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Hepatitis C

Welcome to Hepatitis C Management Discussion Board! The Hepatitis C Management Discussion Board provides Infectious Disease Clinicians a platform to connect with colleagues to exchange information, case studies, complications, and new developments on matters concerning hepatitis C treatment and management. Certain case studies will be developed into clinical vignettes and will be available to Infectious Disease Clinicians for future reference. Please be respectful of all participants and their respective comments. Please read our Terms of Use and Discussion Forum Guidelines.


Any diagnostic or therapeutic recommendations and all opinions presented are those of the individual contributor. They do not necessarily represent the views of IDSA. The reader assumes all risks in using this information. The IDSA Hepatitis C Discussion Forum is in full compliance with HIPPA. IDSA bears no responsibility for the accuracy of participant comments and will bear no legal liability for discussion results.

If a participant wishes to post an issue on the IDSA Hepatitis C Discussion Forum, the participant is strongly urged to provide contact information for possible offline discussion via phone or email concerning the posted issue.

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AbbVie steps closer to FDA filing as first hep C PhIII delivers promising results
Posted: Monday, November 18, 2013 1:45 PM
Joined: 2/20/2013
Posts: 40

"AbbVie's all-oral "3D" regimen scored high sustained virological response rates among 631 treatment-naive patients after 12 weeks of treatment, hitting 96% for the treatment arm. The patients were all in the hard-to-treat genotype 1 category, with SVR rates of 95% and 98% for GT1a and GT1b patients. The discontinuation rate was low, only 0.6%, with a 1.7% relapse rate."

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