Overview

Comparison of Tazarotene and Minocycline Therapies for Maintenance of Facial Acne Vulgaris

Status:
Completed
Trial end date:
2002-08-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of the study is to compare the efficacy of three maintenance regimens (topical tazarotene, oral minocycline, or both) in sustaining improvement in acne.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
KGL, Inc.
Collaborators:
Allergan
Jefferson Medical College of Thomas Jefferson University
Milton S. Hershey Medical Center
New York University School of Medicine
NYU Langone Health
State University of New York - Downstate Medical Center
Treatments:
Minocycline
Nicotinic Acids
Tazarotene
Criteria
Inclusion Criteria:

Moderate facial acne vulgaris 25-60 facial inflammatory acne lesions 10-100 facial comedos
No more than 2 facial nodular cystic lesions (no more than 5 mm in diameter) For females of
child bearing potential, a regular menstrual cycle Negative urine pregnancy test

Exclusion Criteria:

Uncontrolled systemic disease Acne vulgaris known to be resistant to antibiotics For
females: pregnancy, breastfeeding, or planning pregnancy Use of estrogens or birth control
pills for 12 weeks or less Any skin disease that may interfere with diagnosis or evaluation
of acne vulgaris Known hypersensivity to any components in Tazarac gel or to any
tetracyclines Use of any systemic retinoids in past 2 years Use of any systemic
antibiotics, or participation in another drug or investigational study, in past 30 days Use
of topical anti-acne medication in past 14 days