SalioGen Therapeutics

SalioGen Therapeutics

Biotechnology Research

Lexington, Massachusetts 4,122 followers

Accelerating the impact of genetic medicines for patients with Gene Coding™ technology

About us

SalioGen Therapeutics is a biotechnology company on a mission to accelerate the impact of genetic medicine for patients using its novel Gene Coding™ technology. Gene Coding is a non-viral method of integrating large or multiple whole genes into the genome at precise locations through transposition. This mechanism does not induce double-strand breaks or use guide RNA and has the potential to overcome the safety risks and limitations of other genetic medicine approaches. SalioGen's lead programs focus on one-time treatments for Stargardt disease and cystic fibrosis. The company is also developing its Gene Coding technology for additional indications, such as other inherited retinal diseases, and to engineer CAR-T cells for cancer and autoimmune conditions.

Industry
Biotechnology Research
Company size
51-200 employees
Headquarters
Lexington, Massachusetts
Type
Privately Held
Founded
2020
Specialties
Gene therapy, Genome engineering, Cell therapy, Genetic disease, Inherited disease, and Cell engineering

Locations

  • Primary

    10 Maguire Rd

    Building 1, Suite 200

    Lexington, Massachusetts 02421, US

    Get directions

Employees at SalioGen Therapeutics

Updates

  • View organization page for SalioGen Therapeutics, graphic

    4,122 followers

    Thank you, Foundation Fighting Blindness, for all your work to develop resources for people living with Stargardt disease. Your support of research on Stargardt is leading the way toward potential treatments!

    #ChildrensEyeHealthAndSafetyMonth: What is Stargardt disease? Stargardt disease, often diagnosed in childhood or adolescence, is an inherited form of macular degeneration that causes central vision loss. Sometimes called juvenile or early onset macular degeneration, it can make everyday tasks challenging. But there’s a community ready to support you! Learn more about living with Stargardt disease and the exciting research advancements on our website at: https://lnkd.in/d4j2TWGa Image Description: Dark blue background with Spotlight on Children's Eye Health and Safety Month logo in top left corner with text below reading "Did you know? Stargardt disease is usually an autosomal recessive condition caused by mutations in the gene ABCA4." Foundation Fighting Blindness logo in top right corner. Below is a young boy wearing glasses and smiling.

    • Dark blue background with Spotlight on Children's Eye Health and Safety Month logo in top left corner with text below reading "Did you know? Stargardt disease is usually an autosomal recessive condition caused by mutations in the gene ABCA4." Foundation Fighting Blindness logo in top right corner. Below is a young boy wearing glasses and smiling.
  • View organization page for SalioGen Therapeutics, graphic

    4,122 followers

    This week, we’re headed to the Genome Engineering: CRISPR Frontiers meeting at Cold Spring Harbor Laboratory. Join us for Dr. Nancy Craig's, Senior Vice President for Genetic Engineering, oral presentation about the precision of our Gene Coding™ technology and the high efficiency of our bioengineered transposase enzyme to integrate large genes into targeted sites. Her session begins at 9 a.m. EST on Friday, August 30. #cshlcrispr24

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  • View organization page for SalioGen Therapeutics, graphic

    4,122 followers

    SalioGen is pleased to announce the appointment of Dr. Kali Stasi as Chief Medical Officer. Kali is a board-certified ophthalmologist with 30 years of experience in industry and academia, and a proven track record of advancing genetic medicines for retinal diseases from early- and late-stage clinical development through commercialization. In this position, Dr. Stasi will be responsible for bringing the company’s development candidate SGT-1001 into the clinic by mid-2025 as a one-time treatment for Stargardt disease and continuing to develop the company’s Gene Coding™ technology for other inherited retinal diseases and cystic fibrosis. Learn more: https://bit.ly/3YINyty

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  • View organization page for SalioGen Therapeutics, graphic

    4,122 followers

    View organization page for SalioGen Therapeutics, graphic

    4,122 followers

    August is Children’s Eye Health & Safety Month, a time to raise awareness of the importance of taking care of children’s eyes and detecting vision problems early to optimize care. #Stargardt disease is an inherited form of macular degeneration causing central vision loss, often diagnosed in childhood or adolescence. Today, there is no treatment – but we are committed to changing that for patients and their families. Learn more about our research to develop potentially transformative new therapies for Stargardt and other inherited eye diseases: https://bit.ly/3X2e1Bk

    • No alternative text description for this image
  • View organization page for SalioGen Therapeutics, graphic

    4,122 followers

    August is Children’s Eye Health & Safety Month, a time to raise awareness of the importance of taking care of children’s eyes and detecting vision problems early to optimize care. #Stargardt disease is an inherited form of macular degeneration causing central vision loss, often diagnosed in childhood or adolescence. Today, there is no treatment – but we are committed to changing that for patients and their families. Learn more about our research to develop potentially transformative new therapies for Stargardt and other inherited eye diseases: https://bit.ly/3X2e1Bk

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  • View organization page for SalioGen Therapeutics, graphic

    4,122 followers

    We are truly grateful for the opportunity to host Dr. Mike Marciello this week. His story about developing Stargardt disease later in life, adjusting to progressive vision loss, and actively supporting the community is a strong testament to the idea that anything is possible with determination. Thanks, Mike, for being an inspiration.

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  • View organization page for SalioGen Therapeutics, graphic

    4,122 followers

    Saliogase™ transposase was created by Saliogen. It works by harnessing the power of natural enzymes, called transposases, to move DNA segments around the genome safely for evolutionary purposes. The Saliogase™ enzyme is based on a mammalian transposase that has evolved over thousands of years to adapt to the mammalian environment.

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