Encore Medical
Research

Our mission is to be the best clinical research site in the United States and contribute to the development of new medications by conducting clinical trials at the highest standards.

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Vitiligo Clinical Study Details

Dealing with vitiligo? Join our clinical trial exploring a potential new treatment aimed at restoring skin pigment. Access expert care, advanced therapy, and help shape the future of vitiligo treatment.

Recruiting- Male/Female - 12 to 65 years of age - Compensation Available

Apply To This Study Here

Please enter your name, a valid phone number, and a valid email address where you can be contacted.

Have you had phototherapy, laser therapy, or tanned excessively in the past 8 weeks?

Have you been diagnosed with nonsegmental vitiligo by a healthcare provider?

Have you used any of the following treatments in the past 4 to 6 months?

Are you between 18 and 65 years old?

Does your vitiligo cover between 5% and 50% of your body, including your face?

Do you have any serious or unstable health conditions (heart, liver, kidney, lung, psychiatric, or autoimmune disorders)?

Do you have hepatitis B, hepatitis C, or HIV?

Have you ever had tuberculosis (TB) or tested positive for latent TB?

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Am I the right age to join this study?

You may qualify if you are between 18 and 65 years old.

What type of vitiligo do I need to have?

This study is for individuals with nonsegmental vitiligo, affecting at least 5% but no more than 50% of their body.

How do you measure if I qualify based on my vitiligo?

Your vitiligo will be assessed using specific scoring tools (F-VASI and T-VASI). You may be eligible if your scores meet the required thresholds.

What are the pregnancy and birth control requirements?

If you could become pregnant, you must use highly effective birth control during the study and for 10 days after your last dose. Men also need to use effective contraception.

What if I’m on hormonal birth control?

You may still qualify, but additional precautions like using a second form of contraception (e.g., condoms) are recommended due to possible interactions with the study medication.

What else is expected of me?

You must give written informed consent, be willing to use digital tools, and be able to follow all trial instructions, including study visits and medication schedules.

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Benefits of participating in this study

There are multiple ways you can benefit from joining us in this study. Here are some of them.

Innovative medical treatments

Gain access to investigational treatments not yet available to the public. Receive study-related medical care and close health monitoring at no cost. Help researchers better understand medical conditions and improve future treatment options . Contribute to science in a way that may benefit others — including friends, family, and future generations.

Transportation & meals

Complimentary meals and transportation included for your appointment day.

Compensation

Compensation provided for your time and inconvenience.

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