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Completed Phase 3 Interventional Results available

Bioequivalence Study of Clindamycin Phosphate Topical Lotion, 1% in Subjects With Acne Vulgaris

ClinicalTrials.gov ID: NCT03717506

Public ClinicalTrials.gov record NCT03717506. 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 22, 2026, 2:52 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 Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Comparison Study to Determine the Therapeutic Equivalence of GDC 268 and Clindamycin Phosphate Topical Lotion, 1% in Subjects With Acne Vulgaris

Brief summary

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

The objective of the study is to evaluate the safety, tolerability, and therapeutic equivalence of GDC 268 to Clindamycin Phosphate Topical Lotion, 1% and to compare the efficacy of these two products to the GDC vehicle lotion (i.e., placebo) in the treatment of acne vulgaris.

Study identification

NCT ID
NCT03717506
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Balmoral Medical company
Industry
Enrollment
1,236 participants

Conditions and interventions

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
Oct 10, 2018 (Actual)
Primary completion
Feb 17, 2020 (Actual)
Completion
Apr 16, 2020 (Actual)
Last update posted
May 4, 2021

2018 – 2020

United States locations

U.S. sites
34
U.S. states
19
U.S. cities
34
Facility City State ZIP Site status
Site 07 Fort Smith Arkansas 72916 —
Site 22 Rogers Arkansas 72758 —
Site 25 Fountain Valley California 92708 —
Site 33 Northridge California 91324 —
Site 30 San Diego California 92103 —
Site 44 Aventura Florida 33180 —
Site 36 Brandon Florida 33511 —
Site 45 DeLand Florida 32720 —
Site 41 Largo Florida 33770 —
Site 38 Miami Florida 33145 —
Site 35 Miami Lakes Florida 33014 —
Site 37 North Miami Beach Florida 33162 —
Site 26 St. Petersburg Florida 33709 —
Site 42 Tampa Florida 33609 —
Site 01 West Palm Beach Florida 33406 —
Site 10 Newnan Georgia 30263 —
Site 09 Boise Idaho 83704 —
Site 05 Rolling Meadows Illinois 60008 —
Site 02 Plainfield Indiana 46168 —
Site 27 Overland Park Kansas 66215 —
Site 28 Clarkston Michigan 48346 —
Site 24 Fridley Minnesota 55432 —
Site 49 Omaha Nebraska 68134 —
Site 06 High Point North Carolina 27262 —
Site 32 Raleigh North Carolina 27612 —
Site 19 Dublin Ohio 43016 —
Site 17 Gresham Oregon 97030 —
Site 34 Philadelphia Pennsylvania 19103 —
Site 20 Warwick Rhode Island 02886 —
Site 08 Anderson South Carolina 29621 —
Site 29 Chattanooga Tennessee 37421 —
Site 03 Murfreesboro Tennessee 37130 —
Site 04 Nashville Tennessee 37215 —
Site 43 Sugar Land Texas 77479 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03717506, 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 May 4, 2021 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03717506 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →