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  • Hunterian Medicine
    Hunterian Medicine is a gene editing company poised to unleash the full potential of CRISPR Our patented platform technology solves the CRISPR delivery problem by enabling efficient, on-target delivery through a single adeno-associated virus (AAV)
  • Team — Hunterian Medicine
    Mark joined Hunterian following over 26 years of managing the Ludwig Center for Cancer Genetics and Therapeutics at the Sidney Kimmel Comprehensive Cancer Center of Johns Hopkins University School of Medicine and the Howard Hughes Medical Institute under the world-renowned researcher Dr Bert Vogelstein, M D Mark completed his undergraduate
  • The Technology — Hunterian Medicine
    Hunterian Medicine’s platform technology enables greater versatility to address a much broader scope of diseases Hunterian Medicine Focus Areas Hunterian Medicine is exploring a range of diseases and orphan indications for licensing and or development, including for diseases that cannot be addressed by current CRISPR technologies
  • Hunterian Medicine® Licenses Inscripta’s MAD7™ Nuclease to Advance Gene . . .
    Hunterian solved this problem by enabling CRISPR systems to fit inside a single AAV, the gold standard for gene delivery,” said Dr Vinny Jaskula-Ranga, President and CEO of Hunterian Medicine “Inscripta is similarly reducing barriers to innovation by providing access to its MAD7 nuclease and other improved MADzyme nucleases
  • News — Hunterian Medicine
    Hunterian to use its novel platform technology to develop treatments for cystic fibrosis CAMBRIDGE, Mass —May 27, 2021— Hunterian Medicine LLC, a gene-editing and gene therapy company, has been awarded a Therapeutics Development Award by the Cystic Fibrosis Foundation The award, through the Foundation’s Path to a Cure initiative that seeks to replace, restore or repair cystic fibrosis
  • Our Story — Hunterian Medicine
    Our Story Hunterian’s mission is to cure genetic diseases by correcting DNA mutations using its innovative CRISPR delivery technology Every year, nearly 8 million children are born with genetic diseases caused by mutations in DNA
  • Careers — Hunterian Medicine
    408-310-2168 mark@markbutton info For general information info@hunterian com For licensing or partnering opportunities bob lorette@hunterian com A gene editing company poised to unleash the full potential of CRISPR
  • Press Release — News — Hunterian Medicine
    Hunterian to use its novel platform technology to develop treatments for cystic fibrosis CAMBRIDGE, Mass —May 27, 2021— Hunterian Medicine LLC, a gene-editing and gene therapy company, has been awarded a Therapeutics Development Award by the Cystic Fibrosis Foundation The award, through the Foundation’s Path to a Cure initiative that seeks to replace, restore or repair cystic fibrosis
  • Publication — News — Hunterian Medicine
    June 17, 2019 Vinod Jaskula-Ranga Publication CRISPR start-ups turn attention toward delivery June 17, 2019 Vinod Jaskula-Ranga Publication
  • USPTO Awards Patent for Hunterian Medicine Technology
    Hunterian Medicine LLC, a gene-editing company working to cure genetic diseases, has developed groundbreaking CRISPR delivery technology for which the United States Patent and Trademark Office has granted a patent (No 9,907,863)





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