Report ID: SQMIG35H2365
Skyquest Technology's expert advisors have carried out comprehensive research and identified these companies as industry leaders in the Genome Editing Market. This Analysis is based on comprehensive primary and secondary research on the corporate strategies, financial and operational performance, product portfolio, market share and brand analysis of all the leading Genome Editing industry players.
The genome editing market will continue to grow because of the growing number of genetic disorders, chronic diseases, and cancers, leading to an increasing demand for more precise and effective therapeutics to treat these conditions. Rapid advancements in gene editing technologies, including CRISPR-Cas9, TALEN, and ZFN have provided researchers with increased access to and reduced costs for targeted gene editing, speeding up the pace at which gene editing technology can be implemented clinically as well as within the laboratory setting.
According to SkyQuest Technology “Genome Editing Market By Technology ((CRISPR)/Cas9, TALENs/MegaTALs, ZFN, Meganucleases), By Delivery Mode (ex-Vivo, In-Vivo), By Application (Genetic Engineering, Clinical Applications), By Mode, By Region- Industry Forecast 2025-2032,” Global Genome Editing Market is projected to grow at a CAGR of over 16.8% by 2032, on account of urgent need for automating quantified data. An increasing number of applications within agriculture for using genome editing technology to increase crop yield and disease resistance as well as livestock genetics are driving further growth within this market.
|
Company |
Est. Year |
Headquarters |
Revenue |
Key Services |
|
Thermo Fisher Scientific Inc. |
1956 (Incorporated) |
Waltham, MA, USA |
USD 42.8 Billion |
Genome Editing Tools & Reagents, CRISPR/TALEN/ZFN commercialization, Life Science Services, Diagnostics, Laboratory Products. |
|
Merck KGaA (MilliporeSigma) |
1668 (Parent Co.) |
Darmstadt, Germany |
USD 22.4 Billion |
CRISPR & Gene Editing Tools, Genomic Services, Materials Science, Biopharma Manufacturing & Solutions. |
|
CRISPR Therapeutics AG |
2013 |
Zug, Switzerland/ Cambridge, MA, USA |
USD 37.0 Million |
CRISPR/Cas9 Therapeutics (e.g., Casgevy for SCD/Thalassemia), Ex vivo and In vivo Gene Editing for genetic diseases & oncology. |
|
Intellia Therapeutics |
2014 |
Cambridge, MA, USA |
USD 57.88 Million |
In vivo (e.g., ATTR amyloidosis) and Ex vivo CRISPR/Cas9 Gene Editing, LNP (Lipid Nanoparticle) delivery technology. |
|
Beam Therapeutics |
2017 |
Cambridge, MA, USA |
USD 63.52 Million |
Pioneer in Base Editing (CRISPR-derived non-cutting technology), developing precision therapeutics for genetic diseases and oncology. |
|
Precision BioSciences |
2006 |
Durham, NC, USA |
USD 68.69 Million |
Proprietary ARCUS genome editing platform (a meganuclease), developing Allogeneic CAR T cell therapies and In vivo gene therapies. |
|
Editas Medicine |
2013 |
Cambridge, MA, USA |
USD 32.31 Million |
In vivo (e.g., ocular diseases) and Ex vivo gene editing using CRISPR-Cas9 and CRISPR-Cas12a platforms. |
|
GenScript |
2002 |
Nanjing, China/ Piscataway, NJ, USA |
USD 594.49 Million |
Genome Editing Services (Custom gene synthesis, CRISPR tools/reagents), Cell Line Development, Antibody Drug Discovery Services. |
|
Cellectis |
1999 |
Paris, France |
USD 41.51 Million |
TALEN $^{\circledR}$ technology (Transcription Activator-Like Effector Nucleases), developing allogeneic (off-the-shelf) CAR T cell immunotherapies. |
|
Prime Medicine |
2019 |
Cambridge, MA, USA |
USD 2.98 Million |
Prime Editing technology (searches and replaces DNA segments), aiming for higher precision and fewer off-target effects than traditional CRISPR. |
Thermo Fisher Scientific imports more types of different types of laboratory equipment than anyone else and has a very strong presence in selling products used in genetic engineering research and development.
Merck K.G.A. operates as MilliporeSigma in North America manufactures and sells lab supplies that are foundational to the life sciences industry and is an important supplier to labs worldwide.
Nobel Laureate Jennifer Doudna was an initial investor in CRISPR Therapeutics; CRISPR Therapeutics AG is focused on developing transformative therapies for mankind that allow the application of CRISPR technology for clinical applications. As part of this process, they have successfully completed the clinical trials of Casgevy (the first Food and Drug Administration approved CRISPR-based therapy) to treat sickle cell disease and beta-thalassemia, which represented significant milestones in their development efforts.
Intellia Therapeutics is working to advance the use of CRISPR technology for therapeutic use and to enable its use as a technology to enable in vivo gene editing (i.e., CRISPR has been delivered directly to patients to edit specific genes in living cells). A key strategy for Intellia Therapeutics has been the development of lipid nanoparticles (LNPs) to deliver the biological material needed to apply CRISPR to the affected tissues.
Beam Therapeutics is pioneering Base Editing, a next-generation approach to content. Base editing is a modified version of CRISPR that adds a specific chemical alteration to a base (e.g. A-C) without creating a break in double-stranded DNA like traditional CRISPR (e.g. Cas9).
Precision BioSciences has developed a proprietary gene-editing platform called ARCUS that uses meganucleases. ARCUS is marketed as the smaller and more versatile option compared to Cas9, producing precise gene insertions, deletions, and repairs.
Editas Medicine is a clinical-stage Biopharma, a pioneer in the CRISPR space, utilizing both Cas9 and Cas12 (formerly known as Cpf1) nucleases to target a wider variety of potential mutations.
GenScript is a contract research organization (CRO), with world will help to develop research materials and provide related services and is in the U.S. and China. GenScript's role in the gene editing value ecosystem is to provide quality, custom-made gene synthesis and CRISPR reagents and to support the development of cell lines.
Cellectis is a French clinical-stage biotechnology company developing "off-the-shelf" CAR T-cell immunotherapies for cancer treatment using TALENs to modify T cells extracted from healthy donors. The use of TALENs allows for the development of off-the-shelf therapies with additional advantages over patient-specific therapies in terms of manufacturing simplification and wider availability.
Prime Medicine is focused solely on Prime Editing and is one of the first companies to utilize this exciting new technology. Prime Editing is viewed as the next evolution in gene editing, allowing for more precise control over gene sequences by providing the ability to perform a "search-and-replace" format.
As advances in technology and funding for research continue to grow, the genome editing market is expected to experience rapid growth in its usage in various fields such as healthcare, agriculture and industrial biotechnology. By utilizing personalized medicine, gene therapy, and precision agriculture, genome editing has become a pivotal resource for solving unmet medical needs as well as increasing the overall availability of food security on a global level. As regulatory frameworks change to facilitate safe and ethical usage; this increases confidence in the market. Additionally, with continued maturation of technology we anticipate further collaborations among biotech companies, academic institutions, and healthcare providers which will further drive innovation, reduce costs and increase widespread adoption of genome editing solutions worldwide.
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