Patient Guide: Study of Oral Upadacitinib to Assess Change in Disease Activity and Adverse Events in Adult Participants With Ulcerative Colitis or Crohn's Disease

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 14 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06459297
Status: 🟢 Enrolling Now
Condition: Ulcerative Colitis, Crohn's Disease
Phase: Research Study

Where You Can Participate

This study is available at 14 locations across the country.

Top locations include:
  • • Cheonan-si, Chungcheongnamdo
  • • Daejeon, Daejeon Gwang Yeogsi
  • • 고양시, Gyeonggido
  • • And 11 more locations

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Study of Oral Upadacitinib to Assess Change in Disease Activity and Adverse Events in Adult Participants With Ulcerative Colitis or Crohn's Disease - Join Clinical Trial NCTNCT06459297

How to Join This Clinical Trial - NCTNCT06459297

Learn how to participate in this clinical trial studying an investigational therapy for Ulcerative Colitis, Crohn's Disease. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Ulcerative Colitis, Crohn's Disease. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Ulcerative Colitis, Crohn's Disease
Treatment Being Tested
Investigational treatment
Study Phase
Clinical trial phase - Research study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06459297 - 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 14 locations. Find a study site near you:

Clinical Research Site

Cheonan-si, Chungcheongnamdo 31151 - Korea, Republic of

Status: RECRUITING

Clinical Research Site

Daejeon, Daejeon Gwang Yeogsi 34943 - Korea, Republic of

Status: RECRUITING

Clinical Research Site

고양시, Gyeonggido 10380 - Korea, Republic of

Status: RECRUITING

Clinical Research Site

Daegu, Gyeongsangbugdo 42601 - Korea, Republic of

Status: RECRUITING

Clinical Research Site

Gwangju, Jeonranamdo 61453 - Korea, Republic of

Status: RECRUITING

Clinical Research Site

Dongdaemun-gu, Seoul Teugbyeolsi 02447 - Korea, Republic of

Status: RECRUITING

Clinical Research Site

Seoul, Seoul Teugbyeolsi 03722 - Korea, Republic of

Status: RECRUITING

Clinical Research Site

Seoul, Seoul Teugbyeolsi 06273 - Korea, Republic of

Status: RECRUITING

Clinical Research Site

Seoul, Seoul Teugbyeolsi 06591 - Korea, Republic of

Status: RECRUITING

Clinical Research Site

Seoul, Seoul Teugbyeolsi 07441 - Korea, Republic of

Status: RECRUITING

And 4 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this clinical trial for Ulcerative Colitis, Crohn's Disease:

  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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