The Duchenne Muscular Dystrophy Pipeline report embraces in-depth commercial and clinical assessment of the Duchenne Muscular Dystrophy pipeline products from the pre-clinical developmental phase to the marketed phase.
The report covers a detailed description of the drug including mechanism of action of the drug, clinical studies, NDA approvals (if any), and product development activities comprising the technology, Duchenne Muscular Dystrophy collaborations, mergers, acquisition, funding, designations, and other product-related details.
The expected Launch of potential therapies may increase the market size in the coming years, assisted by an increase in the diagnosed prevalent population of Duchenne Muscular Dystrophy. Owing to the positive outcomes of the several products during the developmental stage by key players the Duchenne Muscular Dystrophy market is expected to witness a significant positive shift during the forecast period.
Some of the key companies in the Duchenne Muscular Dystrophy market include:
Sarepta Therapeutics
FibroGen
Capricor
Santhera Pharmaceutical
Catabasis Pharmaceuticals
Italfarmaco
Daiichi Sankyo
Pfizer
ReveraGen BioPharma
Taiho Pharmaceutical
And others.
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Duchenne Muscular Dystrophy Pipeline Analysis
The report provides insights into:
The report provides detailed insights about companies that are developing therapies for the treatment of Duchenne Muscular Dystrophy with aggregate therapies developed by each company for the same.
It accesses the Different therapeutic candidates segmented into early-stage, mid-stage, and late stage of development for the Duchenne Muscular Dystrophy Treatment.
Duchenne Muscular Dystrophy key companies involved in targeted therapeutics development with respective active and inactive (dormant or discontinued) projects.
Duchenne Muscular Dystrophy Drugs 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.
Detailed analysis of collaborations (company-company collaborations and company-academia collaborations), licensing agreement and financing details for future advancement of 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.
Duchenne Muscular Dystrophy Therapies Covered in the report include:
Casimersen (SRP-4045)
Givinostat (ITF2357)
Edasalonexent (CAT-1004/Edasa)
SRP-9001
Vamorolone
Ifetroban
And many others.
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Report Highlights
A better understanding of disease pathogenesis contributing to the development of novel therapeutics for Duchenne Muscular Dystrophy.
In the coming years, the Duchenne Muscular Dystrophy market is set to change due to the rising awareness of the disease, and incremental healthcare spending across the world; which would expand the size of the market to enable the drug manufacturers to penetrate more into the market.
The companies and academics are working to assess challenges and seek opportunities that could influence Duchenne Muscular Dystrophy Research & Development. The therapies under development are focused on novel approaches to treat/improve the disease condition.
A detailed portfolio of major pharma players who are involved in fueling the Duchenne Muscular Dystrophy treatment market. Several potential therapies for Duchenne Muscular Dystrophy are under investigation. With the expected launch of these emerging therapies, it is expected that there will be a significant impact on the Duchenne Muscular Dystrophy market size in the coming years.
Our in-depth analysis of the Duchenne Muscular Dystrophy pipeline assets (in early-stage, mid-stage, and late stage of development) includes therapeutic assessment and comparative analysis. This will support the clients in the decision-making process regarding their therapeutic portfolio by identifying the overall scenario of the research and development activities.
Table of Content
1. Report Introduction
2. Duchenne Muscular Dystrophy
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. 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. Duchenne Muscular Dystrophy Key Companies
15. Duchenne Muscular Dystrophy Key Products
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 is not exhaustive; the final content may vary.
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