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세계의 CRISPR Cas9 시장 : 시장 기회 및 임상시험 전망(2029년)

Global CRISPR Cas9 Market Opportunity & Clinical Trials Outlook 2029

발행일: | 리서치사: KuicK Research | 페이지 정보: 영문 180 Pages | 배송안내 : 1-2일 (영업일 기준)

    
    
    



※ 본 상품은 영문 자료로 한글과 영문 목차에 불일치하는 내용이 있을 경우 영문을 우선합니다. 정확한 검토를 위해 영문 목차를 참고해주시기 바랍니다.

암, 자가면역 질환, 염증성 질환 및 기타 질병을 관리하기 위해 화학요법, 분자 표적 치료 등 전통적인 치료법이 사용되어 왔지만, 임상 연구자들은 다른 첨단 기술을 발견하기 위해 끈질기게 노력해 왔습니다. 전 세계적으로 유전성 질환이 무서운 속도로 확산되고 효과적인 치료법의 필요성이 증가함에 따라 CRISPR/Cas9 치료법이 발견되었고, 2024년 7월 현재 CRISPR/Cas9 치료법은 베타 지중해 빈혈과 겸상 적혈구 빈혈 치료제로 승인되었으며, 미국, EU, 영국, 사우디아라비아, 바레인, 영국, 사우디아라비아, 바레인에서 사용할 수 있습니다.

향후 5년 내에 CRISPR/Cas9 치료의 첫 번째 물결이 규제 당국의 승인을 받고 시장에 진입할 것으로 예상됩니다. 이러한 치료법이 실제 환경에서 안전성과 효능을 입증함에 따라 CRISPR/Cas9 기반 치료법의 광범위한 수용과 적용을 위한 길이 열릴 것이기 때문입니다. 이와 함께 이 획기적인 유전자 편집 기술의 잠재적 응용은 유전성 질환과 암을 넘어 심혈관 질환, 신경 퇴행성 질환, 중추신경계 질환의 치료에도 활용될 수 있을 것으로 기대됩니다.

지금까지 전 세계 CRISPR/Cas9 치료제의 임상 파이프라인은 해마다 급증하고 있으며, 여러 치료법이 임상시험에 들어갔고, 다른 CRISPR/Cas9 후보물질도 전임상 단계에 있습니다. 현재 진행 중인 CRISPR/Cas9 임상시험은 대부분 개발 후기 단계에 이르렀으며, 5-7년 내에 시장에 진입할 것으로 예상됩니다. 예를 들어, Intellia Therapeutics는 심근증을 동반한 트랜스시레틴 아밀로이드증(ATTR-CM) 환자를 대상으로 CRISPR/Cas9 치료제인 NTLA-2001의 단회 투여의 유효성과 안전성을 위약과 비교 평가하기 위한 임상 3상을 진행 중입니다. 다국가, 다기관, 이중맹검, 위약대조 시험을 시작했습니다. 이 시험(MAGNITUDE)은 2023년 12월에 시작되어 2028년 4월까지 완료될 예정입니다.

이 보고서는 세계 CRISPR Cas9 시장에 대해 조사했으며, 시장 개요와 함께 의약품 동향, 임상시험 동향, 지역별 동향, 시장 진출기업의 경쟁 구도 등을 조사하여 전해드립니다.

목차

제1장 CRISPR-Cas9 요법 요약

제2장 CRISPR-Cas9 전달 방법

  • 물리적 방법에 따르는 CRISPR-Cas9 컴포넌트 전달
  • 바이러스 벡터에 의한 CRISPR-Cas9 컴포넌트 전달
  • 비바이러스 벡터(바이오소재)에 의한 CRISPR-Cas9 컴포넌트 전달

제3장 CRISPR-Cas9 : 다양한 이용 장소

  • CRISPR-Cas9 기술에 따른 이점
  • CRISPR-Cas9와 기타 유전자 편집 툴 비교

제4장 세계의 CRISPR-Cas9 요법, 임상시험 개요

  • 기업별
  • 국가별
  • 적응증별
  • 상별
  • 우선도별

제5장 세계의 CRISPR-Cas9 요법 임상시험 : 기업, 나라, 적응증, 단계별

  • 조사
  • 전임상
  • 제I상
  • 제I/II상
  • 제II상

제6장 승인을 획득한 CRISPR-Cas9 요법 : Casgevy(Exagamglogene Autotemcel) 요법 임상적 통찰

제7장 승인을 획득한 CRISPR-Cas9 요법 : 개요, 가격 결정, 투여량 분석

  • Casgevy(Exagamglogene Autotemcel)
    • 개요
    • 가격과 투여량

제8장 세계의 CRISPR-Cas9 요법 현재 시장 동향과 발전

  • 현재 시장 개요
  • 향후 시장 전망

제9장 CRISPR-Cas9 요법 시장 동향 분석, 지역별

  • 미국
  • 영국
  • 유럽연합
  • 중국
  • 일본
  • 한국

제10장 CRISPR-Cas9 요법 시장 기회와 임상시험 통계 : 적응증별

  • 유전성 혈액 질환
  • 유전성 질환
  • 자가면역 질환 및 염증성 질환
  • 미생물 감염증
  • 심혈관 질환
  • 안질환, 뇌질환, 대사질환 및 기타 질환

제11장 CRISPR-Cas9 요법의 복합 접근

제12장 CRISPR-Cas9 요법 발전을 위한 플랫폼

제13장 세계의 CRISPR-Cas9 요법 시장 역학

  • 시장 성장 촉진요인
  • 시장 약점

제14장 경쟁 구도

  • 4D Molecular Therapeutics
  • Arbor Biotechnologies
  • ASC Therapeutics
  • C4U Corporation
  • Casebia Therapeutics
  • CRISPR Therapeutics
  • Editas Medicine
  • Intellia Therapeutics
  • Nkarta Therapeutics
  • Vertex Pharmaceuticals
LSH 24.08.13

Global CRISPR Cas9 Market Opportunity & Clinical Trials Outlook 2029 Report Offering:

  • Global & Regional: Commercial & Clinical Outlook
  • Global CRISPR-Cas9 Therapy Clinical Trials By Company, County, Indication & Phase
  • Number Of CRISPR-Cas9 Therapies In Trials: > 25 Therapies
  • Approved CRISPR-Cas9 Therapy: Casgevy (Exagamglogene Autotemcel) Therapy Clinical Insight
  • Approved CRISPR-Cas9 Therapy Pricing & Dosing Analysis
  • Technology Platforms For Advancing CRISPR-Cas9 Therapy
  • Delivery Methodologies For CRISPR-Cas9
  • Competitive Landscape

Antecedently, out-of-date bestseller conventional therapies, including chemotherapy or targeted therapies, were utilized for the management of cancer, autoimmune, inflammation and other diseases; yet, clinical researchers were occupied tenaciously with the hypothesis of discovering other cutting edge technologies. The growing rampant of genetic disorders across the globe at a frightening gait as well as the need for an effective cure has led to the discovery of CRISPR/Cas9 therapy. Build on the triumph of gene therapies, these therapies clenches gargantuan plausibility with only one CRISPR/Cas9 therapy; Casgevy, approved into the commercial market, as of July 2024, to treat sickle cell anemia along with beta thalassemia and is currently accessible in US, EU, UK, Saudi Arabia and Bahrain; proposing novel opportunity in the approaching years.

With respect to KuicK Research statistics, we anticipate to perceive the first wave of CRISPR/Cas9 therapies receiving regulatory approvals over and above entering the market in upcoming 5 years due to the fact that as these therapies demonstrate their effectiveness in addition to safety in real-world settings, they will pave the way for broader acceptance and application of CRISPR/Cas9 based treatments. Coupled with this, the potential applications of this groundbreaking gene-editing technology are expected to expand dramatically beyond genetic disorders and cancers and will be utilized to cure cardiovascular, neurodegenerative together with CNS diseases as evident from rising preclinical as well as clinical studies, touching fundamentally every area of medicine and biotechnology.

Until now, the clinical pipeline for global CRISPR/Cas9 therapy is up surging year by year with multiple therapies have entered into clinical trials and other CRISPR/Cas9 candidates are lately in the preclinical stage. Many of ongoing CRISPR/Cas9 clinical trials have reached late stage of development and it is predicable that they will penetrate into the market in the imminent 5-7 years. For instance, Intellia Therapeutics has begun a phase III, multinational, multicenter, double-blind, placebo-controlled study is ongoing which aims to evaluate the efficacy and safety of a single dose of NTLA-2001, a CRISPR/Cas9 therapy, compared to placebo in participants with transthyretin amyloidosis with cardiomyopathy (ATTR-CM). The study (MAGNITUDE) was begun in December 2023 and is anticipated to be complete by April 2028 coupled with clenches an enrollment of 765 participants.

Just as importantly, the over-all market for CRISPR/Cas9 therapies is estimated to grow substantively and will become a multi-billion-dollar industry over the impending eons, driven by the snowballing number of preclinical and clinical trials, the likely regulatory approvals, in conjugation with the increase of indications. Currently, the US dominates the CRISPR/Cas9 sphere in terms of research and development activities, but EU is correspondingly far-sighted momentous evolution in this field.

As well as, the current approved CRISPR/Cas9 therapy; Casgevy, developed by CRISPR Therapeutics and Vertex Pharmaceutical, is launched into the market at an average cost of roughly US$ 2 Million per single course of treatment according to Casgevy developer company SEC filings. Additionally, the anticipated high prices of these therapies, justified by their potential curative nature, are expected to further drive significant market growth in terms of revenue, even with relatively small patient populations.

As a final point, all elucidations aforesaid epitomize that the global CRISPR/Cas9 therapy is growing at a trailblazing gait and is predictable to multiply additional in the forthcoming 10 years. The expanding clinical application as well as together with indication of CRISPR/Cas9, mounting preclinical and clinical trials, rise in technological advancement, presences of key players like Intellia Therapeutics, CRISPR Therapeutics, Editas Medicine, TransCode Therapeutics and many more, combination studies of CRISPR/Cas9 with other therapies coupled with augment in investment, collaborations and government bestow are driving the market penetration, offering opportunism to pharma and biotech companies in future.

Table of Contents

1. Synopsis To CRISPR-Cas9 Therapy

  • 1.1 Overview
  • 1.2 Approved CRISPR-Cas9 Therapies

2. Delivery Methods For CRISPR-Cas9

  • 2.1 Delivery of CRISPR-Cas9 Components Through Physical Methods
    • 2.1.1 Microinjection
    • 2.1.2 Electroporation
    • 2.1.3 Hydrodynamic Delivery
  • 2.2 Delivery of CRISPR-Cas9 Components through Viral Vectors
    • 2.2.1 Adeno-Associated Virus (AAV)
    • 2.2.2 Lentivirus & Adenovirus
  • 2.3 Delivery of CRISPR-Cas9 Components through Non-Viral Vectors (Biomaterials)
    • 2.3.1 Liposomes
    • 2.3.2 Gold Nanoparticles
    • 2.3.3 DNA Nanoclew

3. CRISPR-Cas9: A Home To Variety Of Applications

  • 3.1 Advantages Accompanying CRISPR-Cas9 Technology
  • 3.2 CRISPR-Cas9 Comparison with other Genome Editing Tools

4. Global CRISPR-Cas9 Therapy Clinical Trials Overview

  • 4.1 By Company
  • 4.2 By Country
  • 4.3 By Indication
  • 4.4 By Phase
  • 4.5 By Priority Status

5. Global CRISPR-Cas9 Therapy Clinical Trials By Company, County, Indication & Phase

  • 5.1 Research
  • 5.2 Preclinical
  • 5.3 Phase I
  • 5.4 Phase I/II
  • 5.5 Phase II

6. Approved CRISPR - Cas9 Therapy: Casgevy (Exagamglogene Autotemcel) Therapy Clinical Insight

7. Approved CRISPR-Cas9 Therapy - Overview, Pricing & Dosing Analysis

  • 7.1 Casgevy (Exagamglogene Autotemcel)
    • 7.1.1 Overview
    • 7.1.2 Pricing & Dosing

8. Global CRISPR-Cas9 Therapy Current Market Trend & Developments

  • 8.1 Current Market Outline
  • 8.2 Future Market Outlook

9. CRISPR-Cas9 Therapy Market Trend Analysis By Region

  • 9.1 US
  • 9.2 UK
  • 9.3 EU
  • 9.4 China
  • 9.5 Japan
  • 9.6 South Korea

10. CRISPR-Cas9 Therapy Market Opportunities & Clinical Trial Statistics: By Indications

  • 10.1 Inherited Blood Disorders
  • 10.2 Genetic Disorders
  • 10.3 Cancer
  • 10.4 Autoimmune & Inflammatory Disorders
  • 10.5 Microbial Infections
  • 10.6 Cardiovascular Illnesses
  • 10.7 Eye Disorders, Brain Diseases, Metabolic Illness & Other Conditions

11. Combination Approaches For CRISPR-Cas9 Therapy

12. Platforms For Advancing CRISPR-Cas9 Therapy

  • 12.1 CRISPR-GNDM Modalis Therapeutics Platform
  • 12.2 Intellia Therapeutics - Modular Platform
  • 12.3 Editas Medicine CRISPR Gene Editing Platform
  • 12.4 CRISPR-Cas9 Genome Editing Technology - ERS Genomics
  • 12.5 CRISTARS Gene Editing Technology Innovation Platform- BRL Medicine
  • 12.6 Gene Editing-BDmRNA Platform Shanghai BDgene
  • 12.7 Kamau Therapeutics Next-Generation Gene Editing Platform
  • 12.8 Excision BioTherapeutics CRISPR Gene Editing Technology

13. Global CRISPR-Cas9 Therapy Market Dynamics

  • 13.1 Market Drivers
  • 13.2 Market Achilles Heels

14. Competitive Landscape

  • 14.1 4D Molecular Therapeutics
  • 14.2 Arbor Biotechnologies
  • 14.3 ASC Therapeutics
  • 14.4 C4U Corporation
  • 14.5 Casebia Therapeutics
  • 14.6 CRISPR Therapeutics
  • 14.7 Editas Medicine
  • 14.8 Intellia Therapeutics
  • 14.9 Nkarta Therapeutics
  • 14.10 Vertex Pharmaceuticals
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