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Pipeline

Pipeline

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AAVLinkTM platform, including the AAV-Find platform, the AAV-Stable platform, and the AV-Expand platform, simplifies the development of AAV vectors and expands their capabilities.

  • The AAV-Find platform develops new tissue-targeted AAVs in a simple way, breaking through the barriers of animal-to-human transformation.
  • The AAV-Stable platform integrates all genes required for AAV production into cells, and through induction of viral vector production, solves the current three-plasmid system, difficult amplification, high impurities and high cost.
  • The AV-Expand platform establishes a highly efficient dual AAV to express genes that exceed the packaging capacity of AAV.

Protheragen is actively advancing a diverse range of gene therapy pipelines leveraging its state-of-the-art AAV vector platform. A significant milestone has been reached with the progression of the IVP-021 injection for X-linked juvenile retinoschisis (XLRS) to an investigator-initiated clinical study (IIT). The successful completion of the first subject's vitreous injection has shown promising outcomes, as the subject displayed favorable conditions within 28 days post-administration. Notably, no instances of intraocular inflammation or ocular and systemic adverse events linked to the study drug were reported. In addition, our dedicated team is actively developing several other promising pipelines designed to address a variety of gene therapies.

Program Indication Discovery PCC Efficacy Preclinical Clinical
IVP-003 X-linked Juvenile Retinoschisis (XLRS)
IVP-011 Wet Macular Degeneration (wAMD)
IVP-012 Achromatopsia (ACHM)
IVP-023 Retinal Degeneration
IVP-027 Geographic Atrophy (GA)
IVP-029 RDH12-associated Retinal Degeneration
IVP-039 Transthyretin Amyloidosis (ATTR)
IVP-044 Stroke
IVP-042 Alzheimer's Disease (AD)
IVP-050 Aging Related Diseases

If you are interested in our services, please feel free to contact us for more details and quotation information of related services.

Our AAVLinkTM platform is at the forefront of adeno-associated viral (AAV) vector development, leveraging our extensive expertise and state-of-the-art technologies to drive innovation in gene therapy.

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