Background: There is a lack of head-to-head studies comparing the efficacy of fingolimod (FIN) and natalizumab (NTZ) as second-line therapy for relapsing-remitting multiple sclerosis (RRMS).
Methods: Multicenter, observational study, in which, information of 388 patients randomly selected and treated with FIN or NTZ in routine clinical practice was retrospectively collected with the main objective of comparing the annualized relapse rate (ARR) over the first year, after FIN or NTZ treatment initiation.
Results: Mean ARR during the first year of treatment was 0.28 in FIN group and 0.12 in NTZ group (p = 0.0064); nevertheless, the difference between groups lost statistical significance when the propensity score analysis was performed. Time to disability -progression was similar in both treatment groups (12.3 ± 6.7 months in FIN, and 12.8 ± 0.1 months in NTZ; p = 0.4654). Treatment persistence after the first year of treatment was higher in patients treated with FIN (95%) than in those treated with NTZ (84%; p = 0.0014).
Conclusions: After 12 months of treatment, both FIN and NTZ reduced the ARR, but ARR percent reduction was significantly higher with NTZ. Treatment persistence was higher in patients receiving FIN.
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http://dx.doi.org/10.1159/000505778 | DOI Listing |
Eur Neurol
November 2020
Novartis Farmacéutica S.A., Barcelona, Spain.
Background: There is a lack of head-to-head studies comparing the efficacy of fingolimod (FIN) and natalizumab (NTZ) as second-line therapy for relapsing-remitting multiple sclerosis (RRMS).
Methods: Multicenter, observational study, in which, information of 388 patients randomly selected and treated with FIN or NTZ in routine clinical practice was retrospectively collected with the main objective of comparing the annualized relapse rate (ARR) over the first year, after FIN or NTZ treatment initiation.
Results: Mean ARR during the first year of treatment was 0.
Angew Chem Int Ed Engl
January 2018
Department of Chemistry and Biochemistry, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA, 92093-0358, USA.
A series of enzymatic transformations, which generate visibly emissive isofunctional cofactors based on an isothiazolo[4,3-d]pyrimidine analogue of adenosine ( A), was developed. Nicotinamide adenylyl transferase condenses nicotinamide mononucleotide and ATP to yield N AD , which can be enzymatically phosphorylated by NAD kinase and ATP or ATP to the corresponding N ADP . The latter can be engaged in NADP-specific coupled enzymatic transformations involving conversion to N ADPH by glucose-6-phosphate dehydrogenase and reoxidation to N ADP by glutathione reductase.
View Article and Find Full Text PDFJ Clin Immunol
January 2018
Immunodeficiency Unit, Inflammation Center and Center for Rare Diseases, Children's Hospital, Helsinki University and Helsinki University Hospital, Helsinki, Finland.
J Med Econ
March 2017
b Biogen , Weston , MA , USA.
Background: The safety and efficacy of disease-modifying therapies (DMTs) for relapsing-remitting multiple sclerosis (RRMS) has been established; however, it is not clear which provides optimal value, given benefit-risk profiles and costs.
Aims: To compare the cost-effectiveness of current DMTs for patients with RRMS in the US.
Materials And Methods: A Markov model predicting RRMS course following initiation of a DMT was created comparing outcomes (e.
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