20 Participants Needed

Roflumilast Foam for Vitiligo

AH
Overseen ByAmanda Harvey, Study Coordinator
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests Roflumilast foam to determine its effectiveness for non-segmental vitiligo, a condition causing patches of skin to lose color. Researchers aim to assess whether this foam can effectively treat these patches, particularly on the face. The trial is open to children and teens who have had the condition for at least three months and have noticeable facial patches. Participants should be generally healthy and able to adhere to the study rules. As a Phase 2 trial, this research focuses on measuring the treatment's effectiveness in an initial, smaller group of people.

Will I have to stop taking my current medications?

The trial requires participants to stop certain medications before starting, including any biologic or experimental therapy, phototherapy, immunomodulating treatments, and topical treatments. Additionally, you must discontinue systemic CYP3A4 inhibitors or dual inhibitors. Please consult with the study team to see if your current medications are affected.

Is there any evidence suggesting that Roflumilast Foam 0.3% is likely to be safe for humans?

Research has shown that Roflumilast foam 0.3% is generally safe and well-tolerated. In studies with patients who have seborrheic dermatitis, this foam was used for up to 52 weeks, and few treatment-related side effects occurred. Most side effects were mild to moderate. Additionally, Roflumilast foam has proven effective over time, with results that continue to improve.

Evidence also suggests it might help children with facial vitiligo who haven't had success with other treatments. While this is encouraging, it's important to note that this trial is still in the early stages. This means there is less safety information compared to treatments studied longer. Participants should discuss any concerns with the trial team to better understand the risks and benefits.12345

Why do researchers think this study treatment might be promising for vitiligo?

Unlike the standard of care for vitiligo, which typically involves topical corticosteroids or calcineurin inhibitors to reduce inflammation and promote repigmentation, Roflumilast Foam is unique because it uses a new delivery method with a novel active ingredient. Roflumilast is a phosphodiesterase-4 (PDE4) inhibitor, which works by targeting and reducing inflammation in the skin more precisely. Researchers are excited about Roflumilast Foam because it could offer a more effective and targeted treatment option with potentially fewer side effects, paving the way for improved skin repigmentation in vitiligo patients.

What evidence suggests that Roflumilast foam might be an effective treatment for vitiligo?

Studies have shown that roflumilast foam 0.3% effectively and safely treats skin conditions like seborrheic dermatitis, with benefits lasting over a year. Early research suggests that roflumilast cream 0.3% might help children with vitiligo, especially those unresponsive to other treatments. The foam has consistently demonstrated positive effects and is well-tolerated in individuals aged 12 and older. This trial will evaluate the efficacy of roflumilast foam 0.3% specifically for vitiligo, building on early findings that suggest it could be a helpful treatment.13678

Who Is on the Research Team?

KW

Kelly Warren, MD

Principal Investigator

Derm Texas, PLLC

Are You a Good Fit for This Trial?

This trial is for pediatric patients with Non-Segmental Vitiligo (NSV), a condition where patches of skin lose their pigment. The study is open-label and at a single center, meaning both the researchers and participants know what treatment is being used.

Inclusion Criteria

My parents or guardian and I (if old enough) have agreed to my participation.
I (or my child) can follow the study plan and attend all appointments.
In good health as judged by the Investigator, based on the medical history, and dermatology examination
See 3 more

Exclusion Criteria

Subjects with diagnosis of other forms of vitiligo, other differential diagnosis of vitiligo or other skin depigmentation disorders that would interfere with the evaluations of the effect of the study medication, as determined by the Investigator
Subjects who are family members of the clinical study site, clinical study staff, or sponsor, or family members of enrolled subjects living in the same house
Subjects with any serious medical condition or physical examination abnormality that would prevent study participation or place the subject at significant risk, as judged by the Investigator
See 9 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive Roflumilast foam 0.3% for Non-Segmental Vitiligo

24 weeks
Visits at baseline, weeks 4, 8, 12, 18, and 24

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Roflumilast Foam 0.3%
Trial Overview The trial is testing Roflumilast foam at a concentration of 0.3%, applied topically. It's designed to assess how effective this medication is in treating NSV in children.
How Is the Trial Designed?
1Treatment groups
Experimental Treatment
Group I: Open-label single center, proof of concept study evaluating the efficacy of Roflumilast foam 0.3%Experimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Derm Texas, PLLC

Lead Sponsor

Arcutis Biotherapeutics, Inc.

Industry Sponsor

Trials
22
Recruited
7,600+

Citations

News & MediaZORYVE foam 0.3% was safe, well-tolerated, and demonstrated durable and continuously improving efficacy in the treatment of seborrheic ...
Recalcitrant Pediatric Facial Vitiligo Successfully Treated ...This case series suggests that roflumilast cream 0.3% may have a positive therapeutic effect in pediatric patients with facial vitiligo who are unresponsive to ...
Study Details | NCT07105254 | An Open-label Single ...An Open-label Single Center, Proof of Concept Study Evaluating the Efficacy of Roflumilast Foam 0.3% in Pediatric Patients With Non-Segmental ...
Off-label therapeutic potential of topical roflumilast in ...Further, roflumilast foam 0.3% has shown early and consis- tent efficacy with a high degree of tolerability in patients 12 years and older ...
Roflumilast Foam Shows Long-Term Safety in Seborrheic ...Roflumilast foam 0.3% demonstrated sustained efficacy and safety in managing moderate to severe seborrheic dermatitis over 52 weeks. The study ...
6.pubmed.ncbi.nlm.nih.govpubmed.ncbi.nlm.nih.gov/41175336/
Long-Term Safety and Efficacy of Roflumilast Foam 0.3% in ...The primary endpoints were occurrence of treatment-emergent adverse events (AEs); local tolerability and efficacy (via Investigator Global ...
Recalcitrant Pediatric Facial Vitiligo Successfully Treated ...This case series suggests that roflumilast cream 0.3% may have a positive therapeutic effect in pediatric patients with facial vitiligo who are unresponsive to ...
STRATUM Trial: Roflumilast Foam Works Across Skin ...Roflumilast foam 0.3% was well tolerated, with most treatment-emergent adverse events classified as mild or moderate. Overall, treatment- ...
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