
Low Glycemic Index and Load Diet for the Treatment of Acne
Acne VulgarisDiet ModificationClinical trial to determine the effect of adding a diet with low glycemic index and load to adults for the treatment of moderate acne. Adult patients with acne where recruited in two groups, A and B. Group A received a normal diet according to their metabolic status and group B received a diet with low glycemic index and load. Outcomes were measured at week 12.

Bioequivalence Study of Two Treatments in the Treatment of Acne Vulgaris on the Face
Acne VulgarisTo compare the safety and efficacy of Perrigo's product to an FDA approved product for the treatment of Acne Vulgaris

A Pilot Study to Evaluate the Effect of a Probiotic Mixture in Acne
AcneAcne VulgarisA 12-week randomized, double-blind, placebo-controlled pilot study to evaluate the effect of a probiotic blend in the treatment and clinical and subjective evolution of acne vulgaris in adolescent and adult patients between 12 and 30 years.

Pharmacokinetics and Safety of ALA in Acne Vulgaris
Acne VulgarisThis study will evaluate the pharmacokinetics and safety of ALA in patients with moderate and severe acne vulgaris after single dose in different dosages.

Tazarotene 0.045% Lotion for Treating PIE and PIH in Subjects With Acne
Acne VulgarisPost Inflammatory Hyperpigmentation3 moreThe purpose of the study is to assess the safety and efficacy of Arazlo Lotion (Tazarotene 0.045% Lotion) for treatment of postinflammatory erythema and postinflammatory hyperpigmentation in subjects with acne.

To Evaluate the Efficacy and Safety of Minocycline Hydrochloride Foam in the Treatment of Moderate-to-severe...
Acne VulgarisThis is a randomized, multicenter, double-blind, vehicle-controlled, 2-arm study to evaluate the safety and efficacy in 12 weeks of FMX101 minocycline foam, 4%, compared to vehicle, in the treatment of subjects with moderate to severe facial acne vulgaris.

Open-label Safety and Tolerability Study of LTS-PDT in Healthy Volunteers
Acne VulgarisThe purpose of this study is assess the safety and tolerability of lemuteporfin topical solution (LTS) with exposure to red light (PDT), when applied to the backs of healthy volunteers.

A Safety, Tolerability and Preliminary Efficacy Study of DRM01B Topical Gel
Acne VulgarisThis is a Phase 1/2a study. The purpose of Phase 1 was to evaluate the safety and tolerability of DRM01B Topical Gel in 6 healthy volunteers. The purpose of Phase 2a was to assess the safety, tolerability and preliminary efficacy of DRM01B Topical Gel compared to vehicle in subjects with acne vulgaris on the face.

Double-Blind, Placebo-Controlled Study to Evaluate 3 Doses of a Novel Tetracycline in the Treatment...
Acne VulgarisTo evaluate the safety and effectiveness of 3 strengths of P005672-HCl compared to placebo for the treatment of moderate to severe facial acne vulgaris.

Fractional Ablative Radiofrequency for the Treatment of Acne Scars and Wrinkles
WrinklesAcne ScarsTo assess the safety and efficacy of the Pixel RF (fractional radio frequency) module in the treatment of acne scars and wrinkles.