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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 Sep 5, 2026, 6:21 AM 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 15, 2023
Primary completion
May 20, 2024
Completion
May 20, 2024
Last update posted
Dec 12, 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 12, 2024 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05925127 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →