-
1
-
-
77950332103
-
Rituximab: mechanism of action
-
COI: 1:CAS:528:DC%2BC3cXlslemtLc%3D
-
Weiner GJ. Rituximab: mechanism of action. Sem Hematol. 2010;47:115–23.
-
(2010)
Sem Hematol
, vol.47
, pp. 115-123
-
-
Weiner, G.J.1
-
2
-
-
33646362290
-
B-cell targeting in rheumatoid arthritis and other autoimmune diseases
-
COI: 1:CAS:528:DC%2BD28XjslOhu7g%3D, PID: 16622478
-
Edwards JCW, Cambridge G. B-cell targeting in rheumatoid arthritis and other autoimmune diseases. Nat Rev Immunol. 2006;6:394–403.
-
(2006)
Nat Rev Immunol
, vol.6
, pp. 394-403
-
-
Edwards, J.C.W.1
Cambridge, G.2
-
4
-
-
84857233786
-
Sustained inhibition of progressive joint damage with rituximab plus methotrexate in early active rheumatoid arthritis: 2-year results from the randomised controlled trial IMAGE
-
COI: 1:CAS:528:DC%2BC38Xlt1Wlsr8%3D, PID: 22012969
-
Tak PP, Rigby W, Rubbert-Roth A, et al. Sustained inhibition of progressive joint damage with rituximab plus methotrexate in early active rheumatoid arthritis: 2-year results from the randomised controlled trial IMAGE. Ann Rheum Dis. 2012;71:351–7.
-
(2012)
Ann Rheum Dis
, vol.71
, pp. 351-357
-
-
Tak, P.P.1
Rigby, W.2
Rubbert-Roth, A.3
-
5
-
-
84956767541
-
2015 American College of Rheumatology guideline for the treatment of rheumatoid arthritis
-
PID: 26545940
-
Singh JA, Saag KG, Bridges SL Jr, et al. 2015 American College of Rheumatology guideline for the treatment of rheumatoid arthritis. Arthritis Rheumatol. 2016;68:1–26.
-
(2016)
Arthritis Rheumatol
, vol.68
, pp. 1-26
-
-
Singh, J.A.1
Saag, K.G.2
Bridges, S.L.3
-
6
-
-
77953696525
-
EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs
-
COI: 1:CAS:528:DC%2BC3cXos1GiurY%3D, PID: 20444750
-
Smolen JS, Landewe R, Breedveld FC, et al. EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs. Ann Rheum Dis. 2010;69:964–75.
-
(2010)
Ann Rheum Dis
, vol.69
, pp. 964-975
-
-
Smolen, J.S.1
Landewe, R.2
Breedveld, F.C.3
-
7
-
-
34247535331
-
Immune-mediated inflammatory diseases (IMIDs) and biologic therapy: a medical revolution
-
COI: 1:CAS:528:DC%2BD2sXlvFCgsr0%3D, PID: 17403952
-
Kuek A, Hazleman BL, Ostor AJ. Immune-mediated inflammatory diseases (IMIDs) and biologic therapy: a medical revolution. Postgrad Med J. 2007;83:251–60.
-
(2007)
Postgrad Med J
, vol.83
, pp. 251-260
-
-
Kuek, A.1
Hazleman, B.L.2
Ostor, A.J.3
-
8
-
-
85027169325
-
World Health Organization. Expert Committee on Biological Standardization: Geneva, 19 to
-
Accessed 14 Feb 2017
-
World Health Organization. Expert Committee on Biological Standardization: Geneva, 19 to 23 October 2009. Guidelines on evaluation of similar biotherapeutic products (SBPs). 2009. http://www.who.int/biologicals/areas/biological_therapeutics/BIOTHERAPEUTICS_FOR_WEB_22APRIL2010.pdf. Accessed 14 Feb 2017.
-
(2009)
Guidelines on evaluation of similar biotherapeutic products (SBPs)
, pp. 2009
-
-
-
9
-
-
85027113930
-
Committee for Medicinal Products for Human Use (CHMP). European Medicines Agency. Guideline on Similar Biological Medicine Products
-
Accessed 14 Feb 2017
-
Committee for Medicinal Products for Human Use (CHMP). European Medicines Agency. Guideline on Similar Biological Medicine Products. 23 October 2014. CHMP/437/04 Rev 1. 2014. http://www.ema.europa.eu/docs/en_GB/document_library/Scientific_guideline/2014/10/WC500176768.pdf. Accessed 14 Feb 2017.
-
(2014)
CHMP/437/04 Rev 1.
, pp. 2014
-
-
-
10
-
-
85027100427
-
Quality considerations in demonstrating biosimilarity of a therapeutic protein product to a reference product
-
US Department of Health and Human Services; Food and Drug Administration; Center for Drug Evaluation and Research (CDER); Center for Biologics Evaluation and Research (CBER) Accessed 14 Feb 2017
-
US Department of Health and Human Services; Food and Drug Administration; Center for Drug Evaluation and Research (CDER); Center for Biologics Evaluation and Research (CBER). Quality considerations in demonstrating biosimilarity of a therapeutic protein product to a reference product. Guidance for Industry. 2015. http://www.fda.gov/downloads/drugs/guidancecomplianceregulatoryinformation/guidances/ucm291134.pdf. Accessed 14 Feb 2017.
-
(2015)
Guidance for Industry
-
-
-
11
-
-
84987818368
-
A multicentre randomised controlled trial to compare the pharmacokinetics, efficacy and safety of CT-P10 and innovator rituximab in patients with rheumatoid arthritis
-
PID: 27624791
-
Yoo DH, Suh C, Shim SC, et al. A multicentre randomised controlled trial to compare the pharmacokinetics, efficacy and safety of CT-P10 and innovator rituximab in patients with rheumatoid arthritis. Ann Rheum Dis. 2017;76(3):566–70.
-
(2017)
Ann Rheum Dis
, vol.76
, Issue.3
, pp. 566-570
-
-
Yoo, D.H.1
Suh, C.2
Shim, S.C.3
-
12
-
-
85020577993
-
Efficacy and safety of rituximab biosimilar candidate (CT-P10) and innovator rituximab in patients with rheumatoid arthritis: results from phase I randomized controlled trial over 72 weeks [abstract]
-
Yoo DH, Suh C, Shim SC, et al. Efficacy and safety of rituximab biosimilar candidate (CT-P10) and innovator rituximab in patients with rheumatoid arthritis: results from phase I randomized controlled trial over 72 weeks [abstract]. Arthritis Rheumatol. 2015;67(Suppl 10):2449–52.
-
(2015)
Arthritis Rheumatol
, vol.67
, pp. 2449-2452
-
-
Yoo, D.H.1
Suh, C.2
Shim, S.C.3
-
14
-
-
0028815803
-
Modified disease activity scores that include twenty-eight-joint counts development and validation in a prospective longitudinal study of patients with rheumatoid arthritis
-
COI: 1:STN:280:DyaK2M7hvVeqtA%3D%3D, PID: 7818570
-
Prevoo MLL, van’t Hof MA, Kuper HH, et al. Modified disease activity scores that include twenty-eight-joint counts development and validation in a prospective longitudinal study of patients with rheumatoid arthritis. Arthritis Rheum. 1995;38:44–8.
-
(1995)
Arthritis Rheum
, vol.38
, pp. 44-48
-
-
Prevoo, M.L.L.1
van’t Hof, M.A.2
Kuper, H.H.3
-
15
-
-
0030068817
-
Development and validation of the European League Against Rheumatism response criteria for rheumatoid arthritis. Comparison with the preliminary American College of Rheumatology and the World Health Organization/International League Against Rheumatism Criteria
-
PID: 8546736
-
van Gestel AM, Prevoo ML, van’t Hof MA, et al. Development and validation of the European League Against Rheumatism response criteria for rheumatoid arthritis. Comparison with the preliminary American College of Rheumatology and the World Health Organization/International League Against Rheumatism Criteria. Arthritis Rheum. 1996;39:34–40.
-
(1996)
Arthritis Rheum
, vol.39
, pp. 34-40
-
-
van Gestel, A.M.1
Prevoo, M.L.2
van’t Hof, M.A.3
-
16
-
-
37149035531
-
Safety and efficacy of additional courses of rituximab in patients with active rheumatoid arthritis: an open-label extension analysis
-
COI: 1:CAS:528:DC%2BD1cXnt1Olsg%3D%3D, PID: 18050221
-
Keystone E, Fleischmann R, Emery P, et al. Safety and efficacy of additional courses of rituximab in patients with active rheumatoid arthritis: an open-label extension analysis. Arthritis Rheum. 2007;56:3896–908.
-
(2007)
Arthritis Rheum
, vol.56
, pp. 3896-3908
-
-
Keystone, E.1
Fleischmann, R.2
Emery, P.3
-
17
-
-
84870330803
-
Multiple courses of rituximab produce sustained clinical and radiographic efficacy and safety in patients with rheumatoid arthritis and an inadequate response to 1 or more tumor necrosis factor inhibitors: 5-year data from the REFLEX study
-
COI: 1:CAS:528:DC%2BC3sXhslWgsLY%3D, PID: 23027887
-
Keystone EC, Cohen SB, Emery P, et al. Multiple courses of rituximab produce sustained clinical and radiographic efficacy and safety in patients with rheumatoid arthritis and an inadequate response to 1 or more tumor necrosis factor inhibitors: 5-year data from the REFLEX study. J Rheumatol. 2012;39:2238–46.
-
(2012)
J Rheumatol
, vol.39
, pp. 2238-2246
-
-
Keystone, E.C.1
Cohen, S.B.2
Emery, P.3
-
18
-
-
77949673916
-
Long-term safety of patients receiving rituximab in rheumatoid arthritis clinical trials
-
PID: 20110520
-
Van Vollenhoven RF, Emery P, Bingham CO, et al. Long-term safety of patients receiving rituximab in rheumatoid arthritis clinical trials. J Rheumatol. 2010;37:558–67.
-
(2010)
J Rheumatol
, vol.37
, pp. 558-567
-
-
Van Vollenhoven, R.F.1
Emery, P.2
Bingham, C.O.3
-
19
-
-
84899132159
-
Epoetin zeta in the management of anemia associated with chronic kidney disease, differential pharmacology and clinical utility
-
PID: 24790409
-
Davis-Ajami ML, Wu J, Downton K, et al. Epoetin zeta in the management of anemia associated with chronic kidney disease, differential pharmacology and clinical utility. Biologics. 2014;8:155–67.
-
(2014)
Biologics
, vol.8
, pp. 155-167
-
-
Davis-Ajami, M.L.1
Wu, J.2
Downton, K.3
-
20
-
-
84918518708
-
Switching from originator to biosimilar human growth hormone using dialogue teamwork: single-center experience from Sweden
-
PID: 24392303
-
Flodmark CE, Lilja K, Woehling H, et al. Switching from originator to biosimilar human growth hormone using dialogue teamwork: single-center experience from Sweden. Biol Ther. 2013;3:35–43.
-
(2013)
Biol Ther
, vol.3
, pp. 35-43
-
-
Flodmark, C.E.1
Lilja, K.2
Woehling, H.3
-
21
-
-
41149131276
-
Comparison of the therapeutic effects of epoetin zeta to epoetin alfa in the maintenance phase of renal anaemia treatment
-
COI: 1:CAS:528:DC%2BD1cXkvValtb4%3D, PID: 18208642
-
Wizemann V, Rutkowski B, Baldamus C, et al. Comparison of the therapeutic effects of epoetin zeta to epoetin alfa in the maintenance phase of renal anaemia treatment. Curr Med Res Opin. 2008;24:625–37.
-
(2008)
Curr Med Res Opin
, vol.24
, pp. 625-637
-
-
Wizemann, V.1
Rutkowski, B.2
Baldamus, C.3
-
22
-
-
84965014483
-
Efficacy and safety of switching from reference infliximab to CT-P13 compared with maintenance of CT-P13 in ankylosing spondylitis: 102-week data from the PLANETAS extension study
-
PID: 27117698
-
Park W, Yoo DH, Miranda P, et al. Efficacy and safety of switching from reference infliximab to CT-P13 compared with maintenance of CT-P13 in ankylosing spondylitis: 102-week data from the PLANETAS extension study. Ann Rheum Dis. 2016;76:346–54.
-
(2016)
Ann Rheum Dis
, vol.76
, pp. 346-354
-
-
Park, W.1
Yoo, D.H.2
Miranda, P.3
-
23
-
-
84966417145
-
Efficacy and safety of CT-P13 (biosimilar infliximab) in patients with rheumatoid arthritis: comparison between switching from reference infliximab to CT-P13 and continuing CT-P13 in the PLANETRA extension study
-
PID: 27130908
-
Yoo DH, Prodanovic N, Jaworski J, et al. Efficacy and safety of CT-P13 (biosimilar infliximab) in patients with rheumatoid arthritis: comparison between switching from reference infliximab to CT-P13 and continuing CT-P13 in the PLANETRA extension study. Ann Rheum Dis. 2016;76:355–63.
-
(2016)
Ann Rheum Dis
, vol.76
, pp. 355-363
-
-
Yoo, D.H.1
Prodanovic, N.2
Jaworski, J.3
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