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Webinar: PrEP Beyond Pills – New Technologies in Biomedical HIV Prevention

HIV Prevention, Webcast

Facilitated by Christopher B. Hurt, MD
Associate Professor of Medicine
Director, North Carolina HIV Training & Education Center
Site PI, Ryan White HIV/AIDS Program Part D, UNC ID Clinic
Co-Leader, UNC CFAR Collaborative HIV Epidemiology & Prevention Scientific Working Group
Institute for Global Health & Infectious Diseases
University of North Carolina at Chapel Hill
School of Medicine
September 23, 2020

Objectives

  • List three ways in which pre-exposure prophylaxis may be delivered in the future.
  • Describe the results of HPTN 083 and what this means for PrEPin the near term.
  • Identify the agent currently under investigation as implantable PrEP.
  • Explain how broadly neutralizing antibodies work to prevent HIV infections.

Presentation

Slides

Facilitated by Christopher B. Hurt, MD
Associate Professor of Medicine
Director, North Carolina HIV Training & Education Center
Site PI, Ryan White HIV/AIDS Program Part D, UNC ID Clinic
Co-Leader, UNC CFAR Collaborative HIV Epidemiology & Prevention Scientific Working Group
Institute for Global Health & Infectious Diseases
University of North Carolina at Chapel Hill
School of Medicine
September 23, 2020

Objectives

  • List three ways in which pre-exposure prophylaxis may be delivered in the future.
  • Describe the results of HPTN 083 and what this means for PrEPin the near term.
  • Identify the agent currently under investigation as implantable PrEP.
  • Explain how broadly neutralizing antibodies work to prevent HIV infections.

Presentation

Slides

Facilitated by Christopher B. Hurt, MD
Associate Professor of Medicine
Director, North Carolina HIV Training & Education Center
Site PI, Ryan White HIV/AIDS Program Part D, UNC ID Clinic
Co-Leader, UNC CFAR Collaborative HIV Epidemiology & Prevention Scientific Working Group
Institute for Global Health & Infectious Diseases
University of North Carolina at Chapel Hill
School of Medicine
September 23, 2020

Objectives

  • List three ways in which pre-exposure prophylaxis may be delivered in the future.
  • Describe the results of HPTN 083 and what this means for PrEPin the near term.
  • Identify the agent currently under investigation as implantable PrEP.
  • Explain how broadly neutralizing antibodies work to prevent HIV infections.

Presentation

Slides