabry Disease Therapeutics Market Analysis Summary

Brazil Fabry Disease Therapeutics Market is valued at around $0.01 thousand in 2022 and is projected to reach $0.01 thousand by 2030, exhibiting a CAGR of 8.65% during the forecast period 2023-2030.

Fabry disease is a rare X-chromosome-linked genetic disease which is caused by deficient activity of a lysosomal enzyme called α-galactosidase. This results in the dysfunction of glycosphingolipid (fat) metabolism. α-galactosidase enzyme is responsible for breaking down of complex sugar-lipid molecules called glycolipids or digesting particular compounds. The deficiency of this enzyme may result in cell abnormalities and organ system dysfunction which is caused by an abnormal buildup of a specific fatty matter called globotriaosylceramide in multiple tissues of the body including eyes, skin, kidney, gastrointestinal system, brain, heart, and central nervous system. Since there is no known cure for Fabry's disease, treatment options often focus on managing difficulties brought on by the disease's development and relieving symptoms. Current treatments include enzyme replacement therapy (ERT), chaperone treatment, and substrate reduction therapy (SRT). Development in oral chaperone therapy is taking place which is projected to drive the market in future years. The popularity of substrate reduction therapies and gene therapies in the market is also expected to increase.

Market Dynamics

Drivers of Brazil Fabry disease Therapeutics Market

Increase in incidence and prevalence of Fabry disease – As the patient population suffering from this disease increase this acts as a market growth driver.

An increase in awareness about the disease globally is a market growth driver

The increase in prevalence and adoption of novel therapies like chaperone treatment, substrate therapy and gene therapy acts as a market growth driver. Chaperone therapy includes oral small molecules, which aim to stabilize and enhance the function of the deficient enzyme.

Extensive research and development activities and collaborations between pharmaceutical companies and research organizations also act as market growth drivers.

Orphan Drug Designations provided by regulatory bodies also act as a growth driver.

Development in Fabry Disease Therapeutics Market Analysis:

Elfabrio® (pegunigalsidase alfa-iwxj), a medication for the treatment of adults with Fabry disease, has received FDA approval. Elfabrio is a neutral glycosphingolipid-specific hydrolytic lysosomal enzyme. It is believed that the product exerts enzymatic activity and lowers accumulated Gb3 in the lysosomes after being absorbed and delivered there. The approval was based on information from two clinical trials: a phase 3, double-blind, active-controlled trial in ERT-experienced adults with Fabry disease and an open-label dose-ranging study in patients who were ERT-nave or who had not received ERT for more than 26 weeks and had a negative test for anti-pegunigalsidase alfa-iwxj IgG antibodies.

Restraints of Brazil Fabry disease Therapeutics Market

Side effects associated with treatment options and high treatment costs act as a market growth restraint

A lower rate of diagnosis due to a lack of technologies and the late onset of symptoms also acts as a market growth restraint.

Key players

Sanofi Pfizer Shire plc BioMarin Pharmaceutical Inc. Catalyst Biosciences uniQure Ionis Pharmaceuticals Alnylam Pharmaceuticals Intercept Pharmaceuticals Novartis

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 Brazil Fabry Disease Therapeutics Market

By Type

Classic Fabry disease
Atypical late-onset Fabry disease

By Treatment type

Enzyme replacement therapy (ERT)
Chaperone treatment
Substrate reduction therapy (SRT)
Others

By Mechanism of action

Alpha-galactosidase A (Alpha-Gal A) agonist
Globotriaosylceramide (GL-3) deposition reducer
Pancreatic replacement enzymes
Pain management
Others

By Route of Administration

Oral
Parenteral

By end users

Hospitals
Homecare
speciality clinics
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.