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市場調查報告書
針對癌症之免疫療法
Immunotherapy in Oncology: Gaining Momentum
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針對癌症之免疫療法 是由出版商BioSeeker Group AB在2006年08月所出版的。
這份英文市場調查報告書包含228 pages 價格從美金4278起跳。
針對癌症之免疫療法領域中近來不斷有熱銷藥品研發成功，治療子宮頸癌的疫苗Gardasil在最近也受到承認。對該產業而言今後的課題是尋找有效的抗原及免疫調節劑，並且發展適當的給藥技術。
因醫藥及生物科技領域調查分析在近年來快速成長的瑞典市調公司 BioSeeker Group，出版了一本關於針對癌症之免疫療法的報告書 "Immunotherapy in Oncology: Gaining Momentum" 。
本報告書內容包括：癌症免疫療法市場的競爭環境、腫瘤抗原之檢驗及免疫調節策略、新一代抗體及施打疫苗技術的趨勢等。內容綱要摘記如下：
第1章 實施概要
第2章 方法論
第3章 目次
第4章 疫苗策略：課題與機會
第5章 主要抗體開發策略
第6章 癌症疫苗的競爭趨勢
- 國家與企業：誰在領導趨勢？
- 前10家企業研發比例佔總體的3分之1：不包含大型企業
- 獲得許可的癌症疫苗：功效
- 癌症疫苗相關交易與合作
- 近年來癌症疫苗相關企業的購併
- 前列腺癌相關交易
- 乳癌相關交易
- 白血病及淋巴腺癌相關交易
- 癌症疫苗施打技術相關交易
- 輔助性藥物相關交易
第7章 增加中的抗體交易
第8章 腫瘤抗原
- 腫瘤抗原：一般性意見
- 尋找抗原
- 特定的抗原加工技術促進發現新的抗原
第9章 癌症疫苗中的免疫調節劑及輔助性藥物
- 概要
- 細胞激素
- 與介白素（interleukin-2）合用的疫苗
- 腫瘤壞死的主要原因
- 抗癌干擾素
- 輔助藥物
- 其他免疫調節策略
第10章 施打癌症疫苗
第11章 抗體施打與設計的新策略：新一代
- 小型化與差異化的方法
- 持續施打中生物材料之應用
- 施打基因
第12章 研發中的癌症疫苗：症狀別
- 一般腫瘤學概要
- 進展分析：黑色素瘤
- 進展分析：乳癌
- 進展分析：前列腺癌
- 進展分析：肺癌
- 進展分析：結腸直腸癌
- 進展分析：子宮頸癌
第13章 臨床發展中的抗體
- 前列腺癌治療
- 乳癌治療
- 結腸直腸癌治療
- 黑色素瘤治療
- 血癌治療
- 第三臨床發展階段的抗體
- 第二臨床發展階段的抗體
第14章 免責事項
第15章 藥物索引
第16章 企業索引
Abstract
Introduction
The immunotherapy field in cancer has never been more potent than it is right
now, including block buster drugs like Avastin, Erbitux, and Rituxan.
Antibodies are making the headlines but cancer vaccines are not far away. The
recent approval of Gardasil, a cervical cancer vaccine, will certainly become
a strong representative of its kind. Future challenges for the industry lie in
discovering strong antigens, effective immunomodulators and developing
suitable delivery technologies.
Scope of this report
- In-depth competitive landscape assessment of the cancer immunotherapy
market place; Including more than 200 immunotherapy drugs and pharmaceutical
companies
- Thorough review of tumor antigen discovery, immunomodulating strategies
and adjuvants
- Thorough review of antibody and vaccine delivery and technologies
surrounding it - The next generation
- Progress analysis of six major cancer vaccine indications and late stage
antibody development projects, including players, drugs, clinical progress and
pitfalls
Research and analysis highlights
Among the targeted therapies for cancer, immunotherapy is probably the most
versatile treatment strategy for the eradication of tumors, metastatic spread
or not. Main strategies of cancer immunotherapy aim at exploiting the
therapeutic potential of tumor-specific antibodies and cellular immune
effector mechanisms (vaccines). Active immunotherapy, aiming at the generation
of a tumor-specific immune response combining both humoral and cytotoxic T
cell effector mechanisms by the host's immune system, is advancing over
passive antibody therapy, which relies on the repeated application of large
quantities of tumor antigen-specific antibodies.
Table of Contents
1 Executive Summary
2 Methodology
3 Table of Contents
- 3.1 List of Boxes
- 3.2 List of Figures
- 3.3 List of Tables
4 Vaccine Strategies: Challenges & Opportunities
5 Key Antibody Developmental Strategies
6 Competitive Landscape in Cancer Vaccines
- 6.1 Countries & Players: Who are In the Lead?
- 6.1.1 Top 10 Players Constitute Up to One Third of R&D: Big Pharma Not
Included!
- 6.1.2 Approved Cancer Vaccine Drugs: Performance
- 6.2 Deals & Alliances in Cancer Vaccines
- 6.2.1 Recent Mergers & Acquisitions in Cancer Vaccines
- 6.2.2 Deals in Prostate Cancer
- 6.2.3 Deals in Breast Cancer
- 6.2.4 Deals in Leukemia & Lymphoma
- 6.2.5 Drug Delivery Deals in Cancer Vaccines
- 6.2.6 Adjuvant Deals
7 Antibody Deals on the Rise
- 7.1 Antibody Deals in Phase III
- 7.1.1 Deal Situation: MDX 010
- 7.1.2 Deal Situation: WX G250
- 7.1.3 Deal Situation: Zanolimumab
- 7.2 Antibody Deals in Phase II
- 7.2.1 Deal Situation: Mapatumumab
- 7.2.2 Deal Situation: GCR 3888
- 7.2.3 Deal Situation: MDX 070
- 7.2.4 Deal Situation: CDP 860
- 7.2.5 Deal Situation: Tru-Scint OV
- 7.2.6 Deal Situation: SC 1
- 7.2.7 Deal Situation: PRO 70769
- 7.2.8 Deal Situation: XR 303
- 7.2.9 Deal Situation: HumaRAD-HN
8 Tumor Antigens
- 8.1 Tumor Antigens: General Comments
- 8.2 Antigen Discovery
- 8.2.1 Classical Immunology Approach
- 8.2.2 The Reverse Immunology Approach
- 8.2.3 Company Platforms
- 8.2.3.1 Epitope Identification System - EIS®
- 8.2.3.2 EPIQUEST system
- 8.2.3.3 MolecularBreeding™ & MaxyScan™
- 8.2.3.4 ProtEx™ technology
- 8.2.3.5 Rapid Identification of Alternative Splicing (RIAS) System
- 8.2.3.6 SMARTOMICS™
- 8.3 Specific Antigen Processing Technologies Increasing Antigen
Presentation
9 Immunomodulators & Adjuvants in Cancer Vaccines
- 9.1 Overview
- 9.2 Cytokines
- 9.2.1 Vaccines in Combination with Interleukin-2
- 9.2.2 Tumor Necrosis Factor
- 9.2.3 Interferons
- 9.3 Adjuvants
- 9.4 Other Immunomodulating Strategies
- 9.4.1 An Immune Response Modifying Protein
- 9.4.2 Immunostimulatory DNA
- 9.4.3 Ex Vivo Stimulated Immune Cells
- 9.4.4 Fusion Protein Gain Potent Immune Response
- 9.4.5 Macrophage and Natural Killer Cells Activation
- 9.4.6 Selective Suppression of the Immune System to An Antigen
- 9.4.7 TAP Technology
10 Cancer Vaccine Delivery
- 10.1 Viral Delivery
- 10.1.1 Introduction
- 10.1.2 Viral Constructs Put into Use
- 10.1.2.1 Replicon-based RNA and DNA vaccines
- 10.1.2.1.1 The Alphavaccine Platform System - ArV™
- 10.1.2.1.2 MVA-BN
- 10.1.2.2 Retroviruses
- 10.1.2.2.1 The SDSV-platform
- 10.1.2.3 Lentivirus
- 10.1.2.3.1 LentiPak™
- 10.1.2.3.2 LentiVector™/ pEGASUS™
- 10.1.2.4 Adenoviruses
- 10.1.2.4.1 Failed Adenovirus Delivery Platforms
- 10.1.2.4.2 GVAX
- 10.1.2.4.3 TNFerade™
- 10.1.2.4.4 INGN-225
- 10.1.2.5 Adeno-associated viruses
- 10.1.2.5.1 Failed AAV Delivery Platforms
- 10.1.2.5.2 Genzyme Acquires AAV vector Technology
- 10.1.2.5.3 MediGene's AAV Platform
- 10.1.2.6 Herpes Simplex Viruses
- 10.1.2.6.1 DISC-HSV
- 10.1.2.6.2 ImmunoVEX
- 10.1.2.7 Poxviruses
- 10.1.2.7.1 Hi-8™ PrimeBoost™ platform
- 10.1.2.7.2 PROSTVAC-VF
- 10.1.2.7.3 Transgene's MVA Platform
- 10.1.2.7.4 TroVax
- 10.1.2.8 Other Poxvirus Systems
- 10.1.2.9 Baculovirus
- 10.1.2.9.1 Chimeric virus -like particles (CVLPs)
- 10.2 Bacterias
- 10.3 Cell Therapy: Dendritic-cell Based & Cancer-Cell Based Therapies
- 10.3.1 Introduction
- 10.3.2 Cell Therapy Strategies
- 10.3.2.1 Processed Tumor Cells
- 10.3.2.2 Lysed Tumor Cell Line
- 10.3.2.3 The Dendritic Cell Strategy that Didn't Work Out
- 10.3.2.4 HSPs
- 10.3.2.5 Provenge™
- 10.3.2.6 Dendritophages
- 10.3.2.7 Cell-targeting Antibodies
- 10.3.2.8 Increase Dendritic Cell Number
- 10.3.2.9 DCVax®
- 10.3.2.10 ACTIVATE™
- 10.4 Synthetic Delivery Systems & Strategies
- 10.4.1 Introduction
- 10.4.2 Biotransport™
- 10.4.3 Biotype®vector
- 10.4.4 DNAVax Gene Delivery System
- 10.4.5 FusitAb™
- 10.4.6 GeneDrug™
- 10.4.7 Molecular Conjugates
- 10.4.8 Naked DNA Delivery
- 10.4.9 PVLP Technology
- 10.4.10 Sphingosomal Drug Delivery Technology
- 10.4.11 STEALTH
- 10.4.12 Failed Liposomal Systems
11 New Approaches in Antibody Delivery and Design - The Next Generation
- 11.1 How to Make Them Smaller and Different?
- 11.2 Biomaterials in Sustained Delivery Applications
- 11.3 Gene delivery - the Future?
- 11.3.1 Delivery Vehicles for DNA
- 11.3.2 Gene Delivery in Commercialization
12 Cancer Vaccines in Development: By Major Indications
- 12.1 General Oncology Overview
- 12.2 Progress Analysis - Melanoma
- 12.3 Progress Analysis - Breast Cancer
- 12.4 Progress Analysis - Prostate Cancer
- 12.5 Progress Analysis - Lung Cancer
- 12.6 Progress Analysis - Colorectal Cancer
- 12.7 Progress Analysis - Cervical Cancer
13 Antibodies in Clinical Development
- 13.1.1 Prostate Cancer Therapeutics
- 13.1.2 Breast Cancer Therapeutics
- 13.1.3 Colorectal Cancer Therapeutics
- 13.1.4 Melanoma Therapeutics
- 13.1.5 Hematological Cancers Therapeutics
- 13.2 Antibodies in Phase III Clinical Development
- 13.2.1 Progress Analysis: IGN 101
- 13.2.1.1 Breast Cancer
- 13.2.1.2 Lung Cancer
- 13.2.1.3 Colorectal cancer
- 13.2.2 Progress Analysis: MDX 010
- 13.2.2.1 Melanoma
- 13.2.2.2 Breast Cancer
- 13.2.2.3 Prostate Cancer
- 13.2.2.4 Kidney Cancer
- 13.2.3 Progress Analysis: ONYVAX 105
- 13.2.3.1 Colorectal cancer
- 13.2.3.2 Other Indications
- 13.2.4 Progress Analysis: Ovarex
- 13.2.5 Progress Analysis: Panitumumab
- 13.2.5.1 Solid tumors
- 13.2.5.2 Colorectal cancer
- 13.2.5.3 Lung Cancer
- 13.2.5.4 Kidney Cancer
- 13.2.6 Progress Analysis: RENCAREX
- 13.2.7 Progress Analysis: Nimotuzumab
- 13.2.7.1 Brain cancer
- 13.2.7.2 Pancreatic cancer
- 13.2.7.3 Head and neck cancer
- 13.2.7.4 Lung Cancer
- 13.2.8 Progress Analysis: TransMID
- 13.2.9 Progress Analysis: Lintuzumab
- 13.2.10 Progress Analysis: Zanolimumab
- 13.3 Antibodies in Phase II Clinical Development
- 13.3.1 Progress Analysis: ABT-510
- 13.3.1.1 Kidney Cancer
- 13.3.1.2 Soft Tissue Sarcoma
- 13.3.1.3 Lung Cancer
- 13.3.2 Progress Analysis: BB 10901
- 13.3.2.1 Lung Cancer
- 13.3.2.2 Multiple Myeloma
- 13.3.3 Progress Analysis: CP 675206
- 13.3.4 Progress Analysis: CNTO-328
- 13.3.4.1 Kidney Cancer
- 13.3.4.2 Multiple Myeloma
- 13.3.4.3 Prostate cancer
- 13.3.5 Progress Analysis: Ecromeximab
- 13.3.6 Progress Analysis: EMD 273063
- 13.3.7 Progress Analysis: WX-G250RIT
- 13.3.7.1 Billary Cancer
- 13.3.7.2 Kidney Cancer
- 13.3.8 Progress Analysis: HGS-ETR1
- 13.3.8.1 Lung Cancer
- 13.3.8.2 Lymphoma
- 13.3.8.3 Colorectal Cancer
- 13.3.8.4 HGS-ETR2
- 13.3.9 Progress Analysis: HuMax-CD20
- 13.3.10 Progress Analysis: HuMax-EGFr
- 13.3.10.1 Head and Neck Cancer
- 13.3.11 Progress Analysis: Galiximab
- 13.3.12 Progress Analysis: PROXINIUM
- 13.3.12.1 Head and Neck Cancer
- 13.3.12.2 Bladder Cancer
- 13.3.13 Progress Analysis: RAV12
- 13.3.13.1 Colorectal Cancer
- 13.3.14 Progress Analysis: SGN-15
- 13.3.14.1 Lung Cancer
- 13.3.14.2 Prostate Cancer
- 13.3.14.3 Metastatic Breast and Colorectal Cancer
- 13.3.15 Progress Analysis: SGN-30
- 13.3.16 Progression Analysis: VEGF-Trap
- 13.3.17 Progress Analysis: MEDI 522
- 13.3.17.1 Colorectal Cancer
- 13.3.17.2 Melanoma
- 13.3.18 Progress Analysis: Volociximab
14 Disclaimer
- 14.1 Liability
- 14.2 Completeness
15 Drug Index
16 Company Index
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