- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07600983
Clinical Trial of the 24-valent Pneumococcal Polysaccharide Conjugate Vaccine (CRM197/Tetanus Toxoid)
2026년 5월 15일 업데이트: 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.
연구 개요
상태
아직 모집하지 않음
정황
개입 / 치료
- 생물학적: 24-valent pneumococcal polysaccharide conjugate vaccine (CRM197/tetanus toxoid) (referred to as PCV24) (dose M)
- 생물학적: PCV24 vaccine (dose H)
- 생물학적: PCV24 vaccine (dose H)
- 생물학적: PCV24 vaccine (dose H)
- 생물학적: PCV24 vaccine (dose M)
- 생물학적: PCV24 vaccine (dose M)
- 생물학적: PCV24 vaccine (dose M)
- 생물학적: 23-valent pneumococcal polysaccharide vaccine (referred to as PPV23)
- 생물학적: 13-valent pneumococcal polysaccharide conjugate vaccine (referred to as PCV13)
- 생물학적: PPV23 vaccine
- 생물학적: PCV13 vaccine
- 생물학적: PCV13 vaccine
- 생물학적: PCV13 vaccine
- 생물학적: PCV13 vaccine
- 생물학적: PCV13 vaccine
- 생물학적: PCV13 vaccine
- 생물학적: PCV24 vaccine (dose L)
- 생물학적: PCV24 vaccine (dose L or M or H)
- 생물학적: PCV24 vaccine (dose L or M or H)
상세 설명
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.
연구 유형
중재적
등록 (추정된)
854
단계
- 2 단계
- 1단계
연락처 및 위치
이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.
연구 연락처
- 이름: Haojie Liu
- 전화번호: 022-58213600-6051
- 이메일: haojie.liu@cansinotech.com
참여기준
연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.
자격 기준
공부할 수 있는 나이
- 어린이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
예
설명
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
공부 계획
이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 방지
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 네 배로
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: 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)
|
|
실험적: 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.
|
|
실험적: 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.
|
|
활성 비교기: 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
|
|
실험적: 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.
|
|
활성 비교기: 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
|
|
실험적: 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.
|
|
활성 비교기: 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
|
|
실험적: 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.
|
|
활성 비교기: 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.
|
|
실험적: 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.
|
|
활성 비교기: 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.
|
|
실험적: 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.
|
|
활성 비교기: 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.
|
|
실험적: 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.
|
|
활성 비교기: 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.
|
|
실험적: 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.
|
|
활성 비교기: 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.
|
|
실험적: 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.
|
|
활성 비교기: 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.
|
|
실험적: 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.
|
|
활성 비교기: 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
|
|
실험적: 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.
|
|
활성 비교기: 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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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
기간 |
|---|---|
|
Phase I: Incidence of adverse reactions
기간: 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
기간: 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)
기간: 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
기간: 4 days after vaccination
|
4 days after vaccination
|
|
Phase I: Incidence of abnormalities in complete blood count
기간: 4 days after vaccination
|
4 days after vaccination
|
|
Phase I: Incidence of abnormalities in blood chemistry
기간: 4 days after vaccination
|
4 days after vaccination
|
|
Phase I: Incidence of abnormalities in coagulation function
기간: 4 days after vaccination
|
4 days after vaccination
|
|
Phase II (≥50 years old group): Geometric mean concentration (GMC) of serotype-specific pneumococcal IgG antibodies
기간: 30 days after vaccination
|
30 days after vaccination
|
|
Phase II (≥50 years old group): ≥4-fold increase of serotype-specific pneumococcal IgG antibodies
기간: 30 days after vaccination
|
30 days after vaccination
|
|
Phase II (≥50 years old group): Geometric mean increment (GMI) of serotype-specific pneumococcal IgG antibodies
기간: 30 days after vaccination
|
30 days after vaccination
|
|
Phase II (≥50 years old group): Serotype-specific pneumococcal OPA antibody titers in some trial participants
기간: 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
기간: 30 days after vaccination
|
30 days after vaccination
|
|
Phase II (≥50 years old group): Incidence of adverse reactions
기간: Within 7 days of vaccination
|
Within 7 days of vaccination
|
|
Phase II (≥50 years old group): Incidence of adverse reactions
기간: 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)
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: Within 30 days of each dose
|
Within 30 days of each dose
|
2차 결과 측정
결과 측정 |
기간 |
|---|---|
|
Phase I: Incidence of adverse reactions
기간: 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
기간: Within 30 days of vaccination
|
Within 30 days of vaccination
|
|
Phase II (2-month-old group [minimum 6 weeks]): Incidence of adverse reactions
기간: 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)
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 30 days after vaccination
|
30 days after vaccination
|
|
Phase I (≥50 years old group): ≥4-fold increaseof Serotype-specific pneumococcal IgG antibody
기간: 30 days after vaccination
|
30 days after vaccination
|
|
Phase I (≥50 years old group): GMI of Serotype-specific pneumococcal IgG antibody
기간: 30 days after vaccination
|
30 days after vaccination
|
|
Phase I (≥50 years old group): Serotype-specific pneumococcal OPA antibody titers
기간: 30 days after vaccination
|
30 days after vaccination
|
|
Phase I (≥50 years old group): Proportion of serotype-specific pneumococcal OPA antibody titers ≥1:8
기간: 30 days after vaccination
|
30 days after vaccination
|
|
Phase II (≥50 years old group): Incidence of SAE
기간: Within 180 days of vaccination
|
Within 180 days of vaccination
|
|
Phase II (2-month-old group [minimum 6 weeks]): Incidence of SAE
기간: 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
|
공동 작업자 및 조사자
여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.
수사관
- 수석 연구원: Zhiqiang Xie, Master, Henan Provincial Center for Disease Control and Prevention
연구 기록 날짜
이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.
연구 주요 날짜
연구 시작 (추정된)
2026년 5월 24일
기본 완료 (추정된)
2026년 11월 24일
연구 완료 (추정된)
2027년 12월 30일
연구 등록 날짜
최초 제출
2026년 5월 15일
QC 기준을 충족하는 최초 제출
2026년 5월 15일
처음 게시됨 (실제)
2026년 5월 22일
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
2026년 5월 22일
QC 기준을 충족하는 마지막 업데이트 제출
2026년 5월 15일
마지막으로 확인됨
2026년 5월 1일
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- CTP-PCV24-001
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
아니
미국 FDA 규제 기기 제품 연구
아니
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .
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