A Study to Compare the Efficacy and Safety of Topical Administration of FMX-101 for Treatment of Moderate-to-Severe Acne



Status:Completed
Conditions:Acne, Acne, Dermatology
Therapuetic Areas:Dermatology / Plastic Surgery
Healthy:No
Age Range:9 - Any
Updated:11/7/2018
Start Date:May 2016
End Date:October 13, 2017

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A Randomized, Double-Blind Study to Compare the Efficacy, Safety and Long-Term Safety of Topical Administration of FMX-101 for 1 Year in the Treatment of Moderate-to-Severe Acne Vulgaris, Study FX2014-04

This is a Phase 3 study to evaluate the efficacy, safety and long-term safety of the topical
administration of FMX-101, 4% minocycline foam for the treatment of moderate-to-severe acne
vulgaris.


Inclusion Criteria:

- Has facial acne vulgaris with:

- 20 to 50 inflammatory lesions (papules, pustules, and nodules);

- 25 to 100 noninflammatory lesions (open and closed comedones);

- no more than 2 nodules on the face; and

- IGA score of moderate (3) to severe (4)

- Willing to use only the supplied non-medicated cleanser (Cetaphil Gentle Skin
Cleanser) and to refrain from use of any other acne medication, medicated cleanser,
excessive sun exposure, and tanning booths for the duration of the study

Exclusion Criteria:

- Acne conglobata, acne fulminans, secondary acne (chloracne, drug induced acne) or any
dermatological condition of the face or facial hair (eg, beard, sideburns, mustache)
that could interfere with the clinical evaluations

- Sunburn on the face

- Severe systemic disease, which might interfere with the conduct of the study or the
interpretation of the results.

- Abnormal baseline laboratory values that are considered clinically significant

- Allergy to tetracycline-class antibiotics or to any ingredient in the study drug

- Pseudomembranous colitis or antibiotic-associated colitis
We found this trial at
29
sites
Bridgeport, West Virginia 26330
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Oakbrook Terrace, Illinois 60181
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Omaha, NE
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Washington,
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West Jordan, UT
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