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注册号: Registration number: |
ChiCTR2500113402 |
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最近更新日期: Date of Last Refreshed on: |
2025-11-27 16:47:14 |
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注册时间: Date of Registration: |
2025-11-27 00:00:00 |
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注册号状态: |
补注册 |
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Registration Status: |
Retrospective registration |
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注册题目: |
立他司特滴眼液用于治疗干眼症的有效性和安全性的多中心、随机、双盲、安慰剂对照的 III 期临床试验 |
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Public title: |
A multicenter, randomized, double-blind, placebo-controlled phase III clinical trial of the efficacy and safety of Lifitegrast Ophthalmic Solution for the treatment of dry eye disease |
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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: |
立他司特滴眼液用于治疗干眼症的有效性和安全性的多中心、随机、双盲、安慰剂对照的 III 期临床试验 |
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Scientific title: |
A multicenter, randomized, double-blind, placebo-controlled phase III clinical trial of the efficacy and safety of Lifitegrast Ophthalmic Solution for the treatment of dry eye disease |
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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: |
宋林 |
研究负责人: |
孙兴怀 |
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Applicant: |
Lin song |
Study leader: |
Xinghuai Sun |
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申请注册联系人电话: Applicant telephone: |
+86 189 8218 2468 |
研究负责人电话:
Study leader's |
+86 189 1776 1818 |
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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: |
songlin@cnkh.com |
研究负责人电子邮件: Study leader's E-mail: |
xhsun@shmu.edu.cn |
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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: |
四川省成都市金牛区蜀西路108号 |
研究负责人通讯地址: |
上海市-上海市-徐汇区汾阳路83号 |
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Applicant address: |
108 Shuxi Road, Jinniu District, Chengdu, Sichuan, China |
Study leader's address: |
No. 83, Fenyang Road, Xuhui District, Shanghai |
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申请注册联系人邮政编码: Applicant postcode: |
研究负责人邮政编码: Study leader's postcode: |
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申请人所在单位: |
成都康弘药业集团股份有限公司 |
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Applicant's institution: |
Chengdu Kanghong Pharmaceutical Group Co., Ltd |
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研究负责人所在单位: |
复旦大学附属眼耳鼻喉科医院 |
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Affiliation of the Leader: |
Eye & ENT Hospital of Fudan University |
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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: |
[2022]伦审字第(2021135-2)号 |
伦理委员会批件附件: Approved file of Ethical Committee: |
查看附件View |
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批准本研究的伦理委员会名称: |
复旦大学附属眼耳鼻喉科医院伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of Eye & ENT Hospital of Fudan University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2021-11-23 00:00:00 | ||
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伦理委员会联系人: |
闫晶超 |
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Contact Name of the ethic committee: |
Jingchao Yan |
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伦理委员会联系地址: |
上海市徐汇区汾阳路83号 |
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Contact Address of the ethic committee: |
No. 83, Fenyang Road, Xuhui District, Shanghai |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 21 6437 7434 |
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: |
复旦大学附属眼耳鼻喉科医院 |
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Primary sponsor: |
Eye & ENT Hospital of Fudan University |
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研究实施负责(组长)单位地址: |
上海市-上海市-徐汇区汾阳路83号 |
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Primary sponsor's address: |
No. 83, Fenyang Road, Xuhui District, Shanghai |
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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: |
成都康弘药业集团股份有限公司 |
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Source(s) of funding: |
Chengdu Kanghong Pharmaceutical Group Co., Ltd |
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研究疾病: |
干眼 |
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Target disease: |
Dry Eye Disease |
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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: |
评价立他司特滴眼液治疗干眼的有效性和安全性 |
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Objectives of Study: |
To evaluate the efficacy and safety of Lifitegrast Ophthalmic Solution in the treatment of dry eye disease |
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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: |
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Inclusion criteria |
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排除标准: |
1.现患眼疱疹或任何其他眼部感染或炎症,或在筛选前 30 天内有眼疱疹或任何其他眼部感染史。 2.患有眼睑边缘结构异常(睑外翻、睑内翻、眼睑松弛等)、严重的结膜松弛、 Salzmann 结节状角膜变性、结膜杯状细胞受损(如维生素 A缺 乏症)、进行性翼状胬肉、湿性老年性黄斑变性(wAMD)、糖尿病视网膜病变、视网膜静脉阻塞等眼部疾病,且研究者认为该疾病可能增加 受试者风险或可能影响试验结果者。 3.筛选前 3 个月内使用过抗青光眼药物,或曾经接受过非激光青光眼手术,或在筛选访视前 6 个月内进行过青光眼激光手术者。 4.经研究者评估认为可能会影响受试者依从性或结果评估的眼部继发性疤痕(如:照射可见疤痕、化学烧伤、 Steven-Johnson 综合征、瘢痕性类 天疱疮等)者。 5.患有其他自身免疫性疾病(如类风湿性关节炎、系统性红斑狼疮、多发性硬化症、炎症性肠病)者。除非该受试者同时满足以下条件: (1)未使用类固醇药物、免疫调节或免疫抑制类药物治疗该疾病; (2) 研究者认为其医疗状况不会对试验结果造成影响。 6.曾进行器官或骨髓移植者。 7.筛选前 30 天内佩戴过角膜接触镜者。 8.基线期访视(第 2 次访视)前 30 天内口服过阿司匹林或含阿司匹林的药物,或使用(包括眼用或系统性使用)过非甾体药物、会导致眼睛干涩 的药物(如抗胆碱能药物、 5-羟色胺再摄取抑制剂、 β-受体阻滞剂、利尿剂等)。除非受试者在基线期访视前已稳定使用该药物至少 30天,且 试验期间预期用药剂量无变化。 9.在基线期(第 2 次访视)前的规定时间内使用下列药物: (1)眼用或系统性使用抗组胺药,任意眼部用药(含人工泪液):基线期访视(第 2 次访视)前 72 小时内; (2)眼用环孢素、他克莫司:基线期访视(第 2 次访视)前 6 周内; (3)眼用或系统性使用糖皮质激素、肥大细胞稳定剂:基线期访视(第 2次访视)前 14 天内。 10.在筛选前 12 周内植入过泪点塞/泪道栓或有泪点灼烧术史者;除非受试者仅植入过临时泪点塞/泪道栓,且经研究者评估目前受试者泪道中无泪 点塞/泪道栓的时间>=12 周。 11.在筛选前 6 个月内,开展过钇铝石榴石激光后囊膜切开术;在筛选前 12个月内开展过角膜屈光手术(如 LASIK 手术),或任何其他眼科手 术。 12.已知对荧光素过敏者、对多种物质过敏或患有严重过敏性疾病者。 13.有其他难以控制的临床问题(如严重慢性感染、严重的心肺疾病、控制不佳的高血压【定义为经降压药物治疗后,收缩压仍>=150mmHg或舒 张压>=100mmHg】、恶性肿瘤等)。 14.妊娠检测呈阳性或哺乳期受试者(仅限女性)。 15.在筛选前 30 天或 5 个半衰期(以较长时间为准)内参加任何药物临床试验者,或在筛选期访视(第 1 次访视)前 30 天参加任何医疗器械试 验者。 16.研究者认为不应入组的其他情况。 |
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Exclusion criteria: |
1. Currently suffering from ocular herpes or any other ocular infection or inflammation, or having a history of ocular herpes or any other ocular infection within 30 days prior to screening. 2. Suffering from ocular diseases such as abnormal eyelid margin structure (ectropion, entropion, eyelid relaxation, etc.), severe conjunctival relaxation, Salzmann nodular corneal degeneration, damage to conjunctival goblet cells (such as vitamin A deficiency), progressive pterygium, wet age-related macular degeneration (wAMD), diabetic retinopathy, retinal vein occlusion, etc. And those whose researchers believe that the disease may increase the risk of the subjects or may affect the results of the trial. 3. Those who have used anti-glaucoma drugs within 3 months prior to the screening, or have undergone non-laser glaucoma surgery, or have had laser glaucoma surgery within 6 months prior to the screening visit. 4. Ocular secondary scars (such as visible scars from irradiation, chemical burns, Steven-Johnson syndrome, cicatricoid pemphigoid, etc.) that the researcher evaluated may affect the compliance or outcome assessment of the subjects. 5. Those suffering from other autoimmune diseases (such as rheumatoid arthritis, systemic lupus erythematosus, multiple sclerosis, inflammatory bowel disease). Unless the subject simultaneously meets the following conditions: (1) No steroid drugs, immunomodulatory or immunosuppressive drugs have been used to treat the disease; (2) The researchers believe that their medical condition will not have an impact on the trial results. 6. Those who have undergone organ or bone marrow transplants. 7. Those who have worn contact lenses within 30 days before screening. 8. Within 30 days before the baseline visit (the second visit), oral aspirin or aspirin-containing drugs were taken, or non-steroidal drugs that cause dry eyes (such as anticholinergic drugs, serotonin reuptake inhibitors, beta-blockers, diuretics, etc.) were used (including ophthalmic or systemic use). Unless the subject had been stably using the drug for at least 30 days before the baseline visit and the expected dosage remained unchanged during the trial period. 9.Use the following medications within the specified time before the baseline period (the second visit) : (1) For ocular or systemic use of antihistamines, any ocular medication (including artificial tears) : within 72 hours before the baseline visit (the second visit); (2) Ophthalmic cyclosporine and tacrolimus: within 6 weeks before the baseline visit (the second visit); (3) Ocular or systemic use of steroids or mast cell stabilizers: within 14 days before the baseline visit (the second visit). 10. Those who have had lacrimal punctum plugs/lacrimal duct plugs implanted or have a history of lacrimal punctum cauterization within 12 weeks before screening; Unless the subject has only had a temporary lacrimal punctum plug/lacrimal duct plug implanted, and the researcher assesses that the current time without the lacrimal punctum plug/lacrimal duct plug in the subject's lacrimal duct is >=12 weeks. 11. Within 6 months prior to the screening, yttrium aluminum garnet laser posterior capsulotomy was performed. Have undergone corneal refractive surgery (such as LASIK surgery) or any other ophthalmic surgery within 12 months prior to screening. 12.People who are known to be allergic to fluorescein, allergic to multiple substances, or suffering from severe allergic diseases. 13.There are other difficult-to-control clinical problems (such as severe chronic infections, severe heart and lung diseases, poorly controlled hypertension [defined as systolic blood pressure remaining >=150mmHg or diastolic blood pressure >=100mmHg after antihypertensive drug treatment], malignant tumors, etc.). 14.Pregnancy test positive or lactating subjects (female only). 15.Those who participated in any drug clinical trial 30 days before screening or within 5 half-lives (whichever is longer), or those who participated in any medical device trial 30 days before the screening visit (the first visit). 16.Other situations that the researchers consider should not be included in the group. |
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研究实施时间: Study execute time: |
从 From 2022-02-17 00:00:00至 To 2023-06-19 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2022-02-17 00:00:00 至 To 2023-06-19 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: |
结束 /Completed |
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): |
本试验采用区组随机化方法,应用中央随机化系统进行随机。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Randomization was performed with the use of a central randomization system with the use of block randomization. |
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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,不仅包括研究者,受试者还包括申办方 |
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Blinding: |
Double-blind, including not only the investigators but also the participants and sponsors |
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是否共享原始数据: IPD sharing |
否No |
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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): |
太美医疗科技临床研究电子数据采集系统 https://www.trialos.com.cn/login/(文章发表后6个月) |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
eCollect (EDC) provided by Taimei technology Ltd. https://www.trialos.com.cn/login/(within 6 months of publication) |
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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: |
太美医疗科技提供的eCollect(EDC)临床研究电子数据采集系统 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
eCollect (EDC) provided by Taimei technology Ltd. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |