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Generated: January 24, 2019

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CLINICAL TRIALS PROFILE FOR FLUOCINONIDE

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Clinical Trials for Fluocinonide

Trial ID Title Status Sponsor Phase Summary
NCT00297011 Valacyclovir+Temovate Gel for the Treatment of Herpes Labialis Completed GlaxoSmithKline Phase 2 A randomized study comparing the combination of valacyclovir and temovate gel (clobetasol gel) versus placebo for the treatment of recurrent herpes labialis (cold sores).
NCT00297011 Valacyclovir+Temovate Gel for the Treatment of Herpes Labialis Completed University of Utah Phase 2 A randomized study comparing the combination of valacyclovir and temovate gel (clobetasol gel) versus placebo for the treatment of recurrent herpes labialis (cold sores).
NCT00667589 Sorafenib-induced Hand- Foot Skin Reaction Treatment Terminated Bayer Phase 2 The purpose of this study is to evaluate treatments for a rash caused by sorafenib.
NCT00667589 Sorafenib-induced Hand- Foot Skin Reaction Treatment Terminated Northwestern University Phase 2 The purpose of this study is to evaluate treatments for a rash caused by sorafenib.
NCT00819507 VANOS Cream and Skin Barrier Function Unknown status Medicis Pharmaceutical Corporation Phase 4 The purpose of this study is to determine the effect of short-term therapy using "VANOS Cream," a super-potent topical steroid cream on skin barrier function in patients with atopic dermatitis. This cream is already approved for this indication, but the investigators will further examine its effects on the skin barrier. This cream is a novel formulation of fluocinonide designed to enhance compliance with a cream base, but have the skin barrier repair properties of an ointment.
NCT00819507 VANOS Cream and Skin Barrier Function Unknown status Oregon Health and Science University Phase 4 The purpose of this study is to determine the effect of short-term therapy using "VANOS Cream," a super-potent topical steroid cream on skin barrier function in patients with atopic dermatitis. This cream is already approved for this indication, but the investigators will further examine its effects on the skin barrier. This cream is a novel formulation of fluocinonide designed to enhance compliance with a cream base, but have the skin barrier repair properties of an ointment.
NCT01049243 A Study Evaluating the Efficacy of Fluocinonide Cream 0.1% (Vanos) in Subjects With Atopic Dermatitis Completed Medicis Pharmaceutical Corporation Phase 4 The purpose of this research study is to better understand how fluocinonide cream 0.1% (Vanos®) works when people use it to treat atopic dermatitis for just a few days.
Trial ID Title Status Sponsor Phase Summary

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Clinical Trial Conditions for Fluocinonide

Condition Name

Condition Name for Fluocinonide
Intervention Trials
Atopic Dermatitis 3
Hand-foot Skin Reaction 1
Breast Carcinoma 1
Rash 1
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Condition MeSH

Condition MeSH for Fluocinonide
Intervention Trials
Eczema 3
Dermatitis, Atopic 3
Dermatitis 3
Mycosis Fungoides 1
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Clinical Trial Locations for Fluocinonide

Trials by Country

Trials by Country for Fluocinonide
Location Trials
United States 7
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Trials by US State

Trials by US State for Fluocinonide
Location Trials
North Carolina 3
Oregon 2
Illinois 1
Utah 1
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Clinical Trial Progress for Fluocinonide

Clinical Trial Phase

Clinical Trial Phase for Fluocinonide
Clinical Trial Phase Trials
Phase 4 2
Phase 2 3
N/A 3
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Clinical Trial Status

Clinical Trial Status for Fluocinonide
Clinical Trial Phase Trials
Completed 4
Terminated 1
Unknown status 1
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Clinical Trial Sponsors for Fluocinonide

Sponsor Name

Sponsor Name for Fluocinonide
Sponsor Trials
Medicis Pharmaceutical Corporation 3
Wake Forest University Health Sciences need to be deleted 2
Rochester Skin Lymphoma Medical Group, PLLC 1
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Sponsor Type

Sponsor Type for Fluocinonide
Sponsor Trials
Other 9
Industry 6
NIH 1
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Serving hundreds of leading biopharmaceutical companies globally:

Harvard Business School
Queensland Health
Daiichi Sankyo
Fish and Richardson
Chubb
QuintilesIMS
Accenture
Deloitte
Boehringer Ingelheim

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