Duchenne Muscular Dystrophy 2014 New Study Released

Fast Market Research recommends “Duchenne Muscular Dystrophy – Pipeline Review, H1 2014″ from Global Markets Direct, now available

Boston, MA — (SBWIRE) — 04/17/2014 — Global Markets Direct’s, ‘Duchenne Muscular Dystrophy – Pipeline Review, H1 2014′, provides an overview of the Duchenne Muscular Dystrophy’s therapeutic pipeline.

This report provides comprehensive information on the therapeutic development for Duchenne Muscular Dystrophy, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type, along with latest updates, and featured news and press releases. It also reviews key players involved in the therapeutic development for Duchenne Muscular Dystrophy and special features on late-stage and discontinued projects.

View Full Report Details and Table of Contents

Global Markets Direct’s report features investigational drugs from across globe covering over 20 therapy areas and nearly 3,000 indications. The report is built using data and information sourced from Global Markets Direct’s proprietary databases, Company/University websites, SEC filings, investor presentations and featured press releases from company/university sites and industry-specific third party sources, put together by Global Markets Direct’s team. Drug profiles/records featured in the report undergoes periodic updation following a stringent set of processes that ensures that all the profiles are updated with the latest set of information. Additionally, processes including live news & deals tracking, browser based alert-box and clinical trials registries tracking ensure that the most recent developments are captured on a real time basis.

The report enhances decision making capabilities and help to create effective counter strategies to gain competitive advantage. It strengthens R&D pipelines by identifying new targets and MOAs to produce first-in-class and best-in-class products.

Note*: Certain sections in the report may be removed or altered based on the availability and relevance of data for the indicated disease.


– The report provides a snapshot of the global therapeutic landscape of Duchenne Muscular Dystrophy
– The report reviews key pipeline products under drug profile section which includes, product description, MoA and R&D brief, licensing and collaboration details & other developmental activities
– The report reviews key players involved in the therapeutics development for Duchenne Muscular Dystrophy and enlists all their major and minor projects
– The report summarizes all the dormant and discontinued pipeline projects
– A review of the Duchenne Muscular Dystrophy products under development by companies and universities/research institutes based on information derived from company and industry-specific sources
– Pipeline products coverage based on various stages of development ranging from pre-registration till discovery and undisclosed stages
– A detailed assessment of monotherapy and combination therapy pipeline projects

Companies Mentioned in this Report: Sanofi, Eli Lilly and Company, Daiichi Sankyo Company, Limited, Nippon Shinyaku Co., Ltd., Sarepta Therapeutics, Inc., NicOx S.A., Galapagos NV, Summit Corporation plc, Santhera Pharmaceuticals Holding AG, Shenzhen Beike Biotechnology Co., Ltd., Italfarmaco S.p.A., Prosensa Holding BV, Catabasis Pharmaceuticals, Inc., Nobelpharma Co., Ltd., PTC Therapeutics, Inc., Fate Therapeutics, Inc., N-Gene Research Laboratories, Inc., Asklepios BioPharmaceutical, Inc., Genethon, miRagen Therapeutics, Inc., Prosensa Therapeutics B.V., EryDel SPA, Myomics, Inc., Prothelia, Inc., ReveraGen BioPharma, Inc., Retrophin, LLC

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