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A Study to Evaluate the Safety and Efficacy of CB-03-01 Cream, 1% in Subjects With Facial Acne Vulgaris (26)

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ClinicalTrials.gov Identifier: NCT02608476
Recruitment Status : Recruiting
First Posted : November 18, 2015
Last Update Posted : October 26, 2017
Sponsor:
Information provided by (Responsible Party):
Cassiopea SpA

Brief Summary:
The primary objective of this study is to determine the safety and efficacy of CB-03-01 cream, 1%, versus the vehicle cream applied twice daily for 12 weeks in subjects with facial acne vulgaris.

Condition or disease Intervention/treatment Phase
Acne Vulgaris Drug: CB-03-01 cream, 1% Drug: Vehicle cream Phase 3

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 700 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Investigator)
Primary Purpose: Treatment
Official Title: A Phase 3, Multicenter, Randomized, Double-Blind, Vehicle-Controlled Study to Evaluate the Safety and Efficacy of Cortexolone 17α-Propionate (CB-03-01) Cream, 1% Applied Twice Daily for 12 Weeks in Subjects With Facial Acne Vulgaris
Study Start Date : November 2015
Estimated Primary Completion Date : December 2017
Estimated Study Completion Date : March 2018

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Acne

Arm Intervention/treatment
Experimental: CB-03-01 cream
CB-03-01 cream, 1% applied twice daily for 12 weeks
Drug: CB-03-01 cream, 1%
CB-03-01 (cortexolone 17α-propionate) is a steroidal antiandrogen that is being developed as a 1% cream for the topical treatment of acne vulgaris.
Other Name: cortexolone 17α-propionate

Placebo Comparator: Vehicle cream
Vehicle cream applied twice daily for 12 weeks
Drug: Vehicle cream
Vehicle cream manufactured to mimic look and feel of CB-03-01 but without the active ingredient cortexolone 17α-propionate.




Primary Outcome Measures :
  1. Success rate in Investigator's Global Assessment (IGA) [ Time Frame: Week 12 ]
    Proportion of subjects in each treatment group achieving "success" at Week 12, with "success" defined as an IGA score of "clear (score=0)" or "almost clear (score=1)" and at least a two-point reduction in IGA compared to Baseline.

  2. Change from baseline in non-inflammatory lesion counts [ Time Frame: Baseline and Week 12 ]
    Absolute change from Baseline in non-inflammatory lesion counts in each treatment group at Week 12.

  3. Change from baseline in inflammatory lesion counts [ Time Frame: Baseline and Week 12 ]
    Absolute change from Baseline in inflammatory lesion counts in each treatment group at Week 12.


Secondary Outcome Measures :
  1. Change from baseline in total lesion counts [ Time Frame: Baseline and Week 12 ]
    Absolute change from Baseline in total lesions counts in each treatment group at Week 12.

  2. Percent change from baseline in total lesion counts [ Time Frame: Baseline and Week 12 ]
    Percent change from Baseline in total lesions counts in each treatment group at Week 12.

  3. Percent change from baseline in non-inflammatory lesion counts [ Time Frame: Baseline and Week 12 ]
    Percent change from Baseline in non-inflammatory lesions count in each treatment group at Week 12.

  4. Percent change from baseline in inflammatory lesion counts [ Time Frame: Baseline and Week 12 ]
    Percent change from Baseline in inflammatory lesions count in each treatment group at Week 12.


Other Outcome Measures:
  1. Local Site Reactions [ Time Frame: Baseline, Weeks 4, 8, and 12 ]
    Local Site Reactions (LSRs) including telangiectasia, skin atrophy, striae rubrae, erythema, edema, scaling/dryness, stinging/burning, and pruritus scored by frequency and severity at every visit (Baseline, Weeks 4, 8, and 12).



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Ages Eligible for Study:   9 Years and older   (Child, Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Subject is male or non-pregnant female, 9 years of age or older. Females must be post-menopausal, surgically sterile, or using highly effective birth control methods. Women of child-bearing potential must have a negative urine pregnancy test (UPT) at the Screening/Baseline Visit.
  2. Subject has provided written and verbal informed consent/assent. A subject under 18 years of age must provide written informed assent and be accompanied by the parent or legal guardian at the time of assent/consent signing.
  3. Subject has an Investigator's Global Assessment (IGA) score of 3 (moderate) or 4 (severe) [0 (clear) to 4 (severe) scale].
  4. Subject has facial acne vulgaris with at least 30 to a maximum of 75 inflammatory lesions (papules, pustules, and nodules) and 30 to a maximum of 100 non-inflammatory lesions (open and closed comedones).
  5. Subject and parent/guardian (if applicable) are willing to comply with study instructions and return to the clinic for required visits.
  6. Subject has used the same type and brand of make-up, other facial products (exclusive of RX/OTC acne cleansers) and hair products (e.g., shampoo, gel, hair spray, mousse, etc.) for at least one (1) month prior to the Baseline Visit and agrees to continue his/her other general skin and hair care products and regimen for the entire study.

Exclusion Criteria:

  1. Subject is pregnant, lactating, or is planning to become pregnant during the study.
  2. Subject has any skin pathology or condition that could interfere with the evaluation of the test products or requires the use of interfering topical or systemic therapy.
  3. Subject has greater than two (2) facial nodules.
  4. Subject has nodulocystic acne.
  5. Subject has any condition which, in the investigator's opinion, would make it unsafe for the subject to participate in this research study.
  6. Subject is currently enrolled in an investigational drug or device study.
  7. Subject has received an investigational drug or has been treated with an investigational device within 30 days prior to the initiation of treatment (Baseline).
  8. Subject has facial hair that could interfere with the study assessments in the opinion of the investigator.
  9. Subject and parent/guardian (if applicable) are unable to communicate or cooperate with the investigator due to language problems, poor mental development, or impaired cerebral function.
  10. Subject may be unreliable for the study including subjects who engage in excessive alcohol intake or drug abuse, or subjects who are unable to return for scheduled follow-up visits.
  11. Subject has known hypersensitivity or previous allergic reaction to any of the active or inactive components of the test articles.
  12. Subject has the need or plans to be exposed to artificial tanning devices or excessive sunlight during the trial.
  13. Subject has used any of the prohibited topical anti-acne treatments or procedures prior to the study unless appropriate washout period is documented.
  14. Subject has used used any of the prohibited systemic anti-acne medications prior to the study unless appropriate washout period is documented.

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 ClinicalTrials.gov identifier (NCT number): NCT02608476


Contacts
Contact: Nicoletta Coceani acnestudy@therapeuticsinc.com
Contact: Katrina Kokjohn acnestudy@therapeuticsinc.com

Locations
United States, Arizona
Johnson Dermatology Active, not recruiting
Fort Smith, Arizona, United States, 72916
Clear dermatology & Aesthetic Center Active, not recruiting
Scottsdale, Arizona, United States, 85255
United States, California
Center for Dermatology and Laser Surgery Active, not recruiting
Sacramento, California, United States, 95819
United States, Florida
Belleair Research Center Active, not recruiting
Pinellas Park, Florida, United States, 33781
United States, Illinois
Arlington Dermatology Active, not recruiting
Arlington Heights, Illinois, United States, 60005
United States, Kansas
Kansas City Dermatology, PA Active, not recruiting
Overland Park, Kansas, United States, 66215
United States, Maryland
Maryland Laser Skin and Vein Institute Active, not recruiting
Hunt Valley, Maryland, United States, 21030
United States, New York
Sadick Research Group, LLC Active, not recruiting
New York, New York, United States, 10075
Skin Specialty Dermatology Recruiting
New York, New York, United States, 10155
Contact: Okechukwu Udogu, MD, MPH    212-223-6599    skinspecialtydermatology@gmail.com   
Principal Investigator: Fran Cook-Bolden, MD         
United States, Rhode Island
Clinical Partners, LLC Active, not recruiting
Johnston, Rhode Island, United States, 02919
United States, Texas
Texas Dermatology and Laser Specialists Recruiting
San Antonio, Texas, United States, 78218
Contact: Carla Ilie       carla@TexasDLS.com   
Principal Investigator: John Browning, MD         
Progressive Clinical Research, PA Active, not recruiting
San Antonio, Texas, United States, 78229
Sponsors and Collaborators
Cassiopea SpA
Investigators
Study Director: Louise Dube, PhD Cassiopea S.p.A.

Additional Information:
Responsible Party: Cassiopea SpA
ClinicalTrials.gov Identifier: NCT02608476     History of Changes
Other Study ID Numbers: CB-03-01/26
First Posted: November 18, 2015    Key Record Dates
Last Update Posted: October 26, 2017
Last Verified: October 2017

Keywords provided by Cassiopea SpA:
acne

Additional relevant MeSH terms:
Acne Vulgaris
Acneiform Eruptions
Skin Diseases
Sebaceous Gland Diseases