Patient Guide: Study Assessing Long-teRm Outcomes of dupiluMAb (DUPIXENT®) Treatment in Adult Patients With Chronic Rhinosinusitis With Nasal Polyposis (CRSwNP)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 81 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04959448
Status: ACTIVE_NOT_RECRUITING
Condition: Chronic Rhinosinusitis With Nasal Polyposis
Phase: Not Specified

Where You Can Participate

This study is available at 81 locations across the country.

Top locations include:
  • • Birmingham, Alabama
  • • Scottsdale, Arizona
  • • La Jolla, California
  • • And 78 more locations

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Study Assessing Long-teRm Outcomes of dupiluMAb (DUPIXENT®) Treatment in Adult Patients With Chronic Rhinosinusitis With Nasal Polyposis (CRSwNP) - Join Clinical Trial NCTNCT04959448

How to Join This Clinical Trial - NCTNCT04959448

Learn how to participate in this Not Specified trial studying an investigational therapy for Chronic Rhinosinusitis With Nasal Polyposis. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Chronic Rhinosinusitis With Nasal Polyposis
Treatment Being Tested
Investigational treatment
Study Phase
Not Specified - Research study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT04959448 - 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 81 locations. Find a study site near you:

Clinical Research Site

Birmingham, Alabama 35244 - United States

Status: Contact for availability

Clinical Research Site

Scottsdale, Arizona 85251 - United States

Status: Contact for availability

Clinical Research Site

La Jolla, California 92037 - United States

Status: Contact for availability

Clinical Research Site

Long Beach, California 90806 - United States

Status: Contact for availability

Clinical Research Site

San Diego, California 92130 - United States

Status: Contact for availability

Clinical Research Site

Torrance, California 90503 - United States

Status: Contact for availability

Clinical Research Site

Walnut Creek, California 94598 - United States

Status: Contact for availability

Clinical Research Site

Coral Gables, Florida 33134 - United States

Status: Contact for availability

Clinical Research Site

Gainesville, Florida 32610 - United States

Status: Contact for availability

Clinical Research Site

Lake Mary, Florida 32746 - United States

Status: Contact for availability

And 71 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 Chronic Rhinosinusitis With Nasal Polyposis:

  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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