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UNC-Chapel Hill gene therapy spinout raises $1.4 million

UNC-Chapel Hill gene therapy spinout raises $1.4 million

by Damon Race | Sep 12, 2022 | In the News

By Zac Ezzone  –  Staff writer, Triangle Business Journal Sep 1, 2022 A UNC-Chapel Hill spinout developing gene therapies focused on rare blood diseases and disorders has raised $1.4 million to support its efforts. The company, GeneVentiv Therapeutics, raised the...
UNC-Chapel Hill gene therapy spinout raises $1.4 million

Bootstrapped UNC spinout lands $300K for gene therapy work

by Damon Race | Jun 14, 2022 | In the News

The Old Well on the UNC-Chapel Hill campus. Mehmet Demirci By Zac Ezzone – Staff writer June 14, 2022, 08:52am EDT After bootstrapping for nearly two years, the CEO of a UNC-Chapel Hill spinout developing gene therapies has received some financial support. In...
Triangle gene therapy startup GeneVentiv Therapeutics awarded $250K loan from NC Biotech Center

Triangle gene therapy startup GeneVentiv Therapeutics awarded $250K loan from NC Biotech Center

by Damon Race | Jun 8, 2022 | In the News

Pixabay image by Jason Parker — June 8, 2022 RALEIGH – GeneVentiv Therapeutics, a Triangle-area pre-clinical gene therapy company, has been awarded a $250,000 Strategic Research Loan (SRL) from the North Carolina Biotechnology Center (NCBC). The loan will enable the...
Startup Spotlight: UNC-linked startup is giving hope to those with hemophilia

Startup Spotlight: UNC-linked startup is giving hope to those with hemophilia

by Damon Race | Feb 8, 2022 | In the News

by Shellie Edge, Innovate Carolina — February 8, 2022 . Editor’s note: Startup Spotlight is a regular weekly feature in WRAL TechWire. This week’s feature comes from UNC-Chapel Hill’s Innovate Carolina.  +++ CHAPEL HILL – For most people, a small cut on the hand or...
GeneVentiv Receives Orphan Drug Designation (ODD) for GENV-HEM for the treatment of Hemophilia A or B with or without inhibitors

GeneVentiv Receives Orphan Drug Designation (ODD) for GENV-HEM for the treatment of Hemophilia A or B with or without inhibitors

by Damon Race | Nov 2, 2021 | Press

Preclinical data provide quantitative evidence of GENV-HEM’s ability to achieve phenotypic correction in animal models of hemophilia, independent of the presence of any clotting factor inhibitors. Estimated 95,000 patients in the U.S. and Europe represent...
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Recent Posts

  • Gene therapy developed at Duke to be commercialized by a local biotechnology company
  • GeneVentiv Announces Global Licensing Agreement for Universal Gene Editing Therapy for Infantile Onset and Late Onset Pompe Disease
  • GeneVentiv Welcomes New Scientific Advisory Board Member, Sylvia Fong
  • GeneVentiv Therapeutics Awarded $2.5 Million SBIR Grant to Advance Gene Therapy for All Hemophilias, with or without Inhibitors
  • New partners to develop universal gene therapy for hemophilia

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