Brazil Hunter Syndrome Therapeutics Market Report 2023 to 2030

Brazil Hunter Syndrome Therapeutics Market Analysis

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Brazil Hunter Syndrome 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. Rare X-linked recessive genetic disorder MPS II (Hunter Syndrome) is brought on by changes in the iduronate-2-sulfatase gene (IDS). Due to the poor understanding of the illness, creating effective treatments for uncommon diseases can be difficult and expensive, which has a negative impact on the market for syndromes. Global Key Players in the Hunter Syndrome Therapeutics Market Include Takeda Pharmaceutical Company Limited, BioMarin Pharmaceutical Inc., Shire (now a part of Takeda), Sanofi Genzyme, Ultragenyx Pharmaceutical Inc., Sangamo Therapeutics, Inc., RegenxBio Inc., Denali Therapeutics Inc., JCR Pharmaceuticals Co., Ltd., and ArmaGen Inc.

ID: IN10BRRD037 CATEGORY: Rare Diseases GEOGRAPHY: Brazil AUTHOR: Nipun Arora

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Brazil Hunter Syndrome Therapeutics Market Analysis Summary

Brazil Hunter Syndrome Therapeutics Market is valued at around $23.18 Mn in 2022 and is projected to reach $48.26 Mn by 2030, exhibiting a CAGR of 9.6% during the forecast period 2023-2030.

One of the set of illnesses known as mucopolysaccharidoses is Hunter syndrome. It is also referred to as MPS II, or mucopolysaccharidosis type II. A rare genetic condition called Hunter syndrome causes the body to improperly digest (break down) sugar molecules. These chemicals can harm physical and mental growth and capacities if they accumulate in organs and tissues over time. Boys virtually always experience the condition. Male patients are generally always the ones with Hunter syndrome. Approximately 1 out of 100,000 to 170,000 guys are diagnosed with it by doctors. It is possible for females to carry the genetic mutation that causes MPS II.

Due to the high cost of care, difficulties in making an accurate diagnosis, and the difficulty in creating viable treatments for uncommon diseases, the market for syndromes is constrained.

Global Key Players in the Hunter Syndrome Therapeutics Market Include BioMarin Pharmaceutical Inc., Shire (now a subsidiary of Takeda), Sanofi Genzyme, Ultragenyx Pharmaceutical Inc., Sangamo Therapeutics, Inc., RegenxBio Inc., Denali Therapeutics Inc., JCR Pharmaceuticals Co., Ltd., and ArmaGen Inc.

Market Dynamics

Market Restraints

High Treatment Cost: Because medicines for rare disorders like Hunter syndrome require extensive research and development, they can be expensive to buy and administer. For patients and healthcare systems, the high cost of treatment may result in accessibility difficulties, problems with reimbursement, and issues with affordability.

Challenges in Diagnosis: Hunter syndrome is a complex condition that may require specialized diagnostic tools and expertise. The challenges in accurately diagnosing the disease, particularly in its early stages, can result in delayed or missed diagnoses, hindering the timely initiation of treatment.

Research and Development Challenges: Developing effective treatments for rare diseases like Hunter syndrome can be challenging due to the limited understanding of the condition and the complex mechanisms involved. The rarity of the disease also poses challenges in conducting clinical trials with a sufficient number of participants.

Market Development

Genetic HMI-203 from Homology Medicine is undergoing a Phase I clinical trial. Intravenous administration is the method used to provide it.

Elaprase from Shire is undergoing a Phase IV clinical trial in people with Hunter syndrome, both adults and children (Mucopolysaccharidosis II).

Undergoing clinical trial research is Denali Therapeutics' DNL310, an investigational enzyme replacement therapy (ERT) that penetrates the central nervous system (CNS) and is intended to treat both the peripheral and CNS aspects of Mucopolysaccharidosis type II (MPS II; Hunter syndrome).

The only approved treatment for Hunter syndrome is enzyme replacement therapy (ERT) with recombinant idursulfase (ELAPRASE®); however, ERT as it is currently administered cannot cross the blood-brain barrier and is unable to meet the needs of MPS II patients with central nervous system (CNS) (neurocognition and behaviour) involvement. The goal of RGX-121 is to introduce a functioning gene into CNS cells. Pediatric patients are now participating in the clinical trial.

Key players

uniQure Ionis Pharmaceuticals Alnylam Pharmaceuticals Pfizer Sanofi Shire plc BioMarin Pharmaceutical Inc. Orchard Therapeutics plc PTC Therapeutics Inc. 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 Hunter Syndrome Therapeutics Market

By Treatment

Enzyme replacement drugs
Stem cell transplant
Therapy
Physical therapy
Speech therapy

By Diagnosis

Urine test
Blood test
Genetic testing

By Distribution Channel

Hospital
Clinic
Pharmacy

Methodology for Database Creation

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Analyzing historical proprietary data collected from multiple projects.
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Searching through academic conferences, published research, citations, and social media platforms
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