Last updated: 02/12/2026 12:10:47
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
GSK study ID
221547
Clinicaltrials.gov ID
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Not yet recruiting
Not yet recruiting
Trial overview
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
Trial description: 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
Primary purpose:
Prevention
Trial design:
Parallel
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Allocation:
Randomized
Primary outcomes:
Number of participants with solicited administration site adverse events (AEs)
Timeframe: Day 1 to Day 7
Number of participants with solicited systemic adverse events (AEs)
Timeframe: Day 1 to Day 7
Number of participants with unsolicited AEs
Timeframe: Day 1 to Day 30
Number of Participants with Serious AEs (SAEs), Adverse Events of Special Interest (AESIs) and AEs Leading to Withdrawal
Timeframe: Day 1 up to trial end (Month 16)
Secondary outcomes:
Not applicable
Interventions:
Biological/vaccine: Pn-MAPS30plus
Combination product: PCV20
Enrollment:
60
Observational study model:
Not applicable
Primary completion date:
2028-03-04
Time perspective:
Not applicable
Clinical publications:
Not applicable
Medical condition
Pneumonia, Bacterial
Product
Not applicable
Collaborators
Not applicable
Study date(s)
July 2026 to April 2028
Type
Interventional
Phase
1
Participation criteria
Sex
Female & Male
Age
42 - 90 Days
Accepts healthy volunteers
Yes
- 1. Participants’ parent(s)/Legally acceptable representative [LAR(s)] who, in the opinion of the investigator, can and will comply with all protocol requirements.
- 2. Written or witnessed/thumb printed informed consent obtained from the participants’ parent(s)/LAR(s) prior to performance of any study-specific procedure.
- 1. History of any reaction or hypersensitivity likely to be exacerbated by any component of the study intervention(s).
- 2. Hypersensitivity to latex.
Inclusion and exclusion criteria
Inclusion criteria:
- 1. Participants’ parent(s)/Legally acceptable representative [LAR(s)] who, in the opinion of the investigator, can and will comply with all protocol requirements. 2. Written or witnessed/thumb printed informed consent obtained from the participants’ parent(s)/LAR(s) prior to performance of any study-specific procedure. 3. Participant is approximately 2 Months of Age [MOA (42 to 90 days, inclusive)] at time of first study intervention administration. 4. Healthy participants as established by medical history and clinical examination before entering the trial. 5. Participant is a full-term infant (≥37 weeks gestation at birth) with a birth weight of >2.5 kg.
Exclusion criteria:
- 1. History of any reaction or hypersensitivity likely to be exacerbated by any component of the study intervention(s). 2. Hypersensitivity to latex. 3. History of microbiologically proven Invasive pneumococcal Disease (IPD). 4. Any confirmed or suspected immunosuppressive or immunodeficient condition, based on medical history and physical examination. 5. Major congenital defects, as assessed by the investigator. 6. Recurrent history or uncontrolled neurological disorders or any neuroinflammatory condition, congenital neurological conditions, encephalopathies, or seizures. 7. Condition that in the judgment of the investigator would make intramuscular injection unsafe. 8. Any other clinical condition that, in the opinion of the investigator, might pose additional risk to the participant due to participation in the study. 9. 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. 10. Previous vaccination with any pneumococcal vaccine. 11. 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. 12. 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. 13. 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. 14. Concurrent participation in another clinical study in which the participant has been or will be exposed to an investigational or non-investigational intervention. 15. Any child of trial personnel or their immediate dependents, family, or household members. 16. Child in care.
Trial location(s)
No location data available.
Study documents
No study documents available.
Results overview
Study Results yet to be posted
Recruitment status
Not yet recruiting
Actual primary completion date
Not applicable
Actual study completion date
Not applicable
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Additional information
Not applicable
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