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市場調查報告書

神經科診斷 ‐ 利用預測生物標記增加收益

Stakeholder Opinions: Diagnostics in Neurology - Predictive biomarkers expand drug revenues

出版商 Datamonitor
出版日期 2008年07月 商品編碼 74908
內容資訊 英文  
價格
本報告書已不再販售

本報告已在2011年07月19日停止出版。

簡介

本報告書內容包括:阿茲海默症、帕金森氏症、多發性硬化症、癲癇、偏頭痛、不眠症、漢金頓症、肌肉萎縮性側索硬化症等的神經學狀態 主要生物標記概要、神經學診斷生物標記達成商業成功所需的因素、提昇阿茲海默症診斷品質增加收益的可能性分析等。內容綱要摘記如下:

關於DATAMONITOR的醫療分析團隊

第1章 實施概要

  • 分析範圍
  • 投稿專家
  • Datamonitor針對神經科診斷的分析
  • 相關報告書

第2章 背景

  • 何謂診斷測試
  • 診斷的規範
  • 診斷測試的價値

第3章 現在的診斷技術及課題

  • 神經學狀態‐不同的疾病病理生態學影響生物標記的潛在需求
  • 阿茲海默症
  • 帕金森氏症
  • 多發性硬化症
  • 癲癇
  • 偏頭痛
  • 不眠症
  • 漢金頓症
  • 肌肉萎縮性側索硬化症

第4章 未來開發的影響

  • 未來的疾病診斷
  • 可能為診斷企業開拓高價值市場的分子生物標記
  • 龐大的製藥企業的利益
  • 重要患者的利益
  • 醫療費負擔者歡迎生物標記

第5章 未來的影像技術

  • 定義
  • 阿茲海默症及輕度認知障礙
  • 帕金森氏症
  • 其他神經疾病

第6章 未來的體外臨床檢查

  • 摘要
  • 血清生物標記及尿生物標記(包含基因體學)
  • 腦髓

參考資訊

附錄

目錄

Abstract

Overview

Introduction

As advances in omics technologies enable the development of high value molecular diagnostics, neurological conditions represent an attractive target for diagnostic companies. In this report, Datamonitor identifies the diseases in which early detection with a biomarker could significantly benefit the patient, gain payer approval, and ultimately expand the pharmaceutical market.

Scope

  • Neurological conditions covered: Alzheimer' s disease, Parkinson' s disease, MS, epilepsy, migraine, insomnia, Huntington' s disease and ALS.
  • Overview of key biomarkers in development for each condition (including genetics).
  • Identification of key factors required for the commercial success of neurological diagnostic biomarkers.
  • Analysis of potential drug revenue gains due to improved diagnostics in Alzheimer' s disease.

Highlights

A battery or algorithm of tests for each disease is likely to be available within the next 10 years. This is already the case for multiple sclerosis, the most mature neurological diagnostic market, with both clinical, imaging and in vitro diagnostics incorporated in a clear algorithm.

Revenue gained from earlier use (identification and incorporation of mild cognitively impaired patients) of potentially disease-modifying drugs in Alzheimer' s disease could generate an additional $5 billion by 2017 across the seven major markets (US, Japan, France, Germany, Italy, Spain and the UK).

Neurology biomarker discovery and development is an attractive market for small biotechnology companies. The regulation of in vitro diagnostics is significantly less stringent than for pharmaceutical drugs. This decreases the considerable financial barriers to entry usually faced by biotechnology companies orientated towards drug discovery.

Reasons to Purchase

  • Assess which diseases have the highest unmet need for new biomarkers.
  • Appreciate the lucrative potential of earlier treatment of neurodegenerative conditions.
  • Forecast the impact of improved diagnostics on neurological drug sales.

Table of Contents

  • ABOUT DATAMONITOR HEALTHCARE
    • About the CNS pharmaceutical analysis team
  • CHAPTER 1 EXECUTIVE SUMMARY
    • Scope of the analysis
    • Contributing experts
    • Datamonitor insight into diagnostics in neurology
    • Related reports
  • CHAPTER 2 BACKGROUND
    • What is a diagnostic test?
      • Biomarkers - objective measures
    • Regulation of diagnostics
      • Imaging
      • In vitro diagnostics
        • European Union
        • United States
    • The value of a diagnostic test
      • Technical performance
      • Clinical performance
      • False positives and false negatives
  • CHAPTER 3 CURRENT DIAGNOSTIC TECHNIQUES AND CHALLENGES
    • Neurological conditions - differing disease pathophysiology influences biomarker unmet need
      • Delay to accurate diagnosis is particularly slow in Alzheimer' s disease at present
    • Alzheimer' s disease
      • Challenges for Alzheimer' s disease biomarkers
        • Proposed criteria for effective biomarkers in Alzheimer' s disease
      • Current diagnostic criteria
        • DSM-IV-TR
        • NINCDS-ADRDA
        • Recent revising suggestion - aiming for earlier detection
      • Functional tests
        • Mini-Mental Status Exam
        • Ruling out other conditions
      • Pathological diagnosis post-mortem
      • Time to accurate diagnosis of Alzheimer' s disease
    • Parkinson' s disease
      • Diagnosis is based on clinician observation of symptoms
        • Primary symptoms used for diagnosis
        • Neurological evaluation of Parkinson' s disease
        • Ruling out disorders that produce parkinsonian symptoms
      • Current imaging techniques used by neurologists
      • Time to accurate diagnosis of Parkinson' s disease
    • Multiple sclerosis
      • Current diagnostic technique includes MRI scans
      • Magnetic resonance imaging
        • Clinical signs and MRI might be enough for diagnosis
      • Spinal tap
      • Evoked Potential Tests
      • Differential diagnosis
      • Time to accurate diagnosis of multiple sclerosis
    • Epilepsy
      • Patient and family reported signs
      • Electroencephalography
        • Portable EEG
      • Magnetic Resonance Imaging
      • Genetic testing
    • Migraine
    • Insomnia
      • Basic requirements
        • Optional requirements
      • Clinical history
      • Sleep history
      • Polysomnography
    • Huntington' s disease
      • Pre-symptomatic diagnosis, but no disease-modifying treatment
        • Predictive genetic test is available, but use is only moderate
        • Pre-implantation screening is rarely undertaken
    • Amyotrophic lateral sclerosis
      • The El Escorial diagnostic criteria
  • CHAPTER 4 IMPACT OF FUTURE DEVELOPMENTS
    • Future disease diagnosis
      • Alzheimer' s disease
        • Future diagnostic algorithm likely to include several biomarkers
      • Parkinson' s disease
        • Disease-modifying drug will stimulate early diagnostics research
      • Multiple sclerosis
        • Comparatively mature diagnostic market with several biomarkers
      • Epilepsy
        • Patient reported events and electroencephalography (EEG) likely to remain the mainstay of diagnosis
      • Migraine and insomnia
      • Amyotrophic lateral sclerosis
    • Molecular biomarkers present high value market for diagnostic companies
      • Imaging companies
      • Genetic testing companies
      • In vitro assay companies
    • Benefit to pharmaceutical companies is substantial
      • Defined patient population leads to more targeted marketing
      • Earlier treatment results in greater revenues
      • Case studies-quantifying the impact of improved biomarkers on drug sales
        • Huntington' s disease-pre-symptomatic "at risk" population-the lucrative untapped market
        • Alzheimer' s disease-incorporation of patients with mild cognitive impairment
    • Benefit to patients is significant
      • Earlier treatment and pre-symptomatic medicine
      • Personalized medicine
      • More sophisticated drug development
    • Payers will welcome the clarity biomarkers offer
  • CHAPTER 5 FUTURE IMAGING TECHNOLOGIES
    • Definitions
    • Alzheimer' s disease and mild cognitive impairment
      • Structural imaging
      • Radiotracer fluorodeoxyglucose
      • Beta-amyloid proves to be the dominant imaging biomarker
        • Beta-amyloid radioligands using PET scans
        • GE Healthcare' s Pittsburgh Compound-B
        • Other beta-amyloid tracers
      • Acetylcholinesterase
    • Parkinson' s disease
      • Radiotracers
        • GE Healthcare' s DaTSCAN
      • Transcranial sonography
    • Other neurological diseases
      • Epilepsy
      • Multiple sclerosis
  • CHAPTER 6 FUTURE IN VITRO DIAGNOSTIC TESTS
    • Summary
    • Serum- and urine-based biomarkers (including genomics)
      • Alzheimer' s disease and mild cognitive impairment
        • Power3' s NuroPro protein serum biomarkers
        • Proteome Sciences' TMT technology mass spectrometry tool for protein biomarker development
        • Nymox Pharmaceutical' s AlzheimAlert urine test
        • Genetic blood testing-DiaGenic and IMGM Laboratories
        • Pronucleon peptides, fluorescently labeled peptides for amyloid detection-Adlyfe
        • Sulfatide, possible specificity for mild Alzheimer' s disease
        • Genomics, genetic susceptibility of sporadic form is becoming clear-Athena Diagnostics and others
      • Parkinson' s disease
        • Neuromelanin-endogenous pigment identifies Parkinson' s disease
        • Genomics, genetic susceptibility of sporadic form is becoming clear-Athena Diagnostics and others
        • Power 3' s NuroPro
      • Multiple sclerosis
        • Anti-glycan antibodies in early stage patients-Glycominds
        • Plasma markers of the disease and Tysabri side effect-BG Medicine
        • Genomics in multiple sclerosis
      • Amyotrophic lateral sclerosis
        • Genomics of ALS-attention shifts to sporadic form
      • Other neurological diseases
    • Cerebrospinal fluid
      • Alzheimer' s disease (AD)
        • Beta-amyloid and tau levels have been extensively studied
        • Isoprostane-8,12-iso-iPF2a-VI
      • Parkinson' s disease
        • Neurofilament heavy-chain' s expose axonal damage
      • Other neurological conditions
        • Amyotrophic lateral sclerosis
        • Multiple sclerosis
  • BIBLIOGRAPHY
    • Journal papers and conference abstracts
    • Websites
    • Datamonitor reports
  • APPENDIX
    • Contributing experts
    • About Datamonitor
      • About Datamonitor Healthcare
    • Datamonitor Healthcare' s therapy area capabilities
      • About the Disease analysis team
      • Disclaimer
  • List of Tables
    • Table 1: Comparative biomarker potential across key neurological diseases
    • Table 2: DSM-IV criteria for Alzheimer' s disease type dementia
    • Table 3: Unified Parkinson' s Disease Rating Scale-cognition, behavior and mood
    • Table 4: New multiple sclerosis diagnostic criteria (McDonald criteria)
    • Table 5: Prevalence rate of mild cognitive impairment (MCI)
    • Table 6: A(1-42 in cerebrospinal fluid
  • List of Figures
    • Figure 1: Typical diagnostic biomarker development process
    • Figure 2: Distribution graph of biomarker accuracy
    • Figure 3: False positives and false negatives - distribution curve
    • Figure 4: Mean time between initial presentation to accurate diagnosis of Alzheimer' s disease, Parkinson' s disease and multiple sclerosis
    • Figure 5: Time (months) from presentation to accurate diagnosis of Alzheimer' s disease, 2006
    • Figure 6: Percentage of neurologists using each diagnostic imaging technique to make a diagnosis of Parkinson' s disease, 2007
    • Figure 7: Time (months) from presentation to accurate diagnosis of Parkinson' s disease, 2007
    • Figure 8: Current diagnostic algorithm for multiple sclerosis
    • Figure 9: MRI scan image of a multiple sclerosis patients brain, and a normal individual
    • Figure 10: Magnetic resonance imaging (MRI) scanner
    • Figure 11: Time (months) from presentation to accurate diagnosis of multiple sclerosis (MS), 2006
    • Figure 12: An electroencephalograph (EEG)
    • Figure 13: Photograph of a portable eletroencephalography (EEG) unit
    • Figure 14: Genetic risk of developing Huntington' s disease
    • Figure 15: Points of diagnosis of Alzheimer' s disease
    • Figure 16: Revenue gain in the Alzheimer' s disease market value with the inclusion of patients with amnestic mild cognitive impairment (amMCI), 2013-17
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