This study evaluated the efficacy of a new formulation of subcutaneous (sc) interferon (IFN)-beta1a in relapsing-remitting multiple sclerosis (RRMS). Patients (n = 180) were randomized (2 : 1) to IFN-beta1a or placebo for 16 weeks; all patients then received IFN-beta1a for 24 weeks. Monthly brain MRI was performed. At week 16, the mean number of combined unique active (CUA) lesions was lower with IFN-beta1a than with placebo (p < 0.001; 69% fewer lesions). The mean cumulative number of CUA lesions was already lower with IFN-beta1a by week 4 (post hoc analysis; p = 0.015). The new formulation of sc IFN-beta1a has rapid beneficial effects on MRI outcomes in RRMS
The objective of this study was to assess the effects of subcutaneous (sc) interferon beta-1a (IFNbe...
Objective: To conduct systematic long-term follow-up (LTFU) of patients in the Prevention of Relapse...
The effect of interferon (IFN) beta-1a (44 and 22 mg subcutaneously [sc] three times weekly [tiw]) o...
This study evaluated the efficacy of a new formulation of subcutaneous (sc) interferon (IFN)-beta1a ...
BACKGROUND: The IMPROVE study demonstrated that the fetal bovine serum (FBS)- and human serum album...
BACKGROUND: The IMPROVE study demonstrated that the fetal bovine serum (FBS)- and human serum albu...
BACKGROUND: Previous trials of interferon beta in multiple sclerosis (MS) have shown efficacy, but t...
AIM: The REbif FLEXible dosing in early MS (REFLEX) study compared several brain MRI outcomes in pat...
Abstract Background In the PRISMS study, interferon beta-1a subcutaneously (IFN β-1a SC) reduced cli...
Objective: To explore the effects of exposure to subcutaneous (sc) interferon (IFN) beta-1a on effic...
The objective of this study was to assess the effects of subcutaneous (sc) interferon beta-1a (IFN b...
The REFLEX study (NCT00404352) established that subcutaneous (sc) interferon (IFN) beta-1a reduced t...
The objective of this study was to assess the effects of subcutaneous (sc) interferon beta-1a (IFNbe...
Objective: To conduct systematic long-term follow-up (LTFU) of patients in the Prevention of Relapse...
The effect of interferon (IFN) beta-1a (44 and 22 mg subcutaneously [sc] three times weekly [tiw]) o...
This study evaluated the efficacy of a new formulation of subcutaneous (sc) interferon (IFN)-beta1a ...
BACKGROUND: The IMPROVE study demonstrated that the fetal bovine serum (FBS)- and human serum album...
BACKGROUND: The IMPROVE study demonstrated that the fetal bovine serum (FBS)- and human serum albu...
BACKGROUND: Previous trials of interferon beta in multiple sclerosis (MS) have shown efficacy, but t...
AIM: The REbif FLEXible dosing in early MS (REFLEX) study compared several brain MRI outcomes in pat...
Abstract Background In the PRISMS study, interferon beta-1a subcutaneously (IFN β-1a SC) reduced cli...
Objective: To explore the effects of exposure to subcutaneous (sc) interferon (IFN) beta-1a on effic...
The objective of this study was to assess the effects of subcutaneous (sc) interferon beta-1a (IFN b...
The REFLEX study (NCT00404352) established that subcutaneous (sc) interferon (IFN) beta-1a reduced t...
The objective of this study was to assess the effects of subcutaneous (sc) interferon beta-1a (IFNbe...
Objective: To conduct systematic long-term follow-up (LTFU) of patients in the Prevention of Relapse...
The effect of interferon (IFN) beta-1a (44 and 22 mg subcutaneously [sc] three times weekly [tiw]) o...