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最新型の遺伝子治療:技術・臨床・規制・競争環境と最新動向

Emerging Gene Therapies - Trends within the Technological, Clinical, Regulatory and Competitive Landscape

発行 GlobalData 商品コード 772747
出版日 ページ情報 英文 99 Pages
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最新型の遺伝子治療:技術・臨床・規制・競争環境と最新動向 Emerging Gene Therapies - Trends within the Technological, Clinical, Regulatory and Competitive Landscape
出版日: 2019年01月03日 ページ情報: 英文 99 Pages
概要

当レポートでは、世界の遺伝子治療市場における最新の製品開発・治験動向について分析し、現在の遺伝子編集技術の概要・水準や問題点、近年上市された製品の特徴、主要企業とその主要なパイプライン製品 (治験の進捗状況など)、既存製品との競合状態、規制面での影響、製薬業界における関心事項といった情報を取りまとめてお届けいたします。

第1章 目次

第2章 イントロダクション

  • 遺伝子治療:定義
  • 分析範囲:遺伝子治療の新たなパイプライン製品
  • 遺伝子治療の歴史
  • 遺伝子移植の限界
  • 標的遺伝子編集の動向
  • 遺伝子編集プラットフォームの概要
    • Zinc Fingers (1996)
    • Transcription Activator-Like Effectors (2011)
    • The CRISPR/Cas System (2013)
    • Effectors for Targeting Domains
    • 遺伝子編集システムの比較
    • 遺伝子編集システムの概要
  • 生体内 (IV) 遺伝子編集の概要
    • 細胞の種類・段階・修復過程に依存する遺伝子編集
    • 提供
    • 編集プラットフォームに対する新たな安全面での懸念
    • 標的細胞のサイクルステージとDNA修復設備に依存する編集製品
    • 遺伝子移植に対する遺伝子編集の利点
    • 「安全港」サイトへの統合
    • 遺伝子編集の複雑化
    • 生体内遺伝子治療の概略

第3章 遺伝子治療 - 短期的な製品パイプライン

  • レーバー先天性黒内症 (LCA)
    • アンメットニーズ
    • 分子遺伝学
    • Luxturna (Voretigene neparvovec)
    • Editas Medicine:EDIT-101
    • 治験のデザイン
    • EDIT-101とオフターゲット効果
    • EDIT-101の潜在的な利点:治療効果の持続期間の長さ
    • サマリー
  • コロイデレミア (Choroideremia)
  • ハーラー症候群 (MPS I)
    • 主な臨床研究
    • Regenex:RGX-111
    • Sangamo Therapeutics:SB-318
  • ハンター症候群 (MPS II)
    • アンメットニーズ
    • Sangamo Therapeutics: SB-913
    • Immusoft Corporation:細胞療法
  • サンフィリポ症候群 (MPS III)
    • Lysogene: LYS-SAF302
  • サマリー:ムコ多糖症 (MPS)
  • 血友病
    • 血友病A
    • 血友病B
  • ヘモグロビン異常症
    • βサラセミア:アンメットニーズ
    • βサラセミア:分子遺伝学
    • 鎌状赤血球貧血:アンメットニーズ
    • 鎌状赤血球貧血:分子遺伝学
  • ヘモグロビン異常症向け細胞療法
    • Blue Bird Bio:BB-305 ('LentiGlobin')
    • CRISPR Therapeutics: CTX-001
    • サマリー:ヘモグロビン異常症向け細胞療法
  • デュシェンヌ型筋ジストロフィー
    • アンメットニーズ
    • 分子遺伝学
    • ExonDys 51 - Sarepta Therapeutics
    • Solid BioSciences: SGT-001
    • Exonics Therapeutics:CRISPRアプローチ
    • サマリー:デュシェンヌ型筋ジストロフィー

第4章 競争環境

  • 遺伝子治療製品の開発に際しての、各種規制への配慮
    • 製品の特性
    • 遺伝子治療製品の治験の設計
    • 疾患ごとの設定
    • 医療費の償還・支払い
    • サマリー:規制面での考慮事項
  • 知的所有権 (IP):CRISPR/Cas
    • ライセンス、権利取得、MPEGツール
  • 企業分析:遺伝子編集企業
    • Sangamo Therapeutics
    • CRISPR Therapeutics
    • Casebia Therapeutics
    • Editas Medicine
    • Intellia Therapeutics
    • Homology Medicines
  • 企業分析:製薬企業
    • Amgen
    • Gilead Sciences
    • Novartis
    • Sanofi
    • GlaxoSmithKline
    • Pfizer

第5章 付録

図表

List of Tables

  • Table 1: Pipeline Products Covered
  • Table 2: Properties of Standard Gene-Editing Nucleases
  • Table 3: Registered Clinical Trials of CAR-T Cell Therapies Using Gene-Editing
  • Table 4: Gene Therapy Clinical Trials Worldwide by Vector
  • Table 5: Gene Editing Landscape, Vector Differentiation by Target Tissue
  • Table 6: Gene Editing Landscape, Key Off-Target Effect Studies
  • Table 7: Pre-existing Immunity to Cas9
  • Table 8: Characterization of the Rate of Homology Directed Repair in Range of Cell Lines
  • Table 9: Comparison of Gene Editing and Gene Transfer Approaches
  • Table 10: Gene Editing Landscape, Pipeline of Targeted Gene Editing Products by Company
  • Table 11: Luxturna Clinical Studies
  • Table 12: EDIT-101 - Phase I/II Trial Design and Comparison to Luxturna Efficacy Study
  • Table 13: Dose Response in CEP290 Gene Editing and CRISPR Expression
  • Table 14: Gene editing landscape, Mucopolysaccharidosis I (MPS I) (Hurler Syndrome), Diagnosed, Prevalent Cases, 2017-2027
  • Table 15: Key Phase I/II Studies in MPS I
  • Table 16: Gene editing landscape, Mucopolysaccharidosis II (MPS II) (Hunter Syndrome), Diagnosed, Prevalent Cases, 2017-2027.
  • Table 17: SB-913 Trial Design
  • Table 18: SB-913 - Interim Results
  • Table 19: LYS-SAF302 Phase II/III Trial Design
  • Table 20: Gene Editing Landscape, MPS Disorders
  • Table 21: Gene Editing Landscape, Hemophilia Epidemiology and Forecast, 2016-2026.
  • Table 22: Scale of Hemophilia Severity
  • Table 23: Phase I/II Hemophilia A Trials
  • Table 24: BMN-270 Factor VIII Levels at 1.5 Years (High Dose)
  • Table 25: Gene Therapy Landscape, Phase I/II Clinical Trial Design for Hemophilia A
  • Table 26: Gene Therapy Landscape, Summary of Key Pipeline Gene Therapies for Hemophilia A
  • Table 27: Phase I/II Clinical Studies
  • Table 28: Gene Therapy Landscape, Overview Of Key Pipeline Products in Hemophilia B
  • Table 29: Gene editing landscape, Thalassemia, Diagnosed, Prevalent Cases, 2017-2027
  • Table 30: Frequent Mutations Causing SCD
  • Table 31: Phase I/II Clinical Studies
  • Table 32: LentiGlobin - Ongoing Phase III Trials in Beta Thalassemia
  • Table 33: Results of LentiGlobin trials in Thalassemia and Sickle Cell Disease
  • Table 34: ST-400 Trial Design Compared with LentiGlobin
  • Table 35: CTX-001 trial design (Left) against ST-400 and LentiGlobin (Right)
  • Table 36: LentiGlobin (BB-305) may Achieve Blockbuster Status by 2023
  • Table 37: Gene Therapy Landscape, DMD, Global Prevalence (%)
  • Table 38: Exondys 51 - Clinical Studies
  • Table 39: SGT- 001 Study Design
  • Table 40: Gene Therapy Landscape, Key Patents in the CRISPR Dispute
  • Table 41: Gene Therapy Landscape, IP Estates of CRISPR Companies
  • Table 42: Gene Therapy Landscape, ERS Genomics EU Licensing 2004-2018
  • Table 43: Sangamo Therapeutics Pipeline, September 2018
  • Table 44: Sangamo Therapeutics Partnerships
  • Table 45: Sangamo Therapeutics SWOT
  • Table 46: CRISPR Therapeutics Pipeline
  • Table 47: CRISPR Therapeutics Pipeline
  • Table 48: CRISPR Therapeutics SWOT
  • Table 49: Casebia Pipeline, September 2018
  • Table 50: Editas Medicine Pipeline, September 2018
  • Table 51: Editas Medicine Pipeline, September 2018.
  • Table 52: Editas Medicine SWOT
  • Table 53: Intellia Therapeutics Pipeline
  • Table 54: Intellia Therapeutics SWOT
  • Table 55: Homology Medicines Pipeline
  • Table 56: Homology Medicines SWOT

List of Figures

  • Figure 1: Nucleases Based on Protein-DNA Interactions
  • Figure 2: Transcription Activator-Like Effector Nucleases (TALENs)
  • Figure 3: The CRISPR/Cas System
  • Figure 4: CRISPR/Cas Binding Mechanism
  • Figure 5: Cas9 Orthologs
  • Figure 6: Gene Therapy Clinical Trials Worldwide by Vector
  • Figure 7: Multiple Sangamo Therapeutics Products Use an Albumin Targeting 'Safe Harbor' Approach
  • Figure 8: Gene Editing Landscape, Progression of Gene Therapy Applications
  • Figure 9: Gene Editing Landscape, Hemophilia A + B
  • Figure 10: SPK-9001: Factor IX Activity after SPK-9011 in 8 Participants that did not Show AAV Capsid-Directed Immune Response
  • Figure 11: Cost of Beta-Thalassemia Major Treatment as of NHS Tariffs at 2013/14 Prices
  • Figure 12: BCL11A is Involved in Fetal Hemoglobin Silencing
目次
Product Code: GBI095CBR

Genomic surgery is increasingly a reality. The last two years have seen the approval of four gene therapies by the FDA - (1) Luxturna, the first in vivo gene transfer therapy (2) Imlygic, an novel immunotherapy, (3) Kymriah and (4) Yescarta, two Chimeric Antigen Receptor T - Cell therapies targeting CD19 for oncological conditions. Over the next two years, a number of key events will determine the clinical tractability and commercial interest of gene editing approaches. These will be pivotal within the gene therapy field.

Until recently, the field has had limited success outside of CAR-T therapies. Ex vivo cell therapy Strimvelis for ADA-SCID was approved in 2016, but has subsequently been sold by its developer GSK, due to lack of profitability. The first exon skipping therapy, ExonDys 51, for Duchenne Muscular Dystrophy was approved controversially by the FDA in 2016, but failed to gain approval in Europe based on its efficacy, and its US sales are reportedly slow.

A key challenge in gene therapy development has been delivering enough product into the target tissue. This has meant many gene therapy products have struggled to achieve a high enough level of therapeutic gene expression to induce a clinical effect. Naturally, selection of therapy areas for the development of novel gene therapy products has been influenced by these technical challenges. Drug developers have prioritized conditions with well-understood pathology, those with simple genetics that are able to be corrected using simpler editing approaches, and those in which the delivery problem is minimized.

Due to the relative ease of achieving high levels of gene therapy product to cells ex vivo, development has been focused in areas where cellular therapy is an established part of clinical procedure - for instance, in the hemoglobinopathies (e.g. beta thalassemia, sickle cell disease) and the lysosomal disorders, where hematopoietic stem cell transfer is commonly used as part of clinical care. Ex vivo products have also seen success in oncology, where ex vivo modification of T-Cells has to express antigens as a method for immunotherapy has achieved remarkable clinical results.

The report "Emerging Gene Therapies - Trends within the Technological, Clinical, Regulatory and Competitive Landscape" provides a comprehensive overview of the emerging gene therapy market. It discusses gene therapy and the technology behind gene editing, outlining the advantages, limitations and current evidence for the platforms under development. The report discusses relevant clinical studies targeting specific therapeutic indications and highlights examples of current challenges within the field, with a focus on therapies that target the eye, liver, and blood.

Additionally, the report provides a background to the CRISPR patent litigation, a key factor within the gene editing company landscape. It provides profiles of six companies developing gene editing platforms, considers the gene therapy interests of the main pharmaceutical companies, and discusses current regulatory trends in the development of gene therapies.

Scope:

  • What are the key emerging products within the gene therapy landscape?
  • Which companies have the strongest pipeline of innovative products?
  • How will gene editing disrupt existing gene therapy products?
  • What are the regulatory trends for emerging gene therapies?
  • What are the interests of pharmaceutical companies within the field?

Reasons to buy:

  • Achieve an up-to-date understanding of the area, with a comprehensive reference of key products within the gene therapy landscape, compared across technology-specific relevant characteristics such as editing mechanism and delivery vector.
  • Conduct competitive analysis using indication-specific, side-by-side comparisons of the latest data for key gene therapy products in the strategically relevant areas of eye, blood, and liver.
  • Conduct strategic analysis using an overview of gene therapy specific considerations for evaluating and developing gene therapy products - the CRISPR patent space, emerging regulatory trends, innovation leaders and the interests of pharma in gene therapy.

Table of Contents

1. Table of Contents

  • 1.1. List of Tables
  • 1.2. List of Figures

2. Introduction

  • 2.1. Gene Therapy - Definitions
  • 2.2. Report Coverage - the Emerging Gene Therapy Pipeline
  • 2.3. History of Gene Therapy
  • 2.4. Limitations of Gene Transfer
  • 2.5. The Development of Targeted Gene Editing
  • 2.6. Overview of Gene Editing Platforms
    • 2.6.1. Zinc Fingers (1996)
    • 2.6.2. Transcription Activator-Like Effectors (2011)
    • 2.6.3. The CRISPR/Cas System (2013)
    • 2.6.4. Effectors for Targeting Domains
    • 2.6.5. Comparison of Gene Editing Systems
    • 2.6.6. Summary of Gene Editing Systems
  • 2.7. Overview of In Vivo Gene Therapy
    • 2.7.1. Editing is Dependent on Cell Type, Stage, and Repair Pathway
    • 2.7.2. Delivery
    • 2.7.3. Emerging Safety Concerns with Editing Platforms
    • 2.7.4. Editing Products are Reliant on the Target Cell's Cycle Stage and DNA Repair Machinery
    • 2.7.5. Advantages of Gene Editing over Gene Transfer
    • 2.7.6. Integration into 'Safe Harbor' Sites
    • 2.7.7. The Increasing Complexity of Gene Therapy
    • 2.7.8. Summary of In Vivo Gene Therapy

3. Gene Therapy - Near Term Product Pipeline

  • 3.1. Leber Congenital Amaurosis
    • 3.1.1. Unmet Need
    • 3.1.2. Molecular Genetics
    • 3.1.3. Luxturna (Voretigene neparvovec)
    • 3.1.4. Editas Medicine: EDIT-101
    • 3.1.5. Trial Design
    • 3.1.6. EDIT-101 and Off-Target Effects
    • 3.1.7. The Potential Advantage of EDIT-101 is the Longevity of its Therapeutic Effect
    • 3.1.8. Summary - LCA
  • 3.2. Choroideremia
  • 3.3. Hurler Syndrome (MPS I)
    • 3.3.1. Key Clinical Studies
    • 3.3.2. Regenex: RGX-111
    • 3.3.3. Sangamo Therapeutics: SB-318
  • 3.4. Hunter Syndrome (MPS II)
    • 3.4.1. Unmet Need
    • 3.4.2. Sangamo Therapeutics: SB-913
    • 3.4.3. Immusoft Corporation: Cell Therapy
  • 3.5. Sanfilippo Syndrome (MPS III)
    • 3.5.1. Lysogene: LYS-SAF302
  • 3.6. Summary - MPS Disorders
  • 3.7. Hemophilia
    • 3.7.1. Hemophilia A
    • 3.7.2. Summary - Hemophilia A
    • 3.7.3. Hemophilia B
    • 3.7.4. Summary - Hemophilia B
  • 3.8. Hemoglobinopathies
    • 3.8.1. Beta Thalassemia: Unmet Need
    • 3.8.2. Beta Thalassemia: Molecular Genetics
    • 3.8.3. Sickle Cell Disease: Unmet Need
    • 3.8.4. Sickle Cell Disease: Molecular Genetics
  • 3.9. Cellular Therapies for Hemoglobinopathies
    • 3.9.1. Blue Bird Bio: BB-305('LentiGlobin')
    • 3.9.2. Sangamo: ST-400
    • 3.9.3. CRISPR Therapeutics: CTX-001
    • 3.9.4. Summary: Cellular Therapies for Hemoglobinopathies
  • 3.10. Duchenne Muscular Dystrophy
    • 3.10.1. Unmet Need
    • 3.10.2. Molecular Genetics
    • 3.10.3. ExonDys 51 - Sarepta Therapeutics
    • 3.10.4. Solid BioSciences: SGT-001
    • 3.10.5. Exonics Therapeutics: CRISPR Approach
    • 3.10.6. Summary - Duchenne Muscular Dystrophy

4. Competitive Landscape

  • 4.1. Regulatory Considerations for Developing Gene Therapy Products
    • 4.1.1. Product Characteristics
    • 4.1.2. Clinical Study Design for Gene Therapy Products
    • 4.1.3. Disease specific guidance
    • 4.1.4. Reimbursement and Payment
    • 4.1.5. Summary - Regulatory Considerations
  • 4.2. Intellectual Property - CRISPR/Cas
    • 4.2.1. Licensing, Exploitation, and MPEG Pool
  • 4.3. Company Analysis: Gene Editing Companies
    • 4.3.1. Sangamo Therapeutics
    • 4.3.2. CRISPR Therapeutics
    • 4.3.3. Casebia Therapeutics
    • 4.3.4. Editas Medicine
    • 4.3.5. Intellia Therapeutics
    • 4.3.6. Homology Medicines
  • 4.4. Company Analysis: Pharma
    • 4.4.1. Amgen
    • 4.4.2. Gilead Sciences
    • 4.4.3. Novartis
    • 4.4.4. Sanofi
    • 4.4.5. GlaxoSmithKline
    • 4.4.6. Pfizer

5. Appendix

  • 5.1. References
  • 5.2. Report Methodology
  • 5.3. About GBI Research
  • 5.4. Disclaimer