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Completed Phase 1Phase 2 Interventional Accepts healthy volunteers

Evaluation of the Safety and Immunogenicity of a SARS-CoV-2 rS Nanoparticle Vaccine With/Without Matrix-M Adjuvant

ClinicalTrials.gov ID: NCT04368988

Public ClinicalTrials.gov record NCT04368988. 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 Jul 21, 2026, 7:45 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 2-Part, Phase 1/2, Randomized, Observer-Blinded Study To Evaluate The Safety And Immunogenicity Of A SARS-CoV-2 Recombinant Spike Protein Nanoparticle Vaccine (SARS-CoV-2 rS) With Or Without MATRIX-M™ Adjuvant In Healthy Subjects

Study identification

NCT ID
NCT04368988
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Novavax
Industry
Enrollment
1,419 participants

Conditions and interventions

Conditions

Interventions

  • SARS-CoV-2 rS - Phase 1 Biological
  • SARS-CoV-2 rS/Matrix-M Adjuvant - Phase 1 Biological
  • Normal saline solution (NSS), Placebo - Phase 1 Other
  • Normal saline solution (NSS), Placebo - Phase 2 Other
  • SARS-CoV-2 rS/Matrix-M Adjuvant, Day 0 - Phase 1 Biological
  • Normal saline solution (NSS), Placebo, Day 21 - Phase 1 Other
  • SARS-CoV-2 rS/Matrix-M Adjuvant - Phase 2 Biological

Biological · Other

Eligibility (public fields only)

Age range
18 Years to 84 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
May 24, 2020
Primary completion
May 31, 2022
Completion
May 31, 2022
Last update posted
Apr 9, 2023

2020 – 2022

United States locations

U.S. sites
8
U.S. states
6
U.S. cities
8
Facility City State ZIP Site status
Meridian Clinical Research-(Savannah Georgia) - Platinum - PPDS - Phase 2 Savannah Georgia 31406
Advanced Clinical Research - Meridian - ERN-PPDS - Phase 2 Meridian Idaho 83642
Alliance for Multispecialty Research, LLC - Phase 2 Newton Kansas 67114
Alliance for Multispecialty Research, LLC - Phase 2 Wichita Kansas 67207
Central Kentucky Research Associates Inc - Phase 2 Lexington Kentucky 40509
Meridian Clinical Research-(Rockville Maryland) - Platinum - PPDS - Phase 2 Rockville Maryland 20854
Synexus Clinical Research US, Inc. - Cincinnati - Phase 2 Cincinnati Ohio 45236
Rapid Medical Research Inc - ERN-PPDS - Phase 2 Cleveland Ohio 44122

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 10 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04368988, 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 Apr 9, 2023 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04368988 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →