New Clinical Trial Opportunity

In order to qualify for this study, you must meet a certain set of requirements, known as inclusion criteria. Some of the key inclusion criteria are as follows:

1. You are 18 to 65 years of age
2. You have been diagnosed with non-segmental vitiligo by a healthcare professional
3. You have white areas on your face which, when added up, cover an area roughly half the size of your palm or larger
4. You may have vitiligo on other parts of your body besides face; however, you won’t be allowed to treat it.
5. You agree to discontinue all treatments you use to treat vitiligo while you are participating in the clinical trial, including creams, phototherapy, and any oral medicines

This trial is now seeking to enroll 24 eligible patients nationwide. It will last for 28 weeks and requires a total 11 visits to the clinic over the course of the study. It is an open-label pilot study, meaning that every patient enrolled will receive the investigational study drug for duration of the trial.

The goal of this study is to determine whether patients regain the pigment in vitiligo spots on the face after 6 months of applying the study drug. We will also record the safety and tolerability of the medication.

The Vitiligo Clinical Trial is being conducted at 5 locations nationwide. The UMass Chan Medical School in Worcester, MA is one of the sites and is currently recruiting patients. Please contact us if you think this clinical trial may be right for you. These are the 5 sites currently recruiting  subjects:

• UMASS, Worcester, Massachusetts
• UT, Southwestern, Dallas, Texas
• Encinitas, California
• Los Angeles, California
• Kappa Meadows, Maryland

Because participants in this study will be required to attend multiple clinic visits over the course of the study, you should contact the site closest to you (contact information on the right).