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首頁 > 市場調查報告書 > 生物科技 > 分子標靶治療學 > 激酶治療藥物:生產線分析與商業預測
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市場調查報告書

激酶治療藥物:生產線分析與商業預測

Kinase Therapeutics: Pipeline Assessment and Commercial Prospects

出版商 Insight Pharma Reports
出版日期 2010年01月 商品編碼 111962
內容資訊 英文 302 pages
價格
US $ 3195 PDF by E-mail ( Single User License)
US $ 3995 PDF by E-mail (Single Site License)
US $ 9950 PDF by E-mail ( Multi User License)


激酶治療藥物:生產線分析與商業預測 是由出版商Insight Pharma Reports在2010年01月所出版的。 這份英文市場調查報告書包含302 pages 價格從美金3195起跳。

簡介

進入臨床開發階段之激酶抑製劑數量近年來大幅度持續增加。包括大型製藥公司,連新進軍企業也加入開發之列。預計2020年止小分子激酶抑製劑年間將會創出250億美金之收益。

本報告為,以激酶為標的之研究開發趨勢,並匯整目前激酶抑製劑產品線、目前為止之商業成果、長短期市場展望、同領域之進軍企業動向,以下列摘要形式闡述。

第1章 激酶

  • 激酶之功能
  • 人類激酶組
  • 激酶之分類
  • 激酶之構造
  • 作為藥劑標的之激酶

第2章 對應

  • 簡介
  • 血管新生疾病
  • 發炎疾病
  • 代謝性疾病
  • 中樞神經系統疾病
  • 新血管疾病

第3章 研究開發趨勢

  • 簡介
  • 激酶之選擇性
  • 結構性特徵
  • 激酶突變
  • 智慧財產權問題

第4章 目前商業成果

  • 簡介
  • 小分子
  • 生物製劑

第5章 目前激酶抑製劑之產品線

  • 簡介
  • 概要
  • 第3階段之激酶抑製劑
  • 第2階段之激酶抑製劑
  • 第1階段之激酶抑製劑
  • 生長因子受體激酶
  • 激酶信號通路
  • 細胞週期抑製劑
  • 激酶
  • 其他激酶
  • 今後展望

第6章 企業動態

  • 簡介
  • 主要企業
  • 專業企業
  • 服務公司

第7章 市場展望

  • 簡介
  • 短期發展
  • 長期預測

第8章 專家訪談

參考資訊

企業索引(附網站位址)

目錄

Abstract

The number of kinase inhibitors entering clinical development has increased significantly in recent years. In addition to major pharmaceutical and biotech companies, an increasing number of emerging companies are focusing on their development. By 2020, small-molecule kinase inhibitors could generate annual revenues > $25 billion.

This report assesses:

  • R&D considerations specific to targeting kinases
  • Current kinase inhibitor pipelines
  • Commercial successes to date
  • Near- and longer-term market outlook
  • Corporate activities of firms involved with kinases

Kinases are now firmly established as a major class of drug targets. It was previously thought that kinases would be intractable drug targets due to the presumed need to compete with ATP and the assumption that sufficient selectivity would be unattainable. However, considerable progress has been made in understanding kinases and their function, and the past few years have seen a number of kinase inhibitors reach the market. Imatinib (Novartis' Gleevec) is currently the most commercially successful, with sales reaching $3.7 billion in 2008. Erlotinib (OSI/Roche' s Tarceva) generated revenues of $1.1 billion the same year.

In recent years, there has been an explosion in the number of kinase inhibitors entering the clinic, and many more are in preclinical development. Kinase Therapeutics: Pipeline Assessment and Commercial Prospects identifies which kinase families and their respective members have attracted the greatest interest for therapeutic development and in which indications these kinases play a physiological or pathophysiological role and thus are most relevant for kinase inhibitor development.

This report extensively reviews small-molecule kinase inhibitors identified as being in active clinical development. Oncology indications accounted for 79% of these inhibitors, while inflammatory indications accounted for nearly half of the kinase inhibitors not being developed to treat cancers. Kinase inhibitors identified as being in clinical development are analyzed by clinical phase (Phases I-III) and by target.

Kinase Therapeutics: Pipeline Assessment and Commercial Prospects examines the considerable discrepancies in the levels of activities amongst major companies regarding kinase inhibitor development. The perceived tractability of kinases as drug targets has led to an increasing number of emerging companies focused on kinase inhibitor development. Many are developing kinase inhibitors in partnership with major companies, while others may be potential acquisition targets. Further, the desire to extensively profile kinase inhibitors has led to the emergence of companies that offer such services. The activities of selected specialist and service companies are also examined.

The period to 2015 should see a number of additional kinase inhibitors reach the market. As a result, annual revenues generated by kinase inhibitors should approximately double by 2015 from the near $8 billion generated in 2008. The large number of kinase inhibitors currently in Phase II should ensure that the period between 2015 and 2020 sees a steady flow of new kinase inhibitors approved for use, ensuring continued growth of their commercial revenues.

About the Author

Peter Norman, PhD, MBA is a pharmaceutical consultant and analyst based in Burnham Beeches, near Windsor, England. He has written and presented widely on various aspects of respiratory disease, drug development, and on the analysis of diverse therapeutic markets. Dr. Norman has over 20 years of experience of the pharmaceutical industry in both R&D and competitive intelligence. His publications include many reviews and 16 original scientific papers and 11 patents, together with a number of management reports. The latter have been published by a number of companies including FT Pharmaceuticals, Urch Publications, SMI and Decision Resources, Informa, and Insight Pharma Reports (a division of Cambridge Healthtech Institute). Dr. Norman holds science degrees from Cambridge University and Brunel University and an MBA degree from the Open University.

Table of Contents

CHAPTER - 1

KINASES

  • 1.1. The Function of Kinases
  • 1.2. The Human Kinome
  • 1.3. Kinase Classification
    • AGC Family
    • CAMK Family
    • CMGC Family
    • CK1 Family
    • STE Family
    • TK Family
    • TKL Family
    • Atypical Protein Kinases
  • 1.4. Kinase Structure
  • 1.5. Kinases as Drug Targets

CHAPTER - 2

INDICATIONS

  • 2.1. Introduction
  • 2.2. Cancer
  • 2.3. Angiogenic Conditions
  • 2.4. Inflammatory Diseases
  • 2.5. Metabolic Disorders
  • 2.6. CNS Conditions
  • 2.7. Cardiovascular Disease

CHAPTER - 3

R&D CONSIDERATIONS

  • 3.1. Introduction
  • 3.2. Kinase Selectivity
    • Profiling
    • Selectivity Profiles of Selected Inhibitors
    • How Selective?
  • 3.3. Structural Features
    • X-Ray Structures and Multiple Conformations
  • 3.4. Kinase Mutations
    • Bcr-Abl
    • Pharmacogenomics
  • 3.5. Intellectual Property Issues

CHAPTER - 4

CURRENT COMMERCIAL SUCCESSES

  • 4.1. Introduction
  • 4.2. Small Molecules
    • Overview
    • Abl Inhibitors
      • Gleevec (imatinib)
      • Tasigna (nilotinib) and Sprycel (dasatinib)
    • EGF Family Inhibitors
      • Tarceva (erlotinib) and Iressa (gefitinib)
      • Tykerb (lapatinib)
    • Multi-Kinase Inhibitors
      • Nexavar (sorafenib)
      • Sutent (sunitinib)
      • Palladia (toceranib) and Masivet (mastinib)
    • mTOR Inhibitors
      • Rapamune (sirolimus)
      • Torisel (temsirolimus), Afinitor/Certican (everolimus), Endeavor (zotarolimus)
    • Rho Inhibitor
      • Eril (fasudil)
  • 4.3. Biological Agents

CHAPTER - 5

CURRENT KINASE INHIBITOR PIPELINES

  • 5.1. Introduction
  • 5.2. Overview
  • 5.3. Kinase Inhibitors in Phase III
    • Enzastaurin and Ruboxistaurin
    • Midostaurin
    • Pan-VEGFR Inhibitors
      • Votrient (pazopanib)
      • Cediranib
      • Motesanib
      • Axitinib
      • Aflibercept
    • Vandetanib
    • BIBW-2992
    • Neratinib
    • Pertuzumab
    • FGFR Inhibitors
      • BIBF-1120
      • Brivanib
    • Alvocidib
    • Bosutinib
    • Lestaurtinib
    • Ridaforolimus
    • Masitinib
    • BMS-907351
    • CP-690550
    • INCB-18424
  • 5.4. Kinase Inhibitors in Phase II Development
  • 5.5. Kinase Inhibitors in Phase I Development
  • 5.6. Growth Factor Receptor Kinases
    • ErbB Family Kinases
      • ErbB2 and ErbB3
      • ErbB2 and EGFR
      • Pan-ErbB
      • Antibodies
    • FGF
    • IGF
    • VEGF
    • Multi-Kinase Inhibitors
    • Flt3
  • 5.7. Popular Kinase Cascades
    • PI3K, Akt, mTOR, S6K
      • Perifosine
      • Triciribine
      • Archexin
    • Ras, Raf, MEK, ERK
      • Roche
      • Ardea Biosciences and Bayer
      • Array and AstraZeneca
    • JAK Family
  • 5.8. Cell Cycle Inhibitors
    • Cyclic-Dependent Kinase (CDK)
    • Checkpoint Kinase (Chk)
    • Polo-Like Kinase (PLK)
      • BI-2536 and BI-6727
  • 5.9. Popular Kinase Targets
    • Abl
    • p38
    • GSK-3
    • Protein Kinase C
    • Aurora
      • Broad Spectrum
      • Pan-Aurora
      • Aurora 1
      • Aurora 2
    • c-Met
    • Rho
    • JNK
    • Src Family
    • Kinases in Inflammatory Diseases
  • 5.10. Other Kinases
    • Serine/Threonine Kinases
    • Tyrosine Kinases
    • Tyrosine-Like, CAMK, and Atypical Kinases
  • 5.11. Outlook

CHAPTER - 6

CORPORATE ACTIVITIES

  • 6.1. Introduction
  • 6.2. Major Companies
    • Abbott
    • Amgen
    • Astellas
    • AstraZeneca
    • Bayer
    • Boehringer Ingelheim
    • Bristol-Myers Squibb
    • Daiichi Sankyo
    • Eisai
    • Eli Lilly
    • GlaxoSmithKline
    • Johnson & Johnson
    • Merck & Co.
    • Merck Serono
    • Novartis
    • Pfizer
    • Roche
    • sanofi-aventis
    • Takeda
  • 6.3. Specialist Companies
    • ACT Biotech
    • Advenchen
    • Array BioPharma
    • Avila Therapeutics
    • Calistoga Pharmaceuticals
    • Cellzome
    • Cyclacel Pharmaceuticals
    • Cylene Pharmaceuticals
    • Deciphera Pharmaceuticals
    • Emiliem
    • Exelixis
    • Intellikine
    • Kai Pharmaceuticals
    • Nerviano Medical Sciences
    • Oncalis
    • OSI Pharmaceuticals
    • Rigel Pharmaceuticals
    • S*Bio
    • Semafore Pharmaceuticals
    • SuperGen
    • TargeGen
    • Vertex Pharmaceuticals
  • 6.4. Service Companies
    • Ambit Biosciences
    • Galapagos
    • Invitrogen
    • KINAXO Biotechnologies
    • ProQinase
    • SignalChem
    • Upstate (Millipore)

CHAPTER - 7

MARKET OUTLOOK

  • 7.1. Introduction
  • 7.2. Near-Term Developments
  • 7.3. Longer-Term Outlook

CHAPTER - 8

EXPERT INTERVIEWS

REFERENCES

COMPANY INDEX WITH WEB ADDRESSES

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