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231226s2023 xx |||||o 00| ||eng c |
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|a 10.1016/j.clim.2023.109749
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|a DE-627
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|a eng
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|a Zhang, Xuan
|e verfasserin
|4 aut
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|a Efficacy and safety of tripterygium wilfordii Hook F plus TNF inhibitor for active rheumatoid arthritis
|b A multicentre, randomized, double-blind, triple-dummy controlled trial
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|c 2023
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|a Text
|b txt
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|a ƒaComputermedien
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|a ƒa Online-Ressource
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|a Date Revised 28.09.2023
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|a published: Print-Electronic
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|a ClinicalTrials.gov: NCT03589833
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|a Citation Status Publisher
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|a Copyright © 2023. Published by Elsevier Inc.
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|a An investigator-initiated, multicentre, randomized, double-blind, triple-dummy, controlled trial was conducted at 14 tertiary rheumatology centers in China to evaluate the efficacy and safety of Tripterygium wilfordii Hook F (TwHF) with recombinant human TNF receptor IgGFc fusion protein (rhTNFR-Fc) in active Rheumatoid Arthritis (RA). Primary endpoint was the proportion of patients achieved a 50% improvement of American College of Rheumatology criteria (ACR50) in TwHF+rhTNFR-Fc vs. methotrexate (MTX) group at week 12. ACR50 was achieved in 57.1% (72/126), 41.3% (52/126), 23.0% (29/126), and 26.2% (33/126) patients receiving TwHF+rhTNFR-Fc, MTX + rhTNFR-Fc, TwHF and MTX monotherapy, respectively, at week 12 (TwHF+rhTNFR-Fc vs. other three groups, all p < 0.05). No statistical difference in serious adverse events or adverse events leading to discontinuation of study across all groups was documented. TwHF+rhTNFR-Fc was superior to MTX for active RA, and was more effective than MTX + rhTNFR-Fc on ACR50, with a similar safety profile. Trial registration:ClinicalTrials.govNCT03589833
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|a Journal Article
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|a Rheumatoid arthritis
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|a TNF receptor IgGFc fusion protein
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|a Tripterygium wilfordii Hook F
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|a Yang, Huaxia
|e verfasserin
|4 aut
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|a Zuo, Xiaoxia
|e verfasserin
|4 aut
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|a Wu, Lijun
|e verfasserin
|4 aut
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|a Peng, Jiangyun
|e verfasserin
|4 aut
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|a Li, Zhenbin
|e verfasserin
|4 aut
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|a Li, Hongbin
|e verfasserin
|4 aut
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|a Ji, Wei
|e verfasserin
|4 aut
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|a Zhang, Liyun
|e verfasserin
|4 aut
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|a Li, Xiaomei
|e verfasserin
|4 aut
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|a Dai, Lie
|e verfasserin
|4 aut
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|a Lu, Liangjing
|e verfasserin
|4 aut
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|a Yang, Niansheng
|e verfasserin
|4 aut
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|a Wei, Wei
|e verfasserin
|4 aut
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|a Shuai, Zongwen
|e verfasserin
|4 aut
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|a Jiang, Ying
|e verfasserin
|4 aut
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|a Liu, Yudong
|e verfasserin
|4 aut
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|a Lipsky, Peter E
|e verfasserin
|4 aut
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|a Chen, Hua
|e verfasserin
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|a YISTAR study group
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|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 255(2023) vom: 30. Okt., Seite 109749
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|g volume:255
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|g month:10
|g pages:109749
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|u http://dx.doi.org/10.1016/j.clim.2023.109749
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