Efficacy and safety of ozanimod in multiple sclerosis: Dose-blinded extension of a randomized phase II study
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu klinické zkoušky, fáze II, časopisecké články, multicentrická studie, randomizované kontrolované studie, práce podpořená grantem
PubMed
30043658
PubMed Central
PMC6681431
DOI
10.1177/1352458518789884
Knihovny.cz E-zdroje
- Klíčová slova
- Clinical trial, MRI, T2 lesions, disease-modifying therapies, multiple sclerosis, relapsing/remitting,
- MeSH
- dospělí MeSH
- dvojitá slepá metoda MeSH
- hodnocení výsledků zdravotní péče * MeSH
- indany aplikace a dávkování škodlivé účinky farmakologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- magnetická rezonanční tomografie MeSH
- mladiství MeSH
- mladý dospělý MeSH
- modulátory receptorů sfingosin-1-fosfátu aplikace a dávkování škodlivé účinky farmakologie MeSH
- oxadiazoly aplikace a dávkování škodlivé účinky farmakologie MeSH
- relabující-remitující roztroušená skleróza diagnostické zobrazování farmakoterapie patofyziologie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladiství MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky, fáze II MeSH
- multicentrická studie MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
- Názvy látek
- indany MeSH
- modulátory receptorů sfingosin-1-fosfátu MeSH
- oxadiazoly MeSH
- ozanimod MeSH Prohlížeč
BACKGROUND: Ozanimod, an oral immunomodulator, selectively targets sphingosine 1-phosphate receptors 1 and 5. OBJECTIVE: Evaluate efficacy, safety, and tolerability of ozanimod in relapsing multiple sclerosis. METHODS: In the RADIANCE Part A phase II study (NCT01628393), participants with relapsing multiple sclerosis were randomized (1:1:1) to once-daily ozanimod hydrochloride (0.5 or 1 mg) or placebo. After 24 weeks, participants could enter a 2-year, dose-blinded extension. Ozanimod-treated participants continued their assigned dose; placebo participants were re-randomized (1:1) to ozanimod hydrochloride 0.5 or 1 mg (equivalent to ozanimod 0.46 and 0.92 mg). RESULTS: A total of 223 (89.6%) of the 249 participants completed the blinded extension. At 2 years of the extension, the percentage of participants who were gadolinium-enhancing lesion-free ranged from 86.5% to 94.6%. Unadjusted annualized relapse rate during the blinded extension (week 24-end of treatment) was 0.32 for ozanimod hydrochloride 0.5 mg → ozanimod hydrochloride 0.5 mg, 0.18 for ozanimod hydrochloride 1 mg → ozanimod hydrochloride 1 mg, 0.30 for placebo → ozanimod hydrochloride 0.5 mg, and 0.18 for placebo → ozanimod hydrochloride 1 mg. No second-degree or higher atrioventricular block or serious opportunistic infection was reported. CONCLUSION: Ozanimod demonstrated sustained efficacy in participants continuing treatment up to 2 years and reached similar efficacy in participants who switched from placebo; no unexpected safety signals emerged.
Biostatistics Celgene Corporation San Diego CA USA
Center for Neurology Łódź Poland
Clinical Development Celgene Corporation San Diego CA USA
Department of Neurology Medical Faculty Heinrich Heine University Düsseldorf Germany
Mellen Center for MS Treatment and Research Cleveland Clinic Cleveland OH USA
NeuroRx Research and Montreal Neurological Institute McGill University Montreal QC Canada
Zobrazit více v PubMed
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