A Dose-ranging Study of DRM01 in Subjects With Acne Vulgaris

Completed · Phase 2

Conditions studied: Acne Vulgaris

In brief

The objectives of this study are to assess the safety and efficacy DRM01 Topical Gel compared to vehicle in patients with acne vulgaris.

Key facts

Study ID

NCT02431052

Run by

Dermira, Inc.

People needed

420

Starts

2015-04-01

Expected to finish

2016-04-01

Last updated by the study team

2021-07-20

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Signed informed consent.
• Male or non-pregnant, non-lactating females.
• Age ≥ 18 years.
• Clinical diagnosis of facial acne vulgaris defined as:
• At least 20 inflammatory lesions
• At least 20 non-inflammatory lesions
• Investigator Global Assessment of 3 or greater.

You may not qualify if…

• Active cystic acne or acne conglobata, acne fulminans, and secondary acne.
• Two or more active nodulocystic lesions.
• Screening clinical chemistry or hematology laboratory value that is considered clinically significant, in the opinion of the Investigator.
• Abnormal findings on screening ECG, deemed clinically significant, by the Investigator.
• Subjects who are actively participating in an experimental therapy study or who have received experimental therapy within 30 days or 5 half-lives (whichever is longer) of the Baseline visit.
• Subjects who are a poor medical risk because of other systemic diseases or active uncontrolled infections, in the opinion of the investigator.
• Treatment with over-the-counter topical medications for the treatment of acne vulgaris including benzoyl peroxide, topical anti-inflammatory medications, corticosteroids, α-hydroxy/glycolic acid on the face within 2 weeks prior to Baseline.
• Treatment with systemic corticosteroids (use of intranasal and inhaled corticosteroids allowed for seasonal allergies and asthma) within 4 weeks prior to Baseline.
• Treatment with systemic antibiotics or systemic anti-acne drugs or systemic anti-inflammatory drugs within 4 weeks prior to Baseline.
• Prescription topical retinoid use on the face within 4 weeks of Baseline (e.g., tretinoin, tazarotene, adapalene).
• Treatment with a new hormonal therapy or dose change to existing hormonal therapy within 12 weeks prior to Baseline. Dose and frequency of use of any hormonal therapy started more than 12 weeks prior to Baseline must remain unchanged throughout the study. Hormonal therapies include, but are not limited to, estrogenic and progestational agents such as birth control pills.
• Prior use of androgen receptor blockers (such as spironolactone or flutamide).
• Oral retinoid use (e.g., isotretinoin) within 12 months prior to Baseline or vitamin A supplements greater than 10,000 units/day within 6 months of Baseline.
• Facial procedures (chemical or laser peel, microdermabrasion, etc.) within the past 8 weeks or during the study.

Where it is running

• Coastal Clinical Research, Inc. — Mobile, Alabama, United States
• T. Joseph Raoof, MD, Inc. — Encino, California, United States
• University Clinical Trials, Inc. — San Diego, California, United States
• Tory Sullivan MD PA — North Miami Beach, Florida, United States
• International Clinical Research - US, LLC — Sanford, Florida, United States
• MOORE Clinical Research, Inc. — Tampa, Florida, United States
• Visions Clinical Research — Wellington, Florida, United States
• DermResearch, PLLC — Louisville, Kentucky, United States
• Lawrence J. Green, MD, LLC — Rockville, Maryland, United States
• Michigan Center for Skin Care Research — Clinton Township, Michigan, United States
• Henry Ford Health System — Detroit, Michigan, United States
• Minnesota Clinical Study Center — Fridley, Minnesota, United States
• Las Vegas Dermatology — Las Vegas, Nevada, United States
• Academic Dermatology Associates — Albuquerque, New Mexico, United States
• Skin Search of Rochester, Inc. — Rochester, New York, United States
• Dermatology Consulting Services — High Point, North Carolina, United States
• The Skin Wellness Center — Knoxville, Tennessee, United States
• International Clinical Research - Tennessee LLC — Murfreesboro, Tennessee, United States
• DermResearch, Inc — Austin, Texas, United States
• J&S Studies, Inc. — College Station, Texas, United States
• Center for Clinical Studies, LTD. LLP — Houston, Texas, United States
• Suzanne Bruce & Associates, PA. The Center for Skin Research — Houston, Texas, United States
• Suzanne Bruce & Associates, PA. The Center for Skin Research — Katy, Texas, United States
• Austin Institute for Clinical Research — Pflugerville, Texas, United States
• Progressive Clinical Research, PA — San Antonio, Texas, United States

Full record on ClinicalTrials.gov

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