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The moderators of this session are actively seeking to move cell and gene therapies into resource-limited parts of the world. The panelists will first briefly describe efforts designed to make this happen, and then discuss how to best engage key stakeholders in the future so that safe, durable, and accessible cures for HIV and sickle cell disease will be available to all of those in need.

3 min
Moderators introduction
Jennifer ADAIR, Fred Hutchinson Cancer Research Center, United States
Mark R. DYBUL, Georgetown University, United States
Moses SUPERCHARGER, Uganda
5 min
Towards Sustainable and Affordable Access of Curative Genetic Interventions for all that need them
Boro DROPULIC, Caring Cross, United States
PDF
5 min
Development of in vivo gene therapies for HIV and SCD
Keith HOOTS, National Institutes of Health (NIH), United States
5 min
Development and distribution of in vivo gene therapies for SCD
Susan STEVENSON, NIBR, United States
5 min
Advocacy for sickle cell disease
Evelyn Harlow MWESIGWA, Ministry of Health of Uganda and Sickle Cell Network Uganda, Uganda
5 min
Promotion of HIV cure research through diverse stakeholder engagement
Izukanji SIKAZWE, Centre for Infectious Disease Research in Zambia, Zambia
PDF
52 min
Panel discussion
Jennifer ADAIR, Fred Hutchinson Cancer Research Center, United States
Evelyn Harlow MWESIGWA, Ministry of Health of Uganda and Sickle Cell Network Uganda, Uganda
Boro DROPULIC, Caring Cross, United States
Susan STEVENSON, NIBR, United States
Mark R. DYBUL, Georgetown University, United States
Keith HOOTS, National Institutes of Health (NIH), United States
Izukanji SIKAZWE, Centre for Infectious Disease Research in Zambia, Zambia
Moses SUPERCHARGER, Uganda
5 min
Guest closing remarks
Francis COLLINS, National Institute of Health, United States

5 min
Closing remarks
Sharon LEWIN, University of Melbourne, Australia