Clinical Trial of the 24-valent Pneumococcal Polysaccharide Conjugate Vaccine (CRM197/Tetanus Toxoid)
2026年8月3日 更新者:CanSino Biologics Inc.
A Randomized, Blinded, Dose-Exploratory, Positive-Control Clinical Trial Evaluating the Safety and Immunogenicity of the 24-Valent Pneumococcal Polysaccharide Conjugate Vaccine (CRM197/Tetanus Toxoid) Following Administration in Individuals Aged 2 Months (Minimum 6 Weeks) and Older
This clinical trial consists of Phase I and Phase II.
The objective is to evaluate the safety and immunogenicity of the 24-valent pneumococcal polysaccharide conjugate vaccine (CRM197/tetanus toxoid) in individuals aged 2 months (minimum 6 weeks) and older.
研究概览
地位
招聘中
条件
干预/治疗
- 生物:24-valent pneumococcal polysaccharide conjugate vaccine (CRM197/tetanus toxoid) (referred to as PCV24) (dose M)
- 生物:PCV24 vaccine (dose H)
- 生物:PCV24 vaccine (dose H)
- 生物:PCV24 vaccine (dose H)
- 生物:PCV24 vaccine (dose M)
- 生物:PCV24 vaccine (dose M)
- 生物:PCV24 vaccine (dose M)
- 生物:23-valent pneumococcal polysaccharide vaccine (referred to as PPV23)
- 生物:13-valent pneumococcal polysaccharide conjugate vaccine (referred to as PCV13)
- 生物:PPV23 vaccine
- 生物:PCV13 vaccine
- 生物:PCV13 vaccine
- 生物:PCV13 vaccine
- 生物:PCV13 vaccine
- 生物:PCV13 vaccine
- 生物:PCV13 vaccine
- 生物:PCV24 vaccine (dose L)
- 生物:PCV24 vaccine (dose L or M or H)
- 生物:PCV24 vaccine (dose L or M or H)
详细说明
Phase I employs a randomized, blinded, dose-escalation, positive-control design with a total sample size of 310 participants.
The study population is divided into five age groups: the 18-49 age group is an open-label design with M and H dose groups; The 7-23-month, 2-5-year-old, and ≥50-year-old groups will use a positive-control, blinded design with M and H dose groups; the 2-month-old (minimum 6 weeks) group will use a positive-control, dose-escalation, and blinded design with L, M, and H dose groups.
The Phase II study was divided into two age groups.
The ≥50-year-old group: a randomized, blinded, active-controlled design with a total sample size of 160 participants, who were randomly assigned to the treatment and control groups in a 1:1 ratio; the 2-month-old (minimum 6 weeks) group: a randomized, blinded, active-controlled design with a total sample size of 384 participants.
Participants were randomly assigned in a 3:1 ratio to the treatment groups (doses L, M, and H) and the control group.
研究类型
介入性
注册 (估计的)
854
阶段
- 阶段2
- 阶段1
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习联系方式
- 姓名:Haojie Liu
- 电话号码:022-58213600-6051
- 邮箱:haojie.liu@cansinotech.com
学习地点
-
-
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Shangqiu、中国
- 尚未招聘
- Ningling County Center for Disease Control and Prevention
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接触:
- Qing Shao
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Xuchang、中国
- 招聘中
- Xiangcheng County Center for Disease Control and Prevention
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接触:
- Longfei Wang
-
-
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 孩子
- 成人
- 年长者
接受健康志愿者
是的
描述
Inclusion Criteria:
Phase I:
- Individuals aged 2 months (minimum 6 weeks), 7 months to 5 years, and 18 years and older who are willing to provide identification
- The trial participant and/or guardian (legal representative) has voluntarily signed the informed consent form after providing informed consent
- Children aged 5 and under who have not previously received a pneumococcal vaccine
- People aged 18 and older who have not received a pneumonia vaccine in the past five years
Phase II (age ≥50 group):
- People aged 50 and older who are willing to provide identification documents
- The trial participants voluntarily signed the informed consent form after providing their informed consent
- People aged 50 and older who have not received a pneumonia vaccine in the past five years
Phase II (2-month-old group (minimum 6 weeks)):
- Individuals aged 2 months or older (minimum 6 weeks) who are willing to provide identification documents
- The guardian (authorized representative) of the trial participant has voluntarily signed the informed consent form after providing informed consent.
- Infants aged 2 months (minimum 6 weeks) who have not previously received a pneumococcal vaccine
Exclusion Criteria:
- Exclusion criteria for the first dose:
- Preterm birth (delivery before 37 weeks of gestation), low birth weight (<2500 g at birth), history of labor abnormalities or resuscitation due to asphyxia; (Applicable to individuals in Phase I and Phase II who are 2 months of age or older (minimum 6 weeks))
- Patients with abnormal results in pre-vaccination blood tests (including complete blood count, blood chemistry, and coagulation function) or urinalysis, which the investigator determines to be clinically significant; (Applicable only to Phase I participants aged 2 years (or 7 months) and older)
- Individuals who are allergic to the active ingredient of the vaccine, any of its inactive ingredients, or substances used in the manufacturing process; or those who have previously experienced an allergic reaction after receiving a similar vaccine; Individuals with a history of severe allergic reactions to vaccines (such as acute allergic reactions, angioedema, or difficulty breathing), or a history of severe allergic reactions to any vaccine, food, or medication, including urticaria, anaphylactic shock, eczema, allergic respiratory distress, angioedema, or a history of asthma
- Individuals with uncontrolled hypertension (as measured on-site: systolic blood pressure ≥160 mmHg and diastolic blood pressure ≥100 mmHg); (Applicable to Stage II participants aged 50 and older and Stage I participants aged 18 and older)
- Women of childbearing age with a positive urine pregnancy test; participants who are breastfeeding; or participants or their partners who plan to become pregnant within the next 6 months; (Applicable to the Phase II group aged 50 or older and the Phase I group aged 18 or older)
- History of epilepsy, seizures (excluding febrile seizures), convulsions, or brain disorders [such as congenital brain malformations, traumatic brain injury, brain tumors, cerebral hemorrhage, cerebral infarction (excluding cerebral infarctions without sequelae and lacunar infarctions), brain infections, chemical poisoning, and other conditions causing damage to brain neural tissue], or a history of mental illness or a family history thereof; or those with other progressive neurological diseases
- Have been diagnosed with a congenital or acquired immunodeficiency, HIV infection, lymphoma, leukemia, systemic lupus erythematosus (SLE), juvenile rheumatoid arthritis (JRA), or other autoimmune diseases
- Known or suspected acute illness or severe chronic disease (including severe respiratory disease, severe cardiovascular disease, liver or kidney disease, severe skin disease, malignant tumors, etc.); or currently experiencing an acute exacerbation of a chronic condition
- Clinically diagnosed coagulation disorders (such as coagulation factor deficiencies, coagulation disorders, or platelet abnormalities) or significant bruising or bleeding disorders
- Asplenia, functional asplenia, and asplenia or splenectomy resulting from any cause
- Patients who have received immunosuppressive therapy within 6 months prior to vaccination or who are scheduled to receive such therapy between enrollment and 1 month after completion of the vaccination series (e.g., long-term systemic corticosteroid use for ≥14 days at a dose >2 mg/kg/day or ≥20 mg/day of prednisone or prednisone-equivalent dose) (excluding topical corticosteroids such as inhaled, nasal spray, intra-articular, eye drops, or ointments; topical use must not exceed the dose recommended in the product label or result in any signs of systemic exposure). Individuals who have used long-acting immunomodulatory drugs (e.g., infliximab) within 6 months prior to the first dose or who plan to use such drugs during the trial (applicable to the Phase II group aged ≥50 years and the Phase I group aged 7 months and older)
- Received blood products (excluding hepatitis B immunoglobulin) within 3 months prior to receiving the investigational drug
- Participation in any other clinical trial involving a drug or vaccine within the 6 months prior to enrollment, or currently participating in such a trial, or plans to participate in such a trial during the study period
- Received an injectable live attenuated vaccine within 14 days prior to receiving the investigational drug, or received any other vaccine within 7 days
- Underarm temperature of 37.3°C or higher prior to vaccination
- According to the researchers' assessment, the trial participants had other factors that made them unsuitable for participation in the clinical trial
Exclusion criteria for the 2nd, 3rd, and 4th doses:
- Individuals who experienced a severe allergic reaction following the previous dose of the vaccine
- Individuals who experienced a serious adverse reaction causally related to a previous dose of the vaccine
- Other potential causes ruled out by the researchers
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:预防
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:四人间
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Phase I, Phase 1, Medium dose, 18~49 year-old
This arm is open to all
|
1 dose ( 0.5ml) of PCV24 vaccine (dose M)
|
|
实验性的:Phase I, Phase 2, High dose, 18~49 year-old
This arm is open to all
|
1 dose ( 0.5ml) of PCV24 vaccine (dose H)
If trial participants are 12-23 months of age, they should receive 2 doses ( 0.5ml) of PCV24 (dose H) , administered two months apart.
If trial participants are 7-11 months of age, they should receive 2 doses ( 0.5ml) of PCV24 ( dose H) as a primary series, administered two months apart; a booster dose should be administered at 12-15 months of age, at least two months after the second dose.
The primary vaccination series consists of 3 doses of the PCV24 vaccine ( 0.5ml) , administered 2 months apart; a single booster dose is administered at 12 to 15 months of age.
|
|
实验性的:Phase I, Phase 2, Medium dose, 50 years of age or older
Participants in this age arm were randomly assigned to the experimental group and the control group in a 2:1 ratio.
|
1 dose ( 0.5ml) of PCV24 vaccine (dose M)
If trial participants are 12-23 months of age, they should receive 2 doses (0.5ml) of PCV24 ( dose M) , administered two months apart.
If trial participants are 7-11 months of age, they should receive 2 doses ( 0.5ml) of PCV24 ( dose M) as a primary series, administered two months apart; a booster dose should be administered at 12-15 months of age, at least two months after the second dose.
The primary vaccination series consists of 3 doses of the PCV24 vaccine ( 0.5ml) , administered 2 months apart; a single booster dose is administered at 12 to 15 months of age.
|
|
有源比较器:Phase I, Phase 2, 50 years of age or older
Participants in this age arm were randomly assigned to the experimental group and the control group in a 2:1 ratio.
|
1 dose ( 0.5ml) of PPV23 vaccine
|
|
实验性的:Phase I, Phase 2, Medium dose, 2~5 year-old
Participants in this age arm were randomly assigned to the experimental group and the control group in a 2:1 ratio.
|
1 dose ( 0.5ml) of PCV24 vaccine (dose M)
If trial participants are 12-23 months of age, they should receive 2 doses (0.5ml) of PCV24 ( dose M) , administered two months apart.
If trial participants are 7-11 months of age, they should receive 2 doses ( 0.5ml) of PCV24 ( dose M) as a primary series, administered two months apart; a booster dose should be administered at 12-15 months of age, at least two months after the second dose.
The primary vaccination series consists of 3 doses of the PCV24 vaccine ( 0.5ml) , administered 2 months apart; a single booster dose is administered at 12 to 15 months of age.
|
|
有源比较器:Phase I, Phase 2, 2~5 year-old
Participants in this age arm were randomly assigned to the experimental group and the control group in a 2:1 ratio.
|
1 dose ( 0.5ml) of PCV13 vaccine
|
|
实验性的:Phase I, Phase 3, High dose, 50 years of age or older
Participants in this age arm were randomly assigned to the experimental group and the control group in a 2:1 ratio.
|
1 dose ( 0.5ml) of PCV24 vaccine (dose H)
If trial participants are 12-23 months of age, they should receive 2 doses ( 0.5ml) of PCV24 (dose H) , administered two months apart.
If trial participants are 7-11 months of age, they should receive 2 doses ( 0.5ml) of PCV24 ( dose H) as a primary series, administered two months apart; a booster dose should be administered at 12-15 months of age, at least two months after the second dose.
The primary vaccination series consists of 3 doses of the PCV24 vaccine ( 0.5ml) , administered 2 months apart; a single booster dose is administered at 12 to 15 months of age.
|
|
有源比较器:Phase I, Phase 3, 50 years of age or older
Participants in this age arm were randomly assigned to the experimental group and the control group in a 2:1 ratio.
|
1 dose ( 0.5ml) of PPV23 vaccine
|
|
实验性的:Phase I, Phase 3, High dose, 2~5 year-old
Participants in this age arm were randomly assigned to the experimental group and the control group in a 2:1 ratio.
|
1 dose ( 0.5ml) of PCV24 vaccine (dose H)
If trial participants are 12-23 months of age, they should receive 2 doses ( 0.5ml) of PCV24 (dose H) , administered two months apart.
If trial participants are 7-11 months of age, they should receive 2 doses ( 0.5ml) of PCV24 ( dose H) as a primary series, administered two months apart; a booster dose should be administered at 12-15 months of age, at least two months after the second dose.
The primary vaccination series consists of 3 doses of the PCV24 vaccine ( 0.5ml) , administered 2 months apart; a single booster dose is administered at 12 to 15 months of age.
|
|
有源比较器:Phase I, Phase 3, 2~5 year-old
Participants in this age arm were randomly assigned to the experimental group and the control group in a 2:1 ratio.
|
1 dose ( 0.5ml) of PCV13 vaccine
If trial participants are 12-23 months of age, they should receive 2 doses (0.5ml) of PCV13, administered two months apart.
If trial participants are 7-11 months of age, they should receive 2 doses ( 0.5ml) of PCV13 as a primary series, administered two months apart; a booster dose should be administered at 12-15 months of age, at least two months after the second dose.
If trial participants are 12-23 months of age, they should receive 2 doses ( 0.5ml) of PCV13 , administered two months apart.
If trial participants are 7-11 months of age, they should receive 2 doses ( 0.5ml) of PCV13 as a primary series, administered two months apart; a booster dose should be administered at 12-15 months of age, at least two months after the second dose.
The primary vaccination series consists of 3 doses ( 0.5ml) of the PCV13 vaccine, administered 2 months apart; a single booster dose is administered at 12 to 15 months of age.
The primary vaccination series consists of 3 doses of the PCV13 vaccine ( 0.5ml) , administered 2 months apart; a single booster dose is administered at 12 to 15 months of age.
A primary vaccination series consisting of 3 doses of the PCV13 vaccine ( 0.5ml) , with a 2-month interval between each dose; a single booster dose should be administered at 12 to 15 months of age.
|
|
实验性的:Phase I, Phase 4, Medium dose, 7~23 month-old
Participants in this age arm were randomly assigned to the experimental group and the control group in a 2:1 ratio.
|
1 dose ( 0.5ml) of PCV24 vaccine (dose M)
If trial participants are 12-23 months of age, they should receive 2 doses (0.5ml) of PCV24 ( dose M) , administered two months apart.
If trial participants are 7-11 months of age, they should receive 2 doses ( 0.5ml) of PCV24 ( dose M) as a primary series, administered two months apart; a booster dose should be administered at 12-15 months of age, at least two months after the second dose.
The primary vaccination series consists of 3 doses of the PCV24 vaccine ( 0.5ml) , administered 2 months apart; a single booster dose is administered at 12 to 15 months of age.
|
|
有源比较器:Phase I, Phase 4, 7~23 month-old
Participants in this age arm were randomly assigned to the experimental group and the control group in a 2:1 ratio.
|
1 dose ( 0.5ml) of PCV13 vaccine
If trial participants are 12-23 months of age, they should receive 2 doses (0.5ml) of PCV13, administered two months apart.
If trial participants are 7-11 months of age, they should receive 2 doses ( 0.5ml) of PCV13 as a primary series, administered two months apart; a booster dose should be administered at 12-15 months of age, at least two months after the second dose.
If trial participants are 12-23 months of age, they should receive 2 doses ( 0.5ml) of PCV13 , administered two months apart.
If trial participants are 7-11 months of age, they should receive 2 doses ( 0.5ml) of PCV13 as a primary series, administered two months apart; a booster dose should be administered at 12-15 months of age, at least two months after the second dose.
The primary vaccination series consists of 3 doses ( 0.5ml) of the PCV13 vaccine, administered 2 months apart; a single booster dose is administered at 12 to 15 months of age.
The primary vaccination series consists of 3 doses of the PCV13 vaccine ( 0.5ml) , administered 2 months apart; a single booster dose is administered at 12 to 15 months of age.
A primary vaccination series consisting of 3 doses of the PCV13 vaccine ( 0.5ml) , with a 2-month interval between each dose; a single booster dose should be administered at 12 to 15 months of age.
|
|
实验性的:Phase I, Phase 5, High dose, 7~23 month-old
Participants in this age arm were randomly assigned to the experimental group and the control group in a 2:1 ratio.
|
1 dose ( 0.5ml) of PCV24 vaccine (dose H)
If trial participants are 12-23 months of age, they should receive 2 doses ( 0.5ml) of PCV24 (dose H) , administered two months apart.
If trial participants are 7-11 months of age, they should receive 2 doses ( 0.5ml) of PCV24 ( dose H) as a primary series, administered two months apart; a booster dose should be administered at 12-15 months of age, at least two months after the second dose.
The primary vaccination series consists of 3 doses of the PCV24 vaccine ( 0.5ml) , administered 2 months apart; a single booster dose is administered at 12 to 15 months of age.
|
|
有源比较器:Phase I, Phase 5, 7~23 month-old
Participants in this age arm were randomly assigned to the experimental group and the control group in a 2:1 ratio.
|
1 dose ( 0.5ml) of PCV13 vaccine
If trial participants are 12-23 months of age, they should receive 2 doses (0.5ml) of PCV13, administered two months apart.
If trial participants are 7-11 months of age, they should receive 2 doses ( 0.5ml) of PCV13 as a primary series, administered two months apart; a booster dose should be administered at 12-15 months of age, at least two months after the second dose.
If trial participants are 12-23 months of age, they should receive 2 doses ( 0.5ml) of PCV13 , administered two months apart.
If trial participants are 7-11 months of age, they should receive 2 doses ( 0.5ml) of PCV13 as a primary series, administered two months apart; a booster dose should be administered at 12-15 months of age, at least two months after the second dose.
The primary vaccination series consists of 3 doses ( 0.5ml) of the PCV13 vaccine, administered 2 months apart; a single booster dose is administered at 12 to 15 months of age.
The primary vaccination series consists of 3 doses of the PCV13 vaccine ( 0.5ml) , administered 2 months apart; a single booster dose is administered at 12 to 15 months of age.
A primary vaccination series consisting of 3 doses of the PCV13 vaccine ( 0.5ml) , with a 2-month interval between each dose; a single booster dose should be administered at 12 to 15 months of age.
|
|
实验性的:Phase I, Phase 5, low dose, 2 months old (minimum 6 weeks)
Participants in this age arm were randomly assigned to the experimental group and the control group in a 2:1 ratio.
|
The primary vaccination series consists of 3 doses ( 0.5ml) of the PCV24 vaccine ( dose L) , administered 2 months apart; a single booster dose is administered at 12 to 15 months of age.
|
|
有源比较器:Phase I, Phase 5, 2 months old (minimum 6 weeks)
Participants in this age arm were randomly assigned to the experimental group and the control group in a 2:1 ratio.
|
1 dose ( 0.5ml) of PCV13 vaccine
If trial participants are 12-23 months of age, they should receive 2 doses (0.5ml) of PCV13, administered two months apart.
If trial participants are 7-11 months of age, they should receive 2 doses ( 0.5ml) of PCV13 as a primary series, administered two months apart; a booster dose should be administered at 12-15 months of age, at least two months after the second dose.
If trial participants are 12-23 months of age, they should receive 2 doses ( 0.5ml) of PCV13 , administered two months apart.
If trial participants are 7-11 months of age, they should receive 2 doses ( 0.5ml) of PCV13 as a primary series, administered two months apart; a booster dose should be administered at 12-15 months of age, at least two months after the second dose.
The primary vaccination series consists of 3 doses ( 0.5ml) of the PCV13 vaccine, administered 2 months apart; a single booster dose is administered at 12 to 15 months of age.
The primary vaccination series consists of 3 doses of the PCV13 vaccine ( 0.5ml) , administered 2 months apart; a single booster dose is administered at 12 to 15 months of age.
A primary vaccination series consisting of 3 doses of the PCV13 vaccine ( 0.5ml) , with a 2-month interval between each dose; a single booster dose should be administered at 12 to 15 months of age.
|
|
实验性的:Phase I, Phase 6, Medium dose, 2 months old (minimum 6 weeks)
Participants in this age arm were randomly assigned to the experimental group and the control group in a 2:1 ratio.
|
1 dose ( 0.5ml) of PCV24 vaccine (dose M)
If trial participants are 12-23 months of age, they should receive 2 doses (0.5ml) of PCV24 ( dose M) , administered two months apart.
If trial participants are 7-11 months of age, they should receive 2 doses ( 0.5ml) of PCV24 ( dose M) as a primary series, administered two months apart; a booster dose should be administered at 12-15 months of age, at least two months after the second dose.
The primary vaccination series consists of 3 doses of the PCV24 vaccine ( 0.5ml) , administered 2 months apart; a single booster dose is administered at 12 to 15 months of age.
|
|
有源比较器:Phase I, Phase 6, 2 months old (minimum 6 weeks)
Participants in this age arm were randomly assigned to the experimental group and the control group in a 2:1 ratio.
|
1 dose ( 0.5ml) of PCV13 vaccine
If trial participants are 12-23 months of age, they should receive 2 doses (0.5ml) of PCV13, administered two months apart.
If trial participants are 7-11 months of age, they should receive 2 doses ( 0.5ml) of PCV13 as a primary series, administered two months apart; a booster dose should be administered at 12-15 months of age, at least two months after the second dose.
If trial participants are 12-23 months of age, they should receive 2 doses ( 0.5ml) of PCV13 , administered two months apart.
If trial participants are 7-11 months of age, they should receive 2 doses ( 0.5ml) of PCV13 as a primary series, administered two months apart; a booster dose should be administered at 12-15 months of age, at least two months after the second dose.
The primary vaccination series consists of 3 doses ( 0.5ml) of the PCV13 vaccine, administered 2 months apart; a single booster dose is administered at 12 to 15 months of age.
The primary vaccination series consists of 3 doses of the PCV13 vaccine ( 0.5ml) , administered 2 months apart; a single booster dose is administered at 12 to 15 months of age.
A primary vaccination series consisting of 3 doses of the PCV13 vaccine ( 0.5ml) , with a 2-month interval between each dose; a single booster dose should be administered at 12 to 15 months of age.
|
|
实验性的:Phase I, Phase 7, High dose, 2 months old (minimum 6 weeks)
Participants in this age arm were randomly assigned to the experimental group and the control group in a 2:1 ratio.
|
1 dose ( 0.5ml) of PCV24 vaccine (dose H)
If trial participants are 12-23 months of age, they should receive 2 doses ( 0.5ml) of PCV24 (dose H) , administered two months apart.
If trial participants are 7-11 months of age, they should receive 2 doses ( 0.5ml) of PCV24 ( dose H) as a primary series, administered two months apart; a booster dose should be administered at 12-15 months of age, at least two months after the second dose.
The primary vaccination series consists of 3 doses of the PCV24 vaccine ( 0.5ml) , administered 2 months apart; a single booster dose is administered at 12 to 15 months of age.
|
|
有源比较器:Phase I, Phase 7, 2 months old (minimum 6 weeks)
Participants in this age arm were randomly assigned to the experimental group and the control group in a 2:1 ratio.
|
1 dose ( 0.5ml) of PCV13 vaccine
If trial participants are 12-23 months of age, they should receive 2 doses (0.5ml) of PCV13, administered two months apart.
If trial participants are 7-11 months of age, they should receive 2 doses ( 0.5ml) of PCV13 as a primary series, administered two months apart; a booster dose should be administered at 12-15 months of age, at least two months after the second dose.
If trial participants are 12-23 months of age, they should receive 2 doses ( 0.5ml) of PCV13 , administered two months apart.
If trial participants are 7-11 months of age, they should receive 2 doses ( 0.5ml) of PCV13 as a primary series, administered two months apart; a booster dose should be administered at 12-15 months of age, at least two months after the second dose.
The primary vaccination series consists of 3 doses ( 0.5ml) of the PCV13 vaccine, administered 2 months apart; a single booster dose is administered at 12 to 15 months of age.
The primary vaccination series consists of 3 doses of the PCV13 vaccine ( 0.5ml) , administered 2 months apart; a single booster dose is administered at 12 to 15 months of age.
A primary vaccination series consisting of 3 doses of the PCV13 vaccine ( 0.5ml) , with a 2-month interval between each dose; a single booster dose should be administered at 12 to 15 months of age.
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实验性的:Phase II, Low or medium or High dose, 50 years of age or older
Participants in this age arm were randomly assigned to the experimental group and the control group in a 1:1 ratio.
|
1 dose ( 0.5ml) of PCV24 vaccine (dose L or M or H)
A primary vaccination series consisting of 3 doses of the PCV24 vaccine ( 0.5ml) , with a 2-month interval between each dose; a single booster dose should be administered at 12 to 15 months of age.
|
|
有源比较器:Phase II, 50 years of age or older
Participants in this age arm were randomly assigned to the experimental group and the control group in a 1:1 ratio.
|
1 dose ( 0.5ml) of PPV23 vaccine
|
|
实验性的:Phase II, Low or medium or High dose, 2 months old (minimum 6 weeks)
Participants in this age arm were randomly assigned to the experimental group and the control group in a 3:1 ratio.
|
1 dose ( 0.5ml) of PCV24 vaccine (dose L or M or H)
A primary vaccination series consisting of 3 doses of the PCV24 vaccine ( 0.5ml) , with a 2-month interval between each dose; a single booster dose should be administered at 12 to 15 months of age.
|
|
有源比较器:Phase II, 2 months old (minimum 6 weeks)
Participants in this age arm were randomly assigned to the experimental group and the control group in a 3:1 ratio.
|
1 dose ( 0.5ml) of PCV13 vaccine
If trial participants are 12-23 months of age, they should receive 2 doses (0.5ml) of PCV13, administered two months apart.
If trial participants are 7-11 months of age, they should receive 2 doses ( 0.5ml) of PCV13 as a primary series, administered two months apart; a booster dose should be administered at 12-15 months of age, at least two months after the second dose.
If trial participants are 12-23 months of age, they should receive 2 doses ( 0.5ml) of PCV13 , administered two months apart.
If trial participants are 7-11 months of age, they should receive 2 doses ( 0.5ml) of PCV13 as a primary series, administered two months apart; a booster dose should be administered at 12-15 months of age, at least two months after the second dose.
The primary vaccination series consists of 3 doses ( 0.5ml) of the PCV13 vaccine, administered 2 months apart; a single booster dose is administered at 12 to 15 months of age.
The primary vaccination series consists of 3 doses of the PCV13 vaccine ( 0.5ml) , administered 2 months apart; a single booster dose is administered at 12 to 15 months of age.
A primary vaccination series consisting of 3 doses of the PCV13 vaccine ( 0.5ml) , with a 2-month interval between each dose; a single booster dose should be administered at 12 to 15 months of age.
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研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
|
Phase I: Incidence of adverse reactions
大体时间:Within 7 days of receiving each dose of the vaccine
|
Within 7 days of receiving each dose of the vaccine
|
|
Phase I: Incidence of adverse reactions
大体时间:Within 30 days of receiving each dose of the vaccine
|
Within 30 days of receiving each dose of the vaccine
|
|
Phase I: Incidence of serious adverse event (SAE)
大体时间:Within 180 days of receiving the first dose of the vaccine through completion of the full vaccination series for each group
|
Within 180 days of receiving the first dose of the vaccine through completion of the full vaccination series for each group
|
|
Phase I: Incidence of abnormalities in urinalysis
大体时间:4 days after vaccination
|
4 days after vaccination
|
|
Phase I: Incidence of abnormalities in complete blood count
大体时间:4 days after vaccination
|
4 days after vaccination
|
|
Phase I: Incidence of abnormalities in blood chemistry
大体时间:4 days after vaccination
|
4 days after vaccination
|
|
Phase I: Incidence of abnormalities in coagulation function
大体时间:4 days after vaccination
|
4 days after vaccination
|
|
Phase II (≥50 years old group): Geometric mean concentration (GMC) of serotype-specific pneumococcal IgG antibodies
大体时间:30 days after vaccination
|
30 days after vaccination
|
|
Phase II (≥50 years old group): ≥4-fold increase of serotype-specific pneumococcal IgG antibodies
大体时间:30 days after vaccination
|
30 days after vaccination
|
|
Phase II (≥50 years old group): Geometric mean increment (GMI) of serotype-specific pneumococcal IgG antibodies
大体时间:30 days after vaccination
|
30 days after vaccination
|
|
Phase II (≥50 years old group): Serotype-specific pneumococcal OPA antibody titers in some trial participants
大体时间:30 days after vaccination
|
30 days after vaccination
|
|
Phase II (≥50 years old group): Proportion of trial participants with serotype-specific pneumococcal OPA antibody titers ≥1:8
大体时间:30 days after vaccination
|
30 days after vaccination
|
|
Phase II (≥50 years old group): Incidence of adverse reactions
大体时间:Within 7 days of vaccination
|
Within 7 days of vaccination
|
|
Phase II (≥50 years old group): Incidence of adverse reactions
大体时间:Within 30 days of vaccination
|
Within 30 days of vaccination
|
|
Phase II (2-month-old group [minimum 6 weeks]): Positive rate of vaccine-serotype-specific pneumococcal IgG antibodies (antibody concentration ≥ 0.35 μg/ml)
大体时间:30 days after the primary series, before the booster dose, and 30 days after the booster dose
|
30 days after the primary series, before the booster dose, and 30 days after the booster dose
|
|
Phase II (2-month-old group [minimum 6 weeks]): Proportion with vaccine-serotype-specific pneumococcal IgG antibody concentrations ≥ 1.0 μg/ml
大体时间:30 days after the primary series, before the booster dose, and 30 days after the booster dose
|
30 days after the primary series, before the booster dose, and 30 days after the booster dose
|
|
Phase II (2-month-old group [minimum 6 weeks]): GMC of serotype-specific pneumococcal IgG antibodies
大体时间:30 days after the primary series, before the booster dose, and 30 days after the booster dose
|
30 days after the primary series, before the booster dose, and 30 days after the booster dose
|
|
Phase II (2-month-old group [minimum 6 weeks]): GMI of serotype-specific pneumococcal IgG antibodies
大体时间:30 days after the primary series, before the booster dose, and 30 days after the booster dose
|
30 days after the primary series, before the booster dose, and 30 days after the booster dose
|
|
Phase II (2-month-old group [minimum 6 weeks]): Serotype-specific pneumococcal OPA antibody titers in some trial participants
大体时间:30 days after the primary series; 30 days after the booster dose
|
30 days after the primary series; 30 days after the booster dose
|
|
Phase II (2-month-old group [minimum 6 weeks]): Proportion of trial participants with serotype-specific pneumococcal OPA antibody titers ≥1:8
大体时间:30 days after the primary series; 30 days after the booster dose
|
30 days after the primary series; 30 days after the booster dose
|
|
Phase II (2-month-old group [minimum 6 weeks]): Incidence of adverse reactions
大体时间:Within 7 days of each dose
|
Within 7 days of each dose
|
|
Phase II (2-month-old group [minimum 6 weeks]): Incidence of adverse reactions
大体时间:Within 30 days of each dose
|
Within 30 days of each dose
|
次要结果测量
结果测量 |
大体时间 |
|---|---|
|
Phase I: Incidence of adverse reactions
大体时间:Within 30 days of receiving each dose of the vaccine
|
Within 30 days of receiving each dose of the vaccine
|
|
Phase II (≥50 years old group): Incidence of adverse reactions
大体时间:Within 30 days of vaccination
|
Within 30 days of vaccination
|
|
Phase II (2-month-old group [minimum 6 weeks]): Incidence of adverse reactions
大体时间:Within 30 days of each dose
|
Within 30 days of each dose
|
|
Phase I (2-month-old group [minimum 6 weeks]): Positive rate of vaccine-serotype-specific pneumococcal IgG antibodies (antibody concentration ≥ 0.35 μg/ml)
大体时间:30 days after the primary series, 30 and 180 days after the booster dose
|
30 days after the primary series, 30 and 180 days after the booster dose
|
|
Phase I (2-month-old group [minimum 6 weeks]): Proportion with vaccine-serotype-specific pneumococcal IgG antibody concentrations ≥ 1.0 μg/ml
大体时间:30 days after the primary series, 30 and 180 days after the booster dose
|
30 days after the primary series, 30 and 180 days after the booster dose
|
|
Phase I (2-month-old group [minimum 6 weeks]): GMC of serotype-specific pneumococcal IgG antibodies
大体时间:30 days after the primary series, 30 and 180 days after the booster dose
|
30 days after the primary series, 30 and 180 days after the booster dose
|
|
Phase I (2-month-old group [minimum 6 weeks]): GMI of serotype-specific pneumococcal IgG antibodies
大体时间:30 days after the primary series, 30 and 180 days after the booster dose
|
30 days after the primary series, 30 and 180 days after the booster dose
|
|
Phase I (2-month-old group [minimum 6 weeks]): Serotype-specific pneumococcal OPA antibody titers
大体时间:30 days after the primary series; 30 days after the booster dose
|
30 days after the primary series; 30 days after the booster dose
|
|
Phase I (2-month-old group [minimum 6 weeks]): Proportion of serotype-specific pneumococcal OPA antibody titers ≥1:8
大体时间:30 days after the primary series; 30 days after the booster dose
|
30 days after the primary series; 30 days after the booster dose
|
|
Phase I (≥50 years old group): GMC of Serotype-specific pneumococcal IgG antibody
大体时间:30 days after vaccination
|
30 days after vaccination
|
|
Phase I (≥50 years old group): ≥4-fold increaseof Serotype-specific pneumococcal IgG antibody
大体时间:30 days after vaccination
|
30 days after vaccination
|
|
Phase I (≥50 years old group): GMI of Serotype-specific pneumococcal IgG antibody
大体时间:30 days after vaccination
|
30 days after vaccination
|
|
Phase I (≥50 years old group): Serotype-specific pneumococcal OPA antibody titers
大体时间:30 days after vaccination
|
30 days after vaccination
|
|
Phase I (≥50 years old group): Proportion of serotype-specific pneumococcal OPA antibody titers ≥1:8
大体时间:30 days after vaccination
|
30 days after vaccination
|
|
Phase II (≥50 years old group): Incidence of SAE
大体时间:Within 180 days of vaccination
|
Within 180 days of vaccination
|
|
Phase II (2-month-old group [minimum 6 weeks]): Incidence of SAE
大体时间:Within 180 days of receiving the first dose of the vaccine through the booster shot
|
Within 180 days of receiving the first dose of the vaccine through the booster shot
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 首席研究员:Zhiqiang Xie, Master、Henan Provincial Center for Disease Control and Prevention
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2026年5月24日
初级完成 (估计的)
2026年11月24日
研究完成 (估计的)
2027年12月30日
研究注册日期
首次提交
2026年5月15日
首先提交符合 QC 标准的
2026年5月15日
首次发布 (实际的)
2026年5月22日
研究记录更新
最后更新发布 (实际的)
2026年8月5日
上次提交的符合 QC 标准的更新
2026年8月3日
最后验证
2026年5月1日
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- CTP-PCV24-001
药物和器械信息、研究文件
研究美国 FDA 监管的药品
不
研究美国 FDA 监管的设备产品
不
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