Greetings,
In the news today is the 46th Annual Meeting of the European Association for the Study of the Liver which will take place in Berlin, Germany, March 30 - April 3, 2011. You may have noticed a link located on the sidebar of this blog which includes the upcoming Oral Presentations and Abstracts/Poster Sessions. The abstracts though published online, are under a press embargo until the conference begins on March 30. You can find abstracts through the link below.
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During the meeting all media updates will be posted on the blog in the order they are received, you will find them under this link also on the sidebar;
The News EASL .
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It can be a challenge to find your way around the EASL site, here are a few direct links
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Telaprevir and VX-222 combined with pegylated-interferon and ribavirin
As noted yesterday in the press release Vertex will be presenting 15 abstracts at the EASL including data from the ongoing Phase 2 study evaluating response-guided, 12- and 24-week regimens of "telaprevir and VX-222" combined with pegylated-interferon and ribavirin.
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What Is VX-222 ?
"VX-222 is an investigational, oral, non-nucleoside inhibitor of HCV NS5B polymerase. VX-222 is currently being evaluated in combination with telaprevir, pegylated-interferon and ribavirin in a Phase 2 study. Vertex has worldwide commercial rights for VX-222."
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What Is Telaprevir ?
"Telaprevir is an investigational, oral inhibitor that acts directly on the HCV protease, an enzyme essential for viral replication. To date, more than 2,500 people with genotype 1 hepatitis C have received telaprevir in Phase 2 and Phase 3 studies. Vertex has received priority review for its applications for the approval of telaprevir by the U.S. FDA and Health Canada."
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A quick reminder about the two drug combo;
Back in October of 2010 the VX-222/telaprevir combo being tested in low doses was stopped because of viral breakthrough. In December the higher dose of the VX-222/telaprevir combo was halted in part of the Vertex study.
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The abstract; VX-222 -with telaprevir alone or in combination with Peginterferon/ribavirin is available at the EASL website.
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Pharmasset PSI-7977 and PSI-938
Speaking of oral drug combos, a few abstracts from Pharmasset ; Combination of PSI-7977 and PSI-938 with and without SOC. Treatment with the two oral drugs "alone" resulted in 94%, ( or 15 out of 16 participants reporting ) undetectable after 14 days, as reported in the interim results from the small study released yesterday. You can view both Vertex and the Pharmasset abstracts here.
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Gilead’s GS-9256 and GS-9190 four-drug combination
Gilead’s four-drug combination of GS-9256 and GS-9190 in combination with SOC=Peg-interferon and ribavirin is also being presented at the annual meeting of the European Association for the Study of the Liver. You can view that abstract here.
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Merck Boceprevir
Excerpt from the press release; In total, more than 20 abstracts highlighting Merck medicines and investigational therapies for chronic hepatitis C virus (HCV) infection will be presented, including 3 oral presentations and 17 posters for VICTRELIS.
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The EASL presentations will also include new analyses of the pivotal Phase III data for VICTRELIS administered in combination with PEGINTRON ® (peginterferon alfa-2b) and ribavirin from the HCV SPRINT-2 and HCV RESPOND-2 studies:
.Response-guided therapy with VICTRELIS in combination with current standard therapy among patients with chronic HCV genotype 1, including special populations such as those with advanced fibrosis / cirrhosis;
Overall safety profile of VICTRELIS administered in combination with current standard therapy for chronic HCV; and
Potential predictive factors for chronic HCV treatment success, including response following 4 weeks of lead-in therapy and IL28B polymorphism.
Overall safety profile of VICTRELIS administered in combination with current standard therapy for chronic HCV; and
Potential predictive factors for chronic HCV treatment success, including response following 4 weeks of lead-in therapy and IL28B polymorphism.
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Quick Search For Abstracts
To Search for abstracts on Boceprevir simply click Search
1-Text to search: Type In Boceprevir
Click; 2-Poster Sessions
Click; 3- Abstract Title
Click; 4- The search button
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You could also search for the Key Poster Presentations named in the press release.
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High Sustained Virologic Response (SVR) Among Genotype 1 Previous Non-Responders and Relapsers to Peginterferon/Ribavirin When Re-Treated With Boceprevir Plus Peginterferon Alfa-2A/Ribavirin. S. Flamm et al. Late-Breaker Abstract 1366. Thursday, March 31.
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Response-Guided Therapy with Boceprevir Plus Peginterferon Alfa-2b/Ribavirin Reduces Duration in Naive and Peginterferon Alfa-2b/Ribavirin Previous-Treatment-Failure Patients with HCV Genotype 1. M.P. Manns et al. Abstract 448. Thursday, March 31.
Overall Safety Profile of Boceprevir Plus Peginterferon Alfa-2b/Ribavirin. M.P. Manns et al. Abstract 449. Thursday, March 31.
Response-Guided Therapy with Boceprevir Plus Peginterferon Alfa-2b/Ribavirin Reduces Duration in Naive and Peginterferon Alfa-2b/Ribavirin Previous-Treatment-Failure Patients with HCV Genotype 1. M.P. Manns et al. Abstract 448. Thursday, March 31.
Overall Safety Profile of Boceprevir Plus Peginterferon Alfa-2b/Ribavirin. M.P. Manns et al. Abstract 449. Thursday, March 31.
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Four-Week Therapy with Peginterferon Alfa-2b/Ribavirin Effectively Predicts Sustained Virologic Response in Treatment-Naïve and Previous-Treatment-Failure Patients with HCV-1 Treated with Boceprevir Plus Peginterferon Alfa-2b/Ribavirin. J.M. Viering et al. Abstract 481. Thursday, March 31.
Four-Week Therapy with Peginterferon Alfa-2b/Ribavirin Effectively Predicts Sustained Virologic Response in Treatment-Naïve and Previous-Treatment-Failure Patients with HCV-1 Treated with Boceprevir Plus Peginterferon Alfa-2b/Ribavirin. J.M. Viering et al. Abstract 481. Thursday, March 31.
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Utility of Historical Data Compared to Lead-In Response in Predicting Sustained Virologic Response in Non-Responders and Relapsers to Peginterferon/Ribavirin When Re-Treated With Boceprevir+Peginterferon Alfa-2b/Ribavirin (P/R). R. Esteban et al. Abstract 418. Thursday, March 31.
Utility of Historical Data Compared to Lead-In Response in Predicting Sustained Virologic Response in Non-Responders and Relapsers to Peginterferon/Ribavirin When Re-Treated With Boceprevir+Peginterferon Alfa-2b/Ribavirin (P/R). R. Esteban et al. Abstract 418. Thursday, March 31.
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Watch For More Updates On The Sidebar
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Updated March 8th;
Links To The; Upcoming Oral Presentations and Abstracts/Poster Sessions To Be Presented At The EASL March 30-April 3, 2011;
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In The News EASL
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