GHIT Fund Announces New Investments in Vaccines for Dengue and Leishmaniasis, and Drug Screening for Malaria and Tuberculosis

TOKYO, Dec. 12, 2018 /PRNewswire/ -- The Global Health Innovative Technology (GHIT) Fund announced today a total of 520 million yen (US$4.6 million*) to support four partnerships to develop new lifesaving drugs and vaccines for malaria, tuberculosis, dengue and leishmaniasis. This includes three new projects and one that will receive continued funding. (Appendix 1)

"At the GHIT Fund, we are delighted to accelerate open innovation between Japanese and non-Japanese R&D entities across the globe," BT Slingsby, the CEO of GHIT said. "With the new partnerships developed through this investment, we are further strengthening our work through global collaboration to meet the needs of neglected populations worldwide."

Including the investment projects announced today, GHIT has invested approximately 14.1 billion yen (US$124 million*) in 77 global product development partnerships that leverage Japanese science and capabilities in pharmaceutical research and development. Currently, 23 discovery projects, 13 preclinical projects, and eight clinical trials are under way in low- and middle-income countries. (Appendix 2)

* USD1 = JPY113.46, the approximate exchange rate on November 30, 2018.

The first of its kind in Japan, the GHIT Fund is an international public-private partnership between the Government of Japan, multiple pharmaceutical companies, the Bill & Melinda Gates Foundation, the Wellcome Trust, and the United Nations Development Programme (UNDP). The GHIT Fund invests and manages a portfolio of development partnerships aimed at neglected diseases, such as malaria, tuberculosis and neglected tropical diseases that afflict the world's poorest people. The GHIT Fund mobilizes Japanese pharmaceutical companies, academic and research organizations to engage in the effort to create new drugs, vaccines, and diagnostics. For more information, please visit https://www.ghitfund.org.



       Appendix.1 New Investment

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                     Project Title 
      The development and production of cGMP lots of a novel tetravalent dengue virus-like particle (VLP) vaccine

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                     Collaboration    Nagasaki University, National Institute of Infectious Diseases (NIID), VLP Therapeutics, Johns Hopkins University (JHU), Latham BioPharm
                        Partners       Group (Latham)

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                        Disease    
      Dengue

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                     Intervention  
      Vaccine

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                         Stage     
      Preclinical Development

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                    Awarded Amount 
      YEN442,209,139 (US$3,897,489)

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                                     Dengue is one of the most serious public health problems worldwide. 50% of the world's population are at risk of dengue. Despite decades of
                                       effort, there is no effective treatment and the currently one licensed vaccine is recommended for use only in those >= 9 years of age. The
                                       current vaccine has been associated with a safety risk in those who were seronegative to dengue at the time of vaccination. Therefore,
                                       there is an urgent need for next-generation vaccines. Virus-like particle (VLP)-based vaccines are an attractive approach. VLP vaccines
                                       have shown to be safe and highly immunogenic because they mimic the conformation of the authentic virus but lack the viral genome. Notably,
                        Summary        VLP vaccines can be administered to all populations including the most vulnerable population of infants and children.



                                      In collaboration with Nagasaki University and National Institute of Infectious diseases, Japan (NIID), VLP Therapeutics has developed a
                                       novel dengue VLP vaccine using our unique technology. In an ongoing project, we have demonstrated the efficacy of our dengue VLP vaccine in
                                       preclinical studies including non-human primates. Here we will produce this VLP vaccine to conduct and lay the groundwork for clinical
                                       trials. The long-term goal of this project is to commercialize the first flavivirus VLP vaccine.



                                      This project involves constructing VLP dengue vaccines across all four Dengue serotypes; establishing master cell banks and manufacturing
                                       vaccines, prepare an IND package and a clinical development plan.

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                    Project Detail 
      
              https://www.ghitfund.org/investment/portfoliodetail/detail/129/en

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            Project Title  
      Immune therapy to prevent VL complications

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            Collaboration     The University of Tokyo, Infectious Disease Research Institute (IDRI), International Center for Diarrheal Disease Research, Bangladesh
                Partners       (icddr,b)

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                Disease    
      Leishmaniasis

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             Intervention  
      Vaccine

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                 Stage     
      Lead Optimization - Preclinical Development

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            Awarded Amount 
      YEN55,831,570 (US$492,082)

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                             Caused by L. donovani infection, visceral leishmaniasis (VL; Kala-azar) is endemic in large areas of the Indian subcontinent. Primary
                               symptoms include splenomegaly, weight loss and anemia and VL has the highest mortality rate among neglected tropical diseases. Improved
                               treatment regimen are being sought to reduce toxicity and drug resistance. Resistance to antimonials has resulted in their replacement with
                               Amphotericin B, paromomycin and miltefosine. Treatment failure occurs in 3-30% of treated cases in VL endemic populations and can be as
                               high as 50-60% for patients co-infected with HIV. Extended observation periods are required to detect relapse and progression to post-
                Summary        Kala azar dermal leishmaniasis (PKDL).



                             Intervention in VL patients at greatest risk of treatment failure, relapse or subsequent development of PKDL is critical for effective
                               disease management. Our published data has identified vaccine candidates that are effective as a prophylaxis in advanced animal models. In
                               this proposal we will build upon this data to determine the candidate antigen best suited for use in the Indian subcontinent (Bangladesh)
                               and use a long term preclinical model of L. donovani infection to develop immune/chemotherapeutic approaches to prevent complications of
                               VL.



                             To develop an effective therapeutic vaccine for VL, selection of good antigen(s) and adjuvant is important. Besides, the vaccine, when used
                               a component of the immune/chemotherapeutics, is not supposed to compromise the effect of chemotherapy. Therefore, this project will
                               comprise three major activities; 1) Patient-instructed selection of vaccine antigen for prevention of PKDL, 2) Evaluation of compatibility
                               of vaccines with Ambisome treatment, 3) Evaluation of efficacy of immune therapy in long term VL model. Based on the success in these
                               activities, all the partners will start preparation for clinical trial of the therapeutic vaccine in combination with Ambisome.

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            Project Detail 
      
                https://www.ghitfund.org/investment/portfoliodetail/detail/130/en

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         Project Title  
     Screening project between the University of Tokyo and MMV

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         Collaboration
             Partners   
     The University of Tokyo, Medicines for Malaria Venture (MMV)

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             Disease    
     Malaria

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          Intervention  
     Drug

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              Stage     
     Hit Identification

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         Awarded Amount 
     YEN15,000,000 (US$132,205)

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             Summary    
     This is a screening project between the University of Tokyo and MMV

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         Project Detail 
     
                https://www.ghitfund.org/investment/portfoliodetail/detail/131/en

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                   Project Title     
              Screening project between Fujifilm and TB Alliance

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                   Collaboration
                       Partners      
              Fujifilm, Global Alliance for TB Drug Development (TB Alliance)

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                       Disease       
              Tuberculosis

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                    Intervention     
              Drug

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                        Stage        
              Hit Identification

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                   Awarded Amount    
              YEN11,000,000 ($96,950)

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                       Summary       
              This is a screening project between Fujifilm and TB Alliance

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                   Project Detail    
              
                https://www.ghitfund.org/investment/portfoliodetail/detail/132/en

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     *All amounts are listed at the exchange rate of USD1 = JPY113.46, the approximate exchange rate on November 30, 2018.

Appendix.2 Investment Overview (As of December 13, 2018)

    1. Investment to date Total Investments 14.1billion yen
       (US$124million*)Total Invested Projects 77?Active projects 44, Completed
       projects 33?
    2. Portfolio Analysis

To know more about GHIT investment, please visit

Investment Overview: https://www.ghitfund.org/investment/overview/en
Portfolio: https://www.ghitfund.org/investment/portfolio/en
Advancing Portfolio: https://www.ghitfund.org/investment/advancingportfolio/en
Clinical Candidates: https://www.ghitfund.org/investment/clinicalcandidates/en

*All amounts are listed at the exchange rate of USD1 = JPY113.46, the approximate exchange rate on November 30, 2018.

For more information, contact:
Katy Lenard at +1-301-280-5719 or klenard@burness.com

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