AASLD 2011: Daclatasvir with Pegylated Interferon/ Ribavirin Produces High Rates of HCV Suppression


Most treatment-naive chronic hepatitis C patients who added the experimental HCV NS5A inhibitor daclatasvir (BMS-790052) to pegylated interferon/ribavirin achieved undetectable viral load at 12 and 24 weeks, according to data presented at the at the 62nd Annual Meeting of the American Association for the Study of Liver Disease (AASLD 2011) last month in San Francisco.

Daclatasvir is the first direct-acting agent to target the HCV NS5A replication complex; the function of NS5A is not fully understood, but it appears to play an important role in viral replication.

Christophe Hézode and fellow investigators with the multinational Phase 2b COMMAND-1 study (AI444010)evaluated triple therapy using daclatasvir plus pegylated interferon/ribavirin vs standard therapy.

The analysis included 395 previously untreated chronic hepatitis C patients. About 70% were men, about 85% were white, and the median age was approximately 50 years; 30% had the favorable IL28B CC gene pattern and liver cirrhosis was not an exclusion criterion. Most had HCV genotype 1 (about 75% with difficult-to-treat subtype 1a), but 30 people had genotype 4.

Participants were randomly assigned to receive 20 mg or 60 mg daclatasvir once-daily plus pegylated interferon and ribavirin for either 24 or 48 weeks, or else pegylated interferon/ribavirin with placebo for 48 weeks. Patients with good virological response at weeks 4 and 12 were eligible for shorter treatment and were re-randomized to receive either triple therapy for another 12 weeks (24 weeks total) or 12 weeks of pegylated interferon/ribavirin alone.


Once-daily daclatasvir plus pegylated interferon/ribavirin "provided higher rates of early virologic response compared with placebo plus pegylated interferon/ribavirin," the researchers concluded.

Adverse event profiles were similar in the daclatasvir and standard therapy arms, they continued, and safety profiles were comparable for daclatasvir used for 12 or 24 weeks.

These findings, Hézode said, "suggest that a vast majority of [IL28B] CC patients can be treated with a shorter duration" of therapy. He added that the new data "strongly support initiation of Phase 3 trials."

Investigator affiliations: CHU Henri Mondor, Creteil, France; Liver Centre, Toronto Western Hospital, Toronto, Ontario, Canada; Vancouver Island Health Authority, University of British Columbia, Victoria, British Columbia, Canada; Monash Medical Centre, Monash University, Melbourne, Victoria, Australia; Fundacion de Investigacion de Diego, San Juan, Puerto Rico; Univ of Alberta, Edmonton, Alberta, Canada; Mercy Medical Center, Baltimore, MD; Options Health Research, LLC, Tulsa, OK; National Liver Institute, Shebeen El Kom , Egypt; Tropical Medicine and Hepatology Department, Cairo University, Cairo, Egypt; Alamo Medical Research, San Antonio, TX; Metropolitan Research, Arlington, VA; Liver Unit, Hôpital Cochin, Paris, France; Copenhagen University Hospital, Hvidovre, Denmark; Scripps Clinic, La Jolla, CA; Hopital Saint Joseph, Marseille, France; Hopital Saint-Antoine, Paris, France; Baylor College of Medicine, Houston, TX; University of North Carolina at Chapel Hill, Chapel Hill, NC; Karolinska Institutet, Stockholm, Sweden; Azienda Ospedaliero Universitaria Pisana, Pisa, Italy; University of Colorado, Aurora, CO; JW Goethe University, Frankfurt, Germany; Indiana University Medical Center, Indianapolis, IN; Johns Hopkins University, Baltimore, MD; Bristol-Myers Squibb, Wallingford, CT.



C Hezode, GM Hirschfield, W Ghesquiere, et al. BMS-790052, A NS5A Replication Complex Inhibitor, Combined with Peginterferon Alfa-2a and Ribavirin in Treatment-Naive HCV- Genotype 1 or 4 Patients: Phase 2b AI444010 Study Interim Week 12 Results. 62nd Annual Meeting of the American Association for the Study of Liver Disease (AASLD 2011). San Francisco, November 4-8, 2011. Abstract 227.

Other Source

Bristol-Myers Squibb. 12-Week On-Treatment Results from Large Phase IIb Study (COMMAND-1) of Bristol-Myers Squibb’s NS5A Inhibitor Daclatasvir Support Anti-HCV Activity and Safety Profile Observed in Earlier Studies. Press release. November 8, 2011.