D&MD' s Expanding Opportunities in Contract Research and Contract Manufacture
of Biotherapeutics/ Biologics market analysis report is a comprehensive
compilation of CROs, CMOs and their numerous secondary interconnections. This
report traces the funding of the CRO network and highlights failure points
along the chain of the biologic' s production including the realization that
pharmaceutical productivity decline is most imminent in Phase II failure rates.
Table of Contents
Chapter 1: Executive Summary
Chapter 2: Economics of Outsourcing BioPharmaceuticals/Biologics
2.1 Funding of Biomedical Research by the Pharmaceutical Industry and
Federal Government in US
2.1.1 Government Funding
2.1.1.1 Industry Support
2.1.1.2 Distribution of Funds between Basic and Clinical Research
2.1.2 R&D Funding for Drug Development in 2006
2.1.3 Regulatory Environment
2.1.4 Funding for Discovery and Preclinical Innovation of Drugs
2.1.5 Failure Analysis of Pharmaceutical Productivity
2.1.6 Small/Mid Tier Pharmaceutical Companies
2.2 CROs Contribution to Drug Discovery, Development, Manufacture and Sale
of BioPharmaceuticals
2.2.1 Meta Analysis of the CRO Markets
2.2.2 CRO Segment Growth Rates
2.3 Outsourcing BioPharmaceutical to Contract Research Organizations
2.3.1 Reasons for Outsourcing Clinical Trials to CROs
2.3.1.1 Drivers of Outsourcing
2.3.1.2 Downward Cost Pressures
2.3.1.3 Upward Cost Pressures
Chapter 3: An FDA Approved Drug Takes 15 Years and Costs Over $1 Billion
3.1 CROs-Integral to the Drug Discovery and Development of Biologics
3.2 An Overview of Biologics Manufacturing
3.2.1 The Drug Discovery and Development (Preclinical) to Clinical FDA
Approval Process
3.2.2 Phases of Drug Development in the US
3.3 Making a Reliable Estimate of Drug Productivity
3.3.1 Current Costs to Develop a New Drug
3.4 Clinical Trials (Phases I to III) Leading to NDA Submissions, Phase IV
and FDA Approval
3.4.1 Tactical, Project, and Strategic Clinical Trial Outsourcing Models
3.4.2 Preclinical Market in 2006
3.4.2.1 Phase I Clinical Study Market
3.4.2.2 Phase II/IIIB Clinical Study Market
3.4.2.3 Phase IIIb/IV Clinical Study Market Projection
3.4.3 Central Laboratory/Clinical Trial Laboratory Service Market
3.4.4 Electronic Data Capture (EDC) and Electronic Health Record (EHR)
3.4.4.1 Electronic Data Capture (EDC)
3.4.4.2 Electronic Health Records (EHR)
3.4.5 Medical Devices Worldwide and US Revenues
3.5 Market Drivers for CROs
3.5.1 CRO Usage by Sponsor Companies
3.5.2 Drivers of CRO Growth
3.6 Estimating Clinical Success and Evaluating Clinical Phase Related
Attrition Rates
3.6.1 CMOs Can Speed Up Time to Market by 30%
Chapter 4: Large Scale Contract Manufacture in Phase IV
4.1 CMOs-A Gateway to Clinical Trials f0r Growing Biotech Companies
4.1.1 Case Study of Wyeth' s Over- and Under- Production of
BioPharmaceuticals
4.2 Biologics Growth Drives the CMO Market
4.2.2 Demand for Biotech Products on the Rise
4.2.3 The Growth of Pharmaceutical/Biotech Company-based Gross Sales
Revenues
4.3 Large Number of Branded Drugs Going Off-Patent Likely to Boost Demand
for Manufacturing
4.4 CMOs Provide Biotech Follow ups for Smaller and Mid Size Biotech and
Pharmaceutical Agencies
4.4.1 CMOs Provide the Means to Entry at a Later Stage of the
Development Process
4.4.2 CMOs Add Value by Increasing the Rate of Manufacturing
4.4.3 Self Manufacture Versus Outsourcing to a CMO
4.5 Capacity Sharing: Symbiotic Relationships between Bio/Pharmaceutical
Companies and Contract Manufacturers of Therapeutic Antibodies
4.5.1 Summary of Market Drivers for CMOs
Chapter 5: Globalized CRO Outsourcing in Asia
5.1 India is the Number One Preferred Offshoring Site for CROs
5.1.1 CROs are Boosting the Indian Biotech Market and Vice Versa
5.1.1.1 Conclusion
5.2 China, Singapore, Malaysia, and South Korea
5.2.1 Production Issues in China in 2007 in a Rapidly Growing Generics
Market
5.2.1.1 Infrastructure and Local Regulations -the Growing Generics
Industry
5.2.1.2 Major Biotech Advances in Taiwan
5.2.1.3 Singapore' s Strategic Imperative
5.2.1.4 South Korea
5.2.2 CROs Market Analysis
Chapter 6: Company Profiles
AAI Pharmaceutical
Averion International
Bioanalytical Systems
Bio-Imaging Technologies
Catalyst Pharmaceutical Group
Charles River Laboratories
Clinigene (Biocon)
ClinPro
Commonwealth Biotechnologies
Constella Group
Covalent Group (Encorium Group)
Covance
Eurofins Scientific
ICON Clinical
Kendle Research
Lab International & LAB Research (Aleka Pharma)
Life Science Research
MDS Pharmaceutical
Medpace
Novum Pharmaceutical
Omnicare CRO Services
Paragon Biomedical
Parexel
Patheon
PPD
PRA International (Genstar Capital)
Pracs Institute
Quest
Quintiles Transnational
SFBC (PharmaNet)
SIRO Clinpharm (3i Group)
TABLE OF EXHIBITS
Exhibit 2.1 Pharmaceutical/BioPharmaceutical and NIH Funding 2004 - 2006
Exhibit 2.2 Domestic Spending for R&D in Biomedical Sector
Exhibit 2.3 2006 Budget for R&D Funding for Drug Development
Exhibit 2.4 Current Legislative Acts Initiated in 2007
Exhibit 2.5 Industry versus Non-Industry Distribution of Funding
Exhibit 2.6 NME Output Normalized for 2004 $s
Exhibit 2.7 Division of NMEs Attributed to Small/Mid-Tier Pharmaceutical
Companies versus Large Pharmaceutical Companies 2001-2006
Exhibit 2.8 Current Deal Term by Stage of Development
Exhibit 2.9 Meta Analyses of Financial Projections for the CRO Market
Exhibit 2.10 Projected CRO Market Revenues Derived from Global
Pharmaceutical Sales
Exhibit 2.11 Contract Clinical Service Represented as a Fraction of
Developmental Budget
Exhibit 2.12 Shifting Share of Clinical Projects from AMC to Independent
Community Based CRO Related Sponsors
Exhibit 2.13 Annual Increase in the Percent of Outsourced R&D Expenditure
Exhibit 2.14 Pharmaceutical R&D Spending Growth is Outpaced by the
Outsourced R&D Growth
Exhibit 2.15 Double Digit Growth of CAGR of Developmental Phases
Exhibit 2.16 Activities Across the Development Process
Exhibit 2.17 2006 Services Offered by CROs
Exhibit 3.1 Pharmaceutical Firm Spending by R&D Phase
Exhibit 3.2 Increasing Numbers of Investigators and Clinical Trial studies
Exhibit 3.3 Clinical Trial Spending on Various Drug Development Phases
Exhibit 3.4 Increase in Number of NMEs in Phase II
Exhibit 3.5 Total 2005 Revenue from Companies with Central Laboratory
Services
Exhibit 3.7 Clinical Trials Service Providers Market Share
Exhibit 3.8 Estimated Market Size of EDC Solutions
Exhibit 3.9 Estimated EHR Market Growth
Exhibit 3.10 Global and Domestic Medical Device Market to 2009
Exhibit 3.11 Relating Cost and Speed
Exhibit 3.12 Overall Costs and Times in the Drug Development Process
Exhibit 4.1 Companies Having $400 Million Cash Reserve
Exhibit 4.2 CMO Related Manufacturing Capacity
Exhibit 4.3 Top 20 Blockbuster Biologic Products (Global) in 2006
Exhibit 4.4 Worldwide 2006 Sale of Bio/Pharmaceutical Biologics
Exhibit 4.5 Number of Biotech Drugs in Pipeline
Exhibit 4.6 Implied Demand For Manufacturing Capacity of Monoclonal
Antibodies
Exhibit 4.7 US Pharmaceutical Sales Under Generic Competition Threat
Exhibit 4.8 Top 10 Generic Companies 2005 US Revenues
Exhibit 4.9 Generic Pharmaceutical Market
Exhibit 4.10 Current Blockbusters that are Expected to be Targeted as
Generics
Exhibit 4.11 Number of Biotechnology Derived Marketed Drugs
Exhibit 4.12 Number of Biotechnology Derived Marketed Drugs
Exhibit 4.13 Assumptions Made in an Economical Model
Exhibit 4.14 Comparison of the CRO Manufacturing versus Self Manufacturing
Advantages
Exhibit 4.15 Cell Culture Manufacturing Capacity of CMOs
Exhibit 5.1 2003 Survey Conducted Across Six Offshoring Operations
Exhibit 5.2 Global Clinical Investigation Spread as Demonstrated by
Increase in 1572 Filings
Exhibit 5.3 Clinical Studies Cost Comparison by Country
Exhibit 5.4 2004 Leading Pharmaceutical Companies in India
Exhibit 5.5 India' s Biotech Firms
Exhibit 5.6 Revenue Forecasts for China' s CRO Activities
Exhibit 5.7 Major Generics being Manufactured in Taiwan
Exhibit 5.8 Top 5 CROs Increasing Market Share
Exhibit 5.9 Public CRO Revenues in 2006
Exhibit 5.10 CAGR Relating to Revenues of Public Traded CROs
Exhibit 5.11 CRO Sector Metrics
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【 英文市場調査報告書 】
生物製剤の委託研究および委託製造における機会拡大
Expanding Opportunities in Contract Research and Contract Manufacture of Biotherapeutics/Biologics
出版日 : 2007/11