“Fabry Disease Pipeline Insight, 2023” report by DelveInsight outlines a comprehensive assessment of the present clinical/non-clinical development activities and growth prospects across the Fabry Disease Market.
The Fabry Disease Pipeline report embraces in-depth commercial and clinical assessment of the pipeline products from the pre-clinical developmental phase to the marketed phase. The report also covers a detailed description of the drug, including the mechanism of action of the drug, clinical studies, NDA approvals (if any), and product development activities comprising the technology, collaborations, mergers, acquisition, funding, designations, and other product-related details.
Fabry Disease Pipeline Analysis
The report provides insights into:
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The report provides detailed insights into the emerging therapies for the treatment of Fabry Disease and the aggregate therapies developed by major pharma companies.
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It accesses the different therapeutic candidates segmented into early-stage, mid-stage, and late-stage of clinical development.
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It outlines the key companies involved in targeted therapeutics development with respective active and inactive (dormant or discontinued) projects.
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The report evaluates the drugs that are under development based on the stage of development, route of administration, target receptor, monotherapy or combination therapy, a different mechanism of action, and molecular type.
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It navigates the major collaborations (company-company collaborations and company-academia collaborations), licensing agreements, financing details, data presentation by the pharma giants, and regulatory approval in the Fabry Disease market.
The report is built using data and information traced from the researcher’s proprietary databases, company/university websites, clinical trial registries, conferences, SEC filings, investor presentations, and featured press releases from company/university websites and industry-specific third-party sources, etc.
Analysis of Emerging Therapies by Phases
The report covers the emerging products under different phases of clinical development like –
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Late-stage products (Phase III)
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Mid-stage products (Phase II)
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Early-stage product (Phase I)
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Pre-clinical and Discovery stage candidates
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Discontinued & Inactive candidates
Route of Administration
Fabry Disease pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Products have been categorized under various ROAs such as
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Oral
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Parenteral
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Intravitreal
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Subretinal
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Topical
Molecule Type
Products have been categorized under various Molecule types such as
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Monoclonal Antibody
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Peptides
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Polymer
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Small molecule
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Gene therapy
Latest Key Developments in the Fabry Disease Therapeutics Market
On May 10, 2023, Chiesi Global Rare Diseases and Protalix BioTherapeutics, Inc. (NYSE American:PLX) announced that the U.S. Food and Drug Administration (FDA) has approved ELFABRIO (pegunigalsidase alfa-iwxj) in the United States for the treatment of adult patients with Fabry disease.
Learn How the Ongoing Clinical & Commercial Activities will Affect the Fabry Disease Therapeutic Segment @
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Fabry Disease Therapeutics Landscape
There are approx. 18+ key companies developing therapies for Fabry Disease. Currently, Protalix Biotherapeutics is leading the therapeutics market with its Fabry Disease drug candidates in the most advanced stage of clinical development.
The Leading Players in the Fabry Disease Therapeutics Market Include:
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Idorsia Pharmaceuticals
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Protalix
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Sanofi Genzyme
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Sangamo Therapeutics
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4D Molecular Therapeutics
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Resverlogix Corp
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AVROBIO
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Freeline Therapeutics
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Ozmosis Research Inc.
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CellGenTech, Inc.
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uniQure
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Codexis
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Canbridge
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Eleva GmbH
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MP6 therapeutics
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Amicus therapeutics
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Sigilon Therapeutics
And Many Others
Fabry Disease Emerging and Marketed Drugs Covered in the Report Include:
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4D 310: 4D Molecular Therapeutics
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Fabrazyme (agalsidase beta): Sanofi-Genzyme
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Pegunigalsidase Alfa: Protalix Biotherapeutics
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PRX-102 (Pegunigalsidase Alfa): Protalix Biotherapeutics
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Replagal (agalsidase alfa): Shire (now a part of Takeda)
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Venglustat: Sanofi Genzyme
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Replagal: Shire/Takeda
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Galafold: Amicus Therapeutics
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PRX-102 (Pegunigalsidase Alfa): Protalix Biotherapeutics
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Venglustat: Sanofi Genzyme
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ST-920: Sangamo Therapeutics
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FLT190: Freeline Therapeutics
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Lucerastat: Idorsia Pharmaceuticals
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Moss-aGal: GREENOVATION BIOTECH GMBH
And Many More
Request the Sample PDF to Get a Better Understanding of the Emerging Drugs and Key Companies @
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Table of Content (TOC)
1. Report Introduction
2. Executive Summary
3. Fabry Disease Current Treatment Patterns
4. Fabry Disease – DelveInsight’s Analytical Perspective
5. Therapeutic Assessment
6. Fabry Disease Late Stage Products (Phase-III)
7. Fabry Disease Mid-Stage Products (Phase-II)
8. Fabry Disease Early Stage Products (Phase-I)
9. Pre-clinical Products and Discovery Stage Products
10. Inactive Products
11. Dormant Products
12. Fabry Disease Discontinued Products
13. Fabry Disease Product Profiles
14. Key Companies in the Fabry Disease Market
15. Key Products in the Fabry Disease Therapeutics Segment
16. Dormant and Discontinued Products
17. Fabry Disease Unmet Needs
18. Fabry Disease Future Perspectives
19. Fabry Disease Analyst Review
20. Appendix
21. Report Methodology
*The Table of Contents (TOC) is not exhaustive; the final content may vary. Refer to the sample report for the complete table of contents.
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About DelveInsight
DelveInsight is a leading Business Consultant and Market Research Firm focused exclusively on life sciences. It supports pharma companies by providing comprehensive end-to-end solutions to improve their performance.
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