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Completed Phase 3 Interventional Results available

Bioequivalence Study of Clindamycin Gel 1% in Treatment of Acne Vulgaris

ClinicalTrials.gov ID: NCT03522441

Public ClinicalTrials.gov record NCT03522441. 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 21, 2026, 11:20 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 Multi-Center, Double-Blind, Randomized, Vehicle-Controlled, Parallel-Group Study Comparing Clindamycin 1% Gel To Clindamycin 1% Gel (Greenstone LLC) and Both Active Treatments to Vehicle Control in the Treatment of Acne Vulgaris

Brief summary

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

This is a randomized, double-blind, multiple-site, placebo-controlled, parallel-group study, designed to compare the efficacy and safety of generic Clindamycin 1% gel (Akorn), and the marketed product Clindamycin 1% gel (Greenstone LLC) in the treatment of acne vulgaris.

Study identification

NCT ID
NCT03522441
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Akorn, Inc.
Industry
Enrollment
1,125 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
12 Years to 40 Years
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
Apr 27, 2018 (Actual)
Primary completion
Apr 22, 2019 (Actual)
Completion
Apr 22, 2019 (Actual)
Last update posted
Oct 5, 2020

2018 – 2019

United States locations

U.S. sites
10
U.S. states
4
U.S. cities
7
Facility City State ZIP Site status
Site 11 Encino California 91436 —
Site 10 Sherman Oaks California 91403 —
Site 1 Brandon Florida 33511 —
Site 4 Miramar Florida 33027 —
Site 5 Miramar Florida 33027 —
Site 2 Tampa Florida 33069 —
Site 3 Tampa Florida 33618 —
Site 12 High Point North Carolina 27262 —
Site 8 El Paso Texas 79902 —
Site 9 El Paso Texas 79925 —

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 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03522441, 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 Oct 5, 2020 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03522441 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →