Sandy Springs, GANCT07533019Now EnrollingIRB Ready

Vitiligo Clinical Trial in Sandy Springs, GA

Access cutting-edge vitiligo treatment through this clinical trial at a research site in Sandy Springs. Study-provided care at no cost to qualified participants.

Sponsored by Eli Lilly and Company

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Expert Care in Sandy Springs

Access vitiligo specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related vitiligo treatment provided free

Apply for This Sandy Springs Location

Check if you qualify for this vitiligo clinical trial in Sandy Springs, GA

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Sandy Springs

    Convenient for GA residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Sandy Springs site if eligible
  4. 4Begin participation

About This Vitiligo Study in Sandy Springs

The purpose of this study is to evaluate how well LY4005130 is tolerated and what side effects may occur in participants with non-segmental vitiligo (NSV) when compared with placebo. The study drug will be administered intravenously (IV) (into a vein in the arm). Blood tests will be performed to investigate how the body processes the study drug and how the study drug affects the body. The study will last approximately 48 weeks, including screening.

Sponsor: Eli Lilly and Company

Who Can Participate

Inclusion Criteria

Eligible participants must have the following at both screening and baseline:
A clinical diagnosis of non-segmented vitiligo (NSV) for at least 3 months
Body surface area (BSA) involvement of 4% to 60%, inclusive, excluding involvement at palms of the hands, soles of the feet, or dorsal aspect of the feet
BSA involvement of ≥0.5% on the face
F-VASI ≥0.5 and T-VASI ≥3, and
Either active or stable disease at both screening and baseline

Exclusion Criteria

Participants who have other types of vitiligo that are not considered active or stable vitiligo
Currently have active forms of other disorders of pigmentation
Currently have active forms of inflammatory skin disease(s) or evidence of skin conditions that would interfere with evaluation of vitiligo or response to treatment
Have a superficial skin infection within 2 weeks before baseline. Participants may be rescreened after the infection is resolved
Have a history of chronic alcohol abuse, IV drug abuse, or other illicit drug abuse within 1 year prior to screening
Have a history or presence of cardiovascular, respiratory, hepatic, gastrointestinal, endocrine, hematological, neurological, or neuropsychiatric disorders or any other serious and/or unstable illness that, in the opinion of the investigator, could constitute an unacceptable risk when taking the study intervention or interfere with the interpretation of data
Any previous JAK inhibitor therapy, systemic or topical (for example, ruxolitinib, tofacitinib, baricitinib, upadacitinib, filgotinib, lestaurtinib, pacritinib) will NOT be allowed. Participant MUST be JAK inhibitor therapy-naïve

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Sandy Springs?

Yes, this clinical trial (NCT07533019) has an active research site in Sandy Springs, GA that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Vitiligo Treatment Options in Sandy Springs, GA

If you're searching for vitiligo treatment options in Sandy Springs, GA, this clinical trial (NCT07533019) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Sandy Springs research site is actively enrolling participants for this clinical trial. You'll receive care from experienced vitiligo specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all vitiligo clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Sandy Springs, GA