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시장보고서
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1529409
세계의 CRISPR Cas9 시장 : 시장 기회 및 임상시험 전망(2029년)Global CRISPR Cas9 Market Opportunity & Clinical Trials Outlook 2029 |
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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.
Global CRISPR Cas9 Market Opportunity & Clinical Trials Outlook 2029 Report Offering:
Antecedently, out-of-date bestseller conventional therapies, including chemotherapy or targeted therapies, were utilized for the management of cancer, autoimmune, inflammation and other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.