Abstract
Overview
The clinical trials industry has clear potential for strong growth in the
future, driven by technological and scientific advances. This trend is
complemented by the development of new trial designs, with a view to
rationalizing and accelerating the drug discovery process by identifying
failures at an earlier stage.
This report provides detailed information regarding new developments in the
field of clinical trials as well as an assessment of the impact these new
technologies and designs are having and will have on the pharmaceutical and
biotech industries.
Key Findings
Overall, a number of trends are set to influence the field of clinical trials.
Phase 0 (human microdosing) will become more common and more desirable, while
Phase I is likely to morph into a shorter testing stage.
Similarly, seamless designs are the future of the combined Phase II and III,
cutting development times and associated costs. The latter change would
advance the trend already observed in the field, with many trials designed to
test efficacy and safety concurrently.
Additionally, post-marketing studies will gain importance as patient, ethical
and regulatory demands increase, as much as the methods for toxicology testing
becomes more sophisticated. Such changes will be supported by the use of
existing and new technology.
Other Highlights
- Human microdosing clearly holds significant promise as an analytical tool.
In the coming years, as research methods and technology involved in Phase 0
trials become more sophisticated, human microdosing may be applied to a number
of drugs that could potentially be administered consecutively.
- Looking further into the future, the trend of combining adaptive designs
with the goals of Phase IIb and Phase III trials is likely to become the norm.
This type of trial, described as - ' seamless adaptive' ,, will aim to become
even more time-efficient, although it may carry higher risks for
first-in-class drugs.
- Phase IV trials will continue to grow at an estimated annual rate of over
20 percent. According to some estimates, companies are likely to invest over
US$12 billion in this area in the course of 2007. Phase IV trials will be
increasingly used to expand a drug' s indications, its geographical reach, as
well as to disseminate information to medical professionals, regulatory
authorities and patients alike.
Key Features of This Report
- Analysis of emerging clinical trial innovations, including microdosing
(Phase 0 trials), adaptive trials, Phase IV clinical trials and information
technology trends in the sector
- Integrated discussion and analysis of regulatory activities affecting new
clinical trial designs and information technology in clinical trials
- A discussion of the future trends in the clinical trials marketplace,
shaped by medical and technological advances as well as demographic and
epidemiological changes and industry needs
- Profiles of the leading companies active in microdosing (Phase 0),
adaptive trials, Phase IV trials and information technology
- Overview of the clinical trials industry
- In-depth information and analysis regarding different types and phases of
clinical trials, including their brief history
Table of Contents
1.Methodology and Executive Summary
- 1.1 Report Objectives
- 1.2 Report Methodology
- 1.3 Executive Summary
- 1.3.1 Microdosing
- 1.3.2 Adaptive Design
- 1.3.3 Phase IV Post Marketing Trials
- 1.3.4 Information Technology
- 1.3.5 Clinical Trials Outlook
2. Clinical Trials - “ Background”
- 2.1 Introduction to Clinical Trials
- 2.2 Clinical Trials Marketplace
- 2.3 Types of Clinical Trials
- 2.4 Phases of Clinical Trials
- 2.5 Brief History of Clinical Trials
- 2.6 Need for Innovation in the Pharmaceutical Industry
- 2.7 Need for Maximization of Drug Development
- 2.8 Major Limitations of Present Clinical Trial Designs
- 2.8.1 Cost
- 2.8.2 Inflexibility
- 2.8.3 Time
- 2.8.4 Use of Animals
- 2.8.5 Early Trial Failures
- 2.8.6 Pharmacogenomics
3. Clinical Trials - “ Overview of New Developments”
- 3.1 Present Situation
- 3.2 Regulatory Environment
- 3.3 Need for Changes
- 3.4 Likely Future Trends in Clinical Trials
- 3.5 Partnerships in the Realm of Clinical Trials
4. Phase 0 Clinical Trials
- 4.1 Overview
- 4.2 Human Microdosing - Technology
- 4.2.1 Accelerator Mass Spectometry (AMS)
- 4.2.1.1 Key Study Details
- 4.2.2 Positron Emission Tomography (PET)
- 4.2.2.1 Key Study Details
- 4.2.3 Liquid Chromatography with Tandem Mass Spectrometry (LC-MS/MS)
- 4.2.4 Liquid Scintillation Counting (LSC)
- 4.2.4.1 Key Study Details
- 4.3 Regulatory Issues
- 4.4 Recent Changes in Regulatory Environment
- 4.5 Microdosing Versus Conventional Clinical Trial Methods - Advantages
and Disadvantages
- 4.6 Microdosing and the Use of Animals
- 4.7 Examples of Phase 0 Clinical Trials
- 4.7.1 Neurocrine Biosciences
- 4.7.1.1 Key Study Details
- 4.7.2 Radiant Research
- 4.7.2.1 Key Study Details
- 4.7.3 Resverlogix
- 4.7.3.1 Key Study Details
- 4.7.4 Speedel Pharmaceuticals
- 4.7.4.1 Key Study Details
- 4.7.5 Tripep
- 4.7.5.1 Key Study Details
- 4.7.6 Vitalea Science
- 4.7.6.1 Key Study Details
- 4.7.7 Xceleron
- 4.7.7.1 Key Study Details
- 4.8 Future of Phase 0 Clinical Trials
5. Adaptive Trials
- 5.1 Overview
- 5.2 Forms of Adaptive Trials
- 5.2.1 Scientifically Predetermined Outcome
- 5.2.2 Continual Reassessment Method (CRM)
- 5.2.3 Adaptive Randomization
- 5.2.4 Group Sequential Trial
- 5.3 Regulatory Issues
- 5.4 Recent Examples of Adaptive Trials
- 5.5 Adaptive Versus Controlled Clinical Trials - “ Advantages and
Disadvantages”
- 5.6 Future of Adaptive Clinical Trials
- 5.7 Adaptive Clinical Trials - Company Overviews
- 5.7.1 Bristol-Myers Squibb (BMS)
- 5.7.2 Eli Lilly
- 5.7.3 Novartis
- 5.7.4 Pfizer
- 5.7.5 Tessella
- 5.7.6 Wyeth
6. Phase IV Clinical Trials
- 6.1 Overview
- 6.2 Regulatory Issues
- 6.2.1 Completion of Promised Post-Marketing Studies
- 6.2.2 Clinical Trials Registries
- 6.2.3 Results Disclosure
- 6.3 Examples of Comparative Phase IV Studies
- 6.3.1 Strattera
- 6.3.2 Magnex
- 6.3.3 Avonex
- 6.4 Examples of Indication Extension Phase IV Studies
- 6.4.1 Remicade
- 6.4.2 Velcade
- 6.4.3 Humira
- 6.4.4 Visicol
- 6.5 Examples of Product Withdrawals Following Phase IV Studies
- 6.5.1 Lipobay/Baycol
- 6.5.2 Rezulin
- 6.5.3 Vioxx
- 6.6 Future of Phase IV Trials
7. Information Technology in Clinical Trials
- 7.1 Overview
- 7.2 Regulatory Developments
- 7.3 Benefits of Information Technology
- 7.4 Examples of IT in Clinical Trials
- 7.5 Electronic Data Capture (EDC)
- 7.5.1 Market Value and Potential
- 7.5.2 Main Benefits of EDC
- 7.5.3 Key Therapeutic Areas for EDC Application
- 7.5.4 Companies Using EDC
- 7.6 Clinical Trials Management System (CTMS)
- 7.6.1 Advantages and Disadvantages of CTMS
- 7.6.2 Companies Developing CTMS
- 7.7 Clinical Data Management System (CDMS)
- 7.7.1 CDMS Subtypes
- 7.7.1.1 Database Management System (DBMS)
- 7.7.1.2 Case Report Form (CRF) Designs
- 7.7.1.3 Data Entry Interface
- 7.7.1.4 Reporting/Analysis
- 7.7.2 Companies Involved in CDMS Design
- 7.8 Clinical Trials and the Internet
- 7.9 Security, Confidentiality and Ethical Concerns
8. Company Profiles
- 8.1 Pharmaceutical Companies
- 8.1.1 Bayer
- 8.1.2 Bristol-Myers Squibb (BMS)
- 8.1.3 Eli Lilly
- 8.1.4 InKine Pharmaceuticals
- 8.1.5 Johnson & Johnson (J&J)
- 8.1.6 Merck & Co
- 8.1.7 Novartis
- 8.1.8 Pfizer
- 8.1.9 Wyeth
- 8.2 Biopharmaceutical Companies
- 8.2.1 Biogen Idec
- 8.2.2 Cambridge Antibody Technology (CAT)
- 8.2.3 Millennium
- 8.2.4 Neurocrine Biosciences
- 8.2.5 Pharmaceutical Profiles
- 8.2.6 Radiant Research
- 8.2.7 Resverlogix Corporation
- 8.2.8 Speedel Pharmaceuticals
- 8.2.9 Tripep AB
- 8.2.10 Vitalea Science
- 8.2.11 Xceleron
- 8.3 Medical Device Companies
- 8.4 Pharmaceutical Software Companies
- 8.4.1 DATATRAK
- 8.4.2 etrials
- 8.4.3 Phase Forward
- 8.4.4 Tessella Support Services
Glossary of Terms
Appendix : Regulatory Guidance
Tables
- Table 2.1 Types of Phase I Trials
- Table 2.2 Phases of Clinical Trials
- Table 2.3 Total Expected Sample Sizes for Alternative Clinical Research
Programs
- Table 2.4 Regulatory Agencies for Pharmaceutical Products in Major Global
Markets
- Table 2.5 Areas of Animal Use
- Table 4.1 Advantages and Disadvantages of AMS
- Table 4.2 Advantages and Disadvantages of Human Microdosing
- Table 4.3 Benefits of Microdosing in Relation to Studies on Animals
- Table 4.4 Drugs Tested with Human Microdosing in the CREAM Trial
- Table 5.1 Advantages and Disadvantages of Adaptive Clinical Trials
- Table 7.1 IT in Clinical Trials
- Table 7.6 Examples of Applying IT to Improve Clinical Trials Performance
- Table 7.3 Improvement of Process and Increase of Business Value through
the Adoption of e-Solutions
- Table 7.4 Technology Map for Clinical Trials
- Table 7.5 Benefits of IT in Clinical Trials
- Table 7.2 Reasons Cited for Not Adopting New Data Collection Methods
Graphs
- Graph 2.1 Decreasing R&D Productivity
- Graph 2.2 R&D Costs and Research Productivity
- Graph 4.1 Semilogarithmic Plot of the Plasma Concentration/Time Profile of
Midazolam
- Graph 7.1 Impact of Technology on Clinical Trials
- Graph 7.2 Cost Comparisons (in US$mn) of EDC Budgets of Four Clinical
Trials with
- Corresponding Paper Model and EDC L2TTP
- Graph 7.3 Comparison of Efficiency of EDC versus Paper Data Collection
Figures
- Figure 2.1 Overview of the Activities Involved in Modern Drug Discovery
and Development
- Figure 2.2 Phases of Pre-clinical and Clinical Development
- Figure 5.1 Graphic Representation of Adaptive Trial Design
- Figure 5.2 Re-Analysis of Pravachol Pac Clinical Trial Using Bayesian
Techniques
- Figure 7.1 Typical Systems That Can Be Integrated with CTMS
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