Patient Guide: A Multicentre, Randomised, Double-blind, Parallel Group, Placebo-controlled, Time-to-first Asthma Exacerbation Phase III Efficacy and Safety Study of Benralizumab in Paediatric Patients With Severe Eosinophilic Asthma (DOMINICA)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 87 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05692180
Status: 🟢 Enrolling Now
Condition: Asthma, Pulmonary Eosinophilia
Phase: PHASE3

Where You Can Participate

This study is available at 87 locations across the country.

Top locations include:
  • • Mobile, Alabama
  • • Montgomery, Alabama
  • • Tucson, Arizona
  • • And 84 more locations

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A Multicentre, Randomised, Double-blind, Parallel Group, Placebo-controlled, Time-to-first Asthma Exacerbation Phase III Efficacy and Safety Study of Benralizumab in Paediatric Patients With Severe Eosinophilic Asthma (DOMINICA) - Join Clinical Trial NCTNCT05692180

How to Join This Clinical Trial - NCTNCT05692180

Learn how to participate in this PHASE3 trial studying an investigational therapy for Asthma, Pulmonary Eosinophilia. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Asthma, Pulmonary Eosinophilia
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT05692180 - 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 87 locations. Find a study site near you:

Clinical Research Site

Mobile, Alabama 36608 - United States

Status: WITHDRAWN

Clinical Research Site

Montgomery, Alabama 36106 - United States

Status: WITHDRAWN

Clinical Research Site

Tucson, Arizona 85724 - United States

Status: RECRUITING

Clinical Research Site

Little Rock, Arkansas 72202 - United States

Status: WITHDRAWN

Clinical Research Site

Madera, California 93636 - United States

Status: WITHDRAWN

Clinical Research Site

Torrance, California 90505 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Washington, District of Columbia 20010 - United States

Status: RECRUITING

Clinical Research Site

Miami, Florida 33144 - United States

Status: RECRUITING

Clinical Research Site

Miami, Florida 33184 - United States

Status: RECRUITING

Clinical Research Site

Ocala, Florida 34471 - United States

Status: COMPLETED

And 77 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 Asthma, Pulmonary Eosinophilia:

  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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