Saving Lives by
Innovative Genetic Engineering

Company

  • Overview

    SL VaxiGen is R&D company dedicated to developing innovative vaccine therapeutics based on complementary platforms for saving lives.

    Our goal is to save lives by various innovative genetic and protein engineering technologies especially for infectious diseases and cancers.

  • Vision

    To become the leading global biotech company by developing innovative in-vivo gene therapeutics

  • Mission

    To save and improve the quality of patient’s lives with intractable diseases

Team

Leadership

  • June Young Park Ph.D.
    CEO, SL VAXiGEN
    Executive VP, SL BIGEN
    VP, Buisness Division, ISU Abxis
    Post-doc fellowship, Harvard Medical School/Bringham and Womens Hospital
    Ph.D. Department of Life Science, POSTECH
    M.S./B.S. Department of life Science, POSTECH
  • Kyeong Ha Lee, KICPA
    CFO, SL VAXiGEN
    Director, Finance Div., Genexine. Inc.
    Senior Consultant, LG CNS Entrue Consulting
    B.S. Department of Business Administration, SungKyunKwan Univ.
  • Kyung Hwa Son
    Head of Development Div., SL VAXiGEN
    Senior VP, Medi-Helpline
    Senior Manager, Business Division, ISU Abxis
    M.S. Department of Life Science, Sogang Univ.
  • Yong Bok Seo Ph.D.
    CTO, SL VAXiGEN
    Senior manager, DNA Vaccine Team, SL BIGEN
    Post-doc fellowship, POSTECH-CATHOLIC Biomedical Engineering Inst.
    Ph.D. Department of Life Science, POSTECH

Board of Director

  • June Young Park Ph.D.
    CEO, SL VAXiGEN
    Executive VP, SL BIGEN
    VP, Buisness Division, ISU Abxis
    Post-doc fellowship, Harvard Medical School/Bringham and Womens Hospital
    Ph.D. Department of Life Science, POSTECH
    M.S./B.S. Department of life Science, POSTECH
  • Kyung Hwa Son
    Head of Development Div., SL VAXiGEN
    Senior VP, Medi-Helpline
    Senior Manager, Business Division, ISU Abxis
    M.S. Department of Life Science, Sogang Univ.
  • Yong Bok Seo Ph.D.
    CTO, SL VAXiGEN
    Senior manager, DNA Vaccine Team, SL BIGEN
    Post-doc fellowship, POSTECH-CATHOLIC Biomedical Engineering Inst.
    Ph.D. Department of Life Science, POSTECH
  • Jun Chang Ph.D.
    POSTECH, Ph.D.
    Post-doc fellowship, University of Virginia
    Professor, College of Pharmacy, Ewha Womans University
  • Ji Won Kim
    CEO, Aju IB Investment
    B.S. Department of Business Administration, Yonsei University
  • Sang Sul Jung Ph.D.
    MD & Ph.D. Catholic University of Korea
    Professor, Head Professor, Department of Surgery, College of Medicine, Catholic University of Korea
    Chairman, Korea Breast Cancer Society
    Chairman, Korean Surgical Society

Scientific Advisory Board

  • Yung Dae Yun. Ph.D.
    Michigan State University, Ph.D.
    MOGAM Institute for Biomedical Research, Vice President
    College of Natural Sciences, Ewha Womans University, Dean
  • Man Ki Song Ph.D.
    POSTECH, Ph.D.
    University of Maryland School of Medicine, Postdoc
    France INSERM, Researcher
    International Vaccine Institute, Senior Research Scientist
  • Eui-Cheol Shin, MD & Ph.D.
    Yonsei University, Ph.D.
    Graduate School of Medical Science and Engineering, KAIST, Professor
    Immunology working group member, ICE-HBV
    26th International Symposium on Hepatitis C Virus and Related Viruses, Organizer

DNA Vaccine Technology

  • Highly efficient vector
  • Antigen engineering

To induce antigen-specific strong and broad immunity, we combined the disease-specific multiple antigens and applied antigen engineering technologies such as codon optimization and gene shuffling in efficient expression vector system.

  • DNA Injection
  • Antigen expression
  • APC recruitment and activation
  • Induction of Ag-specific immune response

Plasmid DNA

B.S.A Platform Technology

  • Targeting vaccine-induced CTL immune response
  • Targeting vaccine-induced antibody immune response

Concept

The adaptive immunity which is mainly composed of T cell and B cell (antibody) plays an crucial role in prevention and/or treatment of diseases. Thus, increasing the specific immune response to a certain pathogen is important for the development immunotherapeutic. BSA, bi-specific adaptive adjuvant, is designed for increasing antigen-specific (or vaccine-induced) adaptive immune responses by binding two or more targets in simultaneously.
We have identified multiple potential mechanistic application of the BSA platform, including the three described below,

  • - Targeting to vaccine-induced CTLs. This version of BSA molecules enable the vaccine-induced CTL (cytotoxic T lymphocyte) to be selectively increased in the course of immune responses.
  • - Targeting to vaccine-induced GC B cells or TFH cells. This version of BSA molecules can stimulate the vaccine-induced GC B cells and/or TFH cell result in increase of vaccine-induced antibody responses.
  • - Simultaneous targeting of multiple co-stimulatory receptors or cytokine receptors, such as those involved in T cell responses and antibody responses. Combination of multiple co-stimulatory or cytokine receptors have resulted in significantly enhanced benefit than targeting any one of the targets of them separately. BSA is being developed for co-stimulation of effector T cell or B cells, could afford the clinical benefit of the combination together with the potential for synergistic, as well as significant advantages in manufacturing, simplified clinical development, and enhanced patient convenience.

Mode of Action (BSA for CTL response)

Mode of Action (BSA for antibody response)

Pipelines

이 표는 구성되어 있습니다.
Category Target Product Indication Development Stage
Research Preclinical Clinical
Infectious Diseases SL-V10 CMV/BKV+ Transplantation
SL-V20 Genital Herpes
SL-V30 CHB
Cancer SL-V60 GBM
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