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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: |
ChiCTR2600123076 |
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最近更新日期: Date of Last Refreshed on: |
2026-04-21 14:51:56 |
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注册时间: Date of Registration: |
2026-04-21 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: |
一项在中国早产儿和足月儿中评价RB0026注射液的有效性和安全性的多中心、随机、双盲、安慰剂对照III期临床试验 |
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Public title: |
A Multicenter, Randomized, Double-Blind, Placebo-Controlled Phase III Clinical Trial Evaluating the Efficacy and Safety of RB0026 Injection in Preterm and Term Infants in China |
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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: |
一项在中国早产儿和足月儿中评价RB0026注射液的有效性和安全性的多中心、随机、双盲、安慰剂对照III期临床试验 |
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Scientific title: |
A Multicenter, Randomized, Double-Blind, Placebo-Controlled Phase III Clinical Trial Evaluating the Efficacy and Safety of RB0026 Injection in Preterm and Term Infants in China |
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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: |
徐聪 |
研究负责人: |
钟南山/孙丽红 |
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Applicant: |
Xu Cong |
Study leader: |
Zhong Nanshan, Sun Lihong |
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申请注册联系人电话: Applicant telephone: |
+86 189 5443 1998 |
研究负责人电话:
Study leader's |
+86 20 8156 6771 |
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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: |
xucong@reyoungbio.com |
研究负责人电子邮件: Study leader's E-mail: |
sunlihong9797@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: |
中国山东省淄博市沂源县青龙山路9号 |
研究负责人通讯地址: |
中国广东省广州市荔湾区沿江西路151号 |
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Applicant address: |
9 Qinglongshan Road, Yiyuan County, Zibo, Shandong, China |
Study leader's address: |
151 Yanjiang Road West, Liwan District, Guangzhou, Guangdong, China |
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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: |
瑞阳(山东)生物制药有限公司 |
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Applicant's institution: |
Reyoung (Shandong) Biopharmaceutical Co., Ltd. |
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研究负责人所在单位: |
广州医科大学附属第一医院 |
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Affiliation of the Leader: |
The First Affiliated Hospital of Guangzhou Medical 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: |
EC-2024-070(YW)-02 |
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: |
广州医科大学附属第一医院医学伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of the First Affiliated Hospital of Guangzhou Medical University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2024-08-09 00:00:00 | ||
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伦理委员会联系人: |
张晓露 |
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Contact Name of the ethic committee: |
Zhang Xiaolu |
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伦理委员会联系地址: |
中国广东省广州市荔湾区桥中中路28号 |
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Contact Address of the ethic committee: |
28 Qiaozhong Middle Road, Liwan District, Guangzhou, Guangdong, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 20 8156 6265 |
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: |
广州医科大学附属第一医院 |
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Primary sponsor: |
The First Affiliated Hospital of Guangzhou Medical University |
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研究实施负责(组长)单位地址: |
中国广东省广州市荔湾区沿江西路151号 |
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Primary sponsor's address: |
151 Yanjiang Road West, Liwan District, Guangzhou, Guangdong, 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: |
瑞阳(山东)生物制药有限公司自筹 |
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Source(s) of funding: |
Reyoung (Shandong) Biopharmaceutical Co., Ltd. Self-Financed |
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研究疾病: |
呼吸道合胞病毒感染 |
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Target disease: |
Respiratory Syncytial Virus Infection |
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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: |
主要目的: 有效性(疗效): 在正在进入或处于其第一个呼吸道合胞病毒(RSV)流行季的婴儿人群中,评价RB0026注射液与安慰剂相比,给药后150天内(即D1-D151)降低RSV引起需医学干预的下呼吸道感染(MALRTI)的有效性。 次要目的: 有效性(疗效): 评价与安慰剂相比,RB0026注射液给药后150天内(即D1-D151)降低RSV所致MALRTI住院治疗的有效性; 安全性: 评价与安慰剂相比,单次肌肉注射RB0026注射液后的安全性和耐受性; 药代动力学(PK): 评价单次肌肉注射RB0026注射液后的PK特征; 药效学(PD): 评价单次肌肉注射RB0026注射液或安慰剂后的PD特征; 免疫原性: 评价单次肌肉注射RB0026注射液后的免疫原性。 探索性目的: RSV耐药性: 通过基因型和表型分析来描述对RB0026注射液的耐药特征; 有效性(疗效): 评价与安慰剂相比,RB0026注射液给药后151-240天内(即D152-D241)RB0026注射液降低RSV引起需医学干预的下呼吸道感染(MALRTI)的有效性; 评价与安慰剂相比,RB0026注射液给药后151-240天内(即D152-D241)降低RSV所致MALRTI住院治疗的有效性。 |
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Objectives of Study: |
Primary Objective: Efficacy (Therapeutic Effect): To evaluate the efficacy of RB0026 injection compared to placebo in reducing medically active lower respiratory tract infections (MALRTI) caused by respiratory syncytial virus (RSV) within 150 days post-administration (i.e., D1-D151) in infants entering or experiencing their first RSV season. Secondary Objectives: Efficacy (Therapeutic Effect): Evaluate the efficacy of RB0026 injection compared to placebo in reducing RSV-induced MALRTI requiring hospitalization within 150 days post-administration (i.e., D1-D151). Safety: Evaluate the safety and tolerability of a single intramuscular injection of RB0026 compared to placebo. Pharmacokinetics (PK): Evaluate PK characteristics following a single intramuscular injection of RB0026 injection. Pharmacodynamics (PD): Evaluate PD characteristics following a single intramuscular injection of RB0026 injection or placebo. Immunogenicity: Evaluate immunogenicity following a single intramuscular injection of RB0026 injection. Exploratory Objectives: RSV Resistance: Describe resistance characteristics to RB0026 injection through genotypic and phenotypic analysis; Efficacy: Evaluate the efficacy of RB0026 injection in reducing medically active lower respiratory tract infections (MALRTI) caused by RSV between days 151 and 240 (D152-D241) post-administration compared to placebo; Evaluate the efficacy of RB0026 injection in reducing hospitalizations for RSV-induced MALRTI between days 152 and 241 (D152-D241) compared to placebo. |
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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: |
1.1周岁以内的健康晚期早产儿和足月儿(胎龄>=35孕周),患有基础疾病(如唐氏综合征和唇裂)但无其他风险因素的婴儿允许参加试验; 2.随机给药时正在进入或处于其第一个RSV感染季的婴儿; 3.受试者的父母/法定监护人已签署知情同意书; 4.受试者的父母/法定监护人能够理解并遵守方案的要求和流程,包括计划的中心随访、电话访视及样本采集。 |
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Inclusion criteria |
1. Healthy late preterm infants and term infants (gestational age >=35 weeks) within 1 year of age; infants with underlying conditions (e.g., Down syndrome and cleft lip) but no other risk factors are permitted to participate; 2. Infants entering or currently experiencing their first RSV infection season at the time of randomization; 3. Informed consent has been obtained from the subject's parent(s)/legal guardian(s); 4. The subject's parent(s)/legal guardian(s) are able to understand and comply with the protocol requirements and procedures, including scheduled center visits, telephone follow-ups, and sample collection. |
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排除标准: |
1.在给药前7天内出现任何发热(体温>=38.0℃,任何体温检测方法)或急性疾病(定义为出现中或重度症状或体征); 2.在给药前7天内发生下呼吸道感染者; 3.既往患有荨麻疹,或已知对多种药物有过敏史,或已知对免疫球蛋白产品、血液制品有过敏史者; 4.目前有活动性RSV感染或既往有RSV感染史; 5.给药前7天内接受过任何医学治疗(如长期或临时给药),但以下情况除外:a)各种维生素、铁剂、DHA等;b)根据研究者的判断,针对儿科常见症状的非处方药物(例如止痛药、外用药),这类药物可偶尔使用; 6.患有自身免疫性疾病、当前正在或根据研究者判断预期会在试验期间接受免疫调节剂治疗(如全身性应用糖皮质激素,但局部用药除外); 7.既往3个月内使用过或预期在试验期间会接受血液制品或免疫球蛋白制品或单克隆/多克隆抗体(试验用药品除外); 8.筛选时已知有肾功能损害或肝功能障碍(包括已知或可疑的活动性或慢性肝炎感染); 9.已知有慢性肺疾病(CLD)/支气管肺发育异常或伴有有临床意义的先天性呼吸道异常; 10.患有伴显著血流动力学改变的先天性心脏病(CHD),但是,单纯性CHD(例如动脉导管未闭、无血流动力学影响的房间隔缺损或小室间隔缺损)除外; 11.患有慢性癫痫或进展性或不稳定性神经系统疾病; 12.既往发生过或疑似发生过威胁生命的急性事件,且经研究者判定当前仍不适合参加临床试验者; 13.已知有免疫功能缺陷,包括感染人类免疫缺陷病毒(HIV); 14.母亲感染了HIV(除非已证明受试者未感染); 15.接受过任何抗RSV单克隆抗体或RSV疫苗,包括母亲妊娠期间接受过RSV疫苗; 16.接受过任何研究用药品或者参加过任何干预性研究; 17.研究者认为的可能会干扰研究药物评估或研究结果解读的任何其他情况; 18.受试者为研究者或其下属研究人员或申办者工作人员的子女。 |
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Exclusion criteria: |
1. Any fever (body temperature >=38.0°C, regardless of measurement method) or acute illness (defined as moderate or severe symptoms or signs) within 7 days prior to dosing; 2. Lower respiratory tract infection within 7 days prior to dosing; 3. History of urticaria, known allergies to multiple medications, or known allergies to immunoglobulin products or blood products; 4. Current active RSV infection or prior history of RSV infection; 5. Receipt of any medical treatment (e.g., long-term or temporary medication) within 7 days prior to dosing, except for: a) Various vitamins, iron supplements, DHA, etc.; b) Over-the-counter medications for common pediatric symptoms (e.g., pain relievers, topical treatments) as occasionally used at the investigator's discretion; 6. Patients with autoimmune diseases currently receiving or expected to receive immunomodulatory therapy during the trial (e.g., systemic glucocorticoids, excluding topical applications) at the investigator's discretion; 7. Use of blood products, immunoglobulin preparations, or monoclonal/polyclonal antibodies within the past 3 months or anticipated use during the trial (excluding the investigational product); 8. Known renal impairment or hepatic dysfunction at screening (including known or suspected active or chronic hepatitis infection); 9. Known chronic lung disease (CLD)/bronchopulmonary dysplasia or clinically significant congenital respiratory anomalies; 10. Congenital heart disease (CHD) with significant hemodynamic changes, except isolated CHD (e.g., patent ductus arteriosus, non-hemodynamically significant atrial septal defect, or small ventricular septal defect); 11. Chronic epilepsy or progressive/unstable neurological disease; 12. History of life-threatening acute events (or suspected occurrence thereof), with investigator determination of current ineligibility for clinical trial participation; 13. Known immunodeficiency, including human immunodeficiency virus (HIV) infection; 14. Maternal HIV infection (unless proven negative in subject); 15. Received any anti-RSV monoclonal antibody or RSV vaccine, including maternal RSV vaccination during pregnancy; 16. Received any investigational drug or participated in any interventional study; 17. Any other condition deemed by the investigator to potentially interfere with the assessment of the study drug or interpretation of study results; 18. Subject is the child of the investigator, a subordinate investigator, or a sponsor staff member. |
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研究实施时间: Study execute time: |
从 From 2024-07-04 00:00:00至 To 2026-01-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2024-10-17 00:00:00 至 To 2025-02-11 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): |
由独立的随机化统计师应用SAS9.4及以上版本产生受试者随机表和药物随机表。受试者随机设计:采用分层区组随机化方法,以随机当日的年龄(<=3.0月龄、>3.0至<=6.0月龄、>6.0月龄)作为分层因素,按照2:1的比例随机进入试验组或安慰剂组。药物随机设计:采用区组随机化方法,按照2:1的比例随机进入试验组或安慰剂组。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
An independent randomization statistician generated subject randomization tables and drug randomization tables using SAS version 9.4 or higher. Subject randomization design: A stratified block randomization method was employed, with age on the randomization date (<=3.0 months, >3.0 to <=6.0 months, >6.0 months) as the stratification factor. Subjects were randomized in a 2:1 ratio to the study group or placebo group. Drug Randomization Design: A block randomization method was employed, with subjects randomized in a 2:1 ratio to the study group or placebo group. |
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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: |
研究使用外观、标签和包装与RB0026注射液一致的安慰剂,以双盲方式进行,研究者、受试者、监查员和临床研究协调员均为盲态。 |
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Blinding: |
The study employed a placebo with identical appearance, labeling, and packaging to RB0026 Injection, conducted in a double-blind manner. The investigator, subjects, monitor, and clinical research coordinator were all blinded. |
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是否共享原始数据: IPD sharing |
是Yes |
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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): |
拟于上市后6个月内在国家生物信息中心共享,国家生物信息中心https://www.cncb.ac.cn/ |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
It is intended to be shared at the National Center for Bioinformation (CNCB, https://www.cncb.ac.cn/) within six months after launch. |
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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: |
电子采集和管理系统 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Electronic Data Capture |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |