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1 bavirin regimens or between the two doses of peginterferon alfa-2b.
2 alfa-2b dose (3 MIU) or the once-weekly (QW) peginterferon alfa-2b (0.5, 1.0, or 1.5 microg/kg).
3  infection were randomly assigned to receive peginterferon alfa-2b 1.5 mug/kg plus ribavirin 800-1400
4 00 mg/day) (n = 58 in the final analysis) or peginterferon alfa 2b (1.5 mcg/kg/wk), ribavirin (1000-1
5 eginterferon alfa 2a (180 microg/wk; 43%) or peginterferon alfa 2b (1.5 microg /kg/wk; 44%) compared
6 .5% (95% CI, 19.9 to 27.2) for standard-dose peginterferon alfa-2b, 20.0% (95% CI, 16.4 to 23.6) for
7 among the regimens: 39.8% with standard-dose peginterferon alfa-2b, 38.0% with low-dose peginterferon
8 3 to 6.0) between standard-dose and low-dose peginterferon alfa-2b and -1.1% (95% CI, -5.3 to 3.0) be
9 16) or low-dose ribavirin (400-1000 mg) plus peginterferon alfa-2b and boceprevir three times a day f
10  (95% CI, -5.3 to 3.0) between standard-dose peginterferon alfa-2b and peginterferon alfa-2a.
11 00-1400 mg daily for 48 weeks (PR48; n=104); peginterferon alfa-2b and ribavirin daily for 4 weeks, f
12 white patients with chronic hepatitis C with peginterferon alfa-2b and ribavirin for 48 weeks.
13 e a lower rate of response to treatment with peginterferon alfa-2b and ribavirin than non-Hispanic wh
14                         In all three groups, peginterferon alfa-2b and ribavirin were administered fo
15                WIN-R (Weight-based dosing of pegINterferon alfa-2b and Ribavirin) was a multicenter,
16 virus oral protease inhibitor, when added to peginterferon alfa-2b and ribavirin.
17 b, 20.0% (95% CI, 16.4 to 23.6) for low-dose peginterferon alfa-2b, and 31.5% (95% CI, 27.9 to 35.2)
18 e peginterferon alfa-2b, 38.0% with low-dose peginterferon alfa-2b, and 40.9% with peginterferon alfa
19 eks of treatment with one of three regimens: peginterferon alfa-2b at a standard dose of 1.5 microg p
20 ate was not dose-related above 1.0 microg/kg peginterferon alfa-2b because of a higher relapse rate a
21                                        All 3 peginterferon alfa-2b doses decreased liver inflammation
22                                        All 3 peginterferon alfa-2b doses significantly (P < or =.042)
23 response during treatment with 1.5 microg/kg peginterferon alfa-2b in patients infected with genotype
24                               In conclusion, peginterferon alfa-2b maintained (0.5 microg/kg) or surp
25 lve by week 8 were randomized to once weekly peginterferon alfa-2b monotherapy (1.5 microg/kg per wee
26                                              Peginterferon alfa-2b monotherapy in acute hepatitis C i
27    Treatment guidelines recommend the use of peginterferon alfa-2b or peginterferon alfa-2a in combin
28 fa-2a (P=0.20 for standard-dose vs. low-dose peginterferon alfa-2b; P=0.57 for standard-dose peginter
29 te among patients treated with 1.5 microg/kg peginterferon alfa-2b, particularly among patients infec
30                    Boceprevir (BOC) added to peginterferon alfa-2b (PegIFN) and ribavirin (RBV) signi
31 up, double-blind dose-finding study compared peginterferon alfa-2b (PegIntron) to interferon alfa-2b
32 imeprevir to either peginterferon alfa 2a or peginterferon alfa 2b plus ribavirin improved SVR in tre
33 fa-2b regimens and between the standard-dose peginterferon alfa-2b regimen and the peginterferon alfa
34 afety and adverse-event profiles between the peginterferon alfa-2b regimens and between the standard-
35 and ribavirin daily for 4 weeks, followed by peginterferon alfa-2b, ribavirin, and boceprevir 800 mg
36 4; n=103) or 44 weeks (PR4/PRB44; n=103); or peginterferon alfa-2b, ribavirin, and boceprevir three t
37 interferon alfa-2b; P=0.57 for standard-dose peginterferon alfa-2b vs. peginterferon alfa-2a).
38                                              Peginterferon alfa-2b was well tolerated.

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