Comparing efficacy and side effects of a weekly intramuscular biogeneric/biosimilar interferon beta-1a with Avonex in relapsing remitting multiple sclerosis: A double blind randomized clinical trial

被引:13
|
作者
Nafissi, Shahriar [1 ]
Azimi, Amirreza [1 ]
Amini-Harandi, Ali [2 ]
Salami, Shiva [3 ]
Shahkarami, Mohammad Amir [3 ]
Heshmat, Ramin [4 ]
机构
[1] Univ Tehran Med Sci, Dept Neurol, Tehran, Iran
[2] Shahid Beheshti Univ Med Sci, Dept Neurol, Tehran, Iran
[3] CinnoVex Collaborating Study Grp, Tehran, Iran
[4] Univ Tehran Med Sci, Endocrinol & Metab Res Ctr, Tehran, Iran
关键词
Interferon; Multiple sclerosis; Efficacy; Expanded Disability Status Scales; Clinical trials; Neutralizing antibodies; Biosimilarity; NEUTRALIZING ANTIBODIES; MAGNETIC-RESONANCE; THERAPY; IMPACT;
D O I
10.1016/j.clineuro.2012.02.039
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: We compared the efficacy and safety of two biosimilar forms of interferon beta-la in the treatment of multiple sclerosis: Avonex (Biogen Idec, USA) and CinnoVex (CinnaGen, Iran). Methods: In a double blind randomized clinical trial study 84 patients with relapsing remitting multiple sclerosis (RRMS) with Expanded Disability Status Scale (EDSS) score of 0-5.5 were randomly allocated to two groups of 42 subjects. Results: Twenty-four patients lost to follow-up. Finally, 31 patients (mean +/- SD of age =33.7 +/- 7.0:7 males and 24 females) in the Avonex and 29 patients (mean +/- SD of age = 32.2 +/- 9.2; 8 males and 21 females) in the CinnoVex group completed full 24 months of study period. Decrease in EDSS was 1.05 +/- 0.24, p = 0.62 in the Avonex and 0.16 +/- 0.88, p = 1.0 in the CinnoVex group after 12 months and 0.27 +/- 1.05, p = 0.46 in the Avonex and 0.16 +/- 1.06, p = 1.0 in the CinnoVex group after 24 months. There was no statistically significant difference in attack number between two groups (1.0 +/- 1.2 in Avonex and 1.2 +/- 1.3 in CinnoVex; p = 0.46). Volume of T2-weighted lesions on MRI showed a progressive significant increase in the 12th month (28056 +/- 23693) in Avonex treated patients compared with first image (16353 +/- 11172) (p = 0.01). But number of gadolinium-enhancing lesions in CinnoVex showed statistically significant decrease after 12 months (0.08 +/- 0.28 vs. 1.00 +/- 1.22; p = 0.03). However, there were no significant differences between groups after 24 months. There were no significant differences between 2 groups regarding frequency and duration of most considerable side effects, as well. Neutralizing antibodies were not positive in any patients. Conclusion: CinnoVex can be used as a safe and effective alternative to Avonex in treatment of RRMS. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:986 / 989
页数:4
相关论文
共 50 条
  • [21] Intramuscular interferon beta-1a therapy in patients with relapsing-remitting multiple sclerosis: a 15-year follow-up study
    Bermel, R. A.
    Weinstock-Guttman, B.
    Bourdette, D.
    Foulds, P.
    You, X.
    Rudick, R. A.
    MULTIPLE SCLEROSIS JOURNAL, 2010, 16 (05) : 588 - 596
  • [22] Effect of interferon beta-1a subcutaneously three times weekly on clinical and radiological measures and no evidence of disease activity status in patients with relapsing–remitting multiple sclerosis at year 1
    Anthony Traboulsee
    David K. B. Li
    Mark Cascione
    Juanzhi Fang
    Fernando Dangond
    Aaron Miller
    BMC Neurology, 18
  • [23] Efficacy of vitamin D3 as add-on therapy in patients with relapsing-remitting multiple sclerosis receiving subcutaneous interferon beta-1a: A Phase II, multicenter, double-blind, randomized, placebo-controlled trial
    Smolders, Joost
    Hupperts, Raymond
    Barkhof, Frederik
    Grimaldi, Luigi M. E.
    Holmoy, Trygve
    Killestein, Joep
    Rieckmann, Peter
    Schluep, Myriam
    Vieth, Reinhold
    Hostalek, Ulrike
    Ghazi-Visser, Lizette
    Beelke, Manolo
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2011, 311 (1-2) : 44 - 49
  • [24] Pharmacokinetics and pharmacodynamics of peginterferon beta-1a in patients with relapsing-remitting multiple sclerosis in the randomized ADVANCE study
    Hu, Xiao
    Cui, Yue
    White, Joleen
    Zhu, Ying
    Deykin, Aaron
    Nestorov, Ivan
    Hung, Serena
    BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2015, 79 (03) : 514 - 522
  • [25] Effect of interferon beta-1a subcutaneously three times weekly on clinical and radiological measures and no evidence of disease activity status in patients with relapsing-remitting multiple sclerosis at year 1
    Traboulsee, Anthony
    Li, David K. B.
    Cascione, Mark
    Fang, Juanzhi
    Dangond, Fernando
    Miller, Aaron
    BMC NEUROLOGY, 2018, 18
  • [26] Impact of daclizumab versus interferon beta-1a on patient-reported outcomes in relapsing-remitting multiple sclerosis
    Liu, Ying
    Vollmer, Timothy
    Havrdova, Eva
    Riester, Katherine
    Lee, Andrew
    Phillips, Glenn
    Wang, Ping
    Sabatella, Guido
    MULTIPLE SCLEROSIS AND RELATED DISORDERS, 2017, 11 : 18 - 24
  • [27] Effects of low dose methotrexate on relapsing-remitting multiple sclerosis in comparison to Interferon β-1α: A randomized controlled trial
    Ashtari, Fereshteh
    Savoj, Mohammad Reza
    JOURNAL OF RESEARCH IN MEDICAL SCIENCES, 2011, 16 (04): : 457 - 462
  • [28] Teriflunomide versus subcutaneous interferon beta-1a in patients with relapsing multiple sclerosis: a randomised, controlled phase 3 trial
    Vermersch, Patrick
    Czlonkowska, Anna
    Grimaldi, Luigi M. E.
    Confavreux, Christian
    Comi, Giancarlo
    Kappos, Ludwig
    Olsson, Tomas P.
    Benamor, Myriam
    Bauer, Deborah
    Truffinet, Philippe
    Church, Meg
    Miller, Aaron E.
    Wolinsky, Jerry S.
    Freedman, Mark S.
    O'Connor, Paul
    MULTIPLE SCLEROSIS JOURNAL, 2014, 20 (06) : 705 - 716
  • [29] Effect of peginterferon beta-1a on MRI measures and achieving no evidence of disease activity: results from a randomized controlled trial in relapsing-remitting multiple sclerosis
    Douglas L Arnold
    Peter A Calabresi
    Bernd C Kieseier
    Sarah I Sheikh
    Aaron Deykin
    Ying Zhu
    Shifang Liu
    Xiaojun You
    Bjoern Sperling
    Serena Hung
    BMC Neurology, 14
  • [30] Use of the FIM™ instrument in a trial of intramuscular interferon β-1a for disease progression in relapsing-remitting multiple sclerosis
    Granger, CV
    Wende, K
    Brownscheidle, CM
    AMERICAN JOURNAL OF PHYSICAL MEDICINE & REHABILITATION, 2003, 82 (06) : 427 - 436