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Recruiting Phase 3 Interventional Accepts healthy volunteers

Study of VYD2311 for the Prevention of COVID-19

ClinicalTrials.gov ID: NCT07298434

Public ClinicalTrials.gov record NCT07298434. 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 May 20, 2026, 3:13 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 3, Randomized, Triple-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of VYD2311 for the Prevention of COVID-19 in Adults and Adolescents

Study identification

NCT ID
NCT07298434
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Invivyd, Inc.
Industry
Enrollment
1,770 participants

Conditions and interventions

Conditions

Interventions

  • Placebo Drug
  • VYD2311-MD Drug
  • VYD2311-SD Drug

Drug

Eligibility (public fields only)

Age range
12 Years to 100 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
Jan 7, 2026
Primary completion
Jul 31, 2026
Completion
Jul 31, 2026
Last update posted
May 14, 2026

2026

United States locations

U.S. sites
20
U.S. states
16
U.S. cities
20
Facility City State ZIP Site status
Invivyd Investigative Site Long Beach California 90806 Recruiting
Inviviyd Investigative Site San Diego California 92103 Recruiting
Invivyd Investigative Site Orlando Florida 32819 Recruiting
Invivyd Investigative Site Hinesville Georgia 31313 Recruiting
Invivyd Investigative Site Melrose Park Illinois 60160 Recruiting
Invivyd Investigative Site Lenexa Kansas 66219 Recruiting
Invivyd Investigative Site Silver Spring Maryland 20904 Recruiting
Invivyd Investigative Site Burlington Massachusetts 01803 Recruiting
Invivyd Investigative Site Southfield Michigan 48034 Recruiting
Invivyd Investigative Site Maplewood Minnesota 55109 Recruiting
Invivyd Investigative Site Independence Missouri 64055 Recruiting
Invivyd Investigative Site Jersey City New Jersey 07306 Recruiting
Invivyd Investigative Site The Bronx New York 10455 Recruiting
Invivyd Investigative Site Philadelphia Pennsylvania 19107 Recruiting
Invivyd Investigative Site Myrtle Beach South Carolina 29572 Recruiting
Invivyd Investigative Site Goodlettsville Tennessee 37072 Recruiting
Invivyd Investigative Site Houston Texas 77065 Recruiting
Invivyd Investigative Site Houston-2 Texas 77065 Recruiting
Invivyd Investigative Site Irving Texas 75061 Recruiting
Invivyd Investigative Site Sugar Land Texas 46254 Recruiting

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 NCT07298434, 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 May 14, 2026 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07298434 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →