A Phase 3, Vehicle-controlled Efficacy and Safety Study of IDP-123 Lotion in the Treatment of Acne Vulgaris (302)
A Phase 3, Multi-Center, Randomized, Double-Blind, Vehicle-Controlled, 2 Arm, Parallel Group Study Comparing the Safety and Efficacy of IDP-123 Lotion and IDP-123 Vehicle Lotion in the Treatment of Acne Vulgaris
1 other identifier
interventional
801
2 countries
45
Brief Summary
This is a multi-center, randomized, double-blind, vehicle-controlled, 12-week study designed to assess the safety, efficacy, and tolerability of IDP-123 Lotion in comparison with IDP-123 Vehicle Lotion.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for phase_3
Started Jul 2017
Shorter than P25 for phase_3
45 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 24, 2017
CompletedFirst Posted
Study publicly available on registry
May 30, 2017
CompletedStudy Start
First participant enrolled
July 11, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 24, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
July 24, 2018
CompletedResults Posted
Study results publicly available
April 1, 2021
CompletedApril 1, 2021
March 1, 2021
1 year
May 24, 2017
February 15, 2021
March 30, 2021
Conditions
Outcome Measures
Primary Outcomes (2)
Absolute Change in Mean Lesion Counts at Week 12
For noninflammatory facial lesions, open comedones (blackheads) and closed comedones (whiteheads) were recorded as a single count. For inflammatory facial lesions, papules (solid, elevated lesion less than 5 mm) and pustules (elevated lesion containing pus less than 5 mm) were recorded as a single count, while nodular lesions (palpable subcutaneous lesion greater than 5 mm) were counted and recorded separately.
Baseline to Week 12
Percentage of Subjects Who Had at Least a 2-grade Reduction From Baseline at Week 12 in the Evaluator's Global Severity Score (EGSS) and Had an EGSS at Week 12 That Equated to "Clear" or "Almost Clear"
Evaluator's Global Severity Score (EGSS) was determined based on evaluator-blinded evaluations of the signs and symptoms of acne vulgaris. Evaluations were scored on a scale of 0-4, with 0 being clear and 4 being severe.
Baseline to Week 12
Secondary Outcomes (4)
Percentage Change in Mean Lesion Counts at Week 12
Baseline to Week 12
Percentage of Subjects Who Had at Least a 2-grade Reduction From Baseline at Week 12 in the Evaluator's Global Severity Score (EGSS)
Baseline to Week 12
Percentage Change in Mean Lesion Counts at Week 8
Baseline to Week 8
Percentage Change in Mean Lesion Counts at Week 4
Baseline to Week 4
Study Arms (2)
IDP-123 Lotion
EXPERIMENTALTazarotene 0.045% Lotion
IDP-123 Vehicle Lotion
PLACEBO COMPARATORVehicle Lotion
Interventions
Eligibility Criteria
You may qualify if:
- Male or female at least 9 years of age and older;
- Written and verbal informed consent must be obtained. Subjects less than age of consent must sign an assent for the study and a parent or a legal guardian must sign the informed consent (if subject reaches age of consent during the study they should be re-consented at the next study visit);
- Subject must have a score of 3 (moderate) or 4 (severe) on the Evaluator's Global Severity assessment at the baseline visit;
- Subjects with facial acne inflammatory lesion (papules, pustules, and nodules) count no less than 20 but no more than 50;
- Subjects with facial acne non-inflammatory lesion (open and closed comedones) count no less than 25 but no more than 100;
- Subjects with two or fewer facial nodules
You may not qualify if:
- Use of an investigational drug or device within 30 days of enrollment or participation in a research study concurrent with this study;
- Any dermatological conditions on the face that could interfere with clinical evaluations such as acne conglobata, acne fulminans, secondary acne, perioral dermatitis, clinically significant rosacea, gram-negative folliculitis, dermatitis, eczema;
- Any underlying disease(s) or some other dermatological condition of the face that requires the use of interfering topical or systemic therapy or makes evaluations and lesion count inconclusive;
- Subjects with a facial beard or mustache that could interfere with the study assessments;
- Subjects with more than two (2) facial nodules;
- Evidence or history of cosmetic-related acne
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (45)
Valeant Site 41
Mobile, Alabama, 36608, United States
Valeant Site 22
Rogers, Arkansas, 72758, United States
Valeant Site 34
Carlsbad, California, 92008, United States
Valeant Site 12
Fremont, California, 94538, United States
Valeant Site 06
San Diego, California, 92123, United States
Valeant Site 13
San Diego, California, 92123, United States
Valeant Site 31
San Diego, California, 92123, United States
Valeant Site 36
Santa Ana, California, 92701, United States
Valeant Site 25
Denver, Colorado, 80220, United States
Valeant Site 05
Boynton Beach, Florida, 33437, United States
Valeant Site 29
Clearwater, Florida, 33761, United States
Valeant Site 38
Jupiter, Florida, 33458, United States
Valeant Site 02
Miami, Florida, 33144, United States
Valeant Site 26
West Palm Beach, Florida, 33406, United States
Valeant Site 44
Snellville, Georgia, 30078, United States
Valeant Site 32
Louisville, Kentucky, 40241, United States
Valeant Site 19
Rockville, Maryland, 20850, United States
Valeant Site 08
Bay City, Michigan, 48706, United States
Valeant Site 30
Clarkston, Michigan, 48346, United States
Valeant Site 37
Clinton Township, Michigan, 48038, United States
Valeant Site 20
Fort Gratiot, Michigan, 48059, United States
Valeant Site 24
Fridley, Minnesota, 55432, United States
Valeant Site 03
Morristown, New Jersey, 07960, United States
Valeant Site 42
Albuquerque, New Mexico, 87106, United States
Valeant Site 10
New York, New York, 10155, United States
Valeant Site 43
Rochester, New York, 14623, United States
Valeant Site 33
Stony Brook, New York, 11790, United States
Valeant Site 11
Oklahoma City, Oklahoma, 73112, United States
Valeant Site 28
Broomall, Pennsylvania, 19008, United States
Valeant Site 16
Warwick, Rhode Island, 02886, United States
Valeant Site 18
Knoxville, Tennessee, 37922, United States
Valeant Site 14
Murfreesboro, Tennessee, 37130, United States
Valeant Site 23
College Station, Texas, 77845, United States
Valeant Site 07
Dallas, Texas, 75234, United States
Valeant Site 27
Pflugerville, Texas, 78660, United States
Valeant Site 04
San Antonio, Texas, 78218, United States
Valeant Site 39
Sugar Land, Texas, 77479, United States
Valeant Site 09
Layton, Utah, 84041, United States
Valeant Site 15
West Jordan, Utah, 84088, United States
Valeant Site 21
Charlottesville, Virginia, 22911, United States
Valeant Site 35
Walla Walla, Washington, 99362, United States
Valeant Site 01
Surrey, British Columbia, V3VOC6, Canada
Valeant Site 45
Winnipeg, Manitoba, R3M3Z4, Canada
Valeant Site 40
Windsor, Ontario, N8W5L7, Canada
Valeant Site 17
Saint-Jérôme, Quebec, J7Z3B8, Canada
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Results Point of Contact
- Title
- Study Director
- Organization
- Bausch Health Americas, Inc
Study Officials
- STUDY DIRECTOR
Anya Loncaric
Valeant Pharmaceuticals
Publication Agreements
- PI is Sponsor Employee
- No
- Restriction Type
- OTHER
- Restrictive Agreement
- Yes
Study Design
- Study Type
- interventional
- Phase
- phase 3
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 24, 2017
First Posted
May 30, 2017
Study Start
July 11, 2017
Primary Completion
July 24, 2018
Study Completion
July 24, 2018
Last Updated
April 1, 2021
Results First Posted
April 1, 2021
Record last verified: 2021-03