“Myotonic Dystrophy Pipeline Insight, 2022” report by DelveInsight outlines a comprehensive assessment of the present clinical/non-clinical development activities and growth prospects across the Myotonic Dystrophy Market.
The Myotonic 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.
Myotonic Dystrophy Pipeline Analysis
The report provides insights into:
The report provides detailed insights into the emerging therapies for the treatment of Myotonic Dystrophy and the aggregate therapies developed by major pharma companies.
It accesses the different therapeutic candidates segmented into early-stage, mid-stage, and late-stage of clinical development.
It outlines the key companies involved in targeted therapeutics development with respective active and inactive (dormant or discontinued) projects.
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.
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 Myotonic 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.
Major Clinical, Commercial, and Regulatory Activities in the Myotonic Dystrophy Therapeutics Market
In January 2021, Dewpoint Therapeutics announced a new research collaboration with Pfizer for the development of potential therapeutics for the treatment of myotonic dystrophy type 1, DM1, a rare genetic disorder, and one of two types of myotonic dystrophy. Under the agreement, Dewpoint received an upfront payment and is eligible to receive research, development, and sales milestone payments totaling up to $239 million, should all milestones be achieved.
In August 2022, Arthex Biotech’s lead investigational product, ATX-01, was granted Orphan Drug Designation (ODD) by the US. Food and Drug Administration (FDA). ATX-01 is under development for treating Myotonic Dystrophy Type 1 (DM1), a serious, debilitating, and life-threatening disease with no known cure or currently available drug treatment.
DelveInsight’s Myotonic dystrophy pipeline report covers around 28+ products under different phases of clinical development like –
Late-stage products (Phase III)
Mid-stage products (Phase II)
Early-stage product (Phase I)
Pre-clinical and Discovery stage candidates
Discontinued & Inactive candidates
Route of Administration
The Myotonic Dystrophy Pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Myotonic dystrophy Products have been categorized under various ROAs, such as
Intravenous
Oral
Subcutaneous
Molecule Type
The Report Covers the Pipeline Products Under various Molecule types, such as
Small Molecule
Antidepressants
Learn How the Ongoing Clinical & Commercial Activities will Affect the Myotonic Dystrophy Therapeutic Segment @
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Myotonic Dystrophy Therapeutics Landscape
There are approx. 25+ key companies which are developing therapies for Myotonic dystrophy. Currently, Lupin is leading the therapeutics market with its Myotonic dystrophy drug candidates in the most advanced stage of clinical development among all the key players.
The Leading Companies in Myotonic Dystrophy Therapeutics Market Include
Lupin
AMO Pharma
Harmony Biosciences
Avidity Biosciences
Dyne Therapeutics
Nexien BioPharma
Locana, Inc.
Entrada Therapeutics
Arthex Biotech
NeuBase Therapeutics
Enzerna
Astellas Gene Therapies
Dyne Therapeutics
Pepgen Corporation
Sangamo Therapeutics
Syros Pharmaceuticals
And Many Others
Myotonic Dystrophy Drugs Covered in the Report Include:
Mexiletine: Lupin
AMO-02: AMO Pharma
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. Myotonic Dystrophy Current Treatment Patterns
4. Myotonic Dystrophy – DelveInsight’s Analytical Perspective
5. Therapeutic Assessment
6. Myotonic Dystrophy Late Stage Products (Phase-III)
7. Myotonic Dystrophy Mid-Stage Products (Phase-II)
8. Myotonic Dystrophy Early Stage Products (Phase-I)
9. Pre-clinical Products and Discovery Stage Products
10. Inactive Products
11. Dormant Products
12. Myotonic Dystrophy Discontinued Products
13. Myotonic Dystrophy Product Profiles
14. Key Companies in the Myotonic Dystrophy Market
15. Key Products in the Myotonic Dystrophy Therapeutics Segment
16. Dormant and Discontinued Products
17. Myotonic Dystrophy Unmet Needs
18. Myotonic Dystrophy Future Perspectives
19. Myotonic 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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