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A 2-year observational study of patients with relapsing-remitting multiple sclerosis converting to glatiramer acetate from other disease-modifying therapies: the COPTIMIZE trial

Ziemssen, Tjalf (author)
Klinikum Carl Gustav Carus, Germany
Bajenaru, Ovidiu A. (author)
Carol Davila University of Medical and Pharm, Romania
Carra, Adriana (author)
Hospital Britanico Buenos Aires, Argentina
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de Klippel, Nina (author)
Virga Jessaziekenhuis, Belgium
de Sa, Joao C. (author)
Hospital Santa Mari, Belgium
Edland, Astrid (author)
Central Hospital Buskerud, Norway
Frederiksen, Jette L. (author)
University of Copenhagen, Denmark
Heinzlef, Olivier (author)
Hop Tenon, France
Karageorgiou, Klimentini E. (author)
Gen Hospital Athens, Greece
Lander Delgado, Rafael H. (author)
Landtblom, Anne-Marie (author)
Östergötlands Läns Landsting,Linköpings universitet,Avdelningen för neurovetenskap,Hälsouniversitetet,Centrum för medicinsk bildvetenskap och visualisering, CMIV,Neurologiska kliniken,Medicinska specialistkliniken,Department of Neurology and Department of Clinical and Experimental Medicine, University of Linköping, Linköping, Sweden
Macias Islas, Miguel A. (author)
Central University of Guadalajara, Mexico
Tubridy, Niall (author)
Dublin City University, Ireland
Gilgun-Sherki, Yossi (author)
Teva Pharmaceut Ind Ltd, Israel
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 (creator_code:org_t)
2014-08-14
2014
English.
In: Journal of Neurology. - : Springer Verlag (Germany). - 0340-5354 .- 1432-1459. ; 261:11, s. 2101-2111
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Studies suggest that patients with relapsing-remitting multiple sclerosis (RRMS) who do not benefit from other disease-modifying treatments (DMTs) may benefit from converting to glatiramer acetate (GA). COPTIMIZE was a 24-month observational study designed to assess the disease course of patients converting to GA 20 mg daily from another DMT. Eligible patients had converted to GA and had received prior DMT for 3-6 months, depending on the reasons for conversion. Patients were assessed at baseline and at 6, 12, 18, and 24 months. In total, 672 patients from 148 centers worldwide were included in the analysis. Change of therapy to GA was prompted primarily by lack of efficacy (53.6 %) or intolerable adverse events (AEs; 44.8 %). Over a 24-month period, 72.7 % of patients were relapse free. Mean annual relapse rate decreased from 0.86 [95 % confidence interval (CI) 0.81-0.91] before the change to 0.32 (95 % CI 0.26-0.40; p less than 0.0001) at last observation, while the progression of disability was halted, as the Kurtzke Expanded Disability Status Scale (EDSS) scores remained stable. Patients improved significantly (p less than 0.05) on measures of fatigue, quality of life, depression, and cognition; mobility scores remained stable. The results indicate that changing RRMS patients to GA is associated with positive treatment outcomes.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)

Keyword

Disease-modifying therapy; Glatiramer acetate; Multiple sclerosis; RRMS

Publication and Content Type

ref (subject category)
art (subject category)

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