Last reviewed · How we verify

TOZINAMERAN

FDA-approved approved Vaccine component ✓ Verified May 2026 Quality 5/100

TOZINAMERAN is a drug. It is currently FDA-approved (first approved 2020).

Tozinameran, also known as BNT-162B2, is a vaccine antigen that targets the spike glycoprotein. It is used as a component in COVID-19 vaccines, including Comirnaty, and has been studied in various clinical trials for its efficacy in conditions such as HIV, organ transplantation, lymphoma, and multiple myeloma.

At a glance

Generic nameTOZINAMERAN
ModalityVaccine component
Therapeutic areaImmunology
PhaseFDA-approved
First approval2020
Annual revenue4367

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results
SEC EDGARRevenue + earnings

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:

Frequently asked questions about TOZINAMERAN

What is TOZINAMERAN?

TOZINAMERAN is a Vaccine component drug.

When was TOZINAMERAN approved?

TOZINAMERAN was first approved on 2020.

What development phase is TOZINAMERAN in?

TOZINAMERAN is FDA-approved (marketed).

What is TOZINAMERAN's annual revenue?

TOZINAMERAN generated approximately $0.0B in annual revenue.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing