Patient Guide: A Study to Assess Change in Disease Activity and Adverse Events (AE)s in Adult Participants With Immunoglobulin Light Chain (AL) Amyloidosis Receiving Etentamig (ABBV-383) as an Intravenous (IV) Infusion

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 20 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06158854
Status: 🟢 Enrolling Now
Condition: Immunoglobulin Light Chain (AL) Amyloidosis
Phase: PHASE1, PHASE2

Where You Can Participate

This study is available at 20 locations across the country.

Top locations include:
  • • Miami, Florida
  • • Boston, Massachusetts
  • • Rochester, Minnesota
  • • And 17 more locations

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A Study to Assess Change in Disease Activity and Adverse Events (AE)s in Adult Participants With Immunoglobulin Light Chain (AL) Amyloidosis Receiving Etentamig (ABBV-383) as an Intravenous (IV) Infusion - Join Clinical Trial NCTNCT06158854

How to Join This Clinical Trial - NCTNCT06158854

Learn how to participate in this PHASE1, PHASE2 trial studying an investigational therapy for Immunoglobulin Light Chain (AL) Amyloidosis. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Immunoglobulin Light Chain (AL) Amyloidosis. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Immunoglobulin Light Chain (AL) Amyloidosis
Treatment Being Tested
Investigational treatment
Study Phase
PHASE1, PHASE2 - Safety and effectiveness study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06158854 - 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 20 locations. Find a study site near you:

Clinical Research Site

Miami, Florida 33136 - United States

Status: RECRUITING

Clinical Research Site

Boston, Massachusetts 02118 - United States

Status: RECRUITING

Clinical Research Site

Rochester, Minnesota 55905-0001 - United States

Status: RECRUITING

Clinical Research Site

New York, New York 10032-3729 - United States

Status: RECRUITING

Clinical Research Site

New York, New York 10065-6007 - United States

Status: RECRUITING

Clinical Research Site

Charlotte, North Carolina 28204 - United States

Status: RECRUITING

Clinical Research Site

Winston-Salem, North Carolina 27157 - United States

Status: RECRUITING

Clinical Research Site

Portland, Oregon 97239 - United States

Status: RECRUITING

Clinical Research Site

Seattle, Washington 98109 - United States

Status: RECRUITING

Clinical Research Site

Milwaukee, Wisconsin 53226 - United States

Status: RECRUITING

And 10 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE1, PHASE2 clinical trial for Immunoglobulin Light Chain (AL) Amyloidosis:

  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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