Patient Guide: A Study to Investigate the Efficacy and Safety of Anifrolumab Administered as Subcutaneous Injection and Added to Standard of Care Compared With Placebo Added to Standard of Care in Adult Participants With Idiopathic Inflammatory Myopathies (Polymyositis and Dermatomyositis)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 210 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06455449
Status: 🟢 Enrolling Now
Condition: Dermatomyositis, Myositis, Polymyositis
Phase: PHASE3

Where You Can Participate

This study is available at 210 locations across the country.

Top locations include:
  • • Irvine, California
  • • Aurora, Colorado
  • • Denver, Colorado
  • • And 207 more locations

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A Study to Investigate the Efficacy and Safety of Anifrolumab Administered as Subcutaneous Injection and Added to Standard of Care Compared With Placebo Added to Standard of Care in Adult Participants With Idiopathic Inflammatory Myopathies (Polymyositis and Dermatomyositis) - Join Clinical Trial NCTNCT06455449

How to Join This Clinical Trial - NCTNCT06455449

Learn how to participate in this PHASE3 trial studying an investigational therapy for Dermatomyositis, Myositis, Polymyositis. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Dermatomyositis, Myositis, Polymyositis
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06455449 - 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 210 locations. Find a study site near you:

Clinical Research Site

Irvine, California 92617 - United States

Status: RECRUITING

Clinical Research Site

Aurora, Colorado 80045 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Denver, Colorado 80230 - United States

Status: WITHDRAWN

Clinical Research Site

New Haven, Connecticut 06519 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Washington, District of Columbia 20037 - United States

Status: RECRUITING

Clinical Research Site

Boca Raton, Florida 33486 - United States

Status: RECRUITING

Clinical Research Site

Boynton Beach, Florida 33472 - United States

Status: WITHDRAWN

Clinical Research Site

Gainesville, Florida 32603 - United States

Status: WITHDRAWN

Clinical Research Site

Margate, Florida 33063 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Miami, Florida 33126 - United States

Status: WITHDRAWN

And 200 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 Dermatomyositis, Myositis, Polymyositis:

  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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