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NCT07425392 · ClinicalTrials.gov registry record · Phase 3

Safety, Tolerability, and Immunogenicity of VAX-31 in Adults ≥50 Years With Prior Pneumococcal Vaccination

A Phase 3 study of Pneumococcal Vaccines, sponsored by Vaxcyte.

Recruiting
Registry status
Phase 3
Development phase
720
Enrollment target
20
Study locations

NCT07425392 is a Phase 3 study of Pneumococcal Vaccines that is actively recruiting participants, run by Vaxcyte. The registered enrollment target is 720 participants, below the 1,443-participant average among 5 other Pneumococcal Vaccines trials with a reported enrollment target (50% lower). The trial reports 20 study locations across 12 states.

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The verdict

NCT07425392, a Phase 3 study of Pneumococcal Vaccines, is actively recruiting participants, sponsored by Vaxcyte.

RECRUITING
Registry status
Phase 3
Development phase
720 participants
Enrollment target
20
Study locations

Study Summary

The study will evaluate the safety, tolerability, and immunogenicity of VAX-31 in adults ≥50 years of age.

Conditions Studied

Interventions

  • BIOLOGICAL 31-valent pneumococcal conjugate vaccine
  • BIOLOGICAL PCV20

Study Locations (20)

Florida

  • CenExel (RCA) - Hollywood
  • Eximia (Health Awareness) - Jupiter
  • Eximia (Health Awareness) - Port Saint Lucie
  • Precision Clinical Research - Sunrise
  • The Villages - The Villages

Arizona

  • Chinle Center for Indigenous Health - Chinle
  • Avacare (CCT Research) - Phoenix
  • Whiteriver Center for Indigenous Health - Whiteriver

Missouri

  • AMR - Kansas City
  • DelRicht Research (Command Family Medicine) - Springfield

New Mexico

  • Center of American Indian Health - Gallup
  • Shiprock Center for Indigenous Health - Shiprock

Connecticut

  • Chase Medical Research - Waterbury

Georgia

  • DelRicht Clinical Research - Stockbridge

Indiana

  • Velocity Clinical Valparaiso - Valparaiso

Kansas

  • Johnson County Clin-Trials, LLC - Lenexa

Trial Details

FieldValue
Enrollment Target 720 participants
Start Date 2026-02-09
Est. Completion 2027-03
Phase Phase 3

Sponsor

Vaxcyte

8 total trials

What the Registry Record Tells You About NCT07425392

The ClinicalTrials.gov registry entry for NCT07425392 describes a study currently listed as recruiting, categorized as Phase 3. The registered enrollment target is 720 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,443-participant average among 5 other Pneumococcal Vaccines trials with a reported enrollment target (50% lower). The listed sponsor is Vaxcyte, which has 8 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Pneumococcal Vaccines appearing as the primary indexed condition, and to 2 interventions - of which 31-valent pneumococcal conjugate vaccine is the first listed.

NCT07425392 reports 20 study locations spanning 12 distinct geographic areas - top geographies include Florida, Arizona, Missouri.

Frequently Asked Questions

What is clinical trial NCT07425392 about?

NCT07425392 is a clinical study titled "Safety, Tolerability, and Immunogenicity of VAX-31 in Adults ≥50 Years With Prior Pneumococcal Vaccination". The study will evaluate the safety, tolerability, and immunogenicity of VAX-31 in adults ≥50 years of age.

What is the current status of trial NCT07425392?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 720 participants. The study started on 2026-02-09. Estimated completion is 2027-03.

What conditions does trial NCT07425392 study?

This clinical trial studies the following conditions: Pneumococcal Vaccines.

What interventions are being tested in trial NCT07425392?

The interventions under investigation include: 31-valent pneumococcal conjugate vaccine (BIOLOGICAL), PCV20 (BIOLOGICAL).

Who is sponsoring clinical trial NCT07425392?

This trial is sponsored by Vaxcyte, which has 8 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07425392 being conducted?

This trial has 20 study locations across Arizona, Connecticut, Florida, Georgia, Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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