400
Participants
Start Date
November 30, 2005
Primary Completion Date
May 31, 2006
Study Completion Date
May 31, 2006
Vehicle control, 2x/day
ACZONE (dapsone) Gel, 5%, 2x/day
ACZONE (dapsone) Gel, 5%, 1x/day
MetroGel® (metronidazole gel), 1.0% 1x/day
ACZONE (dapsone) Gel, 5%, 1x/day (AM) + MetroGel (metronidazole gel), 1.0%, 1x/day (PM)
Paddington Testing Co., Inc., Philadelphia
Dermatology Consulting Services, High Point
MedaPhase, Inc., Newnan
University Clinical Research, Inc., Pembroke Pines
FXM Research, Miami
Visions Clinical Research, Boynton Beach
Tampa Bay Medical Research, Clearwater
Radiant Research, Birmingham
Dermatology Research Association, Inc., Nashville
University Dermatology Consultants, Inc., Cincinnati
Dermatology Research Associates Inc., Cincinnati
Madison Skin & Research, Inc., Madison
Dermatology Clinical Trials Unit Washington University, St Louis
Skin Specialists, PC, Omaha
J&S Studies Inc., Bryan
DermResearch, Inc., Austin
Cherry Creek Research, Inc, Denver
Radiant Research, Tucson
Academic Dermatology Associates, Albuquerque
Clincial Research Specialists, Inc., Santa Monica
Therapeutics Clinical Research, San Diego
East Bay Dermatology Medical Group, Inc., Fremont
Northwest Dermatology and Research Center, Portland
Oregon Medical Research Center, Portland
Welborn Clinic, Evansville
The Savin Center, PC, New Haven
Lead Sponsor
Allergan
INDUSTRY