“Duchenne Muscular Dystrophy (DMD) Pipeline Insight, 2022” report by DelveInsight outlines a comprehensive assessment of the present clinical/non-clinical development activities and growth prospects across the Duchenne Muscular Dystrophy Market.
The Duchenne Muscular Dystrophy 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.
Duchenne Muscular Dystrophy Pipeline Analysis
The report provides insights into:
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The report provides detailed insights into the emerging therapies for the treatment of Duchenne Muscular Dystrophy 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 Duchenne Muscular Dystrophy 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.
DelveInsight’s Report covers around 75+ 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 – The Report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Products have been categorized under various ROA, such as –
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Oral
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Intravenous
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Subcutaneous
Molecule Type – Products have been categorized under various Molecule types, such as
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Small molecule
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Cell Therapy
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Peptides
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Polymer
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Small molecule
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Gene therapy
Duchenne Muscular Dystrophy Emerging Therapies – Mechanisms of Action (MOA) Types
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Dipeptidyl peptidase I inhibitors
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Peroxisome proliferator-activated receptor delta modulators
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Cell replacements
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Dystrophin expression stimulants
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Connective tissue growth factor inhibitors
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Dystrophin replacements
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Immunostimulants
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Gene modulators
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Dystrophin expression modulators
Learn How the Ongoing Clinical & Commercial Activities will Affect the Duchenne Muscular Dystrophy Therapeutic Segment @
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Duchenne Muscular Dystrophy Therapeutics Landscape
There are approx. 75+ key companies developing therapies for Duchenne Muscular Dystrophy. Currently, Roche is leading the therapeutics market with its Duchenne Muscular Dystrophy drug candidates in the most advanced stage of clinical development among all the major players in the segment.
The Leading Companies in the Duchenne Muscular Dystrophy Therapeutics Market Include:
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Santhera Pharmaceuticals
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Sarepta Therapeutics
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Italfarmaco
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Wave Life Sciences Ltd
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FibroGen
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Edgewise Therapeutics
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Fordadistrogene movaparvovec
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Daiichi Sankyo
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Sarepta Therapeutics, Inc.
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ENCell
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Taiho Pharmaceutical
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Solid Biosciences
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Capricor
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Nippon Shinyaku
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Hansa Biopharma
And Many Others
Duchenne Muscular Dystrophy Drugs Covered in the Report Include:
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Vamorolone: Santhera
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Givinostat: Italfarmaco
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Pamrevlumab: Fibrogen
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WVE N531: WaVe lifeSciences
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CRISPR/Cas9 gene editing therapy: Vertex Pharmaceuticals
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MA-0211: Mitobridge
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BLS-M22: Bioleaders Corporation
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CAP 1002: Capricor
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DS-5141: Daiichi Sankyo
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TAS-205: Taiho Pharmaceutical
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. Duchenne Muscular Dystrophy Current Treatment Patterns
4. Duchenne Muscular Dystrophy – DelveInsight’s Analytical Perspective
5. Therapeutic Assessment
6. Duchenne Muscular Dystrophy Late Stage Products (Phase-III)
7. Duchenne Muscular Dystrophy Mid-Stage Products (Phase-II)
8. Duchenne Muscular Dystrophy Early Stage Products (Phase-I)
9. Pre-clinical Products and Discovery Stage Products
10. Inactive Products
11. Dormant Products
12. Duchenne Muscular Dystrophy Discontinued Products
13. Duchenne Muscular Dystrophy Product Profiles
14. Key Companies in the Duchenne Muscular Dystrophy Market
15. Key Products in the Duchenne Muscular Dystrophy Therapeutics Segment
16. Dormant and Discontinued Products
17. Duchenne Muscular Dystrophy Unmet Needs
18. Duchenne Muscular Dystrophy Future Perspectives
19. Duchenne Muscular Dystrophy 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.
Download Sample PDF to Explore the Key Offerings of the Report @
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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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