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A Phase 3, Randomized, Double-Blind Study to Evaluate the Safety, Serum Virus Neutralizing Antibody Responses, and Pharmacokinetics of VYD2311, a COVID-19 Vaccine, and Coadministered VYD2311 With a COVID-19 Vaccine
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT07655180-Jul 28, 2026
NCT ID
NCT07655180
Status
RECRUITING
Phase
Phase 3
Sponsor
Invivyd, Inc.
Executive brief
Investment-Ready Snapshot
Invivyd, Inc. is advancing VYD2311, a COVID-19 vaccine, through a Phase 3 clinical trial aimed at evaluating its safety, tolerability, and immunogenicity compared to existing COVID-19 vaccines. The trial's design includes a randomized, double-blind methodology with a focus on both standalone and coadministration scenarios with a COVID-19 vaccine. Given the ongoing global demand for effective COVID-19 vaccines, successful outcomes could position VYD2311 favorably in a competitive market, particularly against established players. The trial is currently recruiting participants, with an estimated completion date in August 2026, indicating a strategic timeline for potential market entry. The results could have significant implications for public health and pandemic management, especially in addressing emerging variants of SARS-CoV-2.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT07655180
Indication
COVID-19
Modality
RNA therapy
Target
SARS-CoV-2 virus, specifically targeting the virus's ability to infect cells through neutralizing antibodies.
Intervention
COVID-19 mRNA vaccine, VYD2311, Placebo (Normal Saline)
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.