Tuesday, 4 October 2016

Fibrinogen Deficiency Treatment Pipeline Review H1 2016


Summary
‘Fibrinogen Deficiency (Factor I Deficiency) - Pipeline Review, H2 2016’, provides an overview of the Fibrinogen Deficiency (Factor I Deficiency) pipeline landscape.
The report provides comprehensive information on the therapeutics under development for Fibrinogen Deficiency (Factor I Deficiency), complete with analysis by stage of development, drug target, mechanism of action (MoA), route of administration (RoA) and molecule type. The report also covers the descriptive pharmacological action of the therapeutics, its complete research and development history and latest news and press releases. Additionally, the report provides an overview of key players involved in therapeutic development for Fibrinogen Deficiency (Factor I Deficiency) and features dormant and discontinued projects.
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 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. Drug profiles featured in the report undergoes periodic review following a stringent set of processes to ensure that all the profiles are updated with the latest set of information. Additionally, various dynamic tracking processes ensure that the most recent developments are captured on a real time basis.
The report 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.

Scope
- The report provides a snapshot of the global therapeutic landscape of Fibrinogen Deficiency (Factor I Deficiency) 
- The report reviews pipeline therapeutics for Fibrinogen Deficiency (Factor I Deficiency) by companies and universities/research institutes based on information derived from company and industry-specific sources 
- The report covers pipeline products based on various stages of development ranging from pre-registration till discovery and undisclosed stages 
- The report features descriptive drug profiles for the pipeline products which includes, product description, descriptive MoA, R&D brief, licensing and collaboration details & other developmental activities 
- The report reviews key players involved Fibrinogen Deficiency (Factor I Deficiency) therapeutics and enlists all their major and minor projects 
- The report assesses Fibrinogen Deficiency (Factor I Deficiency) therapeutics based on drug target, mechanism of action (MoA), route of administration (RoA) and molecule type 
- The report summarizes all the dormant and discontinued pipeline projects 
- The report reviews latest news related to pipeline therapeutics for Fibrinogen Deficiency (Factor I Deficiency)
Reasons to buy
- Gain strategically significant competitor information, analysis, and insights to formulate effective R&D strategies 
- Identify emerging players with potentially strong product portfolio and create effective counter-strategies to gain competitive advantage 
- Identify and understand important and diverse types of therapeutics under development for Fibrinogen Deficiency (Factor I Deficiency) 
- Identify potential new clients or partners in the target demographic 
- Develop strategic initiatives by understanding the focus areas of leading companies 
- Plan mergers and acquisitions effectively by identifying key players and it’s most promising pipeline therapeutics 
- Devise corrective measures for pipeline projects by understanding Fibrinogen Deficiency (Factor I Deficiency) pipeline depth and focus of Indication therapeutics 
- Develop and design in-licensing and out-licensing strategies by identifying prospective partners with the most attractive projects to enhance and expand business potential and scope 
- Modify the therapeutic portfolio by identifying discontinued projects and understanding the factors that drove them from pipeline

Table of Contents 
Table of Contents 2 
List of Tables 4 
List of Figures 4 
Introduction 5 
Global Markets Direct Report Coverage 5 
Fibrinogen Deficiency (Factor I Deficiency) Overview 6 
Therapeutics Development 7 
Pipeline Products for Fibrinogen Deficiency (Factor I Deficiency) - Overview 7 
Fibrinogen Deficiency (Factor I Deficiency) - Therapeutics under Development by Companies 8 
Fibrinogen Deficiency (Factor I Deficiency) - Pipeline Products Glance 9 
Late Stage Products 9 
Clinical Stage Products 10 
Fibrinogen Deficiency (Factor I Deficiency) - Products under Development by Companies 11 
Fibrinogen Deficiency (Factor I Deficiency) - Companies Involved in Therapeutics Development 12 
Biotest AG 12 
China Biologic Products, Inc. 13 
Grifols, S.A. 14 
LFB S.A. 15 
Octapharma AG 16 
Fibrinogen Deficiency (Factor I Deficiency) - Therapeutics Assessment 17 
Assessment by Monotherapy Products 17 
Assessment by Target 18 
Assessment by Mechanism of Action 19 
Assessment by Route of Administration 20 
Assessment by Molecule Type 22 
Drug Profiles 23 
fibrinogen (human) - Drug Profile 23 
Product Description 23 
Mechanism Of Action 23 
R&D Progress 23 
fibrinogen concentrate (human) - Drug Profile 24 
Product Description 24 
Mechanism Of Action 24 
R&D Progress 24 
fibrinogen concentrate (human) - Drug Profile 25 
Product Description 25 
Mechanism Of Action 25 
R&D Progress 25 
fibrinogen concentrate (human) - Drug Profile 26 
Product Description 26 
Mechanism Of Action 26 
R&D Progress 26 
fibrinogen concentrate (human) - Drug Profile 27 
Product Description 27 
Mechanism Of Action 27 
R&D Progress 27 
Fibrinogen Deficiency (Factor I Deficiency) - Dormant Projects 28 
Fibrinogen Deficiency (Factor I Deficiency) - Discontinued Products 29 
Fibrinogen Deficiency (Factor I Deficiency) - Product Development Milestones 30 
Featured News & Press Releases 30 
Mar 23, 2012: China Biologic Receives SFDA Approval To Begin Clinical Trials For Human Fibrinogen 30 
Appendix 31 
Methodology 31 
Coverage 31 
Secondary Research 31 
Primary Research 31 
Expert Panel Validation 31 
Contact Us 31 
Disclaimer 32


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NORAH TRENT
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