HCV Drug Access for People with Bleeding Disorders

Print
MATERIALS AND LINKS

Meeting Information:
Agenda

Participant List

Presentations:
Veronica Miller
Nina Mani
Jamie Siegel
Mark Antell
Kenneth Sherman
Filip Josephson
Jeffrey Murray
Michelle Berrey
Diana Brainard
Background:
The historical cohort of bleeding disorder patients exposed to contaminated blood products from the late 1970s to 1990 is a population currently experiencing high rates of liver-related morbidity and mortality due to hepatitis C viral (HCV) infection. The October 17, 2011 meeting sponsored by the Forum was the first in a series of meetings that will try and address issues associated with providing access to, if indicated, combination interferon-free experimental direct acting antivirals (DAAs).

Meeting participants included representatives from regulatory agencies, academia, hemophilia treatment centers, non-profits associated with database management for those affected with bleeding and blood clotting disorders, community medical practitioners, patient advocates and pharmaceutical companies.

Objectives:
 
1.   Discuss safety issues that should be considered
2.   Discuss clinical trial entry criteria and diagnostic tests used
      in this population

3.   Discuss possible sites for trials and the specialists who should be involved

Status:
The meeting was held on Monday, October 17, 2011 at UC Washington Center, Washington DC.