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临床试验/2023-506236-32-00
2023-506236-32-00已完成3 期

A Phase 3, Randomized, Double-Blind Study to Evaluate the Safety, Tolerability, and Immunogenicity of V116 in Children and Adolescents With Increased Risk of Pneumococcal Disease.

Merck Sharp & Dohme LLC21 个研究点 分布在 5 个国家目标入组 215 人开始时间: 2024年3月18日最近更新:
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
215
试验地点
21
主要终点
Percentage of participants with solicited injection-site adverse events (AEs)

研究概览

简要总结

  1. To evaluate the safety and tolerability of V116 with respect to the proportion of participants with adverse events (AEs)
  2. To compare the serotype-specific opsonophagocytic (OPA) geometric mean titers (GMTs) at 30 days postvaccination with V116 versus PPSV23.

入排标准

年龄范围
0 years 至 17 years(0-17 Years)
接受健康志愿者

入选标准

  • Has one or more of the following risk conditions for pneumococcal disease: • Diabetes mellitus receiving treatment with antidiabetic medication • Chronic compensated liver disease • Chronic lung disease • Chronic heart disease • Chronic kidney disease, with chronic kidney insufficiency/impairment
  • Receiving stable medical management for the risk conditions listed above for ≥3 months.
  • Has not received pneumococcal vaccine, polyvalent (23-valent) (PPSV23) or has received not more than 1 dose of PPSV23 ≥5 years before study vaccination.

排除标准

  • Had a curative procedure/surgery for chronic heart disease and does not require medication, follow-up, additional interventions, or further management per local guidelines.
  • History of active hepatitis within 3 months before study vaccination
  • History of diabetic ketoacidosis or 2 or more episodes of severe, symptomatic hypoglycemia within 3 months before study vaccination
  • History of severely decreased kidney function
  • History of severe pulmonary hypertension
  • History of invasive pneumococcal disease (IPD) or known history of other culture-positive pneumococcal disease within 3 years before study vaccination

结局指标

主要结局

Percentage of participants with solicited injection-site adverse events (AEs)

Percentage of participants with solicited injection-site adverse events (AEs)

Percentage of participants with solicited systemic AEs

Percentage of participants with solicited systemic AEs

Percentage of participants with vaccine-related serious adverse events (SAEs)

Percentage of participants with vaccine-related serious adverse events (SAEs)

Geometric mean titers (GMTs) of serotype-specific opsonophagocytic activity (OPA) following vaccination

Geometric mean titers (GMTs) of serotype-specific opsonophagocytic activity (OPA) following vaccination

次要结局

  • Geometric mean concentrations (GMCs) of serotype-specific Immunoglobulin G (IgG) after vaccination
  • Geometric mean fold rise (GMFR) from baseline in serotype-specific OPA GMTs
  • Percentage of participants with ≥4-fold rise from baseline in serotype-specific OPAs GMTs
  • GMFR from baseline in serotype-specific IgG GMCs
  • Percentage of participants with ≥4-fold rise from baseline in serotype-specific IgG GMCs

研究者

申办方类型
Pharmaceutical company
责任方
Principal Investigator
主要研究者

Jayani Pathirana

Scientific

Merck Sharp & Dohme LLC

研究点 (21)

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