A Phase 2 Dose Escalating Study to Evaluate the Safety and Efficacy of CB-03-01 Cream in Subjects With Facial Acne Vulgaris

Completed · Phase 2

Conditions studied: Acne Vulgaris

In brief

CB-03-01 is being developed for the topical treatment of acne vulgaris, an androgen-dependent skin disorder. The purpose of this study is to compare the safety and efficacy of multiple concentrations of CB-03-01 to vehicle in the treatment of acne vulgaris.

Key facts

Study ID: NCT01631474
Run by: Intrepid Therapeutics, Inc.
People needed: 363
Starts: 2012-06-01
Expected to finish: 2014-02-01
Last updated by the study team: 2020-11-16

Who can join

Age: 12 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Subject is male or non-pregnant female. Females must be post-menopausal, surgically sterile or using highly effective birth control methods.
Subject has provided written and verbal informed consent/assent.
Subject has facial acne vulgaris (including the nose).
Subject is willing to comply with study instructions and return to the clinic for required visits.
Subject has used the same type and brand of make-up, other facial products (including cleanser) and hair products (e.g., shampoo, gel, hair spray, mousse, etc.) for at least one month prior to the study start and agrees to continue his/her other general skin and hair care products and regimen for the entire study.

You may not qualify if…

Subject is pregnant, lactating, or is planning to become pregnant during the study.
Subject is currently enrolled in an investigational drug or device study.
Subject has received an investigational drug or been treated with an investigational device within 30 days prior to the study start.
Subject has the need or plans to be exposed to artificial tanning devices or excessive sunlight during the trial
Subject has used any of the following topical anti-acne preparations or procedures on the face:
Topical anti-acne treatments including but not limited to over-the-counter acne cleaners or treatments, benzoyl peroxide, antibiotics, azelaic acid, sulfa based products, corticosteroids and salicylic acid within two weeks of the initiation of treatment.
Retinoids, including tazarotene, adapalene, tretinoin, within four weeks of the initiation of treatment.
Light treatments, microdermabrasion or chemical peels within eight weeks of the initiation of treatment.
Subject has used the following systemic anti-acne medications:
Corticosteroids (including intramuscular and intralesional injections) within four weeks of the initiation of treatment. Inhaled, intranasal or ocular corticosteroids are allowed if use is stable (stable use is defined as dose and frequency unchanged for at least four weeks prior to the initiation of treatment).
Antibiotics within four weeks of the initiation of treatment with the exception of five days or less of antibiotic therapy during this period, but with no antibiotics use permitted within one week prior to the initiation of treatment.
Spironolactone within eight weeks of the initiation of treatment with the exception of five days or less of spironolactone therapy during this period, but with no spironolactone use permitted within one week prior to the initiation of treatment.
Retinoid therapy within six months of the initiation of treatment.

Where it is running

Dermatology Research Associates — Los Angeles, California, United States
Therapeutics Clinical Research — San Diego, California, United States
University Clinical Trials — San Diego, California, United States
International Clinical Research - US, LLC — Sanford, Florida, United States
Gwinnett Clinical Research Center, Inc. — Snellville, Georgia, United States
Altman Dermatology Associates — Arlington Heights, Illinois, United States
Indiana Clinical Trials Center — Plainfield, Indiana, United States
Marina I. Peredo, M.D., PC — Smithtown, New York, United States
Penn State Milton S. Hershey Medical Center - Dept. of Dermatology — Hershey, Pennsylvania, United States
Clinical Partners, LLC — Johnston, Rhode Island, United States
J & S Studies — College Station, Texas, United States
UT Houston Health Science Center — Houston, Texas, United States
Virginia Clinical Research — Norfolk, Virginia, United States

Full record on ClinicalTrials.gov

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