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Data updated: Mar 10, 2026

CLOBEX

CLOBETASOL PROPIONATE
Immunology Approved 2003-07-24
3
Indications
--
Phase 3 Trials
22
Years on Market

Details

Status
Prescription
First Approved
2003-07-24
Routes
TOPICAL
Dosage Forms
SHAMPOO, SPRAY, LOTION

CLOBEX Approval History

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What CLOBEX Treats

4 indications

CLOBEX is approved for 4 conditions since its original approval in 2003. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Dermatoses
  • Plaque Psoriasis
  • Rosacea
  • Perioral Dermatitis
Source: FDA Label

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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.

CLOBEX FDA Label Details

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Indications & Usage

FDA Label (PDF)

CLOBEX (clobetasol propionate) Lotion, 0.05% is a corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses, in patients 18 years of age or older. . Limitations of Use: Do not use on the face, axillae or groin. Do not use if atrophy is present at the treatment site. Do not use for rosacea or perioral dermatitis. 1.1 Indication CLOBEX Lotion, 0.05% is a super-high potent topical corticosteroid formulation indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses only in p...

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Data Sources

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