EUCTR2004-004184-29-GB进行中(未招募)1 期
A phase III, randomised, multi-centre, double blind, parallel group, active comparator study to compare the efficacy and safety of SPD476 (mesalazine) 2.4g/day once daily (qd) versus Asacol® 1.6g/day twice daily (BID) in the maintenance of remission in patients with ulcerative colitis. - NA
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 入组人数
- 826
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
入选标准
- •Adults (18 years or older) male or female subjects. Females must be post menopausal, surgically or biologically sterile, or with negative pregnancy test at screening and on adequate contraception.
- •Subjects with previous diagnosis of ulcerative colitis confirmed by histology, considered in remission for 30 days or more, with endoscopy score less than or equal to 1 and a combined symptom score (rectal bleeding and stool frequency) of less than or equal to 1.
- •Subjects should have been on a stable dose of 5-aminosalicylic acid of upto 2.4g/day, for at least 30 days prior to baseline; have had at least 1 acute episode of ulcerative colitis in the past 12 months and at least 2 acute episodes in their medical history.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Subjects with proctitis only at most recent relapse (extent of inflammation less than 15 cm from anus), previous resective colonic surgery, or Crohn’s disease.
- •The use of systemic or rectal steroids within 30 days, immunosuppressants within 6 weeks, antibiotics within 2 weeks, anti-TNF antibody therapy within 12 weeks, repeated use of anti-inflammatory drugs within 7 days or the use of rectal 5-ASA prior to the baseline visit.
- •Subjects with hypersensitivity to salicylates, or known 5-ASA sensitive asthma.
- •Moderate/severe renal impairment (creatinine level >2mg/dL).
- •Subjects will be excluded if they require concurrent treatment with coumarin-type anticoagulants.
- •Subjects with conditions predisposing to the development of myo- or pericarditis.
研究者
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A phase III, randomised, multi-centre, double blind, parallel group, active comparator study to compare the efficacy and safety of SPD476 (mesalazine) 2.4g/day once daily (qd) versus Asacol® 1.6g/day twice daily (BID) in the maintenance of remission in patients with ulcerative colitis.lcerative colitisMedDRA version: 3.2Level: LLTClassification code 10045365EUCTR2004-004184-29-ESShire Pharmaceutical Development Ltd410
未知
不适用
A phase III, randomised, multi-centre, double blind, parallel group, active comparator study to compare the efficacy and safety of SPD476 (mesalazine) 2.4g/day once daily (qd) versus Asacol® 1.6g/day twice daily (BID) in the maintenance of remission in patients with ulcerative colitis. - NAPER-112-07Shire Pharmaceutical Development Ltd.,
进行中(未招募)
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A phase III, randomised, multi-centre, double blind, parallel group, active comparator study to compare the efficacy and safety of SPD476 (mesalazine) 2.4g/day once daily (qd) versus Asacol® 1.6g/day twice daily (BID) in the maintenance of remission in patients with ulcerative colitis. - NAEUCTR2004-004184-29-DKShire Pharmaceutical Development Ltd830
进行中(未招募)
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A phase III, randomised, multi-centre, double blind, parallel group, active comparator study to compare the efficacy and safety of SPD476 (mesalazine) 2.4g/day once daily (qd) versus Asacol® 1.6g/day twice daily (BID) in the maintenance of remission in patients with ulcerative colitis. - NAEUCTR2004-004184-29-SEShire Pharmaceutical Development Ltd830
进行中(未招募)
不适用
A phase III, randomised, multi-centre, double blind, parallel group, active comparator study to compare the efficacy and safety of SPD476 (mesalazine) 2.4g/day once daily (qd) versus Asacol® 1.6g/day twice daily (BID) in the maintenance of remission in patients with ulcerative colitis. - NAlcerative colitisEUCTR2004-004184-29-DEShire Pharmaceutical Development Ltd410
