市場調査レポート
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1441148

二重特異性抗体の世界市場:薬剤販売、特許、価格、臨床試験インサイト(2029年)

Global Bispecific Antibody Market, Drugs Sales, Patent, Price & Clinical Trials Insight 2029

出版日: | 発行: KuicK Research | ページ情報: 英文 1200 Pages | 納期: 即日から翌営業日

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二重特異性抗体の世界市場:薬剤販売、特許、価格、臨床試験インサイト(2029年)
出版日: 2024年03月01日
発行: KuicK Research
ページ情報: 英文 1200 Pages
納期: 即日から翌営業日
  • 全表示
  • 概要
  • 図表
  • 目次
概要

二重特異性抗体は、過去10年来勢いを増しているエキサイティングな新しい治療アプローチです。これらの緻密に設計された分子は、免疫系を利用して悪性細胞やその他の疾患細胞・組織を正確に標的とするユニークな作用機序を提供し、副作用のリスクを最小化する標的アプローチを提供します。過去3年間、二重特異性抗体市場は研究開発と商業活動において急速な盛り上がりを見せており、今後数年間で市場は急速に成長することが予想されます。

二重特異性抗体は、2つの異なる抗原に同時に結合するように設計されたタンパク質であり、通常、異なる細胞型に存在します。その二重標的能力は、病気に対する免疫システムを利用する複数の方法を提供します。がんに対する一般的なアプローチとしては、T細胞やナチュラルキラー細胞を悪性細胞への攻撃に向かわせることが挙げられます。また、免疫細胞と腫瘍細胞を架橋して免疫反応を高めることもできます。さらに、2つの異なるシグナル伝達経路をブロックしたり、免疫細胞を腫瘍微小環境に動員することもできます。

がん以外の適応症では、二重特異性抗体は異なる疾患メディエーターや細胞タイプを二重に標的とすることができます。これにより、炎症、自己免疫、その他の疾患に関与する病原性タンパク質、サイトカイン、細胞を中和または除去する機会が得られます。しかし、適応症によって、二重特異性抗体の作用機序は変わる可能性があります。

二特異性抗体の多様性は、その前身である従来のモノクローナル抗体に比べて、特異性、効力、複数の経路を同時に標的とする柔軟性の向上など、いくつかの利点を提供します。これは、モノクローナル抗体がさまざまながん関連経路を阻害するために多用されているがん治療において、特に重要な意味を持っています。免疫細胞を腫瘍に直接誘導することにより、二重特異性抗体は腫瘍の免疫回避機構を克服することができ、従来の化学療法と比較して有効性の向上と低毒性につながる可能性があります。

米国FDAは2014年にBlinatumomab(市販名Blincyto)を承認し、二重特異性抗体の分野における重要なマイルストーンとなり、再発または難治性の前駆B細胞性急性リンパ芽球性白血病の治療法を根本的に変えました。この成功の後、複数の新しい二重特異性抗体が臨床開発段階にあり、がんを中心に幅広い疾患をカバーしています。それにもかかわらず、がんに加えて、ウイルスや細菌感染、自己免疫疾患などの新たな適応症に対処するために設計された二重特異性候補抗体の数が増加しています。このような多様化は、このクラスの医薬品の治療応用範囲が拡大していることを浮き彫りにしています。

二重特異性抗体は、主要な新薬クラスとしての可能性を検証するのに十分な臨床的成功を収めています。複数の疾患経路を利用できるそのユニークな能力は、モノクローナル抗体を超える新たな治療の可能性を引き出しています。がん領域が先導してきた一方で、他の疾患領域への拡大も加速しています。分子設計とエンジニアリングの継続的な革新により、二重特異性抗体は、幅広いアンメットメディカルニーズにおける治療を変革するエキサイティングな汎用性の高いアプローチとなり、調査も徐々に進んでいます。

当レポートでは、世界の二重特異性抗体市場について調査し、市場の概要とともに、薬剤動向、臨床試験動向、地域別動向、および市場に参入する企業の競合情勢などを提供しています。

目次

第1章 二重特異性抗体のイントロダクション

第2章 二重特異性抗体の組み合わせ戦略

  • 化学療法
  • 標的療法
  • 免疫療法
  • 放射線療法

第3章 商業的に承認された二重特異性抗体に関する洞察

第4章 二重特異性抗体の独自プラットフォーム

第5章 世界および地域の二重特異性抗体市場の見通し

  • 年次および四半期の売上に関する洞察(2019年~2023年)
  • 承認された二重特異性抗体の償還政策
  • 世界の二重特異性抗体市場予測:2029年

第6章 世界の二重特異性抗体市場動向、地域別

  • 米国
  • 欧州
  • 中国
  • 英国
  • 日本
  • 韓国
  • オーストラリア
  • カナダ
  • ラテンアメリカ

第7章 世界の二重特異性抗体の調査と市場動向、適応症別

  • リンパ腫
  • 多発性骨髄腫
  • 白血病
  • 肺がん
  • 黒色腫
  • 血液疾患
  • 消化器がん
  • その他のがん
  • 自己免疫疾患および炎症疾患
  • 微生物病
  • 目の病気

第8章 世界の二重特異性抗体臨床試験の概要

  • 相別
  • 国/地域別
  • 会社別
  • 適応症別
  • 優先順位別
  • 患者セグメント

第9章 Blincyto-臨床、特許、価格、販売に関する洞察

第10章 Hemlibra-臨床、特許、価格、販売に関する洞察

第11章 Rybrevant-臨床、特許、価格に関する洞察

第12章 Kimmtrak-臨床、特許、価格、販売に関する洞察

第13章 Vabysmo-臨床、特許、価格設定および販売に関する洞察

第14章 Lunumio-臨床、特許、価格、販売に関する洞察

第15章 カドニリマブ- 臨床および販売に関する洞察

第16章 Tecvayli-臨床、特許、価格に関する洞察

第17章 Columvi-臨床、特許、価格、販売に関する洞察

第18章 Epkinly-臨床、特許、価格設定、販売に関する洞察

第19章 Talvey-臨床、特許、価格設定に関する洞察

第20章 Elrexfio-臨床、特許、価格に関する洞察

第21章 企業、適応症、および相別の二重特異性抗体の世界の臨床試験

  • 調査
  • 前臨床
  • 第I相
  • 第I/II相
  • 第II相
  • 第II/III相
  • 第III相
  • 事前登録
  • 登録済み

第22章 企業、国、および適応症別の市販二重特異性抗体の臨床的洞察

第23章 競合情勢

  • ABL Bio
  • Abzyme Therapeutics
  • Affimed Therapeutics
  • Akeso Biopharma
  • Alligator Bioscience
  • Amgen
  • Antibody Therapeutics
  • APITBIO
  • Aptevo Therapeutics
  • Astellas Pharma
  • AstraZeneca
  • BioAtla
  • Biosion
  • Biotheus
  • BJ Bioscience
  • EpimAb Biotherapeutics
  • FutureGen Biopharmaceutical
  • Genentech
  • Genmab
  • Gensun Biopharma
  • Harbour BioMed
  • IGM Biosciences
  • I-MAB Biopharma
  • ImmuneOnco Biopharma
  • ImmunoPrecise Antibodies
  • Innovent Biologics
  • Invenra
  • Janssen Research & Development
  • Kenjockety Biotechnology
  • LaNova Medicines Limited
  • Light Chain Bioscience
  • Linton Pharm
  • Lyvgen Biopharma
  • MacroGenics
  • Merus
  • NovaRock Biotherapeutics
  • Pfizer
  • Phanes Therapeutics
  • Prestige BioPharma
  • Regeneron Pharmaceuticals
  • Revitope
  • Roche
  • Virtuoso Therapeutics
  • Xencor
  • Y-Biologics
  • Zhejiang Shimai Pharmaceutical
  • Zymeworks
図表

List of Figures

  • Figure 1-1: Bispecific Antibodies - Advantages
  • Figure 2-1: Antibody-Chemotherapy Combination - Advantages
  • Figure 2-2: Antibody-Chemotherapy Combination - Impending Challenges
  • Figure 3-1: Blincyto - Mechanism of Action
  • Figure 3-2: Hemlibra - Mechanism of Action
  • Figure 3-3: Rybrevant - Mechanism of Action
  • Figure 3-4: Regulatory Designations - Benefits
  • Figure 4-1: Multiclonics - Distinctive Characteristics
  • Figure 4-2: Biclonics - Format
  • Figure 4-3: ADAPTIR Bispecific Structure
  • Figure 4-4: ADAPTIR-FLEX
  • Figure 4-5: BEAT Platform - Multispecific Antibodies
  • Figure 4-6: FIT-Ig - Proprietary Bispecific Platform
  • Figure 4-7: BiClone format
  • Figure 4-8: BioAtla CABs - Features
  • Figure 4-9: BioAtla CABs - Benefits
  • Figure 4-10: IMBiologic Bispecific Antibodies - Strategy
  • Figure 4-11: IMBiologic Bispecific Antibodies - Mechanism of Action
  • Figure 4-12: Novel HBICE
  • Figure 4-13: HBICE - Mechanism of Action 1
  • Figure 4-14: HBICE - Mechanism of Action 2
  • Figure 4-15: Phanes Therapeutics - PACbody Platform
  • Figure 4-16: Phanes Therapeutics - SPECpair Platform
  • Figure 4-17: Phanes Therapeutics - ATACCbody
  • Figure 4-18: Numab Therapeutics - Technology
  • Figure 4-19: Grabody I Platform - Mechanism of Action
  • Figure 4-20: Grabody I Platform - Mechanism of Action
  • Figure 4-21: 3-Step DuoBody Production Process
  • Figure 4-22: DuoHexaBody Molecules - Schematic
  • Figure 4-23: iTAb - Patented Structure
  • Figure 4-24: iTAb - Mechanism of Action
  • Figure 4-25: Synimmune - Proprietary Bispecific Antibody Format
  • Figure 4-26: BiTE - Structure
  • Figure 4-27: BiTE Molecule
  • Figure 4-28: Sanyou Super Trillion Common Light Chain Antibody Discovery Platform
  • Figure 4-29: ALiCE - Characteristics
  • Figure 4-30: ALiCE - Schematic Diagram & Mechanism of Action
  • Figure 4-31: Abz2 Bispecific Platform
  • Figure 4-32: Abz2 Bispecifics - Benefits
  • Figure 4-33: Neo-X-Prime Bispecific Mechanism
  • Figure 4-34: B-Body Bispecific Antibody - Structre
  • Figure 4-35: xLinkBsAb - Structure
  • Figure 4-36: PrecisionGATE Bispecific Antibody - Structure
  • Figure 5-1: Global - Annual Bispecific Antibody Market (US$ Million), 2019-2023
  • Figure 5-2: Global - Quarterly Bispecific Antibody Market (US$ Million), 2023
  • Figure 5-3: Global - Annual Bispecific Antibodies Market by Drug (US$ Million), 2023
  • Figure 5-4: Global - Bispecific Antibodies Market Shares by Drugs (%), 2023
  • Figure 5-5: Global - Annual Bispecific Antibody Market by Region (US$ Billion), 2023
  • Figure 5-6: Global - Bispecific Antibody Market Shares by Region (%), 2023
  • Figure 5-7: Global - Annual Bispecific Antibodies Sales by Drugs (US$ Million), 2022
  • Figure 5-8: Global - Bispecific Antibodies Market Shares by Drugs (%), 2022
  • Figure 5-9: Global - Bispecific Antibody Market by Region (US$ Million), 2022
  • Figure 5-10: Global - Bispecific Antibody Market Shares by Region (%), 2022
  • Figure 5-11: US - Annual Bispecific Antibody Market Value (US$ Million), 2019-2023
  • Figure 5-12: ROW - Global Bispecific Antibody Market Value (US$ Million), 2019-2023
  • Figure 5-13: US - Quarterly Bispecific Antibodies Market (US$ Million), 2023
  • Figure 5-14: ROW - Quarterly Bispecific Antibodies Market (US$ Million), 2023
  • Figure 5-15: Blincyto - Total Treatment Cost & Reimbursement Cost
  • Figure 5-16: Blincyto - In Pocket & Out of Pocket Cost of Treatment
  • Figure 5-17: Hemlibra - Total Treatment Cost & Reimbursement Cost
  • Figure 5-18: Hemlibra - In Pocket & Out of Pocket Cost of Treatment
  • Figure 5-19: Rybrevant - Maximum Coverage by Medicaid (US$), 2023
  • Figure 5-20: Rybrevant - Maximum Coverage by Private Insurance Coverage (US$), 2021
  • Figure 5-21: Vabysmo - Total Treatment Cost & Reimbursement Cost
  • Figure 5-22: Vabysmo - In Pocket & Out of Pocket Cost of Treatment
  • Figure 5-23: Global - Bispecific Antibody Market Opportunity Assessment (US$ Billion), 2024 - 2029
  • Figure 6-1: US - Bispecific Antibodies Approval
  • Figure 6-2: Blincyto - US v/s ROW Sales (US$ Million), 2023
  • Figure 6-3: Blincyto - US v/s ROW Shares (%), 2023
  • Figure 6-4: Blincyto - US v/s ROW Sales (US$ Million), 2022
  • Figure 6-5: Blincyto - US v/s ROW Shares (%), 2022
  • Figure 6-6: Hemlibra - US v/s ROW Sales (US$ Million), 2023
  • Figure 6-7: Hemlibra - US v/s ROW Shares (%), 2023
  • Figure 6-8: Hemlibra - US v/s ROW Sales (US$ Million), 2022
  • Figure 6-9: Hemlibra - US v/s ROW Shares (%), 2022
  • Figure 6-10: Global - US v/s ROW in Bispecific Antibodies Market (US$ Million), 2023
  • Figure 6-11: Global - US v/s ROW Shares in Bispecific Antibodies Market (%), 2023
  • Figure 6-12: Global - US v/s ROW in Bispecific Antibodies Market (US$ Million), 2022
  • Figure 6-13: Global - US v/s ROW Shares in Bispecific Antibodies Market (%), 2022
  • Figure 6-14: Blincyto - US Patent Filing & Expiration Year
  • Figure 6-15: Blincyto - EU Patent Expiration
  • Figure 6-16: Vabysmo - Canada Patent Numbers Expiration & Approval Year
  • Figure 6-17: Hemlibra - Canada Patent Numbers Approval & Expiration Year
  • Figure 6-18: Rybrevant - Canada Patent Numbers Approval & Expiration Year
  • Figure 6-19: Kimmtrak - Canada Patent Number Approval & Expiration Year
  • Figure 7-1: Bispecific Antibodies - Advantages
  • Figure 7-2: TG-1801 Phase 1 Study - Initiation & Completion Year
  • Figure 7-3: Bispecific Antibodies - Future Opportunities
  • Figure 7-4: Mim8 Phase 3 (NCT05053139) Study - Initiation & Completion Year
  • Figure 7-5: Mim8 Phase 3 (NCT05878938) Study - Initiation & Completion Year
  • Figure 7-6: NXT007 Phase 1/2 (NCT05987449) Study - Initiation & Completion Year
  • Figure 7-7: HMB-001 Phase 1/2 (NCT06211634) Study - Initiation & Completion Year
  • Figure 7-8: REGN4018 Phase 1/2 (NCT03564340) Study - Initiation & Completion Year
  • Figure 7-9: PRV-3279 Phase 2 (NCT05087628) Study - Initiation & Completion Year
  • Figure 8-1: Global - Bispecific Antibodies Clinical Pipeline by Phase (Numbers), 2023
  • Figure 8-2: Global - Bispecific Antibodies in Clinical Pipeline by Country (Numbers), 2024 till 2029
  • Figure 8-3: Global - Bispecific Antibodies in Clinical Pipeline by Company (Numbers), 2024 till 2029
  • Figure 8-4: Global - Bispecific Antibodies in Clinical Pipeline by Indication (Numbers), 2023 till 2029
  • Figure 8-5: Global - Bispecific Antibodies in Clinical Pipeline by Orphan Status (Numbers), 2023 till 2029
  • Figure 8-6: Global - Bispecific Antibodies in Clinical Pipeline by Patient Segment (Numbers), 2023 till 2029
  • Figure 9-1: Blincyto - Approval Year by Region
  • Figure 9-2: Blincyto - Patent Filing & Expiration Year
  • Figure 9-3: Blincyto - Treatment Regimen Cycles (Weeks)
  • Figure 9-4: Blincyto - Duration of Treatment Phase & Resting Phase in Induction & Consolidation Cycles for Treatment of MRD-Positive B-cell precursor (Days)
  • Figure 9-5: Blincyto - Cost of Single Cycle & Treatment Course for the Treatment of MRD-positive B-cell Precursor ALL
  • Figure 9-6: Blincyto - Recommended Number of Induction & Consolidation Treatment Cycle for Relapsed B-Cell Precursor ALL
  • Figure 9-7: Blincyto - Duration of Single Induction, Consolidation, Continued Cycle & Full Treatment for Relapsed B-Cell Precursor ALL (Weeks)
  • Figure 9-8: Blincyto - Cost of Single Cycle & Treatment Course for Treatment for Relapsed B-Cell Precursor ALL
  • Figure 9-9: Global - Blincyto Sales (US$ Million), 2019-2023
  • Figure 9-10: Global - Blincyto Sales (US$ Million), Q1 - Q4'2023
  • Figure 9-11: Blincyto - US v/s ROW Sales (US$ Million), 2023
  • Figure 9-12: Global - Blincyto Sales by Region (%), 2023
  • Figure 9-13: US - Blincyto Sales (US$ Million), Q1 - Q4'2023
  • Figure 9-14: ROW - Blincyto Sales (US$ Million), Q1 - Q4'2023
  • Figure 9-15: US - Blincyto Sales ((US$ Million), 2019-2023
  • Figure 9-16: ROW - Blincyto Sales (US$ Million), 2019-2023
  • Figure 10-1: Hemlibra - Approval Years by Region
  • Figure 10-2: Hemlibra - Cost per Unit & Supply of 150 mg/mL Subcutaneous Injection (US$), February'2024
  • Figure 10-3: Hemlibra - Recommended Loading & Maintenance Dose for Treatment of Hemophilia (mg/kg/Week)
  • Figure 10-4: Global - Hemlibra Sales (US$ Million), 2019-2023
  • Figure 10-5: US - Hemlibra Sales (US$ Million), 2019-2023
  • Figure 10-6: Europe - Hemlibra Sales (US$ Million), 2019-2023
  • Figure 10-7: Japan - Hemlibra Sales (US$ Million), 2019-2023
  • Figure 10-8: ROW - Hemlibra Sales (US$ Million), 2019-2023
  • Figure 10-9: Global - US v/s ROW Sales (US$ Million), 2023
  • Figure 10-10: Global - Hemlibra Annual Sales by Region (US$ Million), 2023
  • Figure 10-11: Global - Hemlibra Sales by Region (%), 2023
  • Figure 10-12: Global - Hemlibra Sales (US$ Million), Q1 - Q4'2023
  • Figure 10-13: US - Hemlibra Sales (US$ Million), Q1 - Q4'2023
  • Figure 10-14: Europe - Hemlibra Sales (US$ Million), Q1 - Q4'2023
  • Figure 10-15: Japan - Hemlibra Sales (US$ Million), Q1 - Q4'2023
  • Figure 10-16: ROW - Hemlibra Sales (US$/ US$ Million), Q1 - Q4'2023
  • Figure 11-1: Rybrevant - Price per Unit & Supply of Intravenous Solution (US$), February'2024
  • Figure 11-2: Rybrevant - Recommended Dose Per Cycle by Body Weight (mg)
  • Figure 11-3: Rybrevant - Dose Reduction in Patients with Weight less than 80 kg (mg)
  • Figure 11-4: Rybrevant - Dose Reduction in Patients with Weight more than 80 Kg (mg)
  • Figure 12-1: Kimmtrak - Approval Year by Region
  • Figure 12-2: Kimmtrak - Cost Per Unit & Per Vial (US$), February'2024
  • Figure 12-3: Global - Annual Kimmtrak Sales (US$ Million), 2021-2023
  • Figure 12-4: Global - Quarterly Kimmtrak Sales (US$ Million), 2023
  • Figure 12-5: Kimmtrak - Sales by Region (US$ Million), 2023
  • Figure 12-6: Kimmtrak - US v/s ROW Market Shares (US$ Million), 2023
  • Figure 12-7: Kimmtrak - US v/s ROW Market Shares (%), 2023
  • Figure 12-8: US - Quarterly Kimmtrak Sales (US$ Million), 2023
  • Figure 12-9: EU - Quarterly Kimmtrak Sales (US$ Million), 2023
  • Figure 12-10 ROW - Quarterly Kimmtrak Sales (US$ Million), 2023
  • Figure 13-1: Vabysmo - Approval Year by Region
  • Figure 13-2: Vabysmo - Price per Unit & Supply of Intravitreal Solution (US$), February'2024
  • Figure 13-3: Global - Vabysmo Sales (US$ Million), 2022-2023
  • Figure 13-4: Global - Vabysmo US v/s ROW Sales (US$ Million), 2023
  • Figure 13-5: Global - Vabysmo Annual Sales by Region (US$ Million), 2023
  • Figure 13-6: Global - Vabysmo Annual Sales by Region (%), 2023
  • Figure 13-7: US - Vabysmo Sales (US$ Million), 2022-2023
  • Figure 13-8: Europe - Vabysmo Sales (US$ Million), 2022-2023
  • Figure 13-9: Japan - Vabysmo Sales (US$ Million), 2022-2023
  • Figure 13-10: ROW - Vabysmo Sales (US$ Million), 2022-2023
  • Figure 13-11: Global - Vabysmo Sales (US$ Million), Q1 - Q4'2023
  • Figure 13-12: US - Vabysmo Sales (US$ Million), Q1 - Q4'2023
  • Figure 13-13: Europe - Vabysmo Sales (US$ Million), Q1 - Q4'2023
  • Figure 13-14: Japan - Vabysmo Sales (US$ Million), Q1 - Q4'2023
  • Figure 13-15: ROW - Vabysmo Sales (US$ Million), Q1 - Q4'2023
  • Figure 14-1: Lunsumio - Approval Years by Region
  • Figure 14-2: US - Price per Unit & Supply of Lunsumio Intravenous Solution (US$), February'2024
  • Figure 14-3: EU - Price per Unit & Supply of Lunsumio Intravenous Solution (US$), February'2024
  • Figure 14-4: Global - Lunsumio Sales (US$ Million), 2022-2023
  • Figure 14-5: US - Lunsumio Sales (US$ Million), 2022-2023
  • Figure 14-6: Europe - Lunsumio Sales (US$ Million), 2022-2023
  • Figure 14-7: Global - Lunsumio Annual Sales by Region (US$ Million), 2023
  • Figure 14-8: Global - Lunsumio Annual Sales by Region (%), 2023
  • Figure 14-9:- Global - Lunsumio Sales (US$ Million), Q1 - Q4'2023
  • Figure 14-10: US - Lunsumio Sales (US$ Million), Q1 - Q4'2023
  • Figure 14-11: Europe - Lunsumio Sales (US$ Million), Q1 - Q4'2023
  • Figure 15-1: Annual - Cadonilimab Sales (US$ Million), H2'2022 & H1'2023
  • Figure 16-1: Tecvayli - Approval Years by Region
  • Figure 16-2: Tecvayli - Patent Acceptance & Expiration Years
  • Figure 16-3: US - Cost per Unit & Supply of Tecvayli Subcutaneous Solution (US$), February'2024
  • Figure 16-4: EU - Cost per Unit & Supply of Tecvayli Subcutaneous Solution (US$), February'2024
  • Figure 17-1: Columvi - Approval Year by Region
  • Figure 17-2: US - Price per Unit & Supply of Columvi Intravenous Solution (US$), February'2024
  • Figure 17-3: EU - Price per Unit & Supply of Columvi Intravenous Solution (US$), February'2024
  • Figure 17-4: Global - Columvi Sales by Region (US$ Million), 2023
  • Figure 17-5: Global - Columvi Sales (US$ Million), Q1 - Q4'2023
  • Figure 17-6: US - Columvi Sales (US$ Million), Q1 - Q4'2023
  • Figure 17-7: Europe - Columvi Sales (US$ Million), Q1 - Q4'2023
  • Figure 18-1: Epkinly - Approval Year by Region
  • Figure 18-2: US - Cost per Unit & Supply of Epkinly Subcutaneous Solution (US$), February'2024
  • Figure 18-3: EU - Cost per Unit & Supply of Epkinly Subcutaneous Solution (US$), February'2024
  • Figure 18-4: Global - Epkinly Sales (US$ Million), 2023
  • Figure 18-5: Global - Epkinly Sales (US$ Million), Q1 - Q4'2023
  • Figure 19-1: Talvey - Approval Year by Region
  • Figure 19-2: Talquetamab - FDA & EMA Designation Year
  • Figure 19-3: Talvey - Patent Acceptance & Expiration Year
  • Figure 19-4: US - Price per Unit & Supply of Talvey Intravenous Solution (US$), February'2024
  • Figure 19-5: EU - Price per Unit & Supply of Talvey Intravenous Solution (US$), February'2024
  • Figure 20-1: Elrexfio - Approval Years by Region
  • Figure 20-2: Elranatamab - FDA & EMA Designation Years
  • Figure 20-3: US - Price per Unit & Supply of Elrexfio Subcutaneous Solution (US$), February'2024

List of Tables

  • Table 2-1: Bispecific Antibody & Chemotherapy Combinations in Clinical Trials
  • Table 2-2: Bispecific Antibody & Targeted Therapy Combinations in Clinical Trials
  • Table 2-3: Bispecific Antibody & Immunotherapy Combinations in Clinical Trials
  • Table 2-4: Bispecific Antibody & Radiotherapy Combinations in Clinical Trials
  • Table 3-1: Approved Bispecific Antibodies
  • Table 3-2: US - Bispecific Antibodies with Regulatory Designations
  • Table 3-3: EU - Bispecific Antibodies with Regulatory Designations
  • Table 3-4: EU - Bispecific Antibodies with Regulatory Designations
  • Table 5-1: Epkinly - Billing Unit Application for Doses
  • Table 5-2: Talvey - Coverage Summary
  • Table 5-3: Talvey - Coding Summary
  • Table 5-4: Elrexfio - HCPCS Codes
  • Table 5-5: Elrexfio - HCPCS modifiers
  • Table 6-1: US - FDA IND Applications Accepted, February'2024
  • Table 6-2: EU - Bispecific Antibodies in Late Stage Clinical Trials
  • Table 6-3: Bispecific Antibodies in Clinical Trials in Latin America
  • Table 7-1: Lymphoma - Bispecific Antibodies in Clinical Trials
  • Table 7-2: Multiple Myeloma - Bispecific Antibodies in Clinical Trials
  • Table 7-3: Leukemia - Bispecific Antibodies in Clinical Trials
  • Table 7-4: Lung Cancer - Bispecific Antibodies in Clinical Trials
  • Table 7-5: Melanoma - Bispecific Antibodies in Clinical Trials
  • Table 7-6: Digestive System Cancers - Bispecific Antibodies in Clinical Trials
  • Table 7-7: Breast Cancer - Bispecific Antibodies in Clinical Trials
  • Table 7-8: Gynecological Cancers - Bispecific Antibodies in Clinical Trials
  • Table 7-9: Gynecological Cancers - Bispecific Antibodies in Clinical Trials
  • Table 9-1: Blincyto - Active Patents
  • Table 9-2: Blincyto - Recommended Dosage & Schedule for the Treatment of MRD-positive B-cell Precursor ALL
  • Table 9-3: Blincyto - Recommended Dosage & Schedule for Treatment of Relapsed or Refractory B-cell Precursor ALL
  • Table 9-4: Blincyto - Recommended Dosage & Schedule for Treatment of Relapsed or Refractory B-cell Precursor ALL
  • Table 11-1: Rybrevant - Premedication
  • Table 11-2: Rybrevant - Dose Reductions for Adverse Reactions
  • Table 11-3: Rybrevant - Recommended Dosage Modifications for Adverse Reactions
  • Table 12-1: Kimmtrak - Recommended Dosage for Treatment of Unresectable or Metastatic Uveal Melanoma
  • Table 12-2: Kimmtrak - Dose Modifications for Adverse Reactions
  • Table 14-1: Lunsumio - Recommended Treatment Cycles
  • Table 14-2: Lunsumio - Recommended Premedications
  • Table 14-3: Lunsumio - Recommendations for Management of Cytokine Release Syndrome
  • Table 16-1: Tecvayli - Dosing Schedule
  • Table 16-2: Tecvayli - Recommended Dosage Modifications for Adverse Reactions
  • Table 17-1: Columvi - Dosing Schedule (21-Day Treatment Cycles)
  • Table 17-2: Columvi - Premedications to be Administered
  • Table 17-3: Columvi - Recommendations for Management of Cytokine Release Syndrome
  • Table 17-4: Columvi - Recommended Dosage Modification for Neurologic Toxicity (Including ICANS)
  • Table 17-5: Columvi - Recommended Dosage Modifications for Other Adverse Reactions
  • Table 18-1: Epkinly - Dosage Schedule
  • Table 18-2: Epkinly - Recommendations for Management of Cytokine Release Syndrome
  • Table 18-3: Epkinly - Recommendations for Management of Immune Effector Cell-Associated Neurotoxicity Syndrome (ICANS)
  • Table 18-4: Epkinly - Recommended Dosage Modifications for Other Adverse Reactions
  • Table 19-1: Talvey - Weekly Dosing Schedule
  • Table 19-2: Talvey - Biweekly Dosing Schedule
  • Table 19-3: Talvey - Recommendations for Management of CRS
  • Table 19-4: Talvey - Recommendations for Management of Immune Effector Cell-Associated Neurotoxicity Syndrome (ICANS)
  • Table 19-5: Talvey - Recommendations for Management of Neurologic Toxicity (excluding ICANS)
  • Table 19-6: Talvey - Recommended Dosage Modifications for Other Adverse Reactions
  • Table 20-1: Elrexfio - Dosing Schedule
  • Table 20-2: Elrexfio - Recommendations for Management of CRS
  • Table 20-3: Elrexfio - Recommended Dosage Modifications for Other Adverse Reactions
目次

Global Bispecific Antibody Market, Drugs Sales, Patent, Price & Clinical Trials Insight 2029 Report Highlights:

  • Bispecific Antibodies Development Proprietary Platforms Insight: > 30 Platforms
  • Global Bispecific Antibodies Market Size Yearly & Quarterly Sales (2018 till 2023)
  • Global Bispecific Antibodies Market Size 2023: > USD 8 Billion
  • Global Bispecific Antibodies Market Forecast Till 2029
  • Approved Bispecific Antibodies Yearly & Quarterly Sales (2018 till 2023)
  • Approved Bispecific Antibodies Regional Sales (2018 till 2023)
  • Clinical & Commercial Insight On Approved Bispecific Antibodies: 12 Antibodies
  • Approved Bispecific Antibodies Pricing & Dosage Analysis
  • Global Bispecific Antibodies Clinical Trials By Company, Indication & Phase: > 800 Antibodies
  • FDA & EMA Fast Track Approval, Orphan Designation, Priority Status Insights

Bispecific antibodies represent an exciting new therapeutic approach that has been gaining momentum since the last decade. These meticulously designed molecules offer a unique mechanism of action that harnesses the immune system to target malignant and other diseased cells and tissues with precision, offering a targeted approach that minimizes the risk of adverse effects. In the last three years, the market of bispecific antibodies has experienced a rapid surge in research and development, and commercial activities, setting the market for a speedy growth in the coming years.

Bispecific antibodies are engineered proteins intended to simultaneously bind two different antigens, typically found on distinct cell types. Their dual targeting ability provides multiple ways to exploit the immune systems against diseases. For cancer, common approaches include redirecting T cells or natural killer cells to attack malignant cells. They can also crosslink immune cells with tumor cells to enhance the immune response. Additionally, they can block two different signaling pathways or recruit immune cells to the tumor microenvironment.

For indications apart from cancer, bispecific antibodies enable dual targeting of different disease mediators or cell types. This provides opportunities to neutralize or clear pathogenic proteins, cytokines or cells involved in inflammation, autoimmunity and other diseases. However, depending on the indications, the mechanism by which bispecific antibodies work can change.

The versatility of bispecific antibodies offers several advantages over their predecessors, traditional monoclonal antibodies, including enhanced specificity, potency and flexibility in targeting multiple pathways at the same time. This become especially relevant in cancer treatment, where monoclonal antibodies are utilized heavily to interfere with different cancer-associated pathways. By directly redirecting immune cells to tumors, bispecific antibodies can overcome tumor immune evasion mechanisms, leading to improved efficacy and potentially lower toxicity compared to conventional chemotherapy.

The US FDA approved Blinatumomab (commercially known as Blincyto) in 2014, marking a key milestone in the field of bispecific antibodies and fundamentally changing how relapsed or refractory precursor B-cell acute lymphoblastic leukemia is treated. Following this success, multiple new bispecific antibodies have arisen in clinical development, covering a wide range of medical disorders, with a focus on cancer. Nonetheless, in addition to cancer, there has been an increase in the number of bispecific candidates designed to address emerging indications such as viral and bacterial infections, as well as autoimmune diseases. This diversification highlights the growing range of therapeutic applications for this class of medicines.

Currently, there are over 800 bispecific candidates in active clinical development. Phase 3 trials are underway across a spectrum of solid cancers like triple negative breast cancer, small cell lung cancer, bladder cancer among others, in addition to hematological cancers, including myeloma and leukemia. Further, a few other phase 3 candidates are also being investigated in indications beyond cancer, like hemophilia A and diabetic macular edema, displaying the diversity in indications.

The heightened attention on the development of this novel therapeutic class has been greatly supported by the increasing global value of the bispecific antibodies market. At present, 12 bispecific antibodies have received approvals in different markets around the globe, which together, generated revenue of over US$ 8.5 Billion in the year 2023. This was an increase of over 47% as compared to the total sales of 2022, which was approximately over US$ 5.8 Billion. A bulk of this value comes from the global sales of Hemlibra, a bispecific antibody indicated for the treatment of Hemophilia A, which is the highest selling member of this drug class.

Since bispecific antibodies were introduced in the market, the US has been a major contributor to the overall sales of these drugs. In 2023, the US market alone generated a revenue of US$ 5.6 Billion, with the international market contributing US$ 2.8 Billion to the total sales. This was an increase of 34% compared to the sales recorded in 2022, showing the growing interest of patients and physicians in novel therapeutics, such as bispecific antibodies.

Therefore, bispecific antibodies have demonstrated enough clinical success to validate their potential as a major new drug class. Their unique ability to tap into multiple disease pathways is unlocking new therapeutic possibilities beyond monoclonal antibodies. While oncology has led the way, expansion into other disease areas is accelerating. With continued innovation in molecular designs and engineering, bispecific antibodies represent an exciting versatile approach to transform treatment across a wide range of unmet medical needs, which researchers are slowly progressing to.

Table of Contents

1. Introduction to Bispecific Antibody

  • 1.1. Overview
  • 1.2. Clinical Advancement of Bispecific Antibodies

2. Bispecific Antibodies Combination Strategies

  • 2.1. Chemotherapies
  • 2.2. Targeted Therapies
  • 2.3. Immunotherapies
  • 2.4. Radiotherapy

3. Commercially Approved Bispecific Antibodies Insight

  • 3.1. Company, Indication, Location & MOA
  • 3.2. Bispecific Antibodies Granted FDA & EMA Designations

4. Bispecific Antibodies Proprietary Platforms

5. Global & Regional Bispecific Antibody Market Outlook

  • 5.1. Yearly & Quarterly Sales Insight (2019 to 2023)
  • 5.2. Approved Bispecific Antibodies Reimbursement Policy
  • 5.3. Global Bispecific Antibody Market Forecast 2029

6. Global Bispecific Antibody Market Trends By Region

  • 6.1. US
  • 6.2. Europe
  • 6.3. China
  • 6.4. UK
  • 6.5. Japan
  • 6.6. South Korea
  • 6.7. Australia
  • 6.8. Canada
  • 6.9. Latin America

7. Global Bispecific Antibodies Research & Market Trends by Indications

  • 7.1. Lymphoma
  • 7.2. Multiple Myeloma
  • 7.3. Leukemia
  • 7.4. Lung Cancer
  • 7.5. Melanoma
  • 7.6. Blood Disorders
  • 7.7. Gastrointestinal Cancers
  • 7.8. Other Cancers
  • 7.9. Autoimmune & Inflammatory Diseases
  • 7.10. Microbial Diseases
  • 7.11. Ocular Diseases

8. Global Bispecific Antibodies Clinical Trials Overview

  • 8.1. By Phase
  • 8.2. By Country/Region
  • 8.3. By Company
  • 8.4. By Indication
  • 8.5. By Priority Status
  • 8.6. Patient Segment

9. Blincyto - Clinical, Patent, Pricing & Sales Insight

  • 9.1. Overview & Patent Insight
  • 9.2. Pricing & Dosage Analysis
  • 9.3. Sales Analysis

10. Hemlibra - Clinical, Patent, Pricing & Sales Insight

  • 10.1. Overview
  • 10.2. Pricing & Dosage Insight
  • 10.3. Sales Analysis

11. Rybrevant - Clinical, Patent & Pricing Insight

  • 11.1. Overview
  • 11.2. Pricing & Dosage Insight

12. Kimmtrak - Clinical, Patent, Pricing & Sales Insight

  • 12.1. Overview
  • 12.2. Pricing & Dosage Insight
  • 12.3. Sales Analysis

13. Vabysmo - Clinical, Patent, Pricing & Sales Insight

  • 13.1. Overview
  • 13.2. Pricing & Dosage Insight
  • 13.3. Sales Analysis

14. Lunsumio - Clinical, Patent, Pricing & Sales Insight

  • 14.1. Overview & Patent Insight
  • 14.2. Pricing & Dosage Insight
  • 14.3. Sales Analysis

15. Cadonilimab - Clinical & Sales Insight

16. Tecvayli - Clinical, Patent & Pricing Insight

  • 16.1. Overview & Patent Insight
  • 16.2. Pricing & Dosage Insight

17. Columvi - Clinical, Patent, Pricing & Sales Insight

  • 17.1. Overview & Patent Insight
  • 17.2. Pricing & Dosage Insight
  • 17.3. Sales Analysis

18. Epkinly - Clinical, Patent, Pricing & Sales Insight

  • 18.1. Overview
  • 18.2. Pricing & Dosage Insight
  • 18.3. Sales Analysis

19. Talvey - Clinical, Patent & Pricing Insight

  • 19.1. Overview & Patent Insight
  • 19.2. Pricing & Dosage Insight

20. Elrexfio - Clinical, Patent & Pricing Insight

  • 20.1. Overview
  • 20.2. Pricing & Dosage Insight

21. Global Bispecific Antibodies Clinical Trials By Company, Indication & Phase

  • 21.1. Research
  • 21.2. Preclinical
  • 21.3. Phase-I
  • 21.4. Phase-I/II
  • 21.5. Phase-II
  • 21.6. Phase-II/III
  • 21.7. Phase-III
  • 21.8. Preregistration
  • 21.9. Registered

22. Marketed Bispecific Antibodies Clinical Insight By Company, Country & Indication

23. Competitive Landscape

  • 23.1. ABL Bio
  • 23.2. Abzyme Therapeutics
  • 23.3. Affimed Therapeutics
  • 23.4. Akeso Biopharma
  • 23.5. Alligator Bioscience
  • 23.6. Amgen
  • 23.7. Antibody Therapeutics
  • 23.8. APITBIO
  • 23.9. Aptevo Therapeutics
  • 23.10. Astellas Pharma
  • 23.11. AstraZeneca
  • 23.12. BioAtla
  • 23.13. Biosion
  • 23.14. Biotheus
  • 23.15. BJ Bioscience
  • 23.16. EpimAb Biotherapeutics
  • 23.17. FutureGen Biopharmaceutical
  • 23.18. Genentech
  • 23.19. Genmab
  • 23.20. Gensun Biopharma
  • 23.21. Harbour BioMed
  • 23.22. IGM Biosciences
  • 23.23. I-MAB Biopharma
  • 23.24. ImmuneOnco Biopharma
  • 23.25. ImmunoPrecise Antibodies
  • 23.26. Innovent Biologics
  • 23.27. Invenra
  • 23.28. Janssen Research & Development
  • 23.29. Kenjockety Biotechnology
  • 23.30. LaNova Medicines Limited
  • 23.31. Light Chain Bioscience
  • 23.32. Linton Pharm
  • 23.33. Lyvgen Biopharma
  • 23.34. MacroGenics
  • 23.35. Merus
  • 23.36. NovaRock Biotherapeutics
  • 23.37. Pfizer
  • 23.38. Phanes Therapeutics
  • 23.39. Prestige BioPharma
  • 23.40. Regeneron Pharmaceuticals
  • 23.41. Revitope
  • 23.42. Roche
  • 23.43. Virtuoso Therapeutics
  • 23.44. Xencor
  • 23.45. Y-Biologics
  • 23.46. Zhejiang Shimai Pharmaceutical
  • 23.47. Zymeworks