Patient Guide: A Study to Determine the Recommended Dose and Schedule, and Evaluate the Safety and Preliminary Efficacy of Mezigdomide in Combination With Elranatamab in Participants With Relapsed and/or 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 22 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06988488
Status: 🟢 Enrolling Now
Condition: Multiple Myeloma
Phase: PHASE1, PHASE2

Where You Can Participate

This study is available at 22 locations across the country.

Top locations include:
  • • Birmingham, Alabama
  • • New Haven, Connecticut
  • • Hackensack, New Jersey
  • • And 19 more locations

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A Study to Determine the Recommended Dose and Schedule, and Evaluate the Safety and Preliminary Efficacy of Mezigdomide in Combination With Elranatamab in Participants With Relapsed and/or Refractory Multiple Myeloma - Join Clinical Trial NCTNCT06988488

How to Join This Clinical Trial - NCTNCT06988488

Learn how to participate in this PHASE1, PHASE2 trial studying an investigational therapy for Multiple Myeloma. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Multiple Myeloma
Treatment Being Tested
Investigational treatment
Study Phase
PHASE1, PHASE2 - Safety and effectiveness study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06988488 - 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 22 locations. Find a study site near you:

Clinical Research Site

Birmingham, Alabama 35294-3300 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

New Haven, Connecticut 06510 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Hackensack, New Jersey 07601 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Houston, Texas 77030 - United States

Status: RECRUITING

Clinical Research Site

Calgary, Alberta T2N 5G2 - Canada

Status: NOT_YET_RECRUITING

Clinical Research Site

Vancouver, British Columbia V5Z 4E6 - Canada

Status: NOT_YET_RECRUITING

Clinical Research Site

Halifax, Nova Scotia B3H 2Y9 - Canada

Status: NOT_YET_RECRUITING

Clinical Research Site

Toronto, Ontario M5G 2M9 - Canada

Status: RECRUITING

Clinical Research Site

Suzhou, Jiangsu 215006 - China

Status: NOT_YET_RECRUITING

Clinical Research Site

Shanghai, Shanghai Municipality 200434 - China

Status: NOT_YET_RECRUITING

And 12 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 Multiple Myeloma:

  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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