TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

ZELSUVMI

BERDAZIMER SODIUM
Dermatology Approved 2024-01-05
1
Indication
--
Phase 3 Trials
2
Years on Market

Details

Status
Prescription
First Approved
2024-01-05
Routes
TOPICAL
Dosage Forms
GEL

Companies

Active Ingredient: BERDAZIMER SODIUM

ZELSUVMI Approval History

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What ZELSUVMI Treats

1 indications

ZELSUVMI is approved for 1 conditions since its original approval in 2024. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Molluscum Contagiosum
Source: FDA Label

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Active Pipeline

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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.

ZELSUVMI FDA Label Details

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Indications & Usage

FDA Label (PDF)

ZELSUVMI™ is indicated for the topical treatment of molluscum contagiosum (MC) in adults and pediatric patients 1 year of age and older. ZELSUVMI™ is a nitric oxide (NO) releasing agent indicated for the topical treatment of molluscum contagiosum (MC) in adults and pediatric patients 1 year of age and older.

ZELSUVMI Patents & Exclusivity

Latest Patent: Jul 2035
Exclusivity: Jan 2029

Patents (22 active)

US11723858 Expires Jul 10, 2035
US11040006 Expires Jul 10, 2035
US10736839 Expires Jul 10, 2035
US10322081 Expires Jul 10, 2035
US10258564 Expires Nov 22, 2034
US11285098 Expires Feb 28, 2034
US9855211 Expires Feb 27, 2034
US9289442 Expires Jul 3, 2032
US10265334 Expires Jul 3, 2032
US9526738 Expires Sep 3, 2031
+ 12 more patents

Exclusivity

NCE Until Jan 2029
Source: FDA Orange Book

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Data Sources

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