Irving, TXNCT07355075Now EnrollingIRB Ready

Eczema Atopic Dermatitis Clinical Trial in Irving, TX

Access cutting-edge eczema atopic dermatitis treatment through this phase 2/3 clinical trial at a research site in Irving. Study-provided care at no cost to qualified participants.

Sponsored by Turn Therapeutics

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Expert Care in Irving

Access eczema atopic dermatitis specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related eczema atopic dermatitis treatment provided free

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Check if you qualify for this eczema atopic dermatitis clinical trial in Irving, TX

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Why Participate?

  • No-Cost Study Care

  • Local to Irving

    Convenient for TX 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 Irving site if eligible
  4. 4Begin participation

About This Eczema Atopic Dermatitis Study in Irving

This is a Phase 2, randomized, double-blind, vehicle-controlled clinical study evaluating the efficacy and safety of GX-03 topical ointment in adult subjects with moderate to severe atopic dermatitis (eczema). The study plans to enroll up to 120 eligible patients with a target of at least 100 completing the study and an ability to expand enrollment up to 200 subjects based on a pre-specified interim assessment conducted by an Independent Data Monitoring Committee (IDMC). Subjects will be randomized in a 1:1 ratio to receive either GX-03 or vehicle control for 8 weeks. The study is designed to evaluate improvement in investigator-assessed disease severity, itch, and patient-reported eczema symptoms following topical treatment with GX-03 compared with vehicle control. Efficacy assessments include the Validated Investigator Global Assessment for Atopic Dermatitis (vIGA-AD™), Eczema Area and Severity Index (EASI), Peak Pruritus Numeric Rating Scale (PP-NRS), and Patient-Oriented Eczema Measure (POEM). An interim assessment of conditional power for the primary efficacy endpoint will occur after the first 50 subjects complete the Week 8 visit or withdraw prematurely. Based on pre-specified criteria defined in the IDMC Charter, the IDMC may recommend continuation as planned, expansion of enrollment up to 200 subjects, or early curtailment of enrollment.

Sponsor: Turn Therapeutics

Who Can Participate

Inclusion Criteria

Participants must meet all of the following criteria:
Adults aged 18 to 80 years, inclusive
Male or female subjects in good general health as determined by medical history
Presence of visible eczematous skin with disease severity consistent with moderate to severe eczema, as assessed by:
Eczema Area and Severity Index (EASI) or Validated Investigator Global Assessment for Atopic Dermatitis (vIGA-AD™)
Ability to read, understand, and provide written informed consent in English
Willingness and ability to comply with study procedures, including study visits and daily topical application
Agreement to use only the assigned study product on designated areas of interest for the duration of the study Exclusion Criteria Individuals meeting any of the following criteria will be excluded:
Pregnant, breastfeeding, or planning pregnancy during the study
Presence of any skin condition or dermatologic disease that could interfere with study treatment or assessments
Use of systemic or topical immunosuppressive therapies, including corticosteroids, within 3 weeks prior to enrollment
Use of anti-inflammatory medications (e.g., topical steroids, ibuprofen, celecoxib); steroid nasal or ophthalmic drops are permitted
Use of topical medications at the test sites within 72 hours prior to enrollment
Damaged or altered skin at or near test sites (e.g., sunburn, tattoos, scars, uneven pigmentation) that could confound evaluations
Any medical condition that, in the investigator's judgment, places the subject at undue risk or compromises study integrity

Exclusion Criteria

Individuals meeting any of the following criteria will be excluded:
Pregnant, breastfeeding, or planning pregnancy during the study
Presence of any skin condition or dermatologic disease that could interfere with study treatment or assessments
Use of systemic or topical immunosuppressive therapies, including corticosteroids, within 3 weeks prior to enrollment
Use of anti-inflammatory medications (e.g., topical steroids, ibuprofen, celecoxib); steroid nasal or ophthalmic drops are permitted
Use of topical medications at the test sites within 72 hours prior to enrollment
Damaged or altered skin at or near test sites (e.g., sunburn, tattoos, scars, uneven pigmentation) that could confound evaluations
Any medical condition that, in the investigator's judgment, places the subject at undue risk or compromises study integrity

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 Irving?

Yes, this clinical trial (NCT07355075) has an active research site in Irving, TX 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.

Eczema Atopic Dermatitis Treatment Options in Irving, TX

If you're searching for eczema atopic dermatitis treatment options in Irving, TX, this clinical trial (NCT07355075) 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 Irving research site is actively enrolling participants for this phase 2/3 clinical trial. You'll receive care from experienced eczema atopic dermatitis 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 eczema atopic dermatitis clinical trials near you to find additional studies recruiting in your area.

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See all atopic dermatitis clinical trials recruiting in Irving — not just this study.

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