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NUVAXOVID

Approved / Licensed

Developer: Novavax, Inc.  |  Target Disease: COVID-19

Category Resource

Explore licensed vaccines, adverse event reporting data, and history for this disease.

View COVID-19 Vaccine Guide →
Development Phase Approved / Licensed Primary Status
Platform Technology See FDA product page / label Biologic Architecture
Target Indication COVID-19 Pathogen / Antigen
Last Verified 2026-07-10 Tier 1 Multi-Source Checked

Multi-Jurisdiction Regulatory Status

Official licensing, rolling submissions, or authorization status tracked across major health authorities.

Regulatory Authority Status & Details
US FDA Approved / Authorized Date: 2025FDA approval / licensure action (public FDA materials)
EMA (Europe) Not Filed / Pre-submission
Health Canada Not Filed / Pre-submission
TGA (Australia) Not Filed / Pre-submission

Scientific Profile & Documentation

Platform Architecture
See FDA product page / label
Lead Developer
Novavax, Inc.
Next Expected Milestone
US-licensed — see product label / ACIP for use; further supplements may expand indication
Analyst & Development Notes
FDA CBER licensed / approved vaccine (regulator-confirmed US listing). Protein-based COVID-19 vaccine (US pathway evolved from EUA to licensure/seasonal updates — verify current strain formulation on FDA page). May also have later supplements (strain updates, age expansions); see product page.
Primary Source Documentation
FDA — NUVAXOVID →

Registered Clinical Trials & Studies

Direct registry links to active, completed, or pivotal registration studies across phases.

No primary ClinicalTrials.gov record linked directly. Study data tracked via regulatory submission filings and peer-reviewed releases.

Milestone Overview

  • Stage Verification
    Approved / Licensed confirmed as of 2026-07-10.
  • Target Milestone
    US-licensed — see product label / ACIP for use; further supplements may expand indication

Vaccine Data Navigator Candidate Profile Registry:

This candidate profile is indexed across all clinical development levels (Preclinical through Phase 1–3, Regulatory Filing, and Licensure) from primary registry databases (ClinicalTrials.gov, WHO ICTRP, FDA CBER, EMA, Health Canada, TGA Australia). Data are updated continuously to track global biologic and vaccine pipelines.