EUCTR2004-000687-27-AT进行中(未招募)不适用
A 52 week open-label extension study to evaluate the safety and tolerability of licarbazepine 750-2500 mg/d in the treatment of manic episodes of bipolar I disorder
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 入组人数
- 215
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
- •successful completion of study CLIC477D2303
- •written informed consent provided prior to participation in the extension study
- •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
- •premature discontinuation from study CLIC477D2303
- •failure to comply with the study CLIC477D2303 protocol
研究者
相似试验
进行中(未招募)
不适用
A 52-week open-label extension study to evaluate the safety and tolerability of licarbazepine 750-2000 mg/d in the treatment of manic episodes of bipolar I disorderBipolar I disorder, manic and mixed episodesEUCTR2004-000686-35-FIovartis Pharma AG215
进行中(未招募)
不适用
A 52-week open label extension study to evaluate the safety and tolerability of AIN457 (anti IL-17 monoclonal antibody) in patients with moderate to severe Crohn’sdisease - A2202E1EUCTR2009-011621-14-ATovartis Pharma Services AG72
进行中(未招募)
不适用
A 52-week open label extension study to evaluate the safety and tolerability of AIN457 (anti IL-17 monoclonal antibody) in patients with moderate to severe Crohn’sdisease - n/aModerate to severe Crohn's disease (CDAI = 220 and =450)MedDRA version: 9.1Level: LLTClassification code 10011401Term: Crohn's diseaseEUCTR2009-011621-14-DEovartis Pharma Services AG72
进行中(未招募)
不适用
A 76-week open-label extension study to evaluate the efficacy, safety and tolerability of ACZ885 (anti-interleukin-1ß monoclonal antibody) in patients with active rheumatoid arthritis - not availableMedDRA version: 8.1Level: LLTClassification code 10039073Term: Rheumatoid arthritisRheumatoid ArthritisEUCTR2007-000491-16-BEovartis Pharma Services AG
进行中(未招募)
不适用
A 76-week open-label extension study to evaluate the efficacy, safety and tolerability of ACZ885 (anti-interleukin-1ß monoclonal antibody) in patients with active rheumatoid arthritis - not availableRheumatoid ArthritisEUCTR2007-000491-16-DEovartis Pharma Services AG200
