Patient Guide: A Study to Evaluate the Efficacy and Safety of Fenebrutinib Compared With Ocrelizumab in Adult Participants With Primary Progressive Multiple Sclerosis

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 189 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04544449
Status: ACTIVE_NOT_RECRUITING
Condition: Multiple Sclerosis, Primary Progressive
Phase: PHASE3

Where You Can Participate

This study is available at 189 locations across the country.

Top locations include:
  • • Homewood, Alabama
  • • Berkeley, California
  • • Fullerton, California
  • • And 186 more locations

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A Study to Evaluate the Efficacy and Safety of Fenebrutinib Compared With Ocrelizumab in Adult Participants With Primary Progressive Multiple Sclerosis - Join Clinical Trial NCTNCT04544449

How to Join This Clinical Trial - NCTNCT04544449

Learn how to participate in this PHASE3 trial studying an investigational therapy for Multiple Sclerosis, Primary Progressive. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Multiple Sclerosis, Primary Progressive
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT04544449 - 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 189 locations. Find a study site near you:

Clinical Research Site

Homewood, Alabama 35209 - United States

Status: Contact for availability

Clinical Research Site

Berkeley, California 94705 - United States

Status: Contact for availability

Clinical Research Site

Fullerton, California 92835 - United States

Status: Contact for availability

Clinical Research Site

Sunnyvale, California 94086 - United States

Status: Contact for availability

Clinical Research Site

Aurora, Colorado 80045 - United States

Status: Contact for availability

Clinical Research Site

Fairfield, Connecticut 06824 - United States

Status: Contact for availability

Clinical Research Site

Washington D.C., District of Columbia 20007 - United States

Status: Contact for availability

Clinical Research Site

Maitland, Florida 32751 - United States

Status: Contact for availability

Clinical Research Site

Orlando, Florida 32806 - United States

Status: Contact for availability

Clinical Research Site

Tampa, Florida 33612 - United States

Status: Contact for availability

And 179 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 Multiple Sclerosis, Primary Progressive:

  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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