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Cited by 285

The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.

Exploratory Study of Oral Combination Antiviral Therapy for Hepatitis C

Open access
Poordad, Fred, Lawitz, Eric, Kowdley, Kris V., Cohen, Daniel E., Podsadecki, Thomas, Siggelkow, Sara, Heckaman, Michele, Larsen, Lois, Menon, Rajeev, Koev, Gennadiy, Tripathi, Rakesh, Pilot-Matias, Tami, Bernstein, Barry·2013·New England Journal of Medicine

Abstract

BACKGROUND: There is a need for interferon-free treatment regimens for hepatitis C virus (HCV) infection. The goal of this study was to evaluate ABT-450, a potent HCV NS3 protease inhibitor, combined with low-dose ritonavir (ABT-450/r), in addition to ABT-333, a nonnucleoside NS5B polymerase inhibitor, and ribavirin, for the treatment of HCV infection. METHODS: We conducted a 12-week, phase 2a, open-label study involving patients who had HCV genotype 1 infection without cirrhosis. All patients received ABT-333 (400 mg twice daily) and ribavirin (1000 to 1200 mg per day) and one of two daily doses of ABT-450/r. Groups 1 and 2 included previously untreated patients; group 1 received 250 mg of ABT-450 and 100 mg of ritonavir, and group 2 received 150 mg and 100 mg, respectively. Group 3, which included patients who had had a null or partial response to previous therapy with peginterferon and ribavirin, received daily doses of 150 mg of ABT-450 and 100 mg of ritonavir. The primary end point was an undetectable level of HCV RNA from week 4 through week 12 (extended rapid virologic response). RESULTS: A total of 17 of the 19 patients in group 1 (89%) and 11 of the 14 in group 2 (79%) had an extended rapid virologic response; a sustained virologic response 12 weeks after the end of treatment was achieved in 95% and 93% of the patients, respectively. In group 3, 10 of 17 patients (59%) had an extended rapid virologic response, and 8 (47%) had a sustained virologic response 12 weeks after therapy; 6 patients had virologic breakthrough, and 3 had a relapse. Adverse events included abnormalities in liver-function tests, fatigue, nausea, headache, dizziness, insomnia, pruritus, rash, and vomiting. CONCLUSIONS: This preliminary study suggests that 12 weeks of therapy with a combination of a protease inhibitor, a nonnucleoside polymerase inhibitor, and ribavirin may be effective for treatment of HCV genotype 1 infection. (Funded by Abbott; ClinicalTrials.gov number, NCT01306617.).

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Metadata

Authors
Poordad, F., Lawitz, E., Kowdley, K. V., Cohen, D. E., Podsadecki, T., Siggelkow, S., Heckaman, M., Larsen, L., Menon, R., Koev, G., Tripathi, R., Pilot-Matias, T., & Bernstein, B.
Venue
New England Journal of Medicine
Published
2013-01-03
Volume
368
Issue
1
Pages
45-53
ISSN
  • 0028-4793 (ISSN-L)
  • 1533-4406
OpenAlex
W2142165617
Cited by
285
References
3
FWCI
40.74
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Exploratory Study of Oral Combination Antiviral Therapy for Hepatitis C. https://app.cochat.ai/papers/10.1056/nejmoa1208809
The paper
Poordad, F., Lawitz, E., Kowdley, K. V., Cohen, D. E., Podsadecki, T., Siggelkow, S., Heckaman, M., Larsen, L., Menon, R., Koev, G., Tripathi, R., Pilot-Matias, T., & Bernstein, B. (2013). Exploratory Study of Oral Combination Antiviral Therapy for Hepatitis C. New England Journal of Medicine. https://doi.org/10.1056/nejmoa1208809

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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