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Not yet recruiting NCT07406347

A Trial to Evaluate the Safety and Reactogenicity of an Investigational Pneumococcal Vaccine in Infants Receiving 3-dose Primary Dosing Series Followed by a Booster Dose at 12 to 15 Months of Age

Phase I Interventional Pneumonia, Bacterial

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Pn-MAPS30plus, PCV20.
Who it may be relevant to
Registry conditions: Pneumonia, Bacterial. Basic parameters: 42 Days — 90 Days · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

A Phase 1, Observer-blind, Randomized, Active Controlled Trial to Evaluate the Safety and Reactogenicity of an Investigational Pneumococcal Vaccine in Infants Receiving 3-dose Primary Dosing Series Followed by a Booster Dose at 12 to 15 Months of Age

Overview

The main purpose of this study is to evaluate safety and reactogenicity of the investigational pneumococcal vaccine (called Pn-MAPS30plus). PCV20 will be used as a comparator for this study

Interventions

  • Biological Pn-MAPS30plus
    Pn-MAPS30plus vaccine will be administered intramuscularly.
  • Combination product PCV20
    PCV20 vaccine will be administered intramuscularly.

Primary outcome measures

  • Number of participants with solicited administration site adverse events (AEs) [Time frame: Day 1 to Day 7]
  • Number of participants with solicited systemic adverse events (AEs) [Time frame: Day 1 to Day 7]
  • Number of participants with unsolicited AEs [Time frame: Day 1 to Day 30]
  • Number of Participants with Serious AEs (SAEs), Adverse Events of Special Interest (AESIs) and AEs Leading to Withdrawal [Time frame: Day 1 up to trial end (Month 16)]

Eligibility criteria

Inclusion criteria

  • Participants' parent(s)/Legally acceptable representative \[LAR(s)\] who, in the opinion of the investigator, can and will comply with all protocol requirements.
  • Written or witnessed/thumb printed informed consent obtained from the participants' parent(s)/LAR(s) prior to performance of any study-specific procedure.
  • Participant is approximately 2 Months of Age \[MOA (42 to 90 days, inclusive)\] at time of first study intervention administration.
  • Healthy participants as established by medical history and clinical examination before entering the trial.
  • Participant is a full-term infant (≥37 weeks gestation at birth) with a birth weight of >2.5 kg.

Exclusion criteria

  • History of any reaction or hypersensitivity likely to be exacerbated by any component of the study intervention(s).
  • Hypersensitivity to latex.
  • History of microbiologically proven Invasive pneumococcal Disease (IPD).
  • Any confirmed or suspected immunosuppressive or immunodeficient condition, based on medical history and physical examination.
  • Major congenital defects, as assessed by the investigator.
  • Recurrent history or uncontrolled neurological disorders or any neuroinflammatory condition, congenital neurological conditions, encephalopathies, or seizures.
  • Condition that in the judgment of the investigator would make intramuscular injection unsafe.
  • Any other clinical condition that, in the opinion of the investigator, might pose additional risk to the participant due to participation in the study.
  • Use of any investigational or non-registered product (drug, vaccine, or invasive medical device in the country of enrollment) other than the study intervention(s) during the period beginning 30 days before the dose of study intervention(s), or their planned use during the trial period.
  • Previous vaccination with any pneumococcal vaccine.
  • Planned administration/administration of any inactivated or otherwise non live vaccine in the period starting 14 days before and ending 14 days after each dose of study intervention administration or planned administration/administration of any live vaccine in the period starting 28 days before and ending 28 days after each dose of study intervention(s) administration, with the exception of inactivated influenza vaccine which may be administered but must be given at least 7 days before or 15 days after receipt of any study intervention.
  • Receipt of blood or plasma products or immunoglobulins, since birth, or planned receipt during the trial up to 30 days after last study intervention administration.
  • Chronic administration of immune-modifying drugs and/or planned use of long-acting immune-modifying treatments at any time up to the end of the trial since birth. For corticosteroids, this will mean prednisone equivalent ≥0.5 mg/kg/day with maximum of 20 mg/day. Inhaled and topical steroids are allowed.
  • Concurrent participation in another clinical study in which the participant has been or will be exposed to an investigational or non-investigational intervention.
  • Any child of trial personnel or their immediate dependents, family, or household members.
  • Child in care.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Triple blind
Primary purpose
Prevention

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07406347 · 221547

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