Fibrosis - Pipeline Review, H2 2012

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Market	Healthcare and Medical
Report Type	Market Research
Country	Global
Published	25 November 2012
Number of Pages	81
Report Delivery	Email
Delivery Lead Time	1-3 hours, 24 hour max
Publisher	Global Markets Direct
File Format	PDF

Fibrosis - Pipeline Review, H2 2012 - This report 'Fibrosis - Pipeline Review, H2 2012', provides an overview of the indication's therapeutic pipeline. This report provides information on the therapeutic development for Fibrosis, complete with latest updates, and special features on late-stage and discontinued projects. It also reviews key players involved in the therapeutic development for Fibrosis. Fibrosis - Pipeline Review, Half Year is built using data and information sourced from our 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 our team.

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

Scope

- A snapshot of the global therapeutic scenario for Fibrosis.
- A review of the Fibrosis products under development by companies and universities/research institutes based on information derived from company and industry-specific sources.
- Coverage of products based on various stages of development ranging from discovery till registration stages.
- A feature on pipeline projects on the basis of monotherapy and combined therapeutics.
- Coverage of the Fibrosis pipeline on the basis of route of administration and molecule type.
- Key discontinued pipeline projects.
- Latest news and deals relating to the products.

Reasons to buy

- Identify and understand important and diverse types of therapeutics under development for Fibrosis.
- Identify emerging players with potentially strong product portfolio and design effective counter-strategies to gain competitive advantage.
- Plan mergers and acquisitions effectively by identifying players of the most promising pipeline.
- Devise corrective measures for pipeline projects by understanding Fibrosis 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.

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£1,277.92	Electronic License Electronic License An electronic version (mostly PDF, but can be Excel or PPT), which is either available for immediate download or will be sent via email by the Publisher of the report. The licencing for an electronic version is for use by the purchaser ONLY.
£2,555.85	Site License Site License An electronic version (mostly PDF, but can be Excel or PPT). Where the report(s) is intended for use by more than one individual, across for example, a site, an office, or a division or country.
£3,833.77	Corporate License Corporate License An electronic version (mostly PDF, but can be Excel or PPT). Where the report(s) is/are intended for use by an organisation in its entirety. For example, if reports are put on an Intranet or if they are distributed or used by more than one office, division, or country operation, then a Corporate Licence is required.

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Table of Contents
List of Tables
List of Figures
Introduction
Global Markets Direct Report Coverage
Fibrosis Overview
Therapeutics Development
An Overview of Pipeline Products for Fibrosis
Fibrosis Therapeutics under Development by Companies
Fibrosis Therapeutics under Investigation by Universities/Institutes
Late Stage Products
Comparative Analysis
Mid Clinical Stage Products
Comparative Analysis
Discovery and Pre-Clinical Stage Products
Comparative Analysis
Fibrosis Therapeutics – Products under Development by Companies
Fibrosis Therapeutics – Products under Investigation by Universities/Institutes
Companies Involved in Fibrosis Therapeutics Development
Bristol-Myers Squibb Company
Genzyme Corporation
Quark Pharmaceuticals, Inc.
Lpath, Inc.
Compugen Ltd.
ProMetic Life Sciences Inc.
Hanall Pharmaceutical Co., Ltd.
ProtAffin Biotechnologie AG
Telormedix SA
Promedior, Inc.
Conatus Pharmaceuticals Inc.
Angion Biomedica Corp.
Vantia Therapeutics
Siena Biotech S.p.A.
Stromedix, Inc.
Intercept Pharmaceuticals, Inc.
KineMed, Inc.
Fibrosis – Therapeutics Assessment
Assessment by Monotherapy Products
Assessment by Combination Products
Assessment by Route of Administration
Assessment by Molecule Type
Drug Profiles
fresolimumab - Drug Profile
Lpathomab - Drug Profile
CGEN-857 - Drug Profile
STX-100 - Drug Profile
FAP Inhibitor For Oncology and Fibrosis - Drug Profile
VA-999260 - Drug Profile
Methotrexate + Prednisone - Drug Profile
INT-767 - Drug Profile
emricasan - Drug Profile
imatinib mesylate - Drug Profile
spironolactone - Drug Profile
PBI-4050 - Drug Profile
PBI-4419 - Drug Profile
Tankyrase/Wnt Inhibitor - Drug Profile
AM-095 - Drug Profile
TMX-302 - Drug Profile
MCP-1 Program - Drug Profile
PBI-4494 - Drug Profile
GDF-5 - Drug Profile
siRNAs For Fibrotic Diseases - Drug Profile
RhPTX-2 Fusion Proteins - Drug Profile
AIK-1 - Drug Profile
AIK-3 - Drug Profile
Lathionine AT2 Agonist - Drug Profile
Albumin + Midodrine + Octreotide - Drug Profile
ANG-3281 - Drug Profile
HL-156Fib - Drug Profile
Project MITRA - Drug Profile
Program D: Fibrosis And 2 Additional Targets - Drug Profile
Fibrosis Therapeutics – Drug Profile Updates
Fibrosis Therapeutics - Dormant Products
Appendix
Methodology
Coverage
Secondary Research
Primary Research
Expert Panel Validation
Contact Us
Disclaimer

List of Tables

Number of Products Under Development for Fibrosis, H2 2012
Products under Development for Fibrosis – Comparative Analysis, H2 2012
Number of Products under Development by Companies, H2 2012
Number of Products under Development by Companies, H2 2012 (Contd..1)
Number of Products under Investigation by Universities/Institutes, H2 2012
Comparative Analysis by Late Stage Development, H2 2012
Comparative Analysis by Mid Clinical Stage Development, H2 2012
Comparative Analysis by Discovery and Pre-Clinical Stage Development, H2 2012
Products under Development by Companies, H2 2012
Products under Investigation by Universities/Institutes, H2 2012
Bristol-Myers Squibb Company, H2 2012
Genzyme Corporation, H2 2012
Quark Pharmaceuticals, Inc., H2 2012
Lpath, Inc., H2 2012
Compugen Ltd., H2 2012
ProMetic Life Sciences Inc., H2 2012
Hanall Pharmaceutical Co., Ltd., H2 2012
ProtAffin Biotechnologie AG, H2 2012
Telormedix SA, H2 2012
Promedior, Inc., H2 2012
Conatus Pharmaceuticals Inc., H2 2012
Angion Biomedica Corp., H2 2012
Vantia Therapeutics, H2 2012
Siena Biotech S.p.A., H2 2012
Stromedix, Inc., H2 2012
Intercept Pharmaceuticals, Inc., H2 2012
KineMed, Inc., H2 2012
Assessment by Monotherapy Products, H2 2012
Assessment by Combination Products, H2 2012
Assessment by Stage and Route of Administration, H2 2012
Assessment by Stage and Molecule Type, H2 2012
Fibrosis Therapeutics – Drug Profile Updates
Fibrosis Therapeutics – Dormant Products

List of Figures

Number of Products under Development for Fibrosis, H2 2012
Products under Development for Fibrosis – Comparative Analysis, H2 2012
Products under Development by Companies, H2 2012
Products under Investigation by Universities/Institutes, H2 2012
Late Stage Products, H2 2012
Mid Clinical Stage Products, H2 2012
Discovery and Pre-Clinical Stage Products, H2 2012
Assessment by Monotherapy Products, H2 2012
Assessment by Combination Products, H2 2012
Assessment by Route of Administration, H2 2012
Assessment by Stage and Route of Administration, H2 2012
Assessment by Molecule Type, H2 2012
Assessment by Stage and Molecule Type, H2 2012 43

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