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审核状态: Project audit state: |
通过审核 Successful |
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注册号: Registration number: |
ChiCTR-TRC-13003259 |
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最近更新日期: Date of Last Refreshed on: |
2016-02-08 21:17:44 |
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注册时间: Date of Registration: |
2013-04-07 00:00:00 |
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注册号状态: |
预注册 |
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Registration Status: |
Prospective registration |
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注册题目: |
多中心、随机、双盲、安慰剂和阳性对照试验评估苯烯莫德乳膏在轻、中度银屑病患者中的有效性和安全性 |
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Public title: |
Multi-centre, randomised, double-blind, placebo- and comparator-controlled trial on topically applied benvitimod cream in patients with psoriasis |
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注册题目简写: |
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English Acronym: |
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研究课题的正式科学名称: |
多中心、随机、双盲、安慰剂和阳性对照试验评估苯烯莫德乳膏在轻、中度银屑病患者中的有效性和安全性 |
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Scientific title: |
Multi-centre, randomised, double-blind, placebo- and comparator-controlled trial on topically applied benvitimod cream in patients with psoriasis |
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研究课题代号(代码): Study subject ID: |
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在二级注册机构或其它机构的注册号: The registration number of the Partner Registry or other register: |
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申请注册联系人: |
陈庚辉 |
研究负责人: |
张建中 |
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Applicant: |
Genhui Chen |
Study leader: |
Zhang jian-zhong |
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申请注册联系人电话: Applicant telephone: |
+86 13916173094 |
研究负责人电话:
Study leader's |
+86 10 88325471 |
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申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
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申请注册联系人电子邮件: Applicant E-mail: |
genhui@sfu.ca |
研究负责人电子邮件: Study leader's E-mail: |
rmzjz@126.com |
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申请单位网址(自愿提供): Applicant website(voluntary supply): |
研究负责人网址(自愿提供): Study leader's website(voluntary supply): |
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申请注册联系人通讯地址: |
北京市朝阳区东三环北路3号幸福大厦B座1628室 |
研究负责人通讯地址: |
北京市朝阳区东三环北路3号幸福大厦B座1628室 |
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Applicant address: |
Room1628, Block B Lucky Tower, 3 North Dongsanhuan Road, Chaoyang District, Beijing, China |
Study leader's address: |
11 South Xizhimen Street, Beijing, China |
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申请注册联系人邮政编码: Applicant postcode: |
100027 |
研究负责人邮政编码: Study leader's postcode: |
100044 |
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申请人所在单位: |
北京文丰天济医药科技有限公司 |
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Applicant's institution: |
Beijing Wenfeng Tianji Pharmaceutical Technology |
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研究负责人所在单位: |
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Affiliation of the Leader: |
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是否获伦理委员会批准: |
是 |
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Approved by ethic committee: |
Yes |
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伦理委员会批件文号: Approved No. of ethic committee: |
[2012]院伦审药临字第(07)号 |
伦理委员会批件附件: Approved file of Ethical Committee: |
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批准本研究的伦理委员会名称: |
北京大学人民医院伦理委员 |
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Name of the ethic committee: |
Ethics Committee of People's Hospital of Peking University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2012-11-07 00:00:00 | ||
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伦理委员会联系人: |
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Contact Name of the ethic committee: |
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伦理委员会联系地址: |
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Contact Address of the ethic committee: |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
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研究实施负责(组长)单位: |
北京大学人民医院 |
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Primary sponsor: |
People's Hospital of Peking University |
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研究实施负责(组长)单位地址: |
北京市西城区西直门南大街11号 |
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Primary sponsor's address: |
11 South Xizhimen Street, Xicheng District, Beijing, China |
