Patient Guide: A Trial to Learn How Well Linvoseltamab Works Compared to the Combination of Elotuzumab, Pomalidomide and Dexamethasone for Adult Participants With Relapsed/Refractory Multiple Myeloma

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 157 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05730036
Status: 🟢 Enrolling Now
Condition: Relapsed Refractory Multiple Myeloma (RRMM)
Phase: PHASE3

Where You Can Participate

This study is available at 157 locations across the country.

Top locations include:
  • • Los Angeles, California
  • • Gainesville, Florida
  • • Lexington, Kentucky
  • • And 154 more locations

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A Trial to Learn How Well Linvoseltamab Works Compared to the Combination of Elotuzumab, Pomalidomide and Dexamethasone for Adult Participants With Relapsed/Refractory Multiple Myeloma - Join Clinical Trial NCTNCT05730036

How to Join This Clinical Trial - NCTNCT05730036

Learn how to participate in this PHASE3 trial studying an investigational therapy for Relapsed Refractory Multiple Myeloma (RRMM). This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Relapsed Refractory Multiple Myeloma (RRMM). Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Relapsed Refractory Multiple Myeloma (RRMM)
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT05730036 - 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 157 locations. Find a study site near you:

Clinical Research Site

Los Angeles, California 90095 - United States

Status: ACTIVE_NOT_RECRUITING

Clinical Research Site

Gainesville, Florida 32611-5500 - United States

Status: WITHDRAWN

Clinical Research Site

Lexington, Kentucky 40536-0093 - United States

Status: ACTIVE_NOT_RECRUITING

Clinical Research Site

Louisville, Kentucky 40207 - United States

Status: ACTIVE_NOT_RECRUITING

Clinical Research Site

Stony Brook, New York 11794-8153 - United States

Status: ACTIVE_NOT_RECRUITING

Clinical Research Site

Charlotte, North Carolina 28204 - United States

Status: ACTIVE_NOT_RECRUITING

Clinical Research Site

Durham, North Carolina 27705 - United States

Status: RECRUITING

Clinical Research Site

Portland, Oregon 97227 - United States

Status: ACTIVE_NOT_RECRUITING

Clinical Research Site

Houston, Texas 77030 - United States

Status: ACTIVE_NOT_RECRUITING

Clinical Research Site

Seattle, Washington 98195 - United States

Status: ACTIVE_NOT_RECRUITING

And 147 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 Relapsed Refractory Multiple Myeloma (RRMM):

  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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