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Kid’s Vitiligo Study (12 Months)

For condition: Vitiligo
Enrolling:
INCB18424-312

Kid’s Vitiligo Study (12 Months)

Study Summary

Who Can Participate?

Children aged 2 to under 12 with nonsegmental vitiligo may participate.

 

Inclusion Criteria

      • total body vitiligo area (facial and nonfacial) does not exceed 10% of body surface area (BSA)*
      • pigmented hair within some of the areas of vitiligo on the face.

* 1% of your body surface area is roughly equal to the palm of your hand (no wrists or fingers).

 

Participant Information

      • Participate and receive study treatment at no cost
      • Regular visits with study doctors who specialise in treating vitiligo (11 visits)
      • Will receive either an investigative topical treatment (study drug) or a placebo (vehicle cream)
      • Reimbursement for study-related expenses may be provided

 

How Long Will The Study Last?

      • 52 weeks

Note: Participants will need to stop all other treatments for vitiligo during clinical trial participation.

Click here to Register

For more information about this trial, please visit ClinicalTrials.gov

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Privacy Policy

Last Revised: July 2024

Introductions

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You may withdraw this consent at any time or update your information. To withdraw your consent or to update your information, contact the Privacy Officer by mail at:

Probity Medical Research Inc.
Attention: Privacy Officer
139 Union Street East
Waterloo, Ontario, Canada N2J 1C4

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Your Personal Information is kept in strict confidence; Probity utilizes appropriate security safeguards to keep your information confidential and secure. Only authorized personnel have access to your Personal Information and we do not release your Personal Information to third parties other than those third parties that are necessary to satisfy the Purposes (as defined above) for which the Personal Information was collected, including third party service providers. While we cannot guarantee that errors, loss or unauthorized access to your Personal Information will not occur, our procedures and systems are designed to protect your Personal Information from such events. When your Personal Information is no longer required to fulfill the identified Purposes, the information will be destroyed, erased, or made anonymous.

When you are contacted by a third party to participate in a clinical research study, Probity is no longer involved or responsible for collecting or safeguarding any further Personal Information you may provide to that third party.  As such, we recommend that you obtain information regarding their privacy policies before participating.

As we expect the need for participants in clinical research studies to be ongoing, the Personal Information you provide will be kept indefinitely. If at any time you wish to remove or update your information from our database, please contact our Privacy Officer by mail at:

Probity Medical Research Inc.
Attention: Privacy Officer
139 Union Street East
Waterloo, Ontario, Canada N2J 1C4

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If at any time you wish to access your personal information held by us, please contact us by mail at:

Probity Medical Research Inc.
Attention: Privacy Officer
139 Union Street East
Waterloo, Ontario, Canada N2J 1C4

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Changes to the Policy

Probity reserves the right to modify or amend this Privacy Policy without notice and at any time and for any reason. An up-to-date version of this Privacy Policy may be obtained on our website.

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You have the right to know how we protect your privacy and what you should expect from us. If you have questions or a complaint, you may contact our Privacy Officer by mail at:

Probity Medical Research Inc.
Attention: Privacy Officer
139 Union Street East
Waterloo, Ontario, Canada N2J 1C4

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