Patient Guide: A Single-ascending Dose (Part A) and Repeat-dose (Part B) Study to Investigate the Safety, Pharmacokinetics and Efficacy (Part B Only) of UCB1381 in Healthy Study Participants (Part A) and in Study Participants With Moderate to Severe Atopic Dermatitis (Part B)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 16 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05277571
Status: ACTIVE_NOT_RECRUITING
Condition: Atopic Dermatitis
Phase: PHASE1, PHASE2

Where You Can Participate

This study is available at 16 locations across the country.

Top locations include:
  • • Beverly Hills, California
  • • Glendale, California
  • • Los Angeles, California
  • • And 13 more locations

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A Single-ascending Dose (Part A) and Repeat-dose (Part B) Study to Investigate the Safety, Pharmacokinetics and Efficacy (Part B Only) of UCB1381 in Healthy Study Participants (Part A) and in Study Participants With Moderate to Severe Atopic Dermatitis (Part B) - Join Clinical Trial NCTNCT05277571

How to Join This Clinical Trial - NCTNCT05277571

Learn how to participate in this PHASE1, PHASE2 trial studying an investigational therapy for Atopic Dermatitis. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Atopic Dermatitis
Treatment Being Tested
Investigational treatment
Study Phase
PHASE1, PHASE2 - Safety and effectiveness study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT05277571 - 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 16 locations. Find a study site near you:

Clinical Research Site

Beverly Hills, California 90212 - United States

Status: Contact for availability

Clinical Research Site

Glendale, California 91206 - United States

Status: Contact for availability

Clinical Research Site

Los Angeles, California 90045 - United States

Status: Contact for availability

Clinical Research Site

Northridge, California 91324 - United States

Status: Contact for availability

Clinical Research Site

Tustin, California 92780 - United States

Status: Contact for availability

Clinical Research Site

Valencia, California 91355 - United States

Status: Contact for availability

Clinical Research Site

Clearwater, Florida 33765 - United States

Status: Contact for availability

Clinical Research Site

Miami Lakes, Florida 33014 - United States

Status: Contact for availability

Clinical Research Site

Ocala, Florida 34471 - United States

Status: Contact for availability

Clinical Research Site

St. Petersburg, Florida 33705 - United States

Status: Contact for availability

And 6 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE1, PHASE2 clinical trial for Atopic Dermatitis:

  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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