Overview

Clinical Study Comparing the Efficacy and Safety of IDP-126 Gel in the Treatment of Acne Vulgaris

Status:
Completed
Trial end date:
2021-01-18
Target enrollment:
0
Participant gender:
All
Summary
This is a multicenter, randomized, double-blind, vehicle-controlled, 12-week study designed to assess the safety, tolerability, and efficacy of IDP-126 Gel in comparison IDP-126 Vehicle Gel at Weeks 2, 4, 8, and 12.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Bausch Health Americas, Inc.
Criteria
Inclusion Criteria:

- 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 an Evaluator's Global Severity Score (EGSS) of 3 (moderate) or 4
(severe) at the baseline visit.

- Subjects with a facial acne inflammatory lesion (papules, pustules, and nodules) count
no less than 30, but no more than 100.

- Subjects with a facial acne non-inflammatory lesion (open and closed comedones) count
no less than 35, but no more than 150.

- Subjects with 2 or fewer facial nodules.

Exclusion Criteria:

- 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 more than 2 facial nodules.

- Female subjects who are pregnant, nursing mothers, planning a pregnancy during the
course of the study, or become pregnant during the study.

- Use of estrogens (eg, Depogen, Depo-Testadiol, Gynogen, Valergen, etc) for less than
12 weeks immediately preceding study entry; subjects treated with estrogens 12 or more
consecutive weeks immediately prior to study entry need not be excluded unless the
subject expects to change dose, drug or discontinue estrogen use during the study.

- Treatment of any type of cancer within the last 6 months, with the exception of
complete surgical excision of skin cancer outside the treatment area.

- Subjects who have not undergone specified washout period(s) for topical
preparations/physical treatments used on the face or subjects who require the
concurrent use in the treatment area.

- Subjects who have not undergone specified washout period(s) for systemic medications
or subjects who require the concurrent use of systemic medications.

- Subjects with any underlying disease that the investigator deems uncontrolled, and
poses a concern for the subject's safety while participating in the study.