Program

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Program

The scientific program is available and can be downloaded as pdf.
Please use the download link at the right side of the webpage.


 

We are proud to announce the following list of invited speakers for the 5th Intl. Workshop on Clinical Pharmacology of Hepatitis Therapy:

Ribavirin - still needed, but how does it work 
Jordan Feld, M.D., Toronto Western Hospital Liver Centre, Canada

Round Table Discussion: Regulatory requirements for early clinical testing of novel HCV antiviral drugs: 
 - The US (FDA) regulatory perspective 
   Jeffrey Murray, U.S. Food & Drug Administration
 - The EU (EMEA) regulatory perspective 
   Jean-Michel Pawlotsky, M.D.,Ph.D., Université Paris XII, 
France

Novel Combination Therapies for Hepatitis treatment: 
 - Clinical pharmacology aspects 
   Patrick Smith, Ph.D., Roche, USA
 - Virology aspects 
   Isabel Najera, Ph.D., Roche, USA

The role of PK enchancers/Boosting: 
 - Dale Kempf, Ph.D., Abbott, USA
 - Anita Mathias, Ph.D., Gilead Science, USA

 

Confirmed Invited Speakers Joint Session (Morning 24 June):

The epidemic of HCV; globally and on genotype level. How does maturation of the HCV infected patient population (after 2015) impact drug development? 
Gary Davis, M.D., Baylor University Medical Centre, USA


Dynamics of resistance and the implications for drug development.
Jean-Michel Pawlotsky, M.D., Ph.D., Hôpital Henri Mondor, Université Paris XII, France

New findings in HCV replication and how to apply to potential antiviral targets
Charles Rice, Ph.D., Rockefeller University, USA

Implications of genetic host polymorphism for HCV drug development and patient care
Mark Sulkowski, M.D., Ph.D., Johns Hopkins University, USA

Important dates

Registration Timeline
Early:       1 March - 16 April 2010
Regular:  17 April - 14 May 2010
Late:        15 May - 11 June 2010

Abstract Submission:

Start:       1 March 2010
Deadline:  17 May 2010