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New Pipeline report on Rett Syndrome - Pipeline Review, H1 2017 report provide comprehensive information on the therapeutics under development for Rett Syndrome (Central Nervous System), complete with analysis by stage of development, drug target, mechanism of action (MoA), route of administration (RoA) and molecule type.Browse the 28 Tables and 10 Figures, 16 Company Profiles, Spread across 119 Pages Report Available at http://www.reportsnreports.com/reports/992885-rett-syndrome-pipeline-review-h1-2017.html .
Rett syndrome is a neurodevelopmental disorder. This is caused by genetic mutation on MECP2 gene. Rett syndrome is described in four stages: Stage I or early onset, Stage II or rapid destruction, Stage III, or the plateau and Stage IV, or the late motor deterioration stage. Symptoms include slowed growth, loss of normal movement and coordination, loss of communication abilities, breathing problems, pain, irregular heartbeat and seizures. Risk factors include family history and gender. Treatment includes disease modifying drugs.
Rett Syndrome - Companies Involved in Therapeutics Development - Amorsa Therapeutics Inc, Anavex Life Sciences Corp, Apteeus, ArmaGen Inc, Edison Pharmaceuticals Inc, Eloxx Pharmaceuticals Ltd, GW Pharmaceuticals Plc, Horizon Pharma Plc, Mitochon Pharmaceuticals Inc, Mitsubishi Tanabe Pharma Corp, Neuren Pharmaceuticals Ltd, Neurolixis Inc, Newron Pharmaceuticals SpA, OPKO Health Inc, Sage Therapeutics Inc, Ultragenyx Pharmaceutical Inc
Drug Profile - Rett Syndrome, amlexanox, ANAVEX-273, BHV-5000, Bryostatin-1, CPT-157633, cysteamine DR, desipramine hydrochloride, fingolimod hydrochloride, ELX-02, GWP-42006, LM-22A4, MP-101, NLX-101, Oligonucleotide many more..
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Rett Syndrome (Central Nervous System) pipeline market guide helps in identifying and tracking emerging players in the market and their portfolios, enhances decision making capabilities and helps to create effective counter strategies to gain competitive advantage. The guide is built using data and information sourced from Global Markets Direct's proprietary databases, company/university websites, clinical trial registries, conferences, SEC filings, investor presentations and featured press releases from company/university sites and industry-specific third party sources. Additionally, various dynamic tracking processes ensure that the most recent developments are captured on a real time basis.
Rett Syndrome - Pipeline Review, H1 2017, report provides comprehensive information on the therapeutics under development for Rett Syndrome (Central Nervous System), complete with analysis by stage of development, drug target, mechanism of action (MoA), route of administration (RoA) and molecule type. The guide covers the descriptive pharmacological action of the therapeutics, its complete research and development history and latest news and press releases.
Scope
• The pipeline guide provides a snapshot of the global therapeutic landscape of Rett Syndrome (Central Nervous System).
• The pipeline guide reviews pipeline therapeutics for Rett Syndrome (Central Nervous System) by companies and universities/research institutes based on information derived from company and industry-specific sources.
• The pipeline guide features descriptive drug profiles for the pipeline products which comprise, product description, descriptive licensing and collaboration details, R&D brief, MoA & other developmental activities.
• The pipeline guide reviews key companies involved in Rett Syndrome (Central Nervous System) therapeutics and enlists all their major and minor projects.
• The pipeline guide evaluates Rett Syndrome (Central Nervous System) therapeutics based on mechanism of action (MoA), drug target, route of administration (RoA) and molecule type.
• The pipeline guide encapsulates all the dormant and discontinued pipeline projects.
• The pipeline guide reviews latest news related to pipeline therapeutics for Rett Syndrome (Central Nervous System)
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Website: http://www.reportsnreports.com/reports/992885-rett-syndrome-pipeline-review-h1-2017.html
Release ID: 199076
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