- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT07600983
Clinical Trial of the 24-valent Pneumococcal Polysaccharide Conjugate Vaccine (CRM197/Tetanus Toxoid)
15 de maio de 2026 atualizado por: 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.
Visão geral do estudo
Status
Ainda não está recrutando
Condições
Intervenção / Tratamento
- Biológico: 24-valent pneumococcal polysaccharide conjugate vaccine (CRM197/tetanus toxoid) (referred to as PCV24) (dose M)
- Biológico: PCV24 vaccine (dose H)
- Biológico: PCV24 vaccine (dose H)
- Biológico: PCV24 vaccine (dose H)
- Biológico: PCV24 vaccine (dose M)
- Biológico: PCV24 vaccine (dose M)
- Biológico: PCV24 vaccine (dose M)
- Biológico: 23-valent pneumococcal polysaccharide vaccine (referred to as PPV23)
- Biológico: 13-valent pneumococcal polysaccharide conjugate vaccine (referred to as PCV13)
- Biológico: PPV23 vaccine
- Biológico: PCV13 vaccine
- Biológico: PCV13 vaccine
- Biológico: PCV13 vaccine
- Biológico: PCV13 vaccine
- Biológico: PCV13 vaccine
- Biológico: PCV13 vaccine
- Biológico: PCV24 vaccine (dose L)
- Biológico: PCV24 vaccine (dose L or M or H)
- Biológico: PCV24 vaccine (dose L or M or H)
Descrição detalhada
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.
Tipo de estudo
Intervencional
Inscrição (Estimado)
854
Estágio
- Fase 2
- Fase 1
Contactos e Locais
Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.
Contato de estudo
- Nome: Haojie Liu
- Número de telefone: 022-58213600-6051
- E-mail: haojie.liu@cansinotech.com
Critérios de participação
Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.
Critérios de elegibilidade
Idades elegíveis para estudo
- Filho
- Adulto
- Adulto mais velho
Aceita Voluntários Saudáveis
Sim
Descrição
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
Plano de estudo
Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Prevenção
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Quadruplicar
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: 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)
|
|
Experimental: 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.
|
|
Experimental: 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.
|
|
Comparador Ativo: 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
|
|
Experimental: 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.
|
|
Comparador Ativo: 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
|
|
Experimental: 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.
|
|
Comparador Ativo: 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
|
|
Experimental: 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.
|
|
Comparador Ativo: 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.
|
|
Experimental: 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.
|
|
Comparador Ativo: 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.
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Experimental: 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.
|
|
Comparador Ativo: 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.
|
|
Experimental: 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.
|
|
Comparador Ativo: 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.
|
|
Experimental: 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.
|
|
Comparador Ativo: 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.
|
|
Experimental: 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.
|
|
Comparador Ativo: 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.
|
|
Experimental: 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.
|
|
Comparador Ativo: 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
|
|
Experimental: 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.
|
|
Comparador Ativo: 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.
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Prazo |
|---|---|
|
Phase I: Incidence of adverse reactions
Prazo: 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
Prazo: 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)
Prazo: 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
Prazo: 4 days after vaccination
|
4 days after vaccination
|
|
Phase I: Incidence of abnormalities in complete blood count
Prazo: 4 days after vaccination
|
4 days after vaccination
|
|
Phase I: Incidence of abnormalities in blood chemistry
Prazo: 4 days after vaccination
|
4 days after vaccination
|
|
Phase I: Incidence of abnormalities in coagulation function
Prazo: 4 days after vaccination
|
4 days after vaccination
|
|
Phase II (≥50 years old group): Geometric mean concentration (GMC) of serotype-specific pneumococcal IgG antibodies
Prazo: 30 days after vaccination
|
30 days after vaccination
|
|
Phase II (≥50 years old group): ≥4-fold increase of serotype-specific pneumococcal IgG antibodies
Prazo: 30 days after vaccination
|
30 days after vaccination
|
|
Phase II (≥50 years old group): Geometric mean increment (GMI) of serotype-specific pneumococcal IgG antibodies
Prazo: 30 days after vaccination
|
30 days after vaccination
|
|
Phase II (≥50 years old group): Serotype-specific pneumococcal OPA antibody titers in some trial participants
Prazo: 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
Prazo: 30 days after vaccination
|
30 days after vaccination
|
|
Phase II (≥50 years old group): Incidence of adverse reactions
Prazo: Within 7 days of vaccination
|
Within 7 days of vaccination
|
|
Phase II (≥50 years old group): Incidence of adverse reactions
Prazo: 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)
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: Within 30 days of each dose
|
Within 30 days of each dose
|
Medidas de resultados secundários
Medida de resultado |
Prazo |
|---|---|
|
Phase I: Incidence of adverse reactions
Prazo: 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
Prazo: Within 30 days of vaccination
|
Within 30 days of vaccination
|
|
Phase II (2-month-old group [minimum 6 weeks]): Incidence of adverse reactions
Prazo: 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)
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 30 days after vaccination
|
30 days after vaccination
|
|
Phase I (≥50 years old group): ≥4-fold increaseof Serotype-specific pneumococcal IgG antibody
Prazo: 30 days after vaccination
|
30 days after vaccination
|
|
Phase I (≥50 years old group): GMI of Serotype-specific pneumococcal IgG antibody
Prazo: 30 days after vaccination
|
30 days after vaccination
|
|
Phase I (≥50 years old group): Serotype-specific pneumococcal OPA antibody titers
Prazo: 30 days after vaccination
|
30 days after vaccination
|
|
Phase I (≥50 years old group): Proportion of serotype-specific pneumococcal OPA antibody titers ≥1:8
Prazo: 30 days after vaccination
|
30 days after vaccination
|
|
Phase II (≥50 years old group): Incidence of SAE
Prazo: Within 180 days of vaccination
|
Within 180 days of vaccination
|
|
Phase II (2-month-old group [minimum 6 weeks]): Incidence of SAE
Prazo: 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
|
Colaboradores e Investigadores
É aqui que você encontrará pessoas e organizações envolvidas com este estudo.
Patrocinador
Investigadores
- Investigador principal: Zhiqiang Xie, Master, Henan Provincial Center for Disease Control and Prevention
Datas de registro do estudo
Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.
Datas Principais do Estudo
Início do estudo (Estimado)
24 de maio de 2026
Conclusão Primária (Estimado)
24 de novembro de 2026
Conclusão do estudo (Estimado)
30 de dezembro de 2027
Datas de inscrição no estudo
Enviado pela primeira vez
15 de maio de 2026
Enviado pela primeira vez que atendeu aos critérios de CQ
15 de maio de 2026
Primeira postagem (Real)
22 de maio de 2026
Atualizações de registro de estudo
Última Atualização Postada (Real)
22 de maio de 2026
Última atualização enviada que atendeu aos critérios de controle de qualidade
15 de maio de 2026
Última verificação
1 de maio de 2026
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
- Infecções
- Infecções por Bactérias Gram-Positivas
- Infecções bacterianas
- Infecções Bacterianas e Micoses
- Infecções estreptocócicas
- Infecções Pneumocócicas
- Prática profissional
- Organização e administração
- Administração de Serviços de Saúde
- Fenômenos físicos
- Produtos químicos inorgânicos
- Elementos
- Íons
- Eletrólitos
- Produtos biológicos
- Misturas complexas
- Gases
- Partículas elementares
- Vacinas
- Toxóides
- Cátions, monovalente
- Cátions
- Hidrogênio
- Núcleos
- Referência e consulta
- Prótons
- Vacina pneumocócica de 13 valentes
- Toxóide tétano
- CRM197 (variante não tóxica da toxina da difteria)
Outros números de identificação do estudo
- CTP-PCV24-001
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Não
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Não
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .
Ensaios clínicos em Infecção por Streptococcus Pneumoniae
-
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Chia Tai Tianqing Pharmaceutical Group Co., Ltd.Ainda não está recrutandoPneumonia Bacteriana Adquirida no Hospital/Pneumonia Bacteriana Associada ao VentiladorChina
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Universidad de la SabanaClínica Universidad de La Sabana; Universidad de La Sabana, ColombiaConcluídoPneumonia Pneumocócica | Pneumonia Adquirida na Comunidade (PAC)Colômbia
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Capital Medical UniversityChina-Japan Friendship Hospital; Beijing Municipal Health CommissionAinda não está recrutandoPneumonia Adquirida na Comunidade (PAC)China
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Venatorx Pharmaceuticals, Inc.Biomedical Advanced Research and Development AuthorityRetiradoPneumonia Adquirida em Hospital | Pneumonia associada à ventilação mecânica