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Completed Phase 2 Interventional

Study to Evaluate the Safety and Efficacy of Topical Minocycline Gel in Patients With Papulopustular Rosacea

ClinicalTrials.gov ID: NCT03263273

Public ClinicalTrials.gov record NCT03263273. 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 Jul 22, 2026, 12:16 PM 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, Parallel Group, Vehicle-Controlled Study to Evaluate the Safety and Efficacy of 1% and 3% Topical MIinocycline Gel (HY01) in Patients With Papulopustular Rosacea

Study identification

NCT ID
NCT03263273
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Hovione Scientia Limited
Industry
Enrollment
270 participants

Conditions and interventions

Interventions

  • 1% Topical Minocycline Gel Drug
  • 3% Topical Minocycline Gel Drug
  • Topical Vehicle Gel Other

Drug · Other

Eligibility (public fields only)

Age range
18 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
Oct 29, 2017
Primary completion
Feb 28, 2019
Completion
Jun 30, 2019
Last update posted
Nov 7, 2019

2017 – 2019

United States locations

U.S. sites
23
U.S. states
16
U.S. cities
20
Facility City State ZIP Site status
Clinical Site - 15 Bryant Arkansas 72022
Clinical Site - 20 Rogers Arkansas 72758
Center for Dermatology Clinical Research, Inc. Fremont California 94538
Clinical Site - 19 Santa Monica California 90404
Clinical Site - 5 Tampa Florida 33624
Clinical Site - 16 Boise Idaho 83704
Clinical Site - 22 Boston Massachusetts 02116
Clinical Site - 23 Watertown Massachusetts 02472
Clinical Site - 14 Clinton Township Michigan 48038
Clinical Site - 6 Fridley Minnesota 55432
Clinical Site - 12 Omaha Nebraska 68144
Clinical Site - 21 Berlin New Jersey 08009
Clinical Site - 13 New York New York 10022
Clinical Site - 2 New York New York 10155
Clinical Site - 4 High Point North Carolina 27262
Clinical Site - 17 Portland Oregon 97210
Clinical Site - 11 Fort Washington Pennsylvania 19034
Clinical Site - 8 Goodlettsville Tennessee 37072
Clinical Site - 7 Pflugerville Texas 78660
Clinical Site - 18 San Antonio Texas 78213
Clinical Site - 3 San Antonio Texas 78229
Clinical Site - 9 San Antonio Texas 78229
Clinical Site - 10 Norfolk Virginia 23502

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 NCT03263273, 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 7, 2019 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03263273 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →