Patient Guide: Phase 3 Study of Teclistamab in Combination With Lenalidomide and Teclistamab Alone Versus Lenalidomide Alone in Participants With Newly Diagnosed Multiple Myeloma as Maintenance Therapy Following Autologous Stem Cell Transplantation

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 208 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05243797
Status: 🟢 Enrolling Now
Condition: Multiple Myeloma
Phase: PHASE3

Where You Can Participate

This study is available at 208 locations across the country.

Top locations include:
  • • Phoenix, Arizona
  • • Sacramento, California
  • • San Diego, California
  • • And 205 more locations

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Phase 3 Study of Teclistamab in Combination With Lenalidomide and Teclistamab Alone Versus Lenalidomide Alone in Participants With Newly Diagnosed Multiple Myeloma as Maintenance Therapy Following Autologous Stem Cell Transplantation - Join Clinical Trial NCTNCT05243797

How to Join This Clinical Trial - NCTNCT05243797

Learn how to participate in this PHASE3 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
PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT05243797 - 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 208 locations. Find a study site near you:

Clinical Research Site

Phoenix, Arizona 85004 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Sacramento, California 95817 - United States

Status: RECRUITING

Clinical Research Site

San Diego, California 92093 - United States

Status: RECRUITING

Clinical Research Site

Aurora, Colorado 80045 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Denver, Colorado 80218 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

New Haven, Connecticut 06519 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Newark, Delaware 19718 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Orlando, Florida 32804 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Tampa, Florida 33612 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Chicago, Illinois 60612 - United States

Status: NOT_YET_RECRUITING

And 198 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 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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