Patient Guide: A Study to Evaluate the Efficacy and Safety of Subcutaneous Amlitelimab in Participants Aged 12 Years and Older With Moderate-to-severe Atopic Dermatitis on Background Topical Corticosteroids

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 167 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06224348
Status: ACTIVE_NOT_RECRUITING
Condition: Dermatitis Atopic
Phase: PHASE3

Where You Can Participate

This study is available at 167 locations across the country.

Top locations include:
  • • Birmingham, Alabama
  • • Fort Smith, Arkansas
  • • Encino, California
  • • And 164 more locations

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A Study to Evaluate the Efficacy and Safety of Subcutaneous Amlitelimab in Participants Aged 12 Years and Older With Moderate-to-severe Atopic Dermatitis on Background Topical Corticosteroids - Join Clinical Trial NCTNCT06224348

How to Join This Clinical Trial - NCTNCT06224348

Learn how to participate in this PHASE3 trial studying an investigational therapy for Dermatitis Atopic. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Dermatitis Atopic. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Dermatitis Atopic
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT06224348 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 167 locations. Find a study site near you:

Clinical Research Site

Birmingham, Alabama 35244 - United States

Status: Contact for availability

Clinical Research Site

Fort Smith, Arkansas 72916 - United States

Status: Contact for availability

Clinical Research Site

Encino, California 91436 - United States

Status: Contact for availability

Clinical Research Site

Huntington Beach, California 92647 - United States

Status: Contact for availability

Clinical Research Site

Los Angeles, California 90057 - United States

Status: Contact for availability

Clinical Research Site

Palmdale, California 93551 - United States

Status: Contact for availability

Clinical Research Site

Sacramento, California 95815 - United States

Status: Contact for availability

Clinical Research Site

Santa Ana, California 92701 - United States

Status: Contact for availability

Clinical Research Site

Hollywood, Florida 33021 - United States

Status: Contact for availability

Clinical Research Site

Miami, Florida 33126 - United States

Status: Contact for availability

And 157 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE3 clinical trial for Dermatitis Atopic:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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