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Clinical Trial of the 24-valent Pneumococcal Polysaccharide Conjugate Vaccine (CRM197/Tetanus Toxoid)

15 maggio 2026 aggiornato da: 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.

Panoramica dello studio

Descrizione dettagliata

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 di studio

Interventistico

Iscrizione (Stimato)

854

Fase

  • Fase 2
  • Fase 1

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Bambino
  • Adulto
  • Adulto più anziano

Accetta volontari sani

Descrizione

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

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Prevenzione
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Quadruplicare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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)
Sperimentale: 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.
Sperimentale: 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.
Comparatore attivo: 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
Sperimentale: 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.
Comparatore attivo: 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
Sperimentale: 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.
Comparatore attivo: 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
Sperimentale: 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.
Comparatore attivo: 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.
Sperimentale: 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.
Comparatore attivo: 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.
Sperimentale: 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.
Comparatore attivo: 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.
Sperimentale: 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.
Comparatore attivo: 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.
Sperimentale: 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.
Comparatore attivo: 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.
Sperimentale: 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.
Comparatore attivo: 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.
Sperimentale: 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.
Comparatore attivo: 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
Sperimentale: 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.
Comparatore attivo: 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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Lasso di tempo
Phase I: Incidence of adverse reactions
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 4 days after vaccination
4 days after vaccination
Phase I: Incidence of abnormalities in complete blood count
Lasso di tempo: 4 days after vaccination
4 days after vaccination
Phase I: Incidence of abnormalities in blood chemistry
Lasso di tempo: 4 days after vaccination
4 days after vaccination
Phase I: Incidence of abnormalities in coagulation function
Lasso di tempo: 4 days after vaccination
4 days after vaccination
Phase II (≥50 years old group): Geometric mean concentration (GMC) of serotype-specific pneumococcal IgG antibodies
Lasso di tempo: 30 days after vaccination
30 days after vaccination
Phase II (≥50 years old group): ≥4-fold increase of serotype-specific pneumococcal IgG antibodies
Lasso di tempo: 30 days after vaccination
30 days after vaccination
Phase II (≥50 years old group): Geometric mean increment (GMI) of serotype-specific pneumococcal IgG antibodies
Lasso di tempo: 30 days after vaccination
30 days after vaccination
Phase II (≥50 years old group): Serotype-specific pneumococcal OPA antibody titers in some trial participants
Lasso di tempo: 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
Lasso di tempo: 30 days after vaccination
30 days after vaccination
Phase II (≥50 years old group): Incidence of adverse reactions
Lasso di tempo: Within 7 days of vaccination
Within 7 days of vaccination
Phase II (≥50 years old group): Incidence of adverse reactions
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: Within 30 days of each dose
Within 30 days of each dose

Misure di risultato secondarie

Misura del risultato
Lasso di tempo
Phase I: Incidence of adverse reactions
Lasso di tempo: 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
Lasso di tempo: Within 30 days of vaccination
Within 30 days of vaccination
Phase II (2-month-old group [minimum 6 weeks]): Incidence of adverse reactions
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 30 days after vaccination
30 days after vaccination
Phase I (≥50 years old group): ≥4-fold increaseof Serotype-specific pneumococcal IgG antibody
Lasso di tempo: 30 days after vaccination
30 days after vaccination
Phase I (≥50 years old group): GMI of Serotype-specific pneumococcal IgG antibody
Lasso di tempo: 30 days after vaccination
30 days after vaccination
Phase I (≥50 years old group): Serotype-specific pneumococcal OPA antibody titers
Lasso di tempo: 30 days after vaccination
30 days after vaccination
Phase I (≥50 years old group): Proportion of serotype-specific pneumococcal OPA antibody titers ≥1:8
Lasso di tempo: 30 days after vaccination
30 days after vaccination
Phase II (≥50 years old group): Incidence of SAE
Lasso di tempo: Within 180 days of vaccination
Within 180 days of vaccination
Phase II (2-month-old group [minimum 6 weeks]): Incidence of SAE
Lasso di tempo: 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

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Zhiqiang Xie, Master, Henan Provincial Center for Disease Control and Prevention

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

24 maggio 2026

Completamento primario (Stimato)

24 novembre 2026

Completamento dello studio (Stimato)

30 dicembre 2027

Date di iscrizione allo studio

Primo inviato

15 maggio 2026

Primo inviato che soddisfa i criteri di controllo qualità

15 maggio 2026

Primo Inserito (Effettivo)

22 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

22 maggio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

15 maggio 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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