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1  patients receiving combination treatment or interferon alfa-2a.
2  compared peginterferon alfa-2a (40 kd) with interferon alfa-2a.
3 1 IU/mL before the introduction of pegylated interferon alfa-2a.
4 sed double-blind placebo-controlled trial of interferon alfa-2a (10 million units/m2, daily for 7 day
5                                       Use of interferon alfa-2a/2b and ribavirin, 1000 to 1200 mg/d,
6  trial involving 674 patients, the effect of interferon alfa-2a (3 megaunits three times per week for
7 day), peginterferon alfa-2a plus placebo, or interferon alfa-2a (3 million IU three times a week) plu
8 days, then 750 mg/m2 weekly, and recombinant interferon alfa-2a 9 million units subcutaneously three
9 r 90 mug/week (for arm B) of pegylated (Peg) interferon alfa-2a added to their current ART regimen.
10                                    Pegylated interferon alfa-2a administered once weekly is more effe
11  once weekly is more effective than standard interferon alfa-2a administered three times weekly.
12 ined virologic responses than treatment with interferon alfa-2a alone in patients with chronic hepati
13 llocated (1 to 1) by minimisation to receive interferon alfa-2a alone or combination therapy with int
14 l or progression-free survival compared with interferon alfa-2a alone, immunotherapy might still have
15 ere reported in 113 (23%) patients receiving interferon alfa-2a and 131 (26%) of those receiving comb
16 2 patients were randomly assigned to receive interferon alfa-2a and 504 to receive combined treatment
17 , >17 000 IU/mL) were treated with pegylated interferon alfa-2a and adefovir for 48 weeks.
18        Therapy for HCL includes splenectomy, interferon alfa-2a and alfa-2b, pentostatin, and cladrib
19 jection (CR) in patients receiving pegylated interferon alfa-2a and ribavirin (PEG) to treat recurren
20 8), telaprevir in combination with pegylated interferon alfa-2a and ribavirin (Peg-IFN/RBV) for 15 da
21 zed 1:1:2:2 to receive 24 weeks of pegylated interferon alfa-2a and ribavirin (PegIFN/RBV) in combina
22 th TMC435 (200 mg once daily) plus pegylated interferon alfa-2a and ribavirin (PegIFNalpha-2a and RBV
23  (Virahep-C), 260 men treated with pegylated interferon alfa-2a and ribavirin completed self-administ
24              All patients received pegylated interferon alfa-2a and ribavirin therapy.
25 ng recombinant interleukin-2 and recombinant interferon alfa-2a before and after combination cytotoxi
26 d) provides improved sustained response over interferon alfa-2a, but its effect on HRQL is unknown.
27                    INTERPRETATION: Pegylated interferon alfa-2a can induce durable haematological and
28                                 The doses of interferon alfa-2a given in this regimen did not improve
29 owledge, the antiviral activity of pegylated interferon alfa-2a has not been studied in participants
30                     A variety of regimens of interferon alfa-2a have been used, including use of high
31 e maximum-tolerated dosage (MTD) of IL-2 and interferon alfa-2a (IFN alpha-2a) that can be administer
32                                              Interferon alfa-2a (IFN-alpha2a) was administered at 9 m
33 etyl-L-aspartic acid (PALA), and recombinant interferon alfa-2a (IFNalpha-2a) in a sequential order t
34                            Pegylated (40 kd) interferon alfa-2a (IFNalpha2a) (PEGASYS, Hoffman-La Roc
35 rapy with 13-cis-retinoic acid (13-CRA) plus interferon alfa-2a (IFNalpha2a) is superior to IFNalpha2
36                                          Peg-interferon alfa-2a immunotherapy resulted in control of
37 afety and efficacy of REP 2139 and pegylated interferon alfa-2a in patients with chronic HBV and hepa
38                                    Pegylated interferon alfa-2a induced haematological (66 [80%] of 8
39 astatic renal cell carcinoma combinations of interferon alfa-2a, interleukin-2, and fluorouracil prod
40 on alfa-2a alone or combination therapy with interferon alfa-2a, interleukin-2, and fluorouracil.
41                                    Pegylated interferon alfa-2a is an immunomodulatory agent used to
42                   The side effect profile of interferon alfa-2a is similar to that of other interfero
43                            At week 12 of Peg-interferon alfa-2a monotherapy, viral suppression was ob
44  REP 2139 and 180 mug subcutaneous pegylated interferon alfa-2a once per week for 15 weeks, then mono
45 eks, then monotherapy with 180 mug pegylated interferon alfa-2a once per week for 33 weeks.
46     Seven were treated with corticosteroids, interferon alfa-2a, or both.
47 patitis C (CHC) when combined with pegylated interferon alfa 2a (Peg-IFN-alfa-2a) and ribavirin (RBV)
48   We conducted a phase II study of pegylated interferon alfa-2a (PEG-IFN-alpha-2a) in patients with e
49 of sofosbuvir (SOF), ribavirin (RBV) and peg-interferon-alfa-2a (peg-IFN-alfa-2a) as well as the comb
50 -label subcutaneous treatment with pegylated interferon-alfa-2a (Peg-IFNalfa-2a) 180 mug/wk, or albIF
51 ompared the efficacy and safety of pegylated interferon alfa-2a (peginterferon alfa-2a) plus either r
52  of sofosbuvir in combination with pegylated interferon alfa-2a (peginterferon) and ribavirin in non-
53  plus ribavirin than among those assigned to interferon alfa-2a plus ribavirin (40 percent vs. 12 per
54 a lower likelihood of SVR than was pegylated interferon alfa-2a plus ribavirin (absolute difference,
55 us either ribavirin or placebo with those of interferon alfa-2a plus ribavirin for the treatment of c
56 was significantly more effective than either interferon alfa-2a plus ribavirin or peginterferon alfa-
57 ron alfa-2a plus placebo, and 7 percent with interferon alfa-2a plus ribavirin.
58                                              Interferon alfa-2a resembles other recombinant alpha int
59 imeprevir (150 mg once daily) with pegylated interferon alfa-2a/ribavirin (peg-IFN/RBV) for 12 weeks.
60 ERPRETATION: Combined REP 2139 and pegylated interferon alfa-2a therapy is safe, well tolerated, and
61 cts were assigned to receive 6 million IU of interferon alfa-2a three times weekly for 12 weeks follo
62 .8 months (17.0-23.2) for patients receiving interferon alfa-2a versus 18.6 months (16.5-20.6) for th
63       The initial starting dose of pegylated interferon alfa-2a was 450 mug subcutaneously once per w
64  After 5 weeks, ART was interrupted, and Peg-interferon alfa-2a was continued for up to 12 weeks (the
65 uvant chemoprevention with retinoic acid and interferon alfa-2A was offered.
66                                    Pegylated interferon alfa-2a was well tolerated and exhibited stat
67 V infection received 180 microg of pegylated interferon alfa-2a weekly for 12 weeks.

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