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Trial record 31 of 164 for:    acne AND Vehicle

Safety and Efficacy Study of CLS001Topical Gel Compared to Vehicle in Subjects With Inflammatory Acne Vulgaris

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT02066545
Recruitment Status : Completed
First Posted : February 19, 2014
Last Update Posted : September 17, 2015
Information provided by (Responsible Party):
Maruho Co., Ltd.

Brief Summary:
The primary objective of this study is to evaluate the safety and efficacy of once-daily topical application of CLS001 1%, 1.75% and 2.5% topical gel compared to vehicle topical gel in subjects with inflammatory acne vulgaris

Condition or disease Intervention/treatment Phase
Acne Vulgaris Drug: CLS001 Topical Gel Drug: CLS001 Topical Gel Vehicle Phase 2

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 327 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Investigator)
Primary Purpose: Treatment
Official Title: A Phase 2, Randomized, Vehicle-Controlled, Double-Blind, Multicenter Study to Evaluate the Safety and Efficacy of Three Once-Daily CLS001 Topical Gels Versus Vehicle Administered for 12 Weeks to Subjects With Acne Vulgaris
Study Start Date : April 2014
Actual Primary Completion Date : November 2014

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Acne

Arm Intervention/treatment
Placebo Comparator: Vehicle Gel Drug: CLS001 Topical Gel Vehicle
Experimental: CLS001 topical gel 1%
Topical application once daily
Drug: CLS001 Topical Gel
Experimental: CLS001 topical gel 1.75%
Topical application once daily
Drug: CLS001 Topical Gel
Experimental: CLS001 topical gel 2.5%
Topical application once daily
Drug: CLS001 Topical Gel

Primary Outcome Measures :
  1. Change in inflammatory lesion count from Baseline [ Time Frame: 6, 9 and 12 weeks ]

Secondary Outcome Measures :
  1. Percent change from baseline at each visit in inflammatory lesions, non-inflammatory lesions and total lesions [ Time Frame: 1, 3, 6, 9 and 12 weeks ]
  2. Absolute change from Baseline at each visit in inflammatory lesions, no-inflammatory lesions, and total lesions [ Time Frame: 1, 3, 6, 9 and 12 weeks ]
  3. Percentage of subjects with an Investigator's Global Assessment (IGA) of clear or almost clear (0 or 1) at each visit [ Time Frame: 1, 3, 6, 9, and 12 weeks ]
  4. Percentage of subjects with a 2 grade reduction in the IGA at each visit [ Time Frame: 1, 3, 6, 9, and 12 weeks ]

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

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Ages Eligible for Study:   12 Years and older   (Child, Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Male or non-pregnant female subjects with facial acne vulgaris, 12 years of age or older.
  • Subjects with ≥20 inflammatory facial lesions (papules, pustules) inclusive of the nose, with a maximum of 9 inflammatory pustules.
  • An Investigator's Global Assessment (IGA) of Moderate (3) or Severe (4)

Exclusion Criteria:

  • Subjects with acne conglobate, acne fulminans, and secondary acne (chloracne, drug-induced acne, polycystic ovarian syndrome, etc.)
  • Subjects with greater that 75 facial non-inflammatory lesions (open and/or closed comedones; excluding the nose)
  • Subjects with more than 2 facial nodulocystic lesions

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT02066545

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United States, California
Encino Research Center
Encino, California, United States, 91436
Skin Surgery Medical Group, Inc.
San Diego, California, United States, 92117
Clinical Science Institute
Santa Monica, California, United States, 90404
United States, Florida
Skin Care Research, Inc.
Boca Raton, Florida, United States, 33486
Belleair Research Center
Pinellas Park, Florida, United States, 33781
Moore Clinical Research, Inc.
Tampa, Florida, United States, 33609
Kenneth R. Beer, MD, PA
West Palm Beach, Florida, United States, 33401
United States, Georgia
MedaPhase, Inc.
Newnan, Georgia, United States, 30263
United States, Michigan
Hamzavi Dermatology
Fort Gratiot, Michigan, United States, 48059
United States, Minnesota
Minnesota Clinical Study Center
Fridley, Minnesota, United States, 55432
United States, New Mexico
Academic Dermatology Associates
Albuquerque, New Mexico, United States, 87106
United States, New York
Manhattan Dermatology & Cosmetic Center
New York, New York, United States, 10017
Derm Research Center of New York, Inc.
Stony Brook, New York, United States, 11790
United States, North Carolina
Dermatology Consulting Services
High Point, North Carolina, United States, 27262
Wake Research Associates
Raleigh, North Carolina, United States, 27612
United States, Tennessee
Tennessee Clinical Research Center
Nashville, Tennessee, United States, 37215
United States, Texas
Premier Research
Austin, Texas, United States, 78705
J & S Studies, Inc.
College Station, Texas, United States, 77845
Progressive Clinical Research, PA
San Antonio, Texas, United States, 78229
United States, Washington
Premier Clinical Research
Spokane, Washington, United States, 99204
Sponsors and Collaborators
Maruho Co., Ltd.

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Responsible Party: Maruho Co., Ltd. Identifier: NCT02066545     History of Changes
Other Study ID Numbers: CLS001-CO-PR-003
First Posted: February 19, 2014    Key Record Dates
Last Update Posted: September 17, 2015
Last Verified: September 2015
Additional relevant MeSH terms:
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Acne Vulgaris
Acneiform Eruptions
Skin Diseases
Sebaceous Gland Diseases