海曲泊帕联合rhTPO对实体瘤化疗后重度血小板减少症的疗效及安全性分析

注册号:

Registration number:

ChiCTR2400090506 

最近更新日期:

Date of Last Refreshed on:

2024-10-08 08:23:40 

注册时间:

Date of Registration:

2024-10-08 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

海曲泊帕联合rhTPO对实体瘤化疗后重度血小板减少症的疗效及安全性分析

Public title:

the efficacy and safety of hytrebopag combined with rhTPO treating severe thrombocytopenia after chemotherapy in patients with solid tumors

注册题目简写:

English Acronym:

研究课题的正式科学名称:

海曲泊帕联合rhTPO对实体瘤化疗后重度血小板减少症的疗效及安全性分析

Scientific title:

the efficacy and safety of hytrebopag combined with rhTPO treating severe thrombocytopenia after chemotherapy in patients with solid tumors

研究课题代号(代码):

Study subject ID:

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:

申请注册联系人:

孔天东 

研究负责人:

孔天东 

Applicant:

Tiandong Kong 

Study leader:

Tiandong Kong 

申请注册联系人电话:

Applicant telephone:

+86 133 8384 9341

研究负责人电话:

Study leader's
telephone:

+86 133 8384 9341

申请注册联系人传真 :

Applicant Fax:

研究负责人传真:

Study leader's fax:

申请注册联系人电子邮件:

Applicant E-mail:

kongtiandong@126.com

研究负责人电子邮件:

Study leader's E-mail:

kongtiandong@126.com

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):

申请注册联系人通讯地址:

河南省郑州市南顺城街136号

研究负责人通讯地址:

河南省郑州市南顺城街136号

Applicant address:

the No.136,Nanshuncheng street,Zhengzhou city,Henan province

Study leader's address:

the No.136,Nanshuncheng street,Zhengzhou city,Henan province

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:

申请人所在单位:

郑州市第三人民医院

Applicant's institution:

the 3rd people's hospital of Zhengzhou

研究负责人所在单位:

郑州市第三人民医院

Affiliation of the Leader:

the 3rd people's hospital of Zhengzhou

是否获伦理委员会批准:

Approved by ethic committee:

Yes

伦理委员会批件文号:

Approved No. of ethic committee:

2024-08-017-Y12

伦理委员会批件附件:

Approved file of Ethical Committee:

查看附件View

批准本研究的伦理委员会名称:

郑州市第三人民医院医学伦理委员会

Name of the ethic committee:

Medical Ethics Committee of the Third People's Hospital of Zhengzhou

伦理委员会批准日期:

Date of approved by ethic committee:

2024-08-14 00:00:00

伦理委员会联系人:

许佳佳

Contact Name of the ethic committee:

Jiajia Xu

伦理委员会联系地址:

河南省郑州市南顺城街136号

Contact Address of the ethic committee:

the No.136,Nanshuncheng street,Zhengzhou city,Henan province

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 371 6699 2915

伦理委员会联系人邮箱:

Contact email of the ethic committee:

研究实施负责(组长)单位:

郑州市第三人民医院

Primary sponsor:

The 3rd people's hospital of Zhengzhou

研究实施负责(组长)单位地址:

河南省郑州市南顺城街136号

Primary sponsor's address:

the No.136,Nanshuncheng street,Zhengzhou city,Henan province

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

河南

市(区县):

Country:

China

Province:

Henan

City:

单位(医院):

郑州市第三人民医院

具体地址:

河南省郑州市南顺城街136号

Institution
hospital:

the 3rd people's hospital of Zhengzhou

Address:

the No.136,Nanshuncheng street,Zhengzhou city,Henan province

经费或物资来源:

恒瑞医药

Source(s) of funding:

Hengrui Pharmaceutical Co.

研究疾病:

化疗相关血小板减少症  

Target disease:

Chemotherapy-related thrombocytopenia

研究疾病代码:

Target disease code:

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

I期+II期 

Study phase:

1-2

研究设计:

单臂 

Study design:

Single arm 

研究目的:

明确海曲泊帕和rhTPO联合使用治疗重度化疗相关性血小板减少症的疗效及安全性  

Objectives of Study:

To determine the efficacy and safety of the combination of hetrombopag and rhTPO in the treatment of severe chemotherapy-associated thrombocytopenia

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

Inclusion criteria

排除标准:

(1)预计生存期<3个月;(2)d1、8天方案化疗者;(3)骨髓浸润引起血小板下降患者;(4)血液病引起血小板下降患者;(5)存在活动性细菌或真菌感染或活动性病毒感染的临床证据;(6)依从性差,不能按时化疗或参与设定方案者;(7)治疗期间使用除rhTPO+海曲泊帕外的其它升血小板药物;(8)精神疾患.

Exclusion criteria:

(1) The expected survival time was less than 3 months; (2) d1, 8 days chemotherapy; (3) patients with thrombocytopenia caused by bone marrow infiltration; (4) patients with thrombocytopenia caused by hematological diseases; (5) clinical evidence of active bacterial or fungal infection or active viral infection; (6) poor compliance, unable to receive chemotherapy on time or participate in the setting of regimens; (7) platelet raising drugs other than rhTPO+ ztrombopag were used during treatment; (8) Mental disorders.

研究实施时间:

Study execute time:

From 2024-10-01 00:00:00 To 2025-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2024-10-08 00:00:00 To 2025-06-30 00:00:00

干预措施:

Interventions:

组别:

单臂

样本量:

40

Group:

single

Sample size:

干预措施:

rhTPO300u/Kg+海曲泊帕(2.5mg、5mg、7.5mg)三个剂量级别

干预措施代码:

Intervention:

Three dose levels of rhTPO300u/Kg+ hytrebopag (2.5mg, 5mg, 7.5mg) were used

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

河南 

市(区县):

 

Country:

China

Province:

Henan

City:

单位(医院):

郑州市第三人民医院 

单位级别:

三甲 

Institution
hospital:

The 3rd people's hospital of Zhengzhou

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

血小板<50×109的持续天数

指标类型:

主要指标

Outcome:

Duration of platelet count < 50×109

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

血小板恢复至100×109/L以上所需天数

指标类型:

主要指标

Outcome:

The number of days for platelet recovery to more than 100×109/L

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

采集人体标本:

Collecting sample(s)
from participants:

标本中文名:

血液

组织:

Sample Name:

Blood

Tissue:

人体标本去向

使用后销毁  

说明

Fate of sample:

Destruction after use  

Note:

征募研究对象情况:

Recruiting status:

尚未开始

Not yet recruiting

年龄范围:

Participant age:

最小 Min age 18 years
最大 Max age 75 years

性别:

男女均可

Gender:

Both

随机方法(请说明由何人用什么方法产生随机序列):

Randomization Procedure (please state who generates the random number sequence and by what method):

None

是否公开试验完成后的统计结果:

Calculated Results after the Study Completed public access:

公开/Public

盲法:

Blinding:

试验完成后的统计结果(上传文件):

Calculated Results after
the Study Completed(upload file):

是否共享原始数据:

IPD sharing

否No

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):

2026年06,RESMAN

The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url):

JUN,2026.ResMan

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:

EDC

Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture:

edc

数据与安全监察委员会:

Data and Safety Monitoring Committee:

暂未确定/Not yet

注册人:

Name of Registration:

 2024-10-08 08:23:30