Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

A Study to Evaluate the Safety and Efficacy of CB-03-01 Cream, 1% in Subjects With Facial Acne Vulgaris (25)

ClinicalTrials.gov ID: NCT02608450

Public ClinicalTrials.gov record NCT02608450. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 19, 2026, 11:28 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT02608450
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Cassiopea SpA
Industry
Enrollment
708 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
9 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 21, 2016 (Actual)
Primary completion
Apr 11, 2018 (Actual)
Completion
Apr 11, 2018 (Actual)
Last update posted
Nov 20, 2020

2016 – 2018

United States locations

U.S. sites
44
U.S. states
18
U.S. cities
37
Facility City State ZIP Site status
Gary M. Petrus, MD PA Little Rock Arkansas 72205 —
Center For Dermatology Clinical Research, Inc. Fremont California 94538 —
Vitiligo & Pigmentation Institute of Southern California Los Angeles California 90036 —
San Diego Sports Medicine and Family Health Center San Diego California 92120 —
Rady Childrens Hospital, Pediatric and Adolescent Dermatology San Diego California 92123 —
Southern California Dermatology Santa Ana California 92701 —
Clinical Science Institute Santa Monica California 90404 —
Memorial Research Medical Clinic dba / Orange County Research Center Tustin California 92780 —
Horizons Clinical Research Center, LLC Denver Colorado 80220 —
Site 0190 Boca Raton Florida 33434 —
Study Protocol, Inc. Boynton Beach Florida 33437 —
Site 0196 Miami Florida 33125 —
Site 0197 Miami Florida 33126 —
Site 0198 Miami Florida 33135 —
Site 0199 Miami Florida 33145 —
Site 0191 Miami Florida 33172 —
Site 0192 Miami Florida 33172 —
Site 0195 Miami Florida 33176 —
Tory Sullivan, M.D., P.A. North Miami Beach Florida 33162 —
Meridien Research St. Petersburg Florida 33709 —
MOORE Clinical Research, Inc. Tampa Florida 33609 —
MedaPhase, Inc. Newnan Georgia 30263 —
Site 0152 Carmel Indiana 46032 —
The Indiana Clinical Trials Center Plainfield Indiana 46168 —
Henry Ford Health System Detroit Michigan 48202 —
MediSearch Clinical Trials Saint Joseph Missouri 64506 —
The Center for Dermatology, Cosmetic & Laser Surgery Mount Kisco New York 10549 —
DermResearch Center of New York, Inc. Stony Brook New York 11790 —
Wake Research Associates Raleigh North Carolina 27612 —
Wake Forest University Health Sciences Winston-Salem North Carolina 27157 —
Oregon Dermatology and Research Center Portland Oregon 97210 —
The Pennsylvania State University and the Milton S. Hershey Medical Center Hershey Pennsylvania 17033 —
Omega Medical Research Warwick Rhode Island 02886 —
Greenville Dermatology, LLC Greenville South Carolina 29607 —
International Clinical Research - Tennessee LLC Murfreesboro Tennessee 37130 —
Tennessee Clinical Research Center Nashville Tennessee 37215 —
Westlake Dermatology Clinical Research Center Austin Texas 78746 —
Bellaire Dermatology Associates Bellaire Texas 77401 —
J&S Studies, Inc. College Station Texas 77845 —
The University of Texas Health Science Center at Houston Houston Texas 77030 —
Austin Institute for Clinical Research, Inc. Pflugerville Texas 78660 —
Clinical Research Associates of Tidewater, Inc. Norfolk Virginia 23507 —
Dermatology Associates Seattle Washington 98101 —
Premier Clinical Research Spokane Washington 99202 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 10 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02608450, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 20, 2020 · Synced Oct 19, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02608450 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →