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Completed Phase 2Phase 3 Interventional Accepts healthy volunteers

Phase 2/3 Heterologous Boosting Study With Different Dose Levels of Monovalent SARS-CoV-2 rS Vaccines

ClinicalTrials.gov ID: NCT05925127

Public ClinicalTrials.gov record NCT05925127. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 3:11 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2/3, Randomized, Double-Blind Study to Evaluate the Safety and Immunogenicity of Different Booster Dose Levels of Monovalent SARS-CoV-2 rS Vaccines in Adults ≥ 50 Years Previously Vaccinated With COVID-19 mRNA Vaccines

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a Phase 2/3, randomized, double-blind study to evaluate the safety and immunogenicity of different booster dose levels of the monovalent severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) recombinant (r) spike (S) protein nanoparticle (SARS-CoV-2 rS) vaccines with Matrix-M™ adjuvant (NVX-CoV2373 \[prototype Wuhan vaccine with Matrix-M adjuvant\] or NVX-CoV2601 \[Omicron XBB.1.5 subvariant vaccine with Matrix-M adjuvant\]).

Study identification

NCT ID
NCT05925127
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
Novavax
Industry
Enrollment
994 participants

Conditions and interventions

Conditions

Interventions

Biological

Eligibility (public fields only)

Age range
50 Years to 99 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 16, 2023 (Actual)
Primary completion
May 21, 2024 (Actual)
Completion
May 21, 2024 (Actual)
Last update posted
Dec 13, 2024

2023 – 2024

United States locations

U.S. sites
50
U.S. states
22
U.S. cities
47
Facility City State ZIP Site status
ARS-Birmingham CRU Birmingham Alabama 35216 —
Tucson Neuroscience Research Tucson Arizona 85710 —
Velocity Clinical Research, Banning Banning California 99202 —
Velocity Clinical Research, Chula Vista Chula Vista California 91911 —
Velocity Clinical Research, San Diego La Mesa California 91942 —
Artemis Institute for Clinical Research Riverside California 92503 —
Artemis - San Diego San Diego California 92103 —
WR-MCCR San Diego California 92120 —
Deland CRU DeLand Florida 32720 —
Health Awareness Jupiter Florida 33458 —
Wr-Msra, Llc Lake City Florida 32055 —
Professional Urgent Care Services Largo Florida 33777 —
Research Institute of South Florida Miami Florida 33173 —
Suncoast Research Associates, LLC Miami Florida 33173 —
Headlands Research Orlando LLC Orlando Florida 32819 —
Precision Clinical Research, LLC Sunrise Florida 33351 —
TrueBlue Clinical Research Tampa Florida 33609 —
Neurostudies CRU Decatur Georgia 30030 —
Velocity Clinical Research Savannah Georgia 31406 —
CRA Headlands LLC Stockbridge Georgia 30281 —
Velocity Clinical Research Meridian Idaho 83642 —
Velocity Clinical Research Sioux City Iowa 51106 —
Velocity Clinical Research Baton Rouge Louisiana 70809 —
Velocity Clinical Research - Covington Covington Louisiana 70433 —
Velocity Clinical Research, Metairie Metairie Louisiana 70006 —
Activmed Practices and Research, LLC Methuen Massachusetts 01844 —
Velocity Clinical Research, Gulfport Gulfport Mississippi 39503 —
Velocity Clinical Research Grand Island Nebraska 68803 —
Velocity Clinical Research Norfolk Nebraska 68701 —
Velocity Clinical Research Omaha Nebraska 68134 —
Activmed Practices and Research, LLC Portsmouth New Hampshire 03801 —
Velocity Clinical Research Binghamton New York 13905 —
Hypercore (Lucas Research) New Bern North Carolina 28562 —
M3 Wake Research Inc Raleigh North Carolina 27612 —
Trial Management Associates, LLC Wilmington North Carolina 28403 —
Javara Inc./Wake Forest Health Network, LLC Winston-Salem North Carolina 27157 —
Velocity Clinical Research Cincinnati Ohio 45219 —
Velocity Clinical Research Cincinnati Ohio 45246 —
Tekton Research Edmond Oklahoma 73013 —
Lynn Health Science Institute Oklahoma City Oklahoma 73112 —
Velocity Clinical Research, Grants Pass Grants Pass Oregon 97527 —
Velocity Clinical Research, Providence East Greenwich Rhode Island 02818 —
Velocity Clinical Research, Gaffney Gaffney South Carolina 29340 —
Coastal Carolina Research Center an ALCANZA Clinical Research company North Charleston South Carolina 29405 —
Central Texas Clinical Research, LLC Austin Texas 78705 —
Research Your Health Plano Texas 75093 —
Benchmark Research San Angelo Texas 76904 —
Velocity Clinical Research, Salt Lake City West Jordan Utah 84088 —
Health Research of Hampton Roads, Inc Newport News Virginia 23606 —
Clinical Research Partners Richmond Virginia 23226 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05925127, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 13, 2024 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05925127 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →