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Public-Private collaboration for accessible infectious disease mAbs in LMICs
There are significant gaps in mAbs access and availability in LMICs. Viable models, commercial incentives and pathways to afford access are currently not in place. Find out how Public-Private collaboration will be needed to bridge this gap...
Co-organized by: MPP, IAVI, Unitaid and Wellcome
Goal of session: To foster mAb developer engagement to understand the barriers and define the incentives and enablers that would facilitate affordable access to mAbs in LMICs.
Target audience: those involved in the development, manufacturing, supply, regulation, and procurement of monoclonal antibodies.
10:00 Introduction
Carmen Pérez Casas, Strategy Senior Lead/PPPR Head, Unitaid
10:20 Panel: Challenges and opportunities: What are the barriers and unique considerations for mAbs accessibility/availability in LMICs? What advancements have recently been achieved and how can they be further leveraged for infectious disease mAbs?
Moderator: Shelly Malhotra, Executive Director, Global Access, IAVI
11:20 Panel: Industry perspectives on a path towards access and the role of global health stakeholders
Moderator: Esteban Burrone, MPP
12:20 Wrap up/Closing remarks
Pete Gardiner, Wellcome
Senior Representative, InDevR
A holistic approach will be integral to tackling the AMR pandemic – how is industry ensuring the development of new tools & which interventions are best suited to our priority pathogens?
How are we improving our understanding of RNA technology for next generation vaccines? How will RNA transform therapeutics and cancer treatment?
Senior Representative, Vaxxas
Senior Representative, Mylife Technologies
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·The journey of turning mRNA and protein based vaccines into life-saving vaccines – what else can they do for us in future?
·How do we identify and nurture the next platform that could save more lives and prevent the next pandemic?
·How will government agencies become more nimble and improve its communications with the public?
·How do we ensure more female leadership and diversity in public health?
·What are the synergistic differences between BARDA and HERA?
·What did we learnt from COVID and how do we plan to fix the issues we encountered?
·How will we manage stockpiles more efficiently and fairly?
·What kind of regulatory flexibility and framework is in place to support pandemic vaccines?
·How do we exit out of EUAs to fully approved vaccines rapidly to get the coverage we want?
·Which pathogens need more research and which need to be developed by manufacturers?
·What about the AMR and neglected diseases lists? Where does that fit?
·Do we have the right strategy to enable us to create the next pandemic vaccine even faster than COVID? Prototype families and platformed based pandemic preparedness models
·How do we interpret the lists for vaccine and or mABs development?
·Use of mABs and vaccines in Infants and Children – which should be use and when?
·Future of mABs in global accessibility and cost-effectiveness
Join us in the exhibition hall (level 3) for:
1:10 – 2:30 1-2-1 Partnering
1:30 – 2:20 Start-up pitches
2:00 – 2:30 Poster Presentations
·Correlates for vaccines against RSV, CMV and COVID
·Now we’ve built local manufacturing – is it sustainable?
·Are these decentralized manufacturing hubs working and is the infrastructure also in place to support it?
·How will African producers start matching the multinational manufacturers in production? The role of international and national collaborations
·The need for regulatory strengthening and infrastructure
·How do we ensure vaccine acceptability and uptake of vaccines manufactured from Africa?
·As the adult vaccination choices get more crowded, what are our implementation strategies and key challenges?
·How do we navigate current ACIP recommendations for best vaccine uptake of RSV?
·How will that impact other new adult vaccines reaching the market?
·Co-administrating vaccines vs combination vaccines – how do we evaluate these?
·How do we develop and evaluate the effectiveness second/next generation vaccines?
·Lesson learned in universal flu vaccine efforts
·What developments have been made towards broadly protective vaccines?
Sponsored by Tekton Research
Only those who have paid for the ViE admission can attend.
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-The future of COVID-19 vaccinations: combined annual shots for a seasonal disease with flu and RSV?
-How do we compare the effectiveness of combined respiratory vaccines?
-The future of COVID-19 vaccinations: annual shots for a seasonal disease?
-How have our variant specific bivalent COVID vaccines performed during the fall?
-How do we compare the effectiveness of combined respiratory vaccines?
Senior Representative, Emvenio
Senior Representative, Viroclinics DDL a Cerba Research Company
Senior Representative, PPD, part of Thermo Fisher Scientific
Panellist to be announced
Senior Representative, Flourish Research
Senior representative, Novavax
Senior Representative, Q² Solutions
Senior Representative, Emergent Biosolutions
Speaker TBC
Reserved for NOF America Corporation
Senior Representative, ICON plc
Senior represntative PPD, part of Thermo Fisher Scientific
Reserved for Dr Dave Anderson, CSO, VBI Vaccines
Senior Representative, Allucent
Senior Representative, Trilink Biotechnologies
Invited: Robert Connelly, CEO, Elicio Therapeutics
Senior representative, Q2 solutions
Senior Representative, NIH/Merck
Senior Representative, Parexel
Syneos Health
Invited: Bill Enright, CEO, Vaccitech
Reserved for UTMB
Senior Representative, PDC CRO
Senior Representative, Jurata Thin Film
Invited: Dr Natalie Vokes, Assistant Professor, Department of Thoracic/Head and Neck Medical Oncology, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center
Senior Representative Advanced Technology International
Julie Suman, Vice President Scientific Affairs, AptarPharma
Nektaria Karavas, Global Director of Business Development, Aptar Pharma
Prof Ilhan Celik / Dr Michael Wenger, Vice President, Clinical Development, BioNTech- TBC
Reserved for Novo Nordisk
Senior Representative, Touchlight
Senior Representative, Acclime Australia
Senior Representative, BioCina
Senior Representative, Paratus Clinical
Senior Representative, Wuxi Vaccines
Reserved for NEC OncoImmunity AS
Senior Representative Microbiologics
Invited: Caroline Forkin, Head of Clinical Development Programmes and Operations, CEPIProposed speakers: Senior Representative, Africa CDCSenior Representative, WHO
Senior Representative, IDT Biologika
Senior Representative Osivax
Senior Representative Pappas Capital
More to follow..
Sponsored by Viroclinics-DDL
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Senior Representative, BioNTech
Senior Representative DARPA, Walter Reed Army Institute and ARPA-H
Senior Representative, CDC
Senior Representative, Evaxion Biotech A/S
Senior Representative, Eurofins Viracor BioPharma Services
Senior Representative, NIH
Senior Represenative, Pfizer/Valneva
Senior Representative, Cepheid
Senior Representative AAHI
Senior Representative, VisMederi
Senior representative CDC
Senior Representative, Jurata Thin Film
Senior Representative, Utrecht University
·Which world vaccination programs are under threat?
·The devasting impact on infectious diseases reaching far beyond its origins
·How climate change increases pandemic risk and spillover between humans and animals
·The need to invest in strong health systems now to stay resilient to the inevitable complex changes that climate change will bring
·The role of AI in public health, current and future
·Could AI have helped us to prevent a pandemic? Expanding vaccine libraries, predicting strain drifts, monitoring surveillance, vaccine design
·Success, limitations and risks of AI
·What is the evolving regulatory landscape on AI?