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GeneVentiv targeting gene therapies for hemophilia, Pompe disease

GeneVentiv targeting gene therapies for hemophilia, Pompe disease

by Damon Race | May 16, 2025 | In the News

When Damon Race, a Raleigh-based biopharmaceutical entrepreneur and investor, wanted to start a new company, he didn’t have to go far to find the founding technologies. After looking at “30 to 40 assets” nationally, in October of 2020, Race chose to in-license a gene...
Gene therapy developed at Duke to be commercialized by a local biotechnology company

Gene therapy developed at Duke to be commercialized by a local biotechnology company

by Damon Race | Apr 8, 2025 | In the News

Gene therapy developed at Duke to be commercialized by a local biotechnology company by Fedor Kossakovski Duke University recently signed an exclusive license with GeneVentiv Therapeutics, a Raleigh-based gene therapy company, to commercialize a gene therapy developed...
GeneVentiv Announces Global Licensing Agreement for Universal Gene Editing Therapy for Infantile Onset and Late Onset Pompe Disease

GeneVentiv Announces Global Licensing Agreement for Universal Gene Editing Therapy for Infantile Onset and Late Onset Pompe Disease

by Damon Race | Apr 8, 2025 | Press

RALEIGH, N.C., April 8, 2025 /PRNewswire/ — GeneVentiv Therapeutics, a gene therapy company, today announced it has signed a global licensing agreement with Duke University for the first universal gene editing therapy for both infantile-onset and late-onset...
GeneVentiv Welcomes New Scientific Advisory Board Member, Sylvia Fong

GeneVentiv Welcomes New Scientific Advisory Board Member, Sylvia Fong

by Damon Race | Jul 23, 2024 | Press

July 23, 2024 Damon R. Race, President & CEO RALEIGH, NC – GeneVentiv Therapeutics, a pre-clinical gene therapy company focused on blood diseases and disorders, today announced that Sylvia Fong, Ph.D. has joined the Company’s Scientific Advisory Board as the...
GeneVentiv Therapeutics Awarded $2.5 Million SBIR Grant to Advance Gene Therapy for All Hemophilias, with or without Inhibitors

GeneVentiv Therapeutics Awarded $2.5 Million SBIR Grant to Advance Gene Therapy for All Hemophilias, with or without Inhibitors

by Damon Race | Apr 16, 2024 | In the News

Damon R. Race, President & CEO RALEIGH, N.C., April 16, 2024 /PRNewswire/ — GeneVentiv Therapeutics, developer of GENV-HEM (AAV8.FVa) for all hemophilias, announced today it has been awarded a Direct to Phase II Small Business Innovation Research (SBIR)...
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Recent Posts

  • GeneVentiv targeting gene therapies for hemophilia, Pompe disease
  • 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

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