2014
DOI: 10.1016/s1474-4422(14)70068-7
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Pegylated interferon beta-1a for relapsing-remitting multiple sclerosis (ADVANCE): a randomised, phase 3, double-blind study

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Cited by 354 publications
(460 citation statements)
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“…Studies on MS disease activity, such as clinical drug trials, indicate that the number of new MRI lesions is approximately 4–12 times larger than the number of new clinical relapses during the same time period 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20. Such “clinically silent” MRI lesions stress the importance of monitoring patients with MRI even in the absence of clinical signs of disease activity.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Studies on MS disease activity, such as clinical drug trials, indicate that the number of new MRI lesions is approximately 4–12 times larger than the number of new clinical relapses during the same time period 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20. Such “clinically silent” MRI lesions stress the importance of monitoring patients with MRI even in the absence of clinical signs of disease activity.…”
Section: Resultsmentioning
confidence: 99%
“…While we acknowledge this and would like to emphasize that the MRI frequency and timing should be adapted to the clinical situation, it is our opinion that general recommendations of MRI frequency are still valuable in the clinical care of patients. The recommendations regarding MRI frequency presented here are based on clinical experience and extrapolation of study data on the level of disease activity seen in treated and untreated patients with MS in phase III studies 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20…”
Section: Resultsmentioning
confidence: 99%
“…The methods and results of the ADVANCE study have previously been published. 9 Briefly, patients aged 18 to 65 years with an Expanded Disability Status Scale score between 0.0 and 5.0 and a confirmed diagnosis of relapsing-remitting MS, as defined by the McDonald criteria, 14,15 were included in the study. Patients were randomized to receive peginterferon beta1a 125 μg subcutaneously every 2 or 4 weeks or placebo at 183 sites worldwide.…”
Section: Methodsmentioning
confidence: 99%
“…From the 183 sites that participated in ADVANCE, 84 investigators met the inclusion criteria and were invited to participate. Of 50 ADVANCE investigators who agreed to participate, 30 (ie, responders) completed questionnaire 1 and 29 also completed questionnaire 2 was evaluated during the 2-year, double-blind, randomized, placebo-controlled (year 1 only) ADVANCE study in patients with relapsing-remitting MS. 9 Results from year 1 demonstrated that the use of peginterferon beta1a 125 μg subcutaneously every 2 or 4 weeks significantly reduced the relapse rate, risk of relapse, disability progression, and number of magnetic resonance imaging brain lesions compared with placebo. 9 The most common adverse events in ADVANCE were FLSs and ISRs.…”
Section: Responder Demographicsmentioning
confidence: 99%
“…Several similar preparations have been marketed since, namely intramuscular IFN1βa (Avonex: Biogen, Cambridge, MA) [4], subcutaneous IFN-1βa (Rebif: Merck, Darmstadt, Germany) [5], and, more recently, pegylated IFN-1βa (pegIFN-1βa; Plegridy: Biogen, Cambridge, MA) [6]. They differ mainly in terms of application route and frequency (s.c. vs i.m.…”
Section: Ifn-βmentioning
confidence: 99%