France during the forecast period of 2023-30, the Alport Syndrome therapeutics market is anticipated to increase from $xx Mn in 2023 to $xx Mn by 2030, recording a CAGR of xx percent. Almost always affecting the kidney, Alport syndrome is a multisystem condition that also usually affects the inner ear and the eye. A variety of symptoms that normally start in childhood or adolescence and may get worse over time can be present. Invitae Corporation, Hoffmann-La Roche Ltd., Centogene N.V., and Eurofins Discovery are a few of the leading companies in the worldwide Alport syndrome market.
France Alport Syndrome Therapeutics Market is valued at around $4 Mn in 2022 and is projected to reach $6.43 Mn by 2030, exhibiting a CAGR of 6.1% during the forecast period 2023-2030.
In addition to kidney failure, hearing loss, and vision issues, Alport syndrome is an uncommon hereditary illness. Genes COL4A3, COL4A4, and COL4A5, which are important in the manufacture of proteins like type IV collagen, are mutated, and this disorder is the result. The number of Americans with this condition is less than 50,000.
Nerve deafness in various degrees was one of the most notable extrarenal symptoms mentioned by Alport. The diagnosis of the ailment is made using the patient's family history, clinical symptoms, and specialised testing, such as kidney biopsy. Genetic testing can formally establish the diagnosis. In addition to having nerve deafness, their urine also included blood and protein, however, the degree of these conditions varied between family members.
Increased mortality owing to end-stage disease was another characteristic of affected members.
The two Col4a5 models' X-linked nature predicts a gender skew in the disease's severity and course. Another autosomal kidney disorder with a sex-dependent pattern is polycystic kidney disease. More people with less severe types of Alport syndrome are being found, though, as research into the disorder continues. Future possibilities include exon skipping, chaperones, protein replacement therapy, genome editing, premature termination codon readthrough therapy, stem cell transplantation, and many more. In the ongoing proof-of-concept Phase 2 open-label clinical trial (NCT05448755) in up to eight Alport syndrome patients with nonsense mutations in the Collagen Type 4 genes, Eloxx has now dosed three patients with ELX-02 (COL4A3, COL4A4, and COL4A5). One patient's first decrease in proteinuria was encouraging. Increased prevalence and funding and adoption of home care settings have boosted the Alport Syndrome Therapeutics Market. Invitae Corporation, Hoffmann-La Roche Ltd., Centogene N.V., and Eurofins Discovery are a few of the leading companies in the worldwide Alport syndrome market.
Market Growth Drivers
Market Restraints
Companies are concentrating on clinical trials for the development of drugs for the disease because there is no particular treatment for Alport syndrome. The high expense of development is an additional difficulty.
Key players
Otsuka Pharmaceutical Astellas Pharma Alexion Pharmaceuticals CSL Behring Kedrion Biopharma Baxter International GlycoMimetics Vir Biotechnology Intercept Pharmaceuticals Alnylam Pharmaceuticals1. 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
Genetic Type
Diagnosis
Treatment
End-Users
Distribution Channel
Route of Administration
Dosage form
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