Exploration of Safety and Efficacy of AzA 15% Foam Twice a Day in Rosacea
Papulopustular RosaceaThis exploratory study is being performed to determine whether a new form formulation of azelaic acid 15% is effective in the treatment of papulopustular rosecea.
Systemic Bioavailability Study Of Col-118 Administered Topically as a 0.18 % Facial Gel And Brimonidine...
Erythematous RosaceaPhase II systemic bioavailability crossover study to measure the exposure of Col-118 topical 0.18 % Facial Gel and Brimonidine Ophthalmic Solution 0.2%
Isotretinoin in Papular-Pustular Rosacea
Papular-pustular RosaceaA national, multicentre, prospective, randomised, double-blind, phase III study in 2 parallel groups of isotretinoin versus placebo in patients presenting papular-pustular rosacea resistant to standard therapy. A non-balanced group (2 isotretinoin /1 placebo) design was selected since, given the nature of the study disease, fewer patients will receive the placebo than active isotretinoin. Treatment duration for each patient : 4 months, with monthly evaluation Follow-up at 2 months and 4 months for patients responsive after 4 months of treatment.
Pulsed Dye Laser (PDL) vs. Microsecond 1064-nm Nd:YAG Laser for Treatment of Diffuse Facial Redness...
RosaceaThe primary objective of this study is to compare the efficacy of PDL and the 1064-nm Nd:YAG laser in the treatment of facial redness.
Efficacy of Topical Cyclosporin for Ocular Rosacea
RosaceaThe purpose of this study is to determine whether Restasis (topical cyclosporin) is effective in the treatment of ocular rosacea
Open Label Phase 2 Feasibility Study of BPX-04 Topical Minocycline Gel in Rosacea
Moderate to Severe Papulopustular RosaceaAn open label feasibility study using BPX-04 topical minocycline gel in papulopustular rosacea.
Safety and Efficacy Study of a Topical Minocycline Foam in Patients With Papulopustular Rosacea...
RosaceaPapulopustular RosaceaThe purpose of this study is to see if the study drug, FMX-103, is safe to give and if it helps people with moderate-to-severe papulopustular rosacea. The investigational product is FMX-103 minocycline foam. Two concentrations of the investigational product, 1.5% and 3%, will be studied along with vehicle. The foam will be applied once daily to the face for the 12-week treatment duration of the study. Approximately 210 patients will participate in this study.
To Evaluate the Therapeutic Equivalence and Safety of Azelaic Acid 15% Topical Gel
RosaceaA Multi-Center, Double-Blind, Randomized, Placebo Controlled, Parallel-Group Study
Bioequivalence Study of Two Treatments in the Treatment of Inflammatory Lesions of Rosacea on the...
RosaceaTo compare the bioequivalence of Perrigo's azelaic acid foam product to Finacea Foam for the treatment of Inflammatory Lesions of Rosacea
A Study of DER 45-EV Gel to Treat Rosacea
RosaceaTo identify lowest efficacious dose of DER 45 EV Gel, 1% and 5% verses vehicle in patients with rosacea.