Recruiting
Phase 2

wSp

Sponsor:

Serum Life Science Europe GmbH

Code:

NCT07216430

Conditions

Acute Otitis Media (AOM)

Eligibility Criteria

Sex: All

Age: 0

Healthy Volunteers: Accepted

Interventions

wSp vaccine

Saline (0.9% NaCl)

Study Details

Brief summary:

The goal of this clinical trial is to evaluate whether the wSp vaccine can prevent nasopharyngeal colonization by pneumococcal bacteria in healthy young children who have received routine PCV15 or PCV20 vaccination.

The main questions it aims to answer are:

Does wSp vaccine reduce pneumococcal colonization in the nose? Does wSp vaccine safely stimulate the immune system to produce antibodies and protective immune responses?

Researchers will compare children receiving two injections of wSp vaccine to those receiving saline placebo to see if wSp vaccine reduces colonization and boosts immunity.

Participants will:

Receive two injections of either wSp or saline at approximately 7 and 9 months of age.

Have blood samples taken at 6 and/or 12 months to measure immune responses. Have nasal swabs collected at several time points and during infections from 6-24 months.

Be monitored for ear infections, respiratory illnesses, and other pneumococcal-related infections.

Conditions

Acute Otitis Media (AOM)

Study ID

NCT07216430

Start date

Sep 29, 2025

Status verified date

May, 2026

Completion date

Jun, 2029

Anticipated

Primary completion date

Jun, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 0

Healthy Volunteers: Accepted

Inclusion Criteria:

1. Male or female who is 6 months (- 30 to +75 days) of age at time of enrollment
2. Healthy subject as established by medical history and clinical examination before entering into the study.
3. Received 3 doses of PCV15 or PCV20.
4. Written informed consent obtained from the subject's parent/legal guardian.
5. Parent/legal guardian able and willing to bring subject to all study visits.

Exclusion Criteria:

1. Has a history of invasive pneumococcal disease (positive blood culture and/or positive cerebrospinal fluid culture).
2. Known or suspected impairment of immunological function, based on medical history and physical examination.
3. Has a history of congenital or acquired immunodeficiency.
4. Chronic administration (defined > 14 consecutive days) of immunosuppressants or other immune-modifying drugs.
5. Prior receipt since birth of immunoglobulins and/or any blood products or planned administration during the study period.
6. Expected to receive systemic corticosteroids within 14 days prior to any dose of study vaccine.
7. External auditory canal atresia/stenosis.
8. Has known or history of functional or anatomic asplenia.
9. Has a bleeding disorder in which intramuscular vaccination would be contraindicated.
10. Participation in another investigational or interventional trial within the 28-day period before enrollment and during the conduct of the study. Participation in observational studies is permitted.
11. Direct descendant (child or grandchild) of study site personnel.

Temporary exclusion criteria

For day of vaccination:
12. Fever (transcutaneous temperature ≥38.0°C) or acute illness, at investigator's discretion
13. Has received systemic corticosteroids (equivalent of prednisone > 0.5 mg/kg/day or equivalent) and not completed this course of treatment at least 30 days prior to the study vaccination. Inhaled, topical, and ophthalmic steroids are allowed.

Study Design

Enrollment

320 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Prevention

Interventions and Outcome Measures

Arms

experimental: 2x 1 mg wSp vaccine

Intramuscular (IM) injections of 0.5 mL containing 1 mg of total protein

placebo comparator: 2x 0.5 mL saline

Intramuscular (IM) injections of 0.5 mL saline

Interventions

wSp vaccine

wSp vaccine will be administered as intramuscular (IM) injections of 0.5 mL (thus 1 mg total protein). wSp vaccine is supplied as single-dose glass vials in saline (0.9% sodium chloride) at 2 mg protein/mL, with aluminum hydroxide at 1.2 mg elemental Al/mL. Dose 1 will be given preferably in the left thigh at approximately 7 months of age, and dose 2 will be given preferably in the right thigh at approximately 9 months of age.

Saline (0.9% NaCl)

Saline will be administered as intramuscular (IM) injections of 0.5 mL. Dose 1 will be given preferably in the left thigh at approximately 7 months of age and dose 2 will be given preferably in the right thigh at approximately 9 months of age.

Primary outcome measure

  • Occurrences of Streptococcus pneumoniae in the nasopharynx [ Time Frame: 3, 6, 9 and 15 months after second dosing, if healthy, and 14 days through 15 months after second dosing at the time of AOM, LRTI, and/or URTI episodes ]

Central Contacts and Locations

Central contacts

Locations

Pittsford Pediatrics

Recruiting

Pittsford, New York, United States, 14534

Contacts

Long Pond Pediatrics

Recruiting

Rochester, New York, United States, 14606

Contacts

Westside Pediatric Group

Recruiting

Rochester, New York, United States, 14624

Contacts

Panorama Pediatrics

Recruiting

Rochester, New York, United States, 14625

Contacts

More Information

Sponsor

Serum Life Science Europe GmbH

Last update posted

Jun 2, 2026

Last verified

May, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Serum Life Science Europe GmbH on 2026-06-02.