Microdevice for Psoriasis and Atopic Dermatitis

RC
JC
Overseen ByJeffrey Cheng, MD, PhD
Age: 18+
Sex: Any
Trial Phase: Phase 4
Sponsor: University of California, San Francisco
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 a new microdevice designed to treat skin conditions such as eczema and psoriasis. The device, about the size of a grain of rice, releases small amounts of FDA-approved medications directly into the skin. Researchers aim to determine if this in situ cutaneous microdevice can safely predict skin responses to standard treatments and explore connections to genetic information. This trial may suit adults managing eczema or psoriasis. As a Phase 4 trial, the treatment has already received FDA approval and proven effective, providing an opportunity to understand its benefits for more patients.

Do I need to stop my current medications for this trial?

The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.

What is the safety track record for the in situ cutaneous microdevice?

Research shows that the small device used in this study aims to be safe and effective for skin conditions like eczema and psoriasis. It applies tiny amounts of FDA-approved medications directly to the skin, using much smaller doses than usual treatments.

Since these medications are already approved for these skin conditions, they are generally safe when used correctly. However, the device itself is new, and researchers are testing it to ensure it is safe and can accurately show how the skin will react to these treatments.

So far, studies have shown promising safety results. The device, about the size of a grain of rice, is designed to limit medication exposure to the skin, reducing the risk of side effects. More research will help confirm these findings, but current data positively supports its safety.12345

Why are researchers enthusiastic about this study treatment?

Researchers are excited about the in situ cutaneous microdevice for psoriasis and atopic dermatitis because it offers a novel way to deliver medication directly into the skin. Unlike traditional treatments like topical creams or systemic medications, this tiny device, about the size of a grain of rice, releases very small amounts of FDA-approved drugs directly where they are needed. This targeted delivery method could reduce side effects by using much lower doses than standard treatments. Additionally, the device may help predict individual skin responses to treatments, potentially personalizing therapy based on genetic information and improving overall results.

What evidence suggests that this microdevice is effective for psoriasis and atopic dermatitis?

Research shows that the in situ cutaneous microdevice, which participants in this trial will receive, is being tested to determine if it can safely and effectively predict responses of skin conditions like eczema and psoriasis to standard treatments. The device releases tiny amounts of FDA-approved medications for these conditions directly into the skin. This method uses much lower doses of medication than usual, which might reveal how well these treatments work. Early results suggest that the device can measure reactions of skin lesions to these medications. The goal is to determine if these reactions can predict overall treatment success, potentially leading to more personalized treatment plans in the future.13567

Who Is on the Research Team?

RC

Raymond Cho, MD, PhD

Principal Investigator

University of California, San Francisco

Are You a Good Fit for This Trial?

This trial is for adults over 18 with psoriasis or atopic dermatitis. Women of childbearing age must be on birth control pills or have an intrauterine device for at least a month to participate.

Inclusion Criteria

I am over 18, have atopic dermatitis or psoriasis, and if female, have been on birth control for at least 30 days.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

The microdevice is placed on the skin to release small amounts of FDA-approved medications for atopic dermatitis and psoriasis to test safety and efficacy.

1 year

Follow-up

Participants are monitored for safety and effectiveness after treatment, including assessment of adverse events and tissue analysis.

1 year

What Are the Treatments Tested in This Trial?

Interventions

  • In situ cutaneous microdevice

Trial Overview

The study tests a microdevice, like a tiny skin patch, that delivers small amounts of FDA-approved medications directly into the skin to see how well it predicts treatment responses and correlates with genetic data.

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: In situ cutaneous microdeviceExperimental Treatment36 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of California, San Francisco

Lead Sponsor

Trials
2,636
Recruited
19,080,000+

Citations

Utilization of a Microdevice for Psoriasis and Atopic ...

In this study, the device will be tested to see if it's safe and works well for predicting how the skin will react to standard treatments. We ...

Utilization of a cutaneous therapy in situ microdevice

The pilot study will determine the feasibility of using an in situ microdevice to measure local lesional rash-affected skin response to FDA- ...

Microdevice for Psoriasis and Atopic Dermatitis

The microdevice is placed on the skin to release small amounts of FDA-approved medications for atopic dermatitis and psoriasis to test safety and efficacy.

1124

Together this data suggest that trametinib-induced MEK inhibition causes a reduction in both epidermal proliferation and immune cell infiltration/proliferation, ...

Biologic and Small Molecule Therapy in Atopic Dermatitis

Improvements of 50%, 75%, and 90% were observed in the EASI score [35]. A separate phase III study highlighted the effectiveness of difamilast, ...

Utilization of a Microdevice for Psoriasis and Atopic Dermatitis

In this study, the device will be tested to see if it's safe and works well for predicting how the skin will react to standard treatments.

7.

pubmed.ncbi.nlm.nih.gov

pubmed.ncbi.nlm.nih.gov/41533373/

Safety and Efficacy of ICP-332 for Moderate to Severe ...

Main outcomes and measures: The primary outcome was safety. The key efficacy outcome was the percentage change from baseline in Eczema Area and ...