TheraRadar
Data updated: May 26, 2026

Vaxneuvance (pneumococcal 15-valent conjugate vaccine)

Approved 2021-07-15
1
Indication
--
Phase 3 Trials
4
Years on Market

Details

Status
Prescription
First Approved
2021-07-15
Patent Cliff
2033
Revenue
$161M (Q4-2024)

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Patent cliff and revenue data

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Routes
Intramuscular
Dosage Forms
Injection

Companies

Vaxneuvance Approval History

2022
2023
2024
2025
2026
Original
New Indication
New Form
Label Update
1 FDA actions from 2021 to 2021
Jul 2021 ORIGINAL
Update · CBER biologic (Purple Book)

What Vaxneuvance Treats

1 FDA approvals

Originally approved for its first indication in 2021 .

  • Other (1)
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Clinical Trial Registry

4 trials
Trial Sponsor ID Phase Status Title
NCT06855160 223105 2024-518840-18-00 Ph 3 recruiting A Study on the Immune Response and Safety of an Investigational Chickenpox Vaccine and a Marketed Measles, Mumps and Rubella Vaccine When Administered as Intramuscular Injection to Healthy Children 12 to 15 Months of Age
NCT06806137 214002 2024-516635-27-00 Ph 3 recruiting A Study on the Immune Response and Safety of the Second Dose of an Investigational Chickenpox Vaccine When Given to Healthy Children 3 Months After a First Dose at 12 to 15 Months of Age
NCT06740630 213998 2024-515869-33-00 Ph 3 recruiting A Study on the Immune Response and Safety of an Investigational Chickenpox Vaccine When Given to Healthy Children 12 to 15 Months of Age
NCT06693895 213997 2024-515868-31-00 Ph 3 recruiting A Study on the Safety of an Investigational Chickenpox Vaccine, When Given to Healthy Children, 12 to 15 Months of Age
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Active Pipeline

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Ongoing clinical trials by development phase

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

Vaxneuvance FDA Label Details

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Revenue Insights

  • Q4-2024: $161M
  • Historical trend analysis

Patent Timeline

  • Cliff: 2033
  • Generic/biosimilar risk

Trial Analysis

  • Clinical trial tracking
  • Development stage analysis

Competitive Landscape

  • Competitor tracking
  • Same target/indication analysis
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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.