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Completed Phase 3 Interventional Results available

A Multi-Center Open-Label Evaluation of the Safety of Sarecycline Tablets in the Treatment of Acne Vulgaris

ClinicalTrials.gov ID: NCT02413346

Public ClinicalTrials.gov record NCT02413346. 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 Sep 4, 2026, 2:49 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

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

Open-label study will evaluate the safety of an approximate 1.5 mg/kg/day dose of oral sarecycline in the long-term treatment of participants with moderate to severe facial acne vulgaris.

Study identification

NCT ID
NCT02413346
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Almirall, S.A.
Industry
Enrollment
490 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
9 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
Mar 19, 2015
Primary completion
Aug 25, 2016
Completion
Aug 25, 2016
Last update posted
Jan 31, 2019

2015 – 2016

United States locations

U.S. sites
56
U.S. states
23
U.S. cities
49
Facility City State ZIP Site status
Actavis Investigational Study Site #206 Mobile Alabama 36608
Actavis Investigational Study Site #236 Hot Springs Arkansas 71913
Actavis Investigational Study Site #245 Carlsbad California 92008
Actavis Investigational Study Site #129 Encino California 91436
Actavis Investigational Study Site #209 Fremont California 94538
Actavis Investigational Study Site #147 Sacramento California 95819
Actavis Investigational Study Site #150 San Diego California 92120
Actavis Investigational Study Site #125 San Diego California 92123
Actavis Investigational Study Site #204 San Diego California 92123
Actavis Investigational Study Site #222 Denver Colorado 80220
Actavis Investigational Study Site #148 Wheat Ridge Colorado 80033
Actavis Investigational Study Site #226 Clearwater Florida 33761
Actavis Investigational Study Site #238 Jupiter Florida 33458
Actavis Investigational Study Site #249 Miami Florida 33142
Actavis Investigational Study Site #145 Miami Florida 33175
Actavis Investigational Study Site #211 Miramar Florida 33207
Actavis Investigation Study Site # 140 North Miami Beach Florida 33162
Actavis Investigational Study Site #151 Orange Florida 32073
Actavis Investigational Study Site #203 Tampa Florida 33609
Actavis Investigational Study Site #242 Snellville Georgia 30078
Actavis Investigational Study Site #124 Boise Idaho 83704
Actavis Investigational Study Site #106 Chicago Illinois 60611
Actavis Investigational Study Site #113 South Bend Indiana 46617
Actavis Investigational Study Site #213 Louisville Kentucky 40202
Actavis Investigational Study Site #217 Rockville Maryland 20850
Actavis Investigational Study Site #251 Clarkston Michigan 48346
Actavis Investigational Study Site #235 Clinton Township Michigan 48038
Actavis Investigational Study Site #227 Fort Gratiot Michigan 48059
Actavis Investigational Study Site #111 Warren Michigan 48088
Actavis Investigational Study Site #221 Fridley Minnesota 55432
Actavis Investigational Study Site #231 Omaha Nebraska 68144
Actavis Investigational Study Site #146 New York New York 10016
Actavis Investigational Study Site #208 New York New York 10155
Actavis Investigational Study Site #240 Rochester New York 14623
Actavis Investigational Study Site #230 Stony Brook New York 11790
Actavis Investigational Study Site #229 Raleigh North Carolina 27612
Actavis Investigational Study Site #149 Gresham Oregon 97030
Actavis Investigational Study Site #257 Philadelphia Pennsylvania 19103
Actavis Investigational Study Site #225 Goodlettsville Tennessee 37072
Actavis Investigational Study Site #128 Knoxville Tennessee 37917
Actavis Investigational Study Site #216 Knoxville Tennessee 37922
Actavis Investigational Study Site #109 Nashville Tennessee 37215
Actavis Investigational Study Site #223 Arlington Texas 76011
Actavis Investigational Study Site #252 Arlington Texas 76011
Actavis Investigational Study Site #220 College Station Texas 77845
Actavis Investigational Study Site #104 Dallas Texas 75234
Actavis Investigational Study Site #142 Houston Texas 77004
Actavis Investigational Study Site #105 Houston Texas 77056
Actavis Investigational Study Site #201 Katy Texas 77494
Actavis Investigational Study Site #223 Pflugerville Texas 78660
Actavis Investigational Study Site #101 Plano Texas 75093
Actavis Investigational Study Site #207 San Antonio Texas 78218
Actavis Investigational Study Site #212 West Jordan Utah 84088
Actavis Investigational Study Site #244 Norfolk Virginia 23507
Actavis Investigational Study Site #144 Spokane Washington 99202
Actavis Investigational Study Site #233 Walla Walla Washington 99362

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 NCT02413346, 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 Jan 31, 2019 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02413346 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →