Acne Clinical Trial

Thank you for your interest in our Acne Clinical Trial. Please read the following information to see if you qualify.

**** Please note the following information is not all inclusive, there are other ****
**** inclusion/exclusion criteria that are not listed ****  

Inclusion Criteria: (Must be able to answer “YES” to the following)

• Willing to commit to 9 office visits
• Commit to applying a topical investigational medication to your face once a day for up approximately 14 weeks.
• 12 years of age or older.
• If you are female, must be willing to take a pregnancy test.
  
  

Exclusion Criteria:  (Must be able to answer “NO” to the following)

• Planning for a pregnancy during the trial participation period.
• Topical use of antibiotics, steroids and/or other non-retinoid topical acne products (e.g., erythromycin, azelaic acid, topical dapsone, benzoyl peroxide, salicylic acid, etc.) within two (2) weeks prior to study start (Visit 1) and throughout the duration of the study.
• Topical use of retinoids (e.g., adapalene tretinoin, tazarotne, etc.) within six (6) weeks prior to study start (Visit 1) and throughout the duration of the study.
• No more than 3 nodulocystic acne lesions.
  
  

If you think that you would be a good candidate for this study, please click Register here to register online. A staff member will be calling you to schedule your screening visit. Please note, there is compensation for your time and travel of $25 per visit. Thank you for your interest in University Clinical Trials.