Patient Guide: Safety And Efficacy Study Of Intravenous (IV) Administration Of Elezanumab To Assess Change In Upper Extremity Motor Score (UEMS) In Adult Participants With Acute Traumatic Cervical Spinal Cord Injury (SCI)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 41 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04295538
Status: ACTIVE_NOT_RECRUITING
Condition: Spinal Cord Injury (SCI)
Phase: PHASE2

Where You Can Participate

This study is available at 41 locations across the country.

Top locations include:
  • • Sacramento, California
  • • Atlanta, Georgia
  • • Chicago, Illinois
  • • And 38 more locations

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Safety And Efficacy Study Of Intravenous (IV) Administration Of Elezanumab To Assess Change In Upper Extremity Motor Score (UEMS) In Adult Participants With Acute Traumatic Cervical Spinal Cord Injury (SCI) - Join Clinical Trial NCTNCT04295538

How to Join This Clinical Trial - NCTNCT04295538

Learn how to participate in this PHASE2 trial studying an investigational therapy for Spinal Cord Injury (SCI). Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Spinal Cord Injury (SCI). Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Spinal Cord Injury (SCI)
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT04295538 - 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 41 locations. Find a study site near you:

Clinical Research Site

Sacramento, California 95817 - United States

Status: Contact for availability

Clinical Research Site

Atlanta, Georgia 30309-1426 - United States

Status: Contact for availability

Clinical Research Site

Chicago, Illinois 60611-2927 - United States

Status: Contact for availability

Clinical Research Site

Louisville, Kentucky 40202 - United States

Status: Contact for availability

Clinical Research Site

Boston, Massachusetts 02111 - United States

Status: Contact for availability

Clinical Research Site

Boston, Massachusetts 02115 - United States

Status: Contact for availability

Clinical Research Site

Boston, Massachusetts 02118-2515 - United States

Status: Contact for availability

Clinical Research Site

Boston, Massachusetts 02215-5400 - United States

Status: Contact for availability

Clinical Research Site

Ann Arbor, Michigan 48109-1276 - United States

Status: Contact for availability

Clinical Research Site

Saint Louis, Missouri 63110 - United States

Status: Contact for availability

And 31 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE2 clinical trial for Spinal Cord Injury (SCI):

  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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