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试验主办单位(项目批准或申办者): Secondary sponsor: |
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经费或物资来源: |
北京文丰天济医药科技有限公司 |
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Source(s) of funding: |
Beijing Wenfeng Tianji Pharmaceutical Technology Co., Ltd. |
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研究疾病: |
寻常型银屑病 |
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Target disease: |
Plaque psoriasis |
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研究疾病代码: |
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Target disease code: |
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研究类型: |
干预性研究 |
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Study type: |
Interventional study |
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研究所处阶段: |
III期临床试验 | ||||||||||||||||||||||||||||||||||||||||||||
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Study phase: |
3 |
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研究设计: |
随机平行对照 |
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Study design: |
Parallel |
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研究目的: |
评价苯烯莫德乳膏治疗轻、中度银屑病的有效性和安全性 |
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Objectives of Study: |
To evaluate the efficacy and the safety of topically applied benvitimod cream in patients with psoriasis. |
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药物成份或治疗方案详述: |
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Description for medicine or protocol of treatment in detail: |
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纳入标准: |
1.18~65周岁,稳定寻常型屑病患者;男女不限; 2.皮损面积不超过其身体总表面积的10%; 3.研究者总体评价(PGA)大于2;4. 观察靶部位皮损直径不小于2cm;5、既往无心、肝、肾、消化道、神经系统、精神异常及代谢异常疾病等;6.未怀孕且试验期间不计划怀孕的妇女;7.充分了解试验内容与可能出现的不良反应后,受试者自愿参加试验,已签署知情同意书。 |
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Inclusion criteria |
1. Male and female patients with plaque psoriasis aged 18 to 65 years; |
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排除标准: |
1.有严重中枢神经系统、心血管系统、肾脏、肝脏、消化道、呼吸系统、代谢及骨骼肌肉系统疾病;2.肝功能(LT或AST)大于正常值上限2倍,或肾功能血清肌酐高于正常值上限;3.目前诊断为非寻常型银屑病(如红斑型,点滴型和关节型银屑病),及进展期寻常型银屑病;由药物引起的银屑病; 寻常型银屑病面积大于体表面积10%者;4.掌跖部位银屑病;5. 妊娠期、哺乳期妇女,或计划怀孕的妇女;6.已知对研究药物的活性成分或辅料过敏;7.在试验开始前三个月内参加了任何其他药物的临床研究;8.酒精依赖者;9. 经常使用中草药或镇静剂、安眠药、安定剂及其他成瘾性药物者;10. 患有其他可能干扰银屑病临床评估和/或给患者带来危险的皮肤疾病,或有除银屑病外的其他严重皮肤病史; 11.基线访视之前36周内接受过已知可影响银屑病的系统性生物制剂治疗(如阿法赛特),或既往参加过任何银屑病生物制剂临床试验者;12.基线访视之前4周内接受过紫外线光疗、光化学治疗或系统性银屑病治疗(比如系统性皮质激素,甲氨蝶呤,维甲酸或环孢素等); 13.基线访视之前2周内接受过局部抗银屑病治疗(包括局部使用皮质激素和维生素D类似物);14.受试者可能因为其他原因而不能完成本研究,或研究者认为不适宜参加本研究者。 |
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Exclusion criteria: |
1. Other concomitant serious illness or medical condition (e.g., human immunodeficiency virus, renal insufficiency, clinically significant abnormal laboratory values) that could put a patient at risk during the study; |
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研究实施时间: Study execute time: |
从 From 2013-03-01 00:00:00至 To 2014-09-21 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2013-04-20 00:00:00 至 To 2014-09-21 00:00:00 |
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干预措施: Interventions: |
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研究实施地点: Countries of recruitment and research settings: |
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测量指标: Outcomes: |
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采集人体标本:
Collecting sample(s)
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征募研究对象情况: Recruiting status: |
正在进行 Recruiting |
年龄范围: Participant age: |
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性别: |
男女均可 |
Gender: |
Both |
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随机方法(请说明由何人用什么方法产生随机序列): |
计算机软件 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
computer generation |
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是否公开试验完成后的统计结果: Calculated Results after the Study Completed public access: |
不公开/Private |
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盲法: |
双盲 |
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Blinding: |
double-blind |
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是否共享原始数据: IPD sharing |
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共享原始数据的方式(说明:请填入公开原始数据日期和方式,如采用网络平台,需填该网络平台名称和网址): |
北京文丰天济医药科技有限公司 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Beijing Wenfeng Tianji Pharmaceutical Technology Co., Ltd. |
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数据采集和管理(说明:数据采集和管理由两部分组成,一为病例记录表(Case Record Form, CRF),二为电子采集和管理系统(Electronic Data Capture, EDC),如ResMan即为一种基于互联网的EDC: |
方恩医药发展有限公司 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
FOUNTAIN MEDICAL DEVELOPMENT LTD |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |