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市場調查報告書

帕金森氏症的生物標記

Biomarkers in Parkinson's Disease

出版商 Insight Pharma Reports 商品編碼 309637
出版日期 內容資訊 英文 81 Pages
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帕金森氏症的生物標記 Biomarkers in Parkinson's Disease
出版日期: 2014年08月01日 內容資訊: 英文 81 Pages
簡介

本報告提供帕金森氏症的特定及診斷所採用的生物標記調查,提供生物標記概要,神經退化性疾病整體的生物標記趨勢,特定ALS的現有遺傳基因標記生物標記候補概要,生物標記研究相關的專家採訪,臨床實驗及開發平台趨勢等。

摘要整理

第1章 本報告焦點

第2章 生物標記及其臨床性效用

  • 何謂生物標記
  • 生物標記的優點
  • 臨床指標和替代指標
  • 生物標記作為替代指標的優點
  • 生物標記作為替代指標的缺點
  • 生物標記有效性的確認

第3章 神經退化性疾病的生物標記

第4章 帕金森氏症

  • 何謂帕金森氏症
  • 帕金森氏症相關遺傳因子
    • PARK2 (parkin/ubiquitin E3 ligase)
    • PINK1 (PTEN-induced kinase 1 protein)
    • GBA (glucocerebrosidase)
  • 有潛力的帕金森氏症生物標記
    • SNCA (α-synuclein)
    • PARK7 (DJ-1 protein)
    • LRRK2 (dardarin protein)
    • 其他
  • Andrew West博士的採訪
    • 研究的背景
    • LRRK2 Protein Kinase
    • 帕金森氏症的研究
    • 優點
    • 課題與規定
    • 帕金森氏症的展望

第5章 Penn State Hershey Medical Center

  • 背景
  • 帕金森氏病診斷的核磁共振攝影
  • Xuemei Huang博士的採訪
    • 研究的背景
    • 非侵入性成像工具
    • 優點
    • 課題與規定
    • 帕金森氏症的展望

Atlantic Biomarkers

  • 背景
  • 生物標記的質譜分析化驗
  • 醫療的影響
  • Andreas Jeromin博士的採訪
    • 企業背景
    • 神經生物標記的研究
    • 質譜分析為基礎的化驗

第6章 調查結果

第7章 帕金森氏症臨床實驗及開發平台的資訊

參考

關於Cambridge Healthcare Institute

圖表

目錄

Biomarkers in Parkinson's Disease is focused on the biomarker identification and development in patients with Parkinson's Disease. As a spin-off of Biomarkers: Discovery and Development for a Diagnostic Approach to Neurodegenerative Disorders, this report focuses on the Parkinson's Disease space featured in the parent report, highlighting several biomarker targets under investigation and the progress that has been made in the industry. With regards to employing the use of biomarkers for Parkinson's Disease, Biomarkers in Parkinson's Disease captures market growth of biomarkers, advantages, disadvantages, and validation techniques.

Experts interviewed in this report include:

  • Dr. Andrew West, Associate Professor of Neurology and Neurobiology and Co-Director, Center for Neurodegeneration and Experimental Therapeutics
  • Dr. Xuemei Huang, Professor and Vice Chair, Department of Neurology; Professor of Neurosurgery, Radiology, Pharmacology, and Kinesiology Director; Hershey Brain Analysis Research Laboratory for Neurodegenerative Disorders, Penn State University-Milton, S. Hershey Medical Center Department of Neurology
  • Dr. Andreas Jeromin, CSO and President of Atlantic Biomarkers

Also available in this report is extensive survey data exclusively conducted for this report. Illustrated by 30 figures captured in an in-depth analysis, this section features insight into targets under investigation, challenges, advantages, and desired features of future diagnostic applications.

To add even more to the robustness of this report, Insight Pharma Reports also engineered a table of clinical trial information and pipeline data from multiple databases related to Parkinson's Disease. This table features companies, targets, clinical phases, and brief target/product descriptions.

Executive Summary

Biomarkers have been a heavily studied topic of interest, and recently on the rise is the interest in neurodegenerative disorders, particularly Parkinson's Disease. Although there are many techniques used to track Parkinson's Disease progression, this report will primarily focus on blood-based and cerebrospinal fluid-based biomarkers currently under investigation. In addition to covering extensive background information, this report will also highlight market growth and outlook, and feature clinical trial and pipeline information.

After the introduction, Chapters 2 and 3 highlight background information on neurodegenerative disorders and include definitions and elaborate examples of different types of biomarkers used in the clinic. Chapter 2 concludes with market growth, advantages of biomarkers, disadvantages of biomarkers, and validation techniques. Chapters 3 gives a brief overview of neurodegenerative disorders, also speaking to the market growth and rise in interest in biomarkers over the years.

Chapter 4 gives specifics on Parkinson's Disease, featuring definitions, symptoms, genetic markers, and current research. As the second leading cause of neurodegeneration in the aging population, researchers are scrambling to find biomarkers that will provide enough information for therapeutic action. Featured in this chapter is an interview with Dr. Andrew West, who speaks about his research and successes with the gene LRRK2. This chapter also provides an extensive amount of detail speaking to genetic targets and their use as biomarkers. Furthermore, Chapter 5 features Dr. Xuemei Huang (Professor and Vice Chair, Department of Neurology; Professor of Neurosurgery, Radiology, Pharmacology, and Kinesiology Director; Hershey Brain Analysis Research Laboratory for Neurodegenerative Disorders, Penn State University-Milton, S. Hershey Medical Center Department of Neurology) and Dr. Andreas Jeromin, CSO and President of Atlantic Biomarkers. These chapters provide insight to utilizing biomarkers as a diagnostic for Parkinson's Disease.

Chapter 6 includes an elaborate survey analysis exclusively done for this report. Qualifying participants worked with neurobiomarkers, neurodiagnostics, or both. With over 30 survey figures depicting the general R&D group working in this space, this section provides information including: research demographics, targets under investigation, challenges, advantages, and desired features of future diagnostic applications.

Finally, Insight Pharma Reports also created a table of clinical and pipeline information related to Parkinson's Disease.

Executive Summary

Biomarkers have been a heavily studied topic of interest, and recently on the rise is the interest in neurodegenerative disorders, particularly Parkinson's Disease. Although there are many techniques used to track Parkinson's Disease progression, this report will primarily focus on blood-based and cerebrospinal fluid-based biomarkers currently under investigation. In addition to covering extensive background information, this report will also highlight market growth and outlook, and feature clinical trial and pipeline information.

After the introduction, Chapters 2 and 3 highlight background information on neurodegenerative disorders and include definitions and elaborate examples of different types of biomarkers used in the clinic. Chapter 2 concludes with market growth, advantages of biomarkers, disadvantages of biomarkers, and validation techniques. Chapters 3 gives a brief overview of neurodegenerative disorders, also speaking to the market growth and rise in interest in biomarkers over the years.

Chapter 4 gives specifics on Parkinson's Disease, featuring definitions, symptoms, genetic markers, and current research. As the second leading cause of neurodegeneration in the aging population, researchers are scrambling to find biomarkers that will provide enough information for therapeutic action. Featured in this chapter is an interview with Dr. Andrew West, who speaks about his research and successes with the gene LRRK2. This chapter also provides an extensive amount of detail speaking to genetic targets and their use as biomarkers. Furthermore, Chapter 5 features Dr. Xuemei Huang (Professor and Vice Chair, Department of Neurology; Professor of Neurosurgery, Radiology, Pharmacology, and Kinesiology Director; Hershey Brain Analysis Research Laboratory for Neurodegenerative Disorders, Penn State University-Milton, S. Hershey Medical Center Department of Neurology) and Dr. Andreas Jeromin, CSO and President of Atlantic Biomarkers. These chapters provide insight to utilizing biomarkers as a diagnostic for Parkinson's Disease.

Chapter 6 includes an elaborate survey analysis exclusively done for this report. Qualifying participants worked with neurobiomarkers, neurodiagnostics, or both. With over 30 survey figures depicting the general R&D group working in this space, this section provides information including: research demographics, targets under investigation, challenges, advantages, and desired features of future diagnostic applications.

Finally, Insight Pharma Reports also created a table of clinical and pipeline information related to Parkinson's Disease.

Table of Contents

Executive Summary

CHAPTER 1: The Focus of this Report

CHAPTER 2: Biomarkers and Their Clinical Utility

  • What are Biomarkers?
  • Advantages of Biomarkers
  • Clinical Endpoints vs. Surrogate Endpoints
  • Advantages of Biomarkers as Surrogate Endpoints
  • Disadvantages to Biomarkers as Surrogate Endpoints
  • How are Biomarkers Validated?

CHAPTER 3: Biomarkers in Neurodegenerative Disorders

CHAPTER 4: Parkinson's Disease

  • What is Parkinson's Disease?
  • Genetic Factors Linked to Parkinson's Disease
    • PARK2 (parkin/ubiquitin E3 ligase)
    • PINK1 (PTEN-induced kinase 1 protein)
    • GBA (glucocerebrosidase)
  • Promising Biomarkers for Parkinson's Disease
    • SNCA (α-synuclein)
    • PARK7 (DJ-1 protein)
    • LRRK2 (dardarin protein)
    • Other biomarkers
  • Interview with Dr. Andrew West
    • Research Background
    • LRRK2 Protein Kinase
    • Advantages
    • Challenges and Limitations
    • Parkinson's Disease Outlook

CHAPTER 5: Penn State Hershey Medical Center

  • Research Background
  • MRI for Parkinson's Disease Diagnosis
  • Interview with Dr. Xuemei Huang
    • Research Background
    • Non-Invasive Imaging Tool
    • Advantages
    • Challenges and Limitations
    • Parkinson's Disease Outlook

Atlantic Biomarkers

  • Research Background
  • Mass-Spectrometry Assays for Biomarkers
  • Impact on Healthcare
  • Interview with Dr. Andreas Jeromin
    • Company Background
    • Neurobiomarker Research
    • Mass Spectrometry-Based Assays

CHAPTER 6: Survey Results

CHAPTER 7: Clinical Trials and Pipeline Information in Parkinson's Disease

References

About Cambridge Healthtech Institute

FIGURES

  • Figure 2.1: Growth of Interest in Biomarkers
  • Figure 2.2: Biomarker Presence in Diagnostic Development vs. Therapeutic Development
  • Figure 3.1: Comparison of Disease Categories
  • Figure 3.2: Growth of Interest in Biomarkers for Neurology
  • Figure 3.3: Growth of Interest in Biomarkers for Parkinson's Disease
  • Figure 6.1: How Would You Categorize Your Organization?
  • Figure 6.2: Which Neurodegenerative Condition are You Currently Studying?
  • Figure 6.3: Which Targets for Huntington's Disease (HD) are You Currently Studying?
  • Figure 6.4: What is the Clinical Status of Your Target(s) for HD?
  • Figure 6.5: When Do You Expect Your Targets for HD to Enter Clinical Trials?
  • Figure 6.6: When Do You Expect Your Target to be an Available Therapeutic for HD?
  • Figure 6.7: Which Targets for Amyotrophic Lateral Sclerosis (ALS) are You Currently Studying?
  • Figure 6.8: What is the Clinical Status of Your Target(s) for ALS?
  • Figure 6.9: When Do You Expect Your Targets for ALS to Enter Into Clinical Trials?
  • Figure 6.10: When Do You Expect Your Target to be an Available Therapeutic for ALS?
  • Figure 6.11: Which Targets for Multiple Sclerosis (MS) are You Currently Studying?
  • Figure 6.12: What is the Clinical Status of Your Target(s) for MS?
  • Figure 6.13: When Do You Expect Your Targets for MS to Enter Into Clinical Trials?
  • Figure 6.14: When Do You Expect Your Target for MS to be an Available Therapeutic?
  • Figure 6.15: Which Signatures for Alzheimer's Disease (AD) are You Currently Studying?
  • Figure 6.16: What is the Clinical Status of Your Target(s) for AD?
  • Figure 6.17: When Do You Expect Your Targets for AD to Enter Into Clinical Trials?
  • Figure 6.18: When Do You Expect Your Target to be an Available Therapeutic for AD?
  • Figure 6.19: Which Signatures for Parkinson's Disease (PD) are You Currently Studying?
  • Figure 6.20: What is the Clinical Status of Your Target(s) for PD?
  • Figure 6.21: When Do You Expect Your Targets for PD to Enter Into Clinical Trials?
  • Figure 6.22: When Do You Expect Your Targets for PD to be an Available Therapeutic?
  • Figure 6.23: How Would You Describe Your Line of Research?
  • Figure 6.24: With Respect to Neurodiagnostics, Which Diagnostic Tools are You Developing for Biomarker Signatures?
  • Figure 6.25: With Respect to Neurodiagnostics, What are Challenges You Have Encountered with Your Diagnostic Development?
  • Figure 6.26: With Respect to Biomarker Development, What Tools are You Using to Identify Biomarker Signatures?
  • Figure 6.27: With Respect to Biomarker Development, What are Challenges You Have Encountered with Your Therapeutic Discovery/Development?
  • Figure 6.28: With Respect to Biomarker Therapeutics, What Tools are You Using to Identify Biomarker Signatures?
  • Figure 6.29: With Respect to Biomarker Therapeutics, What are Challenges You Have Encountered with Your Therapeutic Discovery/Development?
  • Figure 6.30: Which Imaging Techniques do You Feel are the Most Beneficial for Studying the Effects of Neurodegenerative Diseases?
  • Figure 6.31: Which Therapeutics do You Feel will be the Most Beneficial for Neurodegenerative Diseases?

TABLE

  • Table 2.1: Clinical Applications of Biomarkers as Surrogate Endpoints
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