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Adalimumab for induction of clinical remission in moderately to severely active ulcerative colitis: results of a randomised controlled trial

医学 阿达木单抗 溃疡性结肠炎 安慰剂 内科学 临床终点 临床试验 胃肠病学 外科 意向治疗分析 随机对照试验 不利影响 回廊的 肿瘤坏死因子α 病理 替代医学 疾病
作者
Walter Reinisch,William J. Sandborn,Daniël W. Hommes,G. D’Haens,Stephen B. Hanauer,Stefanie Schreiber,Remo Panaccione,Richard N. Fedorak,M. B. Tighe,B Huang,Wendy Kampman,A. Lazar,Roopal Thakkar
出处
期刊:Gut [BMJ]
卷期号:60 (6): 780-787 被引量:845
标识
DOI:10.1136/gut.2010.221127
摘要

Objective

The aim of this study was to assess the efficacy and safety of adalimumab (ADA), a recombinant human monoclonal antibody against tumour necrosis factor α (TNF), for the induction of clinical remission in anti-TNF naïve patients with moderately to severely active ulcerative colitis.

Methods

This 8-week, multicentre, randomised, double-blind, placebo-controlled study (NCT00385736), conducted at 94 centres in North America and Europe, enrolled ambulatory adult patients with Mayo score of ≥6 points and endoscopic subscore of ≥2 points despite treatment with corticosteroids and/or immunosuppressants. Under the original study protocol, 186 patients were randomised (1:1) to subcutaneous treatment with ADA160/80 (160 mg at week 0, 80 mg at week 2, 40 mg at weeks 4 and 6) or placebo. Subsequently, at the request of European regulatory authorities, the protocol was amended to include a second induction group (ADA80/40: 80 mg at week 0, 40 mg at weeks 2, 4 and 6). The primary efficacy endpoint was clinical remission (Mayo score ≤2 with no individual subscore >1) at week 8, assessed in 390 patients randomised (1:1:1) to ADA160/80, ADA80/40, or placebo. Safety was assessed in all enrolled patients. Patients, study site personnel, investigators, and the sponsor were blinded to treatment assignment.

Results

At week 8, 18.5% of patients in the ADA160/80 group (p=0.031 vs placebo) and 10.0% in the ADA80/40 group (p=0.833 vs placebo) were in remission, compared with 9.2% in the placebo group. Serious adverse events occurred in 7.6%, 3.8% and 4.0% of patients in the placebo, ADA80/40, and ADA160/80 groups, respectively. There were two malignancies in the placebo group, none in the ADA groups. There were no cases of tuberculosis and no deaths.

Conclusions

ADA160/80 was safe and effective for induction of clinical remission in patients with moderately to severely active ulcerative colitis failing treatment with corticosteroids and/or immunosuppressants.

Clinical trial

NCT00385736.
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