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Completed Phase 3 Interventional

A Study to Investigate the Prevention of COVID-19 WithVYD222 in Adults with Immune Compromise and in Participants Aged 12 Years or Older Who Are At Risk of Exposure to SARS-CoV-2

ClinicalTrials.gov ID: NCT06039449

Public ClinicalTrials.gov record NCT06039449. 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 Nov 1, 2026, 1:21 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 Study to Evaluate the Efficacy and Safety of VYD222 for Prevention of COVID-19 (CANOPY)

Brief summary

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

A study to investigate the prevention of COVID-19 with VYD222 in adults with immune compromise and in participants aged 12 years or older who are at risk of exposure to SARS-CoV-2

Study identification

NCT ID
NCT06039449
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Invivyd, Inc.
Industry
Enrollment
790 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

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

Study timeline

Start date
Sep 8, 2023 (Actual)
Primary completion
Nov 19, 2024 (Actual)
Completion
Nov 19, 2024 (Actual)
Last update posted
Dec 9, 2024

2023 – 2024

United States locations

U.S. sites
18
U.S. states
9
U.S. cities
18
Facility City State ZIP Site status
INVIVYD Investigative Site Fullerton California 92835 —
INVIVYD Investigative Site Long Beach California 90806 —
INVIVYD Investigative Site Rolling Hills Estates California 90274 —
INVIVYD Investigative Site San Diego California 92103 —
INVIVYD Investigative Site Clearwater Florida 33756 —
INVIVYD Investigative Site Miami Florida 33186 —
INVIVYD Investigative Site St. Petersburg Florida 33705 —
INVIVYD Investigative Site Atlanta Georgia 30328 —
INVIVYD Investigative Site Hinesville Georgia 31313 —
INVIVYD Investigative Site Oak Brook Illinois 60523 —
INVIVYD Investigative Site Silver Spring Maryland 20904 —
INVIVYD Investigative Site Burlington Massachusetts 01803 —
INVIVYD Investigative Site Morrisville North Carolina 27560 —
INVIVYD Investigative Site Salisbury North Carolina 28144 —
INVIVYD Investigative Site Edmond Oklahoma 73013 —
INVIVYD Investigative Site Yukon Oklahoma 73099 —
INVIVYD Investigative Site Beaumont Texas 77706 —
INVIVYD Investigative Site Dallas Texas 75230 —

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 NCT06039449, 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 9, 2024 · Synced Nov 1, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06039449 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →