Delivering
Next Generation
Therapeutics

 

 
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Gene Therapy
Delivered

CRISPR/Cas9 is a powerful genome editing tool that makes therapeutic gene editing possible. It is easier to use, faster, and more accurate than previous gene editing techniques and thus has the potential for a wide range of therapeutic applications.

GenEdit is developing non-viral delivery technologies for the CRISPR/Cas9 gene editing system that can safely and efficiently correct gene mutations in patients.

More about us

New Era of Genome Editing

CRISPR/Cas9 is a powerful genome editing tool that makes therapeutic gene editing possible. It is easier to use, faster, and more accurate than previous gene editing techniques and thus has the potential for a wide range of therapeutic applications.

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We solve
the biggest challenge
for CRISPR therapeutics

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CRISPR
Delivery vehicle
& Engineering

CRISPR/Cas9 gene editing has the potential to treat a variety of incurable genetic diseases. However, developing therapeutics based on the CRISPR system has been challenging because of delivery problems.

GenEdit has developed a new delivery vehicle for CRISPR/Cas9 therapeutics, which can encapsulate Cas9 protein, guide RNA, and donor DNA, into a single nanoparticle for safe and efficient genome editing . 

We also work on engineering of core components of CRISPR/Cas9 genome editing system to increase editing efficiency and enable targeted delivery. 

More about our science

 

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News

GenEdit's core technologies have been published in top science journals - Nature Materials and Nature Biomedical Engineering - and featured in science news media. 

 

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CRISPR-Cas9 gene editing reduces repetitive behavior in mice with autism-like syndrome

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Editing autism gene with nano-CRISPR curbs repetitive behaviors.

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Scientists successfully reduce autism symptoms in mice through gene editing