Dr. Maria Elena Bottazzi is an internationally recognized tropical and emerging disease vaccinologist, global health advocate and cocreator of a patent-free, open science COVID-19 vaccine technology that led to the development of Corbevax in India and IndoVac in Indonesia, and with approximately 100 million doses delivered. She pioneers and leads the advancement of a robust infectious and tropical disease vaccine portfolio tackling diseases such as coronavirus, hookworm, schistosomiasis, and Chagas that affect disproportionally the world’s poorest populations. She also has established innovative partnerships in Latin America, Middle East and Southeast Asia, making significant contributions to innovative educational & research programs, catalyze policies and disseminate science information to reach a diverse set of audiences. She is a former Emerging Leader in Health and Medicine Scholar from the US National Academy of Medicine (NAM), a Leshner Leadership Institute Public Engagement Fellow in Infectious Diseases of the American Association for the Advancement of Science and a Hedwig van Ameringen Executive Leadership in Academic Medicine (ELAM) Fellow. As global thought-leader she has received national and international highly regarded awards, has more than 250 scientific papers and participated in more than 300 conferences worldwide. In 2023, she was awarded the Vilcek-Gold Award for Humanism in Healthcare and the Rachael Schneerson - John Robbins Prize. For three years in a row, Forbes selected Dr. Bottazzi as one of 100 Most Powerful Women in Central America. In 2022, alongside Dr. Peter Hotez, she was nominated by Texas Congresswoman Lizzie Fletcher for the Nobel Peace Prize. Dr. Bottazzi obtained her bachelor’s degree in Microbiology and Clinical Chemistry from the National Autonomous University of Honduras and a doctorate in Molecular Immunology and Experimental Pathology from the University of Florida. Her post-doctoral training in Cellular Biology was completed at University of Miami and Pennsylvania, where afterwards worked at the George Washington University prior to relocating to Texas.
2.10pm – 3.10pm Parasitic disease vaccine development short talks:
4x 15min presentations
2.10pm Hookworm anaemia and malaria combination vaccine development
Dr Peter Hotez, Co-Director, Texas Children’s Hospital Center for Vaccine Development, Baylor College of Medicine
2.25pm Early development of a vaccine against visceral leishmaniasis * Title TBC
Dr Angamuthu Selvapandiyan, Professor, Department of Molecular Medicine, School of Interdisciplinary Studies and Technology, JAMIA HAMDARD
2.40pm Joint Presentation: A defined molecular vaccine for intestinal schistosomiasis * title TBC
Darrick Carter, CEO, PAI LifesciencesAfzal Siddiqui, Professor, Department of Internal Medicine, Professor (Tenured), Departments of Internal Medicine and Immunology & Molecular Immunology, Texas Tech University Health Sciences Center
2.55pm Development of vaccines for lymphatic filariasis *Title TBC
Dr Ramaswamy Kalyanasundaram, Department Head, Professor of Microbiology and Immunology, University of Illinois College of Medicine
3.10pm Panel: Challenges in establishing correlates of protection and planning trials for NTD vaccines
· What are the difficulties in establishing COP for NTD vaccines
· Planning for ph2-3 trials – how can we innovate in creating pathways and designs?
Darrick Carter, CEO, PAI Lifesciences
Afzal Siddiqui, Professor, Department of Internal Medicine, Professor (Tenured), Departments of Internal Medicine and Immunology & Molecular Immunology, Texas Tech University Health Sciences Center
Dr Ramaswamy Kalyanasundaram, Department Head, Professor of Microbiology and Immunology, University of Illinois College of Medicine
Michael, Senior Director, Principal Consultant DCS/BPE, Cencora
Additional panelists TBC
4.00pm Panel: Moving the needle: alternative pathways to approval for global health vaccines (Parasitic & Neglected Diseases)
· Considering pathways to approval in different scenarios – in-country experiences
o Enabling different technology pathways
o From a local manufacturing perspective
· Moving from science to deployment – other than strong data what do we need to move these vaccines forward?
o Understanding incentives for production, government incentives to buy, individual country policies and regulatory requirements
o How is this challenge further compounded with diseases that are not fatal but have high morbidity burden?
o Case studies – Marburg, Hookworm,
· Improving stringency of regulatory agencies through new frameworks
· Can combinations deal with the issue of high burden but low interest? What would be the complications of combining these types of vaccines?
Dr Maria Elena Bottazzi, Co-Director of Texas Children’s Hospital Center for Vaccine Development, Baylor College of Medicine
Dr Kelly Warfield, President of Global Research, Sabin Vaccine Institute
Javier Guzman, Director of Global Health Policy and Senior Fellow, Center for Global Development
Petro Terblanche, Managing Director, Afrigen
Prof Tuck Seng Wong, Professor, Sheffield University; Director, UKSEA Vax Hub
Dr William Hausdorff, Public Health Value Proposition Lead, PATH