Patient Guide: A Study to Assess Real-World Use, Safety, and Effectiveness of Oral Upadacitinib in Adult and Adolescent (>=12 Years Old) Participants With Atopic Dermatitis

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 140 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05081557
Status: ACTIVE_NOT_RECRUITING
Condition: Atopic Dermatitis
Phase: Not Specified

Where You Can Participate

This study is available at 140 locations across the country.

Top locations include:
  • • Pilar, Buenos Aires
  • • Ciudad Autonoma de Buenos Aire, Ciudad Autonoma de Buenos Aires
  • • Ciudad Autonoma de Buenos Aire, Ciudad Autonoma de Buenos Aires
  • • And 137 more locations

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A Study to Assess Real-World Use, Safety, and Effectiveness of Oral Upadacitinib in Adult and Adolescent (>=12 Years Old) Participants With Atopic Dermatitis - Join Clinical Trial NCTNCT05081557

How to Join This Clinical Trial - NCTNCT05081557

Learn how to participate in this Not Specified 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
Not Specified - Research study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT05081557 - 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 140 locations. Find a study site near you:

Clinical Research Site

Pilar, Buenos Aires 1629 - Argentina

Status: Contact for availability

Clinical Research Site

Ciudad Autonoma de Buenos Aire, Ciudad Autonoma de Buenos Aires 1055 - Argentina

Status: Contact for availability

Clinical Research Site

Ciudad Autonoma de Buenos Aire, Ciudad Autonoma de Buenos Aires 1425 - Argentina

Status: Contact for availability

Clinical Research Site

Ciudad Autonoma de Buenos Aire, Ciudad Autonoma de Buenos Aires 1425 - Argentina

Status: Contact for availability

Clinical Research Site

Rosario, Santa Fe 2000 - Argentina

Status: Contact for availability

Clinical Research Site

Caba, C1199ABB - Argentina

Status: Contact for availability

Clinical Research Site

Miranda, New South Wales 2228 - Australia

Status: Contact for availability

Clinical Research Site

Woolloongabba, Queensland 4102 - Australia

Status: Contact for availability

Clinical Research Site

Bedford, Park, South Australia 5042 - Australia

Status: Contact for availability

Clinical Research Site

East Melbourne, Victoria 3002 - Australia

Status: Contact for availability

And 130 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this Not Specified 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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