TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

ZILXI

MINOCYCLINE HYDROCHLORIDE
Immunology Approved 2020-05-28
1
Indication
--
Phase 3 Trials
5
Years on Market

Details

Status
Prescription
First Approved
2020-05-28
Routes
TOPICAL
Dosage Forms
AEROSOL, FOAM

Companies

Active Ingredient: MINOCYCLINE HYDROCHLORIDE

ZILXI Approval History

Loading approval history...

What ZILXI Treats

1 indications

ZILXI is approved for 1 conditions since its original approval in 2020. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Rosacea
Source: FDA Label
🔬

Active Pipeline

Pro

Ongoing clinical trials by development phase

Loading...

Key Completed Trials

Pro

Completed studies with published results, ranked by significance

Loading...
📊

Trial Timeline

Full development history with FDA approval milestones

Loading...
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.

ZILXI FDA Label Details

Pro

Indications & Usage

FDA Label (PDF)

ZILXI is indicated for the treatment of inflammatory lesions of rosacea in adults [see Clinical Studies ] . Limitations of Use This formulation of minocycline has not been evaluated in the treatment of infections. To reduce the development of drug-resistant bacteria as well as to maintain the effectiveness of other antibacterial drugs, ZILXI should be used only as indicated [see Warnings and Precautions ] . ZILXI is a tetracycline-class drug indicated for the treatment of inflammatory lesions of rosacea in adults. Limitations of Use This formulation of minocycline has not been evaluated in the...

ZILXI Patents & Exclusivity

Latest Patent: Sep 2030

Patents (9 active)

US10213512 Expires Oct 1, 2030
US8992896 Expires Oct 1, 2030
US9675700 Expires Oct 1, 2030
US8865139 Expires Oct 1, 2030
US10322186 Expires Oct 1, 2030
US10946101 Expires Oct 1, 2030
US12138311 Expires Oct 1, 2030
US10265404 Expires Oct 1, 2030
US8945516 Expires Oct 1, 2030
Source: FDA Orange Book

Want competitive intelligence?

See who's developing similar drugs and track their progress

View Pipeline Dashboard

Data Sources

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