Our customers work more efficiently and benefit from
The global CRISPR and cas genes market size was evaluated at USD 4,710 million in 2024 and is expected to grow around USD 21,140 million by 2034, registering a CAGR of 16.2% from 2025 to 2034.
Industry Worth | Details |
Market Size in 2025 | USD 5,470 Million |
Market Size by 2034 | USD 21,140 Million |
Market Growth Rate from 2025 to 2034 | CAGR of 16.2% |
CRISPR is a gene-editing technology that helps scientists to edit the DNA of living things. It is derived from a naturally occurring bacterial immune system found in nature. The CRISPR-Cas9 system is faster, cheaper, effective, and more accurate than any other genome editing method. Researchers have chosen this method due to its efficiency and accuracy in editing DNA. A small RNA is created that binds to specific target sequences in a cell’s DNA. When it encounters the cells, the guide RNA recognizes the intended DNA sequence, and the Cas9 enzyme cuts the DNA at the targeted location.
The primary focus of CRISPR and Cas gene market dynamics is on gene-editing treatments with its potential to aid in genetic disorders, sickle cell anemia, cystic fibrosis, and muscular dystrophy. CRISPR is also being used in agricultural biotechnology to enhance crop yield, resistance to pets & environment stress, and drug discovery to provide more effective and accurate methods to validate drug targets.
Artificial Intelligence (AI) has been a major game changer in the healthcare industry, helping in the research and development of products to fulfill market expectations and enhance success rates. Some advantages that AI brings into the market of CRISPR and Cas genes are:
“Building on the success of CASGEVY’s launch, we continue to broaden our portfolio across oncology, autoimmune, and cardiometabolic indications. 2025 promises to be a milestone-rich year with clinical data updates across several programs spanning a range of indications. In parallel, we are continuously innovating on our platform with next-generation gene editing and delivery technologies, which have the potential to broaden our ability to address additional diseases with curative treatments.”
“Today is a historic day in science and medicine: this authorization of CASGEVY in Great Britain is the first regulatory authorization of a CRISPR-based therapy in the world.”
The CRISPR and Cas genes market is growing at a rapid rate, and a major part of the market is captured by North America, with Europe showing the fastest growth in the forecasted period of 2025-2034.
North America
North America dominates the CRISPR and Cas gene market throughout the world, with the highest market share of 39% in 2024. The leading companies of the world in the CRISPR and Cas gene market are based in this region and use highly advanced tech for the research and development of products in the healthcare industry. Besides this, the government initiative and investment also boost the growth of the market along with various market research organizations that partake in improving research for such products.
Asia-Pacific
The Asia Pacific region is expected to show the fastest growth in the CRISPR and Cas genes market in the forecasted period of 2025-2034. Technological Advancements and an increase in investment in biotechnology drive the market for the region.
Europe
The CRISPR and cas gene market in Europe is increasing steadily with the increase in investment in agriculture biotechnology to focus on crop modification. The growing interest in precision medicine and gene-edited crops are the key market drivers for the region. An increase in collaboration between big players to develop CRISPR-based therapies supports gene editing and fosters innovation in the market.
The CRISPR and cas genes market is dominated by North America, with the leading companies also operating in the region. Furthermore, with the increase in awareness about the benefits of genome-editing methods a lot of Biotech companies are significantly growing and fighting for the market share. The top 3 companies that hold the major market share worldwide are:
Caribou Biosciences Inc. is a biopharmaceutical company focused on developing transformative genome-edited allogeneic cell therapies with its patented chRDNA (CRISPR hybrid RNA-DNA) technology. Caribou Biosciences Inc is one of the key players in the CRISPR and Cas genes market with its hold in the North American region. The company recorded $ 9.99 million of revenue in the year 2024.
Editas Medicine Inc is a pioneering biotechnology company that is focused on developing transformative medicine and advanced therapies using CRISPR gene editing technology, with its main focus towards the vivo editing in hematopoietic stem cells, the liver, and other tissues. The country has gained a huge market share over the years in the North American region, with a revenue of $32.314 million in the year 2024.
Cellectis is a clinical stage biopharmaceutical company with an expertise of gene editing for the past 25 years specializing in its TALEN technology to develop cell and gene therapies. Cellectis is one of the few companies that have in-house manufacturing to develop new and innovative therapeutic ideas.
For any questions about this dataset or to discuss customization options, please write to us at sales@statifacts.com
Stats ID: | 8175 |
Format: | Databook |
Published: | April 2025 |
Delivery: | Immediate |
Price | US$ 1550 |
Stats ID: | 8175 |
Format: | Databook |
Published: | April 2025 |
Delivery: | Immediate |
Price | US$ 1550 |
You will receive an email from our Business Development Manager. Please be sure to check your SPAM/JUNK folder too.
Unlock unlimited access to all exclusive market research reports, empowering your business.
Get industry insights at the most affordable plan
Stay ahead of the competition with comprehensive, actionable intelligence at your fingertips!
Learn More