Chapter 1. Executive Summary
Chapter 2. An Introduction to Alzheimer's Disease
2.1 Introduction
2.2 Symptoms and Differential Diagnosis
2.3 The Risk Factors for AD
2.4 Type of Protein as a Cause for AD?
2.4.1 Neuronal and Synaptic Loss of AD
2.4.2 Chromosomal Mutations of AD
2.4.3 Inflammation of AD
2.4.4 Using brain scans to detect Alzheimer's
2.5 The Demographics for AD
2.6 Financial Burden of AD
Chapter 3. Pharmacotherapy for Alzheimer's Disease
3.1 Current AD Pharmaceutical Drug Therapies
3.2 Acetylcholinesterase Drugs - How do you Treat Mild to Moderate
AD?
3.2.1 Pfizer/Eisai Aricept (Donepezil hyrdochloride) - The leading
drug choice for AD
3.2.1 Aricept clinical data
3.2.1.1 Pre-clinical data
3.2.1.2 Aricept clinical data outcomes
3.2.1.3 Eisai and Pfizer Aricept post marketing research for AD
3.2.1.4 Eisai severe Alzheimer's disease trials
3.3 Novartis Excelon (Rivastigamine) - Popular Drug Therapy for AD
3.3.1 Excelon mild-to-moderately severe Alzheimer's disease clinical
data
3.3.2 J&J/ Shire Razadyne (Galantamine) is a Mild-to-moderate
Treatment for AD
3.3.3 J&J/ Shire Reminyl (Galantamine) clinical studies
3.3.4 Forest and Lundbeck (Namenda/Ebixa) The Drug Treatments for
Moderate to Severe AD
3.3.4.1 Lundbeck Ebixa (Namenda) severe Alzheimer's disease
clinical data
3.3.4.2 Lundbeck Ebixa (Namenda) mild-to-moderate Alzheimer's
disease clinical data
3.3.5 Comparative efficacy of Clinical Approved AD drugs
3.3.6 Cognex (Tacrine)
3.3.7 Non steroidal anti-inflammatory drugs (NSAIDs)
3.4 Comorbid Conditions
3.5 Depression associated with Alzheimer's disease and its
management
Chapter 4. UK Alzheimer's Disease treatment guidelines
4.1 UK-National Institute for Clinical Excellence guidelines
4.2 NICE 2001 AD guideline
4.2.1 NICE reversal to 2001 AD guidance
4.2.2 Stakeholders' reaction to NICE 2001 AD guidelines reversal
4.2.3 NICE 2006 AD Guidance Review- Aricept, Razadyne, Exelon and
Memantine
4.2.4 Judicial Review of NICE guideline 2007
Chapter 5. Global AD market
5.1 Overview of Global AD market and Geographical analysis
5.2 US Alzheimer's disease market
5.3 US AD Market Drivers and Restraints
5.3.1 Market Drivers
5.3.2 Market Restraints
5.4 Japan Alzheimer's disease Market
5.5 Japan Market Drivers and Restraints
5.5.1 Market Drivers
5.5.2 Market Restraints
5.6 France Alzheimer's disease Market
5.7 France AD Market Drivers and Restraints
5.7.1 Market Drivers
5.7.2 Market Restraints
5.8 Germany Alzheimer's disease Market
5.9 Germany AD Market Drivers and Restraints
5.9.1 Market Drivers
5.9.2 Market Restraints
5.10 UK Alzheimer's disease Market
5.11 UK AD Market Drivers and Restraints
5.11.1 Market Drivers
5.11.2 Market Restraints
5.12 Italy's Alzheimer's disease Market
5.13 Italy AD Market Drivers and Restraints
5.13.1 Market Drivers
5.13.2 Market Restraints
5.14 Spain's Alzheimer's disease Market
5.15 Spain AD Market Drivers and Restraints
5.15.1 Market Drivers
5.15.2 Market Restraints
Chapter 6. Key players in Alzheimer's Disease Pharmacotherapy
6.1 Eisai/Pfizer's Aricept
6.1.1 Eisai Aricept product expansion
6.1.2 Eisai R&D
6.2 Forest Laboratories Namenda /Lundbeck
Ebixa product expansion
6.3 Shire Razadyne product expansion
6.4 Novartis Exelon product expansion
6.4.1 Novartis Exelon TransdermalPatch for AD
6.4.2 Potential Success of Exelon Transdermal Patch
6.4.3 Novartis' Exelon and Forest Namenda combinatorial study
6.5 Will there be generic competition?
6.6 Market growth indications
Chapter 7. Alzheimer's disease R&D and pipeline
7.1 Unmet medical needs for Alzheimer's disease
7.2 Present clinical approaches to delivering AD therapies
7.2.1 Biomarkers a prospective diagnostic tool
7.3 Overview of pipeline products
7.3.1 Pipeline Drugs for AD
7.3.2 Neurochem's Alzhemed (anti-amyloid compound) illuminates strong
therapeutic potential
7.3.3 Forest's Neramexane potential follow-on product for Namenda
7.3.4. Other compounds presently in the pipeline
7.3.4.1 PBT-1 (Coloquinol)
7.3.4.2 Phenserine
7.3.4.3 Allon Therapeutics'AL-108 and AL-208 to inhibit neuronal
death
7.3.4.4 Martek's DHA reduces brain lesions in AD animal models
7.3.4.5 Phytopharm Cogane -an orally active neuroprotective
compound
7.3.4.6 Nicotine Replacement Therapy as a Potential Treatment
for AD
7.4 Emerging Therapies for Alzheimer's disease
7.4.1 Vitamin E (Antioxidants) for AD
7.4.2 Research has revealed that Vitamin E, Vitamin C and other
health foods possess oxidative properties.
7.4.3 OTC Ginko Biloba May Slow AD Symptoms
7.4.4 Oestrogen HRT May Protect Against AD
Chapter 8. Conclusions
8.1 Expansion of Global Population
8.2 Prevalence of Alzheimer's disease in the Major Markets
8.3 FDA Approved Alzheimer's disease Therapies and NICE's
Cost-Effective Analysis
8.4 Alzheimer's disease Drug Sales across Major Markets 2006
8.5 Barriers to Generic entrants
8.6 Alzheimer's disease Revenue ($m) Forecast
8.7 Leading Companies with Products in late-stage Alzheimer's
disease Pipeline
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