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Phase 3 Completed N=606 Randomized Triple-blind Prevention

Safety and Immunogenicity of Catch-up Vaccination Regimens of V114 (V114-024)

Pneumococcal Infections
Source: ClinicalTrials.gov NCT03885934 ↗
Enrolled (actual)
606
Serious AEs
4.6%
Results posted
Sep 2021
Primary outcomePrimary: Geometric Mean Concentration of Serotype-specific Immunoglobulin G - Schedule A: 7-11 Months — 2.47; 3.66; 2.65; 1.71 μg/mL
◆ Published Evidence
Emerging
16citations · ~4 / year
A phase III, multicenter, randomized, double-blind, active comparator-controlled study to evaluate the safety, tolerability, and immunogenicity of catch-up vaccination regimens of V114, a 15-valent pneumococcal conjugate vaccine, in healthy infants, children, and adolescents (PNEU-PLAN).
Vaccine · 2022 · Open access · High-confidence link

Summary

The purpose of this study is 1) to evaluate the safety and tolerability of V114 with respect to the proportion of participants with adverse events (AEs) and 2) to evaluate the anti-pneumococcal polysaccharide (PnPs) serotype-specific Immunoglobulin G (IgG) Geometric Mean Concentrations (GMCs) at 30 days following the last dose for each vaccination group. There is no formal hypothesis testing in this study.

Linked Publications

  • A phase III, multicenter, randomized, double-blind, active comparator-controlled study to evaluate the safety, tolerability, and immunogenicity of catch-up vaccination regimens of V114, a 15-valent pneumococcal conjugate vaccine, in healthy infants, children, and adolescents (PNEU-PLAN).
    Vaccine · 2022 · 16 citations · Open access · High-confidence link

Outcome Measures

OutcomeResultp-value
PRIMARY
Geometric Mean Concentration of Serotype-specific Immunoglobulin G - Schedule A: 7-11 Months
2.47; 3.66; 2.65; 1.71; 2.21; 3.85
PRIMARY
GMC of Serotype-specific IgG - Schedule B: 12-23 Months
3.83; 4.20; 2.96; 1.68; 3.46; 4.89
PRIMARY
GMC of Serotype-specific IgG - Schedule C: 2-17 Years
3.00; 3.99; 1.37; 1.03; 2.53; 5.22
PRIMARY
Percentage of Participants With Solicited Injection-site Adverse Events - Schedule A: 7-11 Months
28.1; 34.4; 17.2; 14.1; 18.8; 7.8
PRIMARY
Percentage of Participants With Solicited Injection-site AEs - Schedule B: 12-23 Months
21.0; 21.9; 8.1; 9.4; 33.9; 23.4
PRIMARY
Percentage of Participants With Solicited Injection-site AEs - Schedule C: 2-17 Years
19.2; 21.1; 6.8; 14.9; 54.8; 56.6
PRIMARY
Percentage of Participants With Solicited Systemic AEs - Schedule A: 7-11 Months
15.6; 18.8; 32.8; 43.8; 21.9; 15.6
PRIMARY
Percentage of Participants With Solicited Systemic AEs - Schedule B: 12-23 Months
22.6; 18.8; 35.5; 21.9; 24.2; 17.2
PRIMARY
Percentage of Participants With Solicited Systemic AEs - Schedule C: 2-17 Years
0.0; 1.7; 2.3; 2.9; 15.8; 17.1
PRIMARY
Percentage of Participants With at Least 1 Vaccine-related Serious Adverse Event - Schedule A: 7-11 Months
0.0; 0.0
PRIMARY
Percentage of Participants With at Least 1 Vaccine-related SAE - Schedule B: 12-23 Months
0.0; 0.0
PRIMARY
Percentage of Participants With at Least 1 Vaccine-related SAE - Schedule C: 2-17 Years
0.0; 0.0
SECONDARY
Percentage of Participants Meeting Serotype-specific IgG Threshold Value of ≥0.35 μg/mL for Each of the 15 Serotypes - Schedule A: 7-11 Months
100.0; 100.0; 100.0; 96.6; 100.0; 100.0
SECONDARY
Percentage of Participants Meeting Serotype-specific IgG Threshold Value of ≥0.35 μg/mL for Each of the 15 Serotypes - Schedule B: 12-23 Months
100.0; 98.3; 98.2; 90.0; 100.0; 96.7
SECONDARY
Percentage of Participants Meeting Serotype-specific IgG Threshold Value of ≥0.35 μg/mL for Each of the 15 Serotypes - Schedule C: 2-17 Years
99.4; 100.0; 95.7; 87.7; 98.8; 100.0

Eligibility Criteria

Inclusion Criteria

  • Not be pregnant or breastfeeding
  • Not be a woman of childbearing potential
  • If of a woman of childbearing potential, agree to follow the contraceptive guidance during the treatment period and for at least 6 weeks after the last dose of study intervention
  • Has a legally acceptable representative who understands the study procedures, alternate treatments available, and risks involved with the study and voluntarily agrees to participate by giving written informed consent

Exclusion Criteria

  • History of invasive pneumococcal disease (IPD)
  • Known hypersensitivity to any component of the PCV or any diphtheria toxoid-containing vaccine
  • Had a recent febrile illness occurring within 72 hours prior to receipt of study vaccine
  • Known or suspected impairment of immunological function
  • History of congenital or acquired immunodeficiency
  • Has or his/her mother has a documented human immunodeficiency virus (HIV) infection
  • Known or history of functional or anatomic asplenia
  • Has failure to thrive based on the clinical judgement of the investigator
  • Has a bleeding disorder contraindicating intramuscular vaccination
  • Has a history of autoimmune disease (including but not limited to systemic lupus erythematosus, antiphospholipid syndrome, Behcet's disease, autoimmune thyroid disease, polymyositis and dermatomyositis, scleroderma, type 1 diabetes mellitus, or other autoimmune disorders)
  • Has known neurologic or cognitive behavioral disorder, including encephalitis/myelitis, acute disseminating encephalomyelitis, pervasive development disorder, and related disorders
  • Is 7 to 23 months of age and has received a dose of a pneumococcal vaccine prior to study entry based on medical record. Participants ≥2 years of age could have received a PCV at least 8 weeks prior to study entry as follows: a partial regimen of Prevnar™,Synflorix™, or Prevnar 13™ or a full regimen of Prevnar™ or Synflorix™ based on local guidelines. Participants should not have received any dose of a pneumococcal polysaccharide vaccine
  • Meets one or more of the following systemic corticosteroid exclusion criteria: has received systemic corticosteroids (equivalent of ≥2 mg/kg total daily dose of prednisone or ≥20 mg/day for persons weighing >10 kg) for ≥14 consecutive days and has not completed this course of treatment at least 30 days prior to the first dose of study vaccine at randomization; has received or is expected to receive systemic corticosteroids exceeding physiologic replacement doses (approximately 5 mg/day prednisone equivalent) within 14 days prior to any dose of study vaccine; or is expected to require systemic corticosteroids within 30 days after any study vaccination during conduct of the study (Note: Topical, ophthalmic and inhaled steroids are permitted)
  • Has received other licensed non-live vaccines within 14 days before receipt of study vaccine. Exception: Inactivated influenza vaccine may be administered but must be given at least 7 days before receipt of study vaccine or at least 15 days after receipt of study vaccine
  • Has received a licensed live vaccine within 30 days before receipt of study vaccine
  • Has received a blood transfusion or blood products, including immunoglobulins, within 6 months before receipt of study vaccine
  • Has participated in another clinical study of an investigational product before the beginning or anytime during the duration of the current clinical study
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03885934) and the linked publication. Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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